Patent Application
20190151421
The present invention relates to the use of plasminogen or plasmin in the prevention and/or treatment of hepatic tissue injury caused by various reasons, thereby providing a brand new therapeutic strategy for treating hepatic tissue injury and its related disorders.
Hepatic injury or hepatic tissue injury is a hepatic parenchymal disease caused by various reasons, and is a general term for a series of pathological changes, such as hepatic tissue inflammation, hepatocyte degeneration, necrosis and hepatic tissue fibrosis. Common causes are inflammation, liver congestion, viral infections, poisoning, drugs, radiation, etc. Some diseases, such as diabetes mellitus, hepatitis, hypertension, and atherosclerosis, also occur with injuries of hepatic tissue cells.
Drugs are very common causes of hepatic tissue damage. Common drugs that cause hepatic tissue damage include: anti-tuberculosis drugs, such as rifampicin, isoniazid, and ethambutol; anti-tumor drugs, such as cyclophosphamide, methotrexate, 5-fluorouracil, carboplatin, and cisplatin; lipid-regulating and lipid-lowering drugs, such as statins (atorvastatin and lovastatin), fenofibrate, clofibrate, and niacin; steroid hormones, such as estrogenic drugs, oral contraceptives, and male anabolic hormones; cardiovascular drugs, such as amiodarone, warfarin, and calcium ion antagonists; anti-rheumatic drugs, such as antifan, fenbufen, aspirin, and indomethacin; antibiotics, such as chloramphenicol, roxithromycin, ketoconazole, penicillins, and sulfonamides; anti-allergic drugs, such as promethazine (Phenergan), chlorpheniramine (Chlorphenamine), and loratadine (Clarityne); anti-ulcer drugs, such as cimetidine, ranitidine, and famotidine; antifungal drugs, such as ribavirin; and so on.
Alcohol is a great threat to the liver. Long-term or intermittent heavy drinking can cause hepatic tissue injury. The greater the drinking amount of alcohol is and the longer the drinking history is, the more severe the consequences are. Alcohol directly poisons hepatocytes and affects their structures and functions.
Alcoholic hepatic injury is a chronic, toxic hepatic injury, a hepatic disease caused by long-term heavy drinking. In the early stage, it is usually manifested as fatty liver, which can then develop into alcoholic hepatitis, hepatic fibrosis and hepatic cirrhosis. Its main clinical features include nausea, vomiting, jaundice, and sometimes hepatomegaly and tenderness. Severe alcoholism can induce extensive hepatocyte necrosis or even hepatic failure. Alcoholic hepatopathy is one of common hepatic diseases in China, and seriously endangers people's health[1].
In addition to the toxic hepatic injury caused by alcohol, other “hepatotropic poisons” such as chemical toxicants and certain drugs in the environment can also cause hepatic injury. As an important detoxification organ for the human body, the liver has dual blood supply from the hepatic arteries and hepatic veins. Chemical substances can enter the liver through the portal veins of the gastrointestinal tract or the systemic circulation for conversion, and thus the liver is vulnerable to toxic substances in chemicals. There are substances that are toxic to the liver in both nature and human industrial production processes, known as “hepatotropic poisons”. People are generally susceptible to these poisons, and they have a short incubation period. The pathological process is directly related to the amount of chemical substances, and these substances may cause different levels of hepatocyte necrosis, steatosis and hepatic cirrhosis in the liver. The pathological manifestations include (1) steatosis. Carbon tetrachloride, yellow phosphorus and the like can interfere with the synthesis and translocation of lipoproteins, forming fatty liver. (2) Lipid peroxidation, which is a special manifestation form of toxic hepatic injury. For example, carbon tetrachloride is metabolized in vivo to produce an intermediate product with strong oxidizing ability, leading to lipid peroxidation on biofilms, destructing membrane phospholipids and changing the structures and functions of cells. (3) Cholestasis, which is mainly associated with damage of the hepatic cell membrane and microvilli, causing bile acid excretion disorder[2].
Radiation can also cause hepatic tissue injury. In general, radiation sources are high-energy electromagnetic waves or high-energy particles produced by natural or artificial energy sources. Either instant irradiation with high-dose rays or prolonged irradiation with low-dose rays may cause tissue injury. The radiation energy destroys the chromosomes and enzymes of cells and disrupts the normal functions of cells.
Diabetic hepatic tissue injury refers to the lesions of liver histology and functions caused by diabetes mellitus. Hepatic injuries known to be caused by diabetes mellitus include: hepatic enzymology abnormalities, which can cause carbon dioxide accumulation, acidosis, reduced oxygen supply and increased oxygen consumption in hepatocytes, resulting in increased activity of liver transaminases and bilirubin metabolism disorder, with severe cases causing hepatocyte necrosis; fatty liver, wherein diabetes mellitus is the third most common cause of fatty liver among all causes of fatty liver, and 21%-78% of diabetics have fatty liver; and hepatitis, cirrhosis and hepatic carcinoma, wherein the prevalence of viral hepatitis in diabetics is about 2-4 times that in normal people, and the incidence of primary hepatic carcinoma is about 4 times that in normal people. Diabetic hepatopathy not only damages the quality of life of millions of patients, but also creates care needed for a huge burden cost and healthcare system strength.
Viral infection of the liver is also a common cause of hepatic injury, such as viral hepatitis B, viral hepatitis C, and viral hepatitis E.
Intrahepatic blood congestion may also cause hepatic tissue injury. Intrahepatic blood congestion is mainly caused by the following factors: hepatic veno-occlusive disease, Budd-Chiari syndrome, chronic right cardiac insufficiency and constrictive pericarditis.
Any disease that blocks the return of inferior vena cava blood to the heart can lead to liver congestion, such as rheumatic valvular heart disease, chronic constrictive pericarditis, hypertensive heart disease, ischemic heart disease, pulmonary heart disease and congenital heart disease.
Congestive hepatic injury initially affects the central lobule region; there are venous congestion and expansion in the central lobules, and the degree of hepatic sinusoid expansion varies depending on the distance between the hepatic sinusoids and veins in the central lobules; hepatocytes in the central lobules are compressed, deformed and atrophied; there are granular deformation in the cytoplasm, with nuclear condensation, nuclear division and cell necrosis, accompanied by brown pigmentation with the brown pigment located in the central lobules potentially caused by cholestasis; and degeneration and necrosis of the hepatic parenchyma near the central veins is the most serious, necrotic tissues extend toward the portal area with the exacerbation of congestion, patients with severe congestion only have normal liver tissues in the portal area, the reticular fibers around the central veins can collapse over time, and it can be seen that reticular fibrous tissues and fine fiber bundles extend from one central vein to another.
Currently, the treatment of hepatic tissue injury mainly includes the control and treatment of causes, as well as supportive treatment. Scientists have been looking for drugs that have a direct, good repair effect on injured liver tissues for a long time. The present inventors have also conducted intensive research on this. It is found through experiments that plasminogen, a protein substance naturally present in the human body, has a good repair effect on hepatic tissue injuries caused by poisoning, radiation, chemotherapeutic drugs and diabetes mellitus. Plasminogen is expected to become a new strategy for treating hepatic tissue injury and its related disorders.
Plasminogen (plg) is an inactive precursor of plasmin, a single-stranded glycoprotein that is composed of 791 amino acids and has a molecular weight of about 92 kDa[3,4]. Plasminogen is mainly synthesized in the liver and is abundantly present in the extracellular fluid. The content of plasminogen in plasma is about 2 μM. Therefore, plasminogen is a huge potential source of proteolytic activity in tissues and body fluids[5,6]. Plasminogen exists in two molecular forms: glutamic acid-plasminogen (Glu-plasminogen) and lysine-plasminogen (Lys-plasminogen). The naturally secreted and uncleaved forms of plasminogen have an amino-terminal (N-terminal) glutamic acid and are therefore referred to as glutamic acid-plasminogen. However, in the presence of plasmin, glutamic acid-plasminogen is hydrolyzed to lysine-plasminogen at Lys76-Lys77. Compared with glutamic acid-plasminogen, lysine-plasminogen has a higher affinity for fibrin and can be activated by PAs at a higher rate. The Arg560-Va1561 peptide bond between these two forms of plasminogen can be cleaved by uPA or tPA, resulting in the formation of plasmin as a disulfide-linked double-strand protease[7]. The amino-terminal portion of plasminogen contains five homotrimeric rings, i.e., the so-called kringles, and the carboxy-terminal portion contains a protease domain. Some kringles contain lysine-binding sites that mediate the specific interaction of plasminogen with fibrin and its inhibitor α2-AP. A newly discovered 38 kDa fragment of plasminogen, comprising kringles 1-4, is a potent inhibitor of angiogenesis. This fragment is named as angiostatin and can be produced by the proteolysis of plasminogen via several proteases.
In one aspect, the present invention relates to the use of plasminogen or plasmin in the manufacture of a medicament, article or kit for preventing and/or treating hepatic tissue injury and its related disorders in a subject. The present invention also relates to a method for manufacturing a medicament, comprising preparing a medicament, article or kit for preventing and/or treating hepatic tissue injury and its related disorders in a subject using plasminogen together with a pharmaceutically acceptable carrier.
In one embodiment, the hepatic tissue injury and its related disorders are hepatic injury and its related disorders caused by radiation or chemical substances. In one embodiment, the radiation or chemical substances causing hepatic injury and its related disorders are radiotherapy or chemotherapy methods and drugs used for the treatment of cancer. In one embodiment, the radiation is radiation caused by an accident or other event such as a work environment. In one embodiment, the hepatic tissue injury and its related disorders are toxic hepatic injury and its related disorders. In one embodiment, the toxic hepatic injury is toxic hepatic injury caused by “hepatotropic poisons” including alcohol. In one embodiment, the hepatic tissue injury and its related disorders are caused by diabetes mellitus and one of the complications of diabetes mellitus. In one embodiment, the hepatic tissue injury and its related disorders are due to hepatitis caused by viral infection of the liver, such as hepatitis caused by hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus or hepatitis E virus. In one embodiment, the hepatic tissue injury and its related disorders are drug-induced hepatic injury and its related disorders. In one embodiment, the hepatic tissue injury and its related disorders are caused by intrahepatic blood congestion (liver congestion). In one embodiment, the hepatic tissue injury and its related disorders are diabetic hepatic injury and its related disorders, toxic hepatic injury and its related disorders, drug-induced hepatic injury or its related disorders, radiation-induced hepatic injury and its related disorders, viral infectious hepatic injury and its related disorders, or congestive hepatic injury and its related disorders. In one embodiment, the hepatic tissue injury and its related disorders include hepatic dysfunction, abnormal hepatic enzymology, liver discomfort and haphalgesia, hepatomegaly, splenomegaly, hepatosplenomegaly, hepatitis, fatty liver, cholangitis, hepatic cirrhosis, hepatic necrosis and hepatic carcinoma caused by hepatic tissue injury.
In one embodiment, the sequence in this patent application refers to the patent document CN 102154253 A. In one embodiment, the plasminogen is a protein that comprises a plasminogen active fragment and still has plasminogen activity.
In one embodiment, the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, δ-plasminogen or any combination thereof. In one embodiment, the plasminogen or plasmin is administered systemically or locally, including topical, intravenous, intramuscular, subcutaneous, inhalation, intraspinal, local injection, intraarticular injection or rectal administration. In one embodiment, the related disorders of diabetic hepatic injury or the related disorders of toxic hepatic injury include: abnormal hepatic enzymology, liver discomfort and haphalgesia, hepatomegaly, splenomegaly, hepatosplenomegaly, hepatitis, fatty liver, cholangitis, hepatic cirrhosis, hepatic necrosis and hepatic carcinoma. In one embodiment, the hepatic injury and its related disorders are caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels. In one embodiment, the plasminogen can be administered in combination with one or more other drugs. In one embodiment, the other drugs include: liver-protecting drugs, antidiabetic drugs, antithrombotic drugs, anticoagulant drugs, hypolipidemic drugs, drugs against cardiovascular and cerebrovascular diseases, and anti-infective drugs.
In one embodiment, the subject is a mammal, preferably human.
In one embodiment, the hepatic injury caused by diabetes mellitus is caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels.
In one embodiment, the subject has a low level of plasmin or plasminogen. Specifically, the low level is innate, secondary and/or local.
In one embodiment, the sequence in this patent application refers to the patent document CN 102154253 A. In one embodiment, the plasminogen is a protein that has 1-100, 1-90, 1-80, 1-70, 1-60, 1-50, 1-45, 1-40, 1-35, 1-30, 1-25, 1-20, 1-15, 1-10, 1-5, 1-4, 1-3, 1-2 or 1 amino acid added, deleted and/or substituted in SEQ ID No. 2, 6, 8, 10 or 12, and still has the activity of plasminogen. In one embodiment, the plasminogen is a protein that comprises a plasminogen active fragment and still has the activity of plasminogen. In one embodiment, the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, δ-plasminogen or any combination thereof. In one embodiment, the plasminogen is a conservatively substituted variant selected from variants of Glu-plasminogen, Lys-plasminogen, mini-plasminogen, δ-plasminogen or micro-plasminogen. In one embodiment, the plasminogen is a human natural plasminogen, such as an ortholog of plasminogen shown in SEQ ID No. 2, e.g., an ortholog of plasminogen from primates or rodents, for example, an ortholog of plasminogen from gorillas, rhesus monkeys, murine, cows, horses and dogs. Most preferably, the amino acid sequence of the plasminogen of the present invention is as shown in SEQ ID No. 2, 6, 8, 10 or 12.
In one embodiment, the plasminogen is administered in combination with a suitable polypeptide carrier or stabilizer. In one embodiment, the plasminogen is administered at a dosage of 0.0001-2000 mg/kg, 0.001-800 mg/kg, 0.01-600 mg/kg, 0.1-400 mg/kg, 1-200 mg/kg, 1-100 mg/kg or 10-100 mg/kg (by per kg of body weight) or 0.0001-2000 mg/cm2, 0.001-800 mg/cm2, 0.01-600 mg/cm2, 0.1-400 mg/cm2, 1-200 mg/cm2, 1-100 mg/cm2 or 10-100 mg/cm2 (by per square centimeter of body surface area) daily, preferably the dosage is repeated at least once, preferably the dosage is administered at least daily. In the case of local administration, the above dosages may also be further adjusted depending on the circumstances.
In one embodiment, the plasminogen is administered by systemic or topical route, preferably by the following routes: topical, intravenous, intramuscular, subcutaneous, inhalation, intraspinal, local injection, intraarticular injection or rectal route. In one embodiment, the local administration is performed by applying a plasminogen-containing catheter in the liver area.
In one aspect, the present invention relates to a method for preventing and/or treating hepatic tissue injury and its related disorders in a subject, comprising administering an effective amount of plasminogen or plasmin to the subject. The present invention also relates to the use of plasminogen or plasmin for preventing and/or treating hepatic tissue injury and its related disorders in a subject.
In one embodiment, the hepatic tissue injury and its related disorders are hepatic injury and its related disorders caused by radiation or chemical substances. In one embodiment, the radiation or chemical substances causing hepatic injury and its related disorders are radiotherapy or chemotherapy methods and drugs used for the treatment of cancer. In one embodiment, the radiation is radiation caused by an accident event. In one embodiment, the hepatic tissue injury and its related disorders are toxic hepatic injury and its related disorders. In one embodiment, the toxic hepatic injury is toxic hepatic injury caused by “hepatotropic poisons” including alcohol. In one embodiment, the hepatic tissue injury and its related disorders are caused by diabetes mellitus and one of the complications of diabetes mellitus. In one embodiment, the hepatic tissue injury and its related disorders are due to hepatitis caused by viral infection of the liver, such as hepatitis caused by hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus or hepatitis E virus. In one embodiment, the hepatic tissue injury and its related disorders are drug-induced hepatic injury and its related disorders. In one embodiment, the hepatic tissue injury and its related disorders are caused by intrahepatic blood congestion (liver congestion). In one embodiment, the hepatic tissue injury and its related disorders are diabetic hepatic injury and its related disorders, toxic hepatic injury and its related disorders, drug-induced hepatic injury or its related disorders, radiation-induced hepatic injury and its related disorders, viral infectious hepatic injury and its related disorders, or congestive hepatic injury and its related disorders. In one embodiment, the hepatic tissue injury and its related disorders include hepatic dysfunction, abnormal hepatic enzymology, liver discomfort and haphalgesia, hepatomegaly, splenomegaly, hepatosplenomegaly, hepatitis, fatty liver, cholangitis, hepatic cirrhosis, hepatic necrosis and hepatic carcinoma caused by hepatic tissue injury.
In one embodiment, the sequence in this patent application refers to the patent document CN 102154253 A. In one embodiment, the plasminogen is a protein that comprises a plasminogen active fragment and still has plasminogen activity. In one embodiment, the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, δ-plasminogen or any combination thereof. In one embodiment, the plasminogen or plasmin is administered systemically or locally, including topical, intravenous, intramuscular, subcutaneous, inhalation, intraspinal, local injection, intraarticular injection or rectal administration. In one embodiment, the related disorders of diabetic hepatic injury or the related disorders of toxic hepatic injury include: abnormal hepatic enzymology, liver discomfort and haphalgesia, hepatomegaly, splenomegaly, hepatosplenomegaly, hepatitis, fatty liver, cholangitis, hepatic cirrhosis, hepatic necrosis and hepatic carcinoma. In one embodiment, the hepatic injury and its related disorders are caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels. In one embodiment, the plasminogen can be administered in combination with one or more other drugs. In one embodiment, the other drugs include: liver-protecting drugs, antidiabetic drugs, antithrombotic drugs, anticoagulant drugs, hypolipidemic drugs, drugs against cardiovascular and cerebrovascular diseases, and anti-infective drugs.
In one embodiment, the subject is a mammal, preferably human.
In one embodiment, the hepatic injury caused by diabetes mellitus is caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels.
In one embodiment, the subject has a low level of plasmin or plasminogen. Specifically, the low level is innate, secondary and/or local.
In one embodiment, the sequence in this patent application refers to the patent document CN 102154253 A. In one embodiment, the plasminogen is a protein that has 1-100, 1-90, 1-80, 1-70, 1-60, 1-50, 1-45, 1-40, 1-35, 1-30, 1-25, 1-20, 1-15, 1-10, 1-5, 1-4, 1-3, 1-2 or 1 amino acid added, deleted and/or substituted in SEQ ID No. 2, 6, 8, 10 or 12, and still has the activity of plasminogen. In one embodiment, the plasminogen is a protein that comprises a plasminogen active fragment and still has the activity of plasminogen. In one embodiment, the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, δ-plasminogen or any combination thereof. In one embodiment, the plasminogen is a conservatively substituted variant selected from variants of Glu-plasminogen, Lys-plasminogen, mini-plasminogen, δ-plasminogen or micro-plasminogen. In one embodiment, the plasminogen is a human natural plasminogen, such as an ortholog of plasminogen shown in SEQ ID No. 2, e.g., an ortholog of plasminogen from primates or rodents, for example, an ortholog of plasminogen from gorillas, rhesus monkeys, murine, cows, horses and dogs. Most preferably, the amino acid sequence of the plasminogen of the present invention is as shown in SEQ ID No. 2, 6, 8, 10 or 12.
In one embodiment, the plasminogen is administered in combination with a suitable polypeptide carrier or stabilizer. In one embodiment, the plasminogen is administered at a dosage of 0.0001-2000 mg/kg, 0.001-800 mg/kg, 0.01-600 mg/kg, 0.1-400 mg/kg, 1-200 mg/kg, 1-100 mg/kg or 10-100 mg/kg (by per kg of body weight) or 0.0001-2000 mg/cm2, 0.001-800 mg/cm2, 0.01-600 mg/cm2, 0.1-400 mg/cm2, 1-200 mg/cm2, 1-100 mg/cm2 or 10-100 mg/cm2 (by per square centimeter of body surface area) daily, preferably the dosage is repeated at least once, preferably the dosage is administered at least daily. In the case of local administration, the above dosages may also be further adjusted depending on the circumstances.
In one embodiment, the plasminogen is administered by systemic or topical route, preferably by the following routes: topical, intravenous, intramuscular, subcutaneous, inhalation, intraspinal, local injection, intraarticular injection or rectal route. In one embodiment, the local administration is performed by applying a plasminogen-containing catheter in the liver area.
In one aspect, the present invention relates to plasminogen or plasmin, a pharmaceutical composition comprising the plasminogen or plasmin, or an article or kit comprising the plasminogen or plasmin, which are useful in the prevention and/or treatment of hepatic tissue injury and its related disorders in a subject.
In one embodiment, the hepatic tissue injury and its related disorders are hepatic injury and its related disorders caused by radiation or chemical substances. In one embodiment, the radiation or chemical substances causing hepatic injury and its related disorders are radiotherapy or chemotherapy methods and drugs used for the treatment of cancer. In one embodiment, the radiation is radiation caused by an accident event. In one embodiment, the hepatic tissue injury and its related disorders are toxic hepatic injury and its related disorders. In one embodiment, the toxic hepatic injury is toxic hepatic injury caused by “hepatotropic poisons” including alcohol. In one embodiment, the hepatic tissue injury and its related disorders are caused by diabetes mellitus and one of the complications of diabetes mellitus. In one embodiment, the hepatic tissue injury and its related disorders are due to hepatitis caused by viral infection of the liver, such as hepatitis caused by hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus or hepatitis E virus. In one embodiment, the hepatic tissue injury and its related disorders are drug-induced hepatic injury and its related disorders. In one embodiment, the hepatic tissue injury and its related disorders are caused by intrahepatic blood congestion (liver congestion). In one embodiment, the hepatic tissue injury and its related disorders are diabetic hepatic injury and its related disorders, toxic hepatic injury and its related disorders, drug-induced hepatic injury or its related disorders, radiation-induced hepatic injury and its related disorders, viral infectious hepatic injury and its related disorders, or congestive hepatic injury and its related disorders. In one embodiment, the hepatic tissue injury and its related disorders include hepatic dysfunction, abnormal hepatic enzymology, liver discomfort and haphalgesia, hepatomegaly, splenomegaly, hepatosplenomegaly, hepatitis, fatty liver, cholangitis, hepatic cirrhosis, hepatic necrosis and hepatic carcinoma caused by hepatic tissue injury.
In one embodiment, the sequence in this patent application refers to the patent document CN 102154253 A. In one embodiment, the plasminogen is a protein that comprises a plasminogen active fragment and still has plasminogen activity. In one embodiment, the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, δ-plasminogen or any combination thereof. In one embodiment, the plasminogen or plasmin is administered systemically or locally, including topical, intravenous, intramuscular, subcutaneous, inhalation, intraspinal, local injection, intraarticular injection or rectal administration. In one embodiment, the related disorders of diabetic hepatic injury or the related disorders of toxic hepatic injury include: abnormal hepatic enzymology, liver discomfort and haphalgesia, hepatomegaly, splenomegaly, hepatosplenomegaly, hepatitis, fatty liver, cholangitis, hepatic cirrhosis, hepatic necrosis and hepatic carcinoma. In one embodiment, the hepatic injury and its related disorders are caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels. In one embodiment, the plasminogen can be administered in combination with one or more other drugs. In one embodiment, the other drugs include: liver-protecting drugs, antidiabetic drugs, antithrombotic drugs, anticoagulant drugs, hypolipidemic drugs, drugs against cardiovascular and cerebrovascular diseases, and anti-infective drugs.
In one embodiment, the subject is a mammal, preferably human.
In one embodiment, the hepatic injury caused by diabetes mellitus is caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels.
In one embodiment, the subject has a low level of plasmin or plasminogen. Specifically, the low level is innate, secondary and/or local.
In one embodiment, the sequence in this patent application refers to the patent document CN 102154253 A. In one embodiment, the plasminogen is a protein that has 1-100, 1-90, 1-80, 1-70, 1-60, 1-50, 1-45, 1-40, 1-35, 1-30, 1-25, 1-20, 1-15, 1-10, 1-5, 1-4, 1-3, 1-2 or 1 amino acid added, deleted and/or substituted in SEQ ID No. 2, 6, 8, 10 or 12, and still has the activity of plasminogen. In one embodiment, the plasminogen is a protein that comprises a plasminogen active fragment and still has the activity of plasminogen. In one embodiment, the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, δ-plasminogen or any combination thereof. In one embodiment, the plasminogen is a conservatively substituted variant selected from variants of Glu-plasminogen, Lys-plasminogen, mini-plasminogen, δ-plasminogen or micro-plasminogen. In one embodiment, the plasminogen is a human natural plasminogen, such as an ortholog of plasminogen shown in SEQ ID No. 2, e.g., an ortholog of plasminogen from primates or rodents, for example, an ortholog of plasminogen from gorillas, rhesus monkeys, murine, cows, horses and dogs. Most preferably, the amino acid sequence of the plasminogen of the present invention is as shown in SEQ ID No. 2, 6, 8, 10 or 12.
In one embodiment, the plasminogen is administered in combination with a suitable polypeptide carrier or stabilizer. In one embodiment, the plasminogen is administered at a dosage of 0.0001-2000 mg/kg, 0.001-800 mg/kg, 0.01-600 mg/kg, 0.1-400 mg/kg, 1-200 mg/kg, 1-100 mg/kg or 10-100 mg/kg (by per kg of body weight) or 0.0001-2000 mg/cm2, 0.001-800 mg/cm2, 0.01-600 mg/cm2, 0.1-400 mg/cm2, 1-200 mg/cm2, 1-100 mg/cm2 or 10-100 mg/cm2 (by per square centimeter of body surface area) daily, preferably the dosage is repeated at least once, preferably the dosage is administered at least daily. In the case of local administration, the above dosages may also be further adjusted depending on the circumstances.
In one embodiment, the plasminogen is administered by systemic or topical route, preferably by the following routes: topical, intravenous, intramuscular, subcutaneous, inhalation, intraspinal, local injection, intraarticular injection or rectal route. In one embodiment, the local administration is performed by applying a plasminogen-containing catheter in the liver area.
In one embodiment, the plasminogen or plasmin is subpackaged in containers. Preferably, the article or kit further comprises other drugs subpackaged in other containers of the kit. The kit can also comprise instructions for use, which indicate that the plasminogen can be used to treat hepatic tissue injury and its related disorders, specifically, for example, diabetic hepatic injury and its related disorders caused by diabetes mellitus, toxic hepatic injury and its related disorders, drug-induced hepatic injury or its related disorders, hepatic injury and its related disorders caused by radiation, hepatic injury and its related disorders caused by virus infection, or hepatic injury and its related disorders caused by congestion, and can further indicate that the plasminogen or plasmin can be administered before, simultaneously with and/or after administration of other drugs or therapies.
The present invention explicitly encompasses all the combinations of technical features belonging to the embodiments of the present invention, and these combined technical solutions have been explicitly disclosed in the present application, as if the above technical solutions were individually and explicitly disclosed. In addition, the present invention also explicitly encompasses all the subcombinations of the various embodiments and elements thereof, and these subcombinations have been disclosed herein, as if each of such subcombinations was individually and explicitly disclosed herein.
“Diabetic hepatic injury” refers to a lesion with the histological and functional changes of the liver caused by diabetes mellitus. It is mainly caused by diabetes mellitus-induced angiopathy of large vessels, small vessels, and microvessels. Hepatic injuries known to be caused by diabetes mellitus include: hepatic enzymology abnormalities, which can cause carbon dioxide accumulation, acidosis, reduced oxygen supply and increased oxygen consumption in hepatocytes, resulting in increased activity of liver transaminases and bilirubin metabolism disorder, with severe cases causing hepatocyte necrosis; fatty liver, wherein diabetes mellitus is the third most common cause of fatty liver among all causes of fatty liver, and 21%-78% of diabetics have fatty liver; and hepatitis, cirrhosis and hepatic carcinoma, wherein the prevalence of viral hepatitis in diabetics is about 2-4 times that in normal people, and the incidence of primary hepatic carcinoma is about 4 times that in normal people.
“Chemical hepatic injury” or “toxic hepatic injury” refers to hepatic damage caused by chemical hepatotoxic substances. These chemical substances include alcohol, chemical toxicants in the environment and certain drugs. There are substances that are toxic to the liver in both nature and human industrial production processes, known as “hepatotropic poisons”. People are generally susceptible to these poisons, and they have a short incubation period. The pathological process is directly related to the amount of chemical substances, and these substances may cause different levels of hepatocyte necrosis, steatosis and hepatic cirrhosis in the liver.
“hepatotropic poisons” refer to a generic term for substances that are toxic to the liver. Alcohol is the most common “hepatotropic poison” in life. In addition to alcohol, chemical toxicants in the environment and certain drugs may also cause hepatic injury. As an important detoxification organ for the human body, the liver has dual blood supply from the hepatic arteries and hepatic veins. Chemical substances can enter the liver through the portal veins of the gastrointestinal tract or the systemic circulation for conversion, and thus the liver is vulnerable to toxic substances in chemicals. There are substances that are toxic to the liver in both nature and human industrial production processes, known as “hepatotropic poisons”. They enter the liver and may cause different levels of hepatocyte necrosis, steatosis and hepatic cirrhosis in the liver. The pathological manifestations include (1) steatosis. Carbon tetrachloride, yellow phosphorus and the like can interfere with the synthesis and translocation of lipoproteins, forming fatty liver. (2) Lipid peroxidation, which is a special manifestation form of toxic hepatic injury. For example, carbon tetrachloride is metabolized in vivo to produce an intermediate product with strong oxidizing ability, leading to lipid peroxidation on biofilms, destructing membrane phospholipids and changing the structures and functions of cells. (3) Cholestasis, which is mainly associated with damage of the hepatic cell membrane and microvilli, causing bile acid excretion disorder.
“Drug-induced hepatic injury”, also known as drug-induced hepatopathy, refers to hepatic injury during drug use caused by the drug itself or/and its metabolites, or the hypersensitivity or reduced tolerance to the drug due to a special constitution of the body, clinically manifested as a variety of acute and chronic hepatopathies. Patients with light illness may recover spontaneously after discontinuation of medication, and serious ones may be life-threatening and require active treatment and rescue. “Drug-induced hepatic injury” can occur in a healthy person who has not previously had a history of hepatopathy or a patient who has had a serious disease previously. It can occur when the medication is overdosed, but it can also occur under normal dosages.
“Radiation-induced hepatic injury” refers to radiation injury caused by high-energy ionizing radiation, including α and β particles, γ rays, χ rays and neutron rays. Either instant irradiation with high-dose rays or prolonged irradiation with low-dose rays may cause tissue injury. The radiation energy destroys the chromosomes and enzymes of cells and disrupts the normal functions of cells.
“Viral infectious hepatic injury” refers to a generic term for hepatic injury caused by viral infection. The viral infection commonly includes infection caused by hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus or hepatitis E virus.
“Congestive hepatic injury” refers to pathology of hepatic tissue injury caused by intrahepatic blood congestion. Any disease that blocks the return of inferior vena cava blood to the heart can lead to liver congestion, such as rheumatic valvular heart disease, chronic constrictive pericarditis, hypertensive heart disease, ischemic heart disease, pulmonary heart disease and congenital heart disease.
“Plasminogen” is the zymogenic form of plasmin, and based on the sequence in the swiss prot and calculated from the amino acid sequence (SEQ ID No. 4) of the natural human-derived plasminogen containing a signal peptide, is a glycoprotein composed of 810 amino acids, which has a molecular weight of about 92 kD and is synthesized mainly in the liver and capable of circulating in the blood; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No3. Full-length plasminogen contains seven domains: a C-terminal serine protease domain, an N-terminal Pan Apple (PAp) domain and five Kringle domains (Kringles 1-5). Referring to the sequence in the swiss prot, the signal peptide comprises residues Met1-Gly19, PAp comprises residues Glu20-Va198, Kringle 1 comprises residues Cys103-Cys181, Kringle 2 comprises residues Glu184-Cys262, Kringle 3 comprises residues Cys275-Cys352, Kringle 4 comprises residues Cys377-Cys454, and Kringle 5 comprises residues Cys481-Cys560. According to the NCBI data, the serine protease domain comprises residues Va1581-Arg804.
Glu-plasminogen is a natural full-length plasminogen and is composed of 791 amino acids (without a signal peptide of 19 amino acids); the cDNA sequence encoding this sequence is as shown in sequence 1; and the amino acid sequence is as shown in SEQ ID No. 2. In vivo, Lys-plasminogen, which is formed by hydrolysis of amino acids at positions 76-77 of Glu-plasminogen, is also present, as shown in SEQ ID No. 6; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 5. δ-plasminogen is a fragment of full-length plasminogen that lacks the structure of Kringle 2-Kringle 5 and contains only Kringle 1 and the serine protease domain[8,9]. The amino acid sequence (SEQ ID No. 8) of δ-plasminogen has been reported in the literature[9], and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 7. Mini-plasminogen is composed of Kringle 5 and the serine protease domain, and has been reported in the literature to comprise residues Va1443-Asn791 (with the Glu residue of the Glu-plasminogen sequence that does not contain a signal peptide as the starting amino acid)[10]; the amino acid sequence is as shown in SEQ ID No. 10; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 9. Micro-plasminogen comprises only the serine protease domain, the amino acid sequence of which has been reported in the literature to comprise residues Ala543-Asn791 (with the Glu residue of the Glu-plasminogen sequence that does not contain a signal peptide as the starting amino acid)[11], and the sequence of which has been also reported in patent document CN 102154253 A to comprise residues Lys531-Asn791 (with the Glu residue of the Glu-plasminogen sequence that does not contain a signal peptide as the starting amino acid) (the sequence in this patent application refers to the patent document CN 102154253 A); the amino acid sequence is as shown in SEQ ID No. 12; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 11.
In the present invention, “plasmin” is used interchangeably with “fibrinolysin” and “fibrinoclase”, and the terms have the same meaning; and “plasminogen” is used interchangeably with “fibrinolytic zymogen” and “fibrinoclase zymogen”, and the terms have the same meaning.
Those skilled in the art can understand that all the technical solutions of the plasminogen of the present invention are suitable for plasmin. Therefore, the technical solutions described in the present invention cover plasminogen and plasmin.
In the course of circulation, plasminogen is in a closed, inactive conformation, but when bound to thrombi or cell surfaces, it is converted into an active plasmin in an open conformation under the mediation of a plasminogen activator (PA). The active plasmin can further hydrolyze the fibrin clots to fibrin degradation products and D-dimers, thereby dissolving the thrombi. The PAp domain of plasminogen comprises an important determinant that maintains plasminogen in an inactive, closed conformation, and the KR domain is capable of binding to lysine residues present on receptors and substrates. A variety of enzymes that can serve as plasminogen activators are known, including: tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, coagulation factor XII (Hagmann factor), and the like.
“Plasminogen active fragment” refers to an active fragment in the plasminogen protein that is capable of binding to a target sequence in a substrate and exerting the proteolytic function. The technical solutions of the present invention involving plasminogen encompass technical solutions in which plasminogen is replaced with a plasminogen active fragment. The plasminogen active fragment of the present invention is a protein comprising a serine protease domain of plasminogen. Preferably, the plasminogen active fragment of the present invention comprises SEQ ID NO: 14, or an amino acid sequence having an amino acid sequence identity of at least 80%, 90%, 95%, 96%, 97%, 98% or 99% with SEQ ID NO: 14. Therefore, plasminogen of the present invention comprises a protein comprising the plasminogen active fragment and still having plasminogen activity.
At present, methods for determining plasminogen and its activity in blood include: detection of tissue plasminogen activator activity (t-PAA), detection of tissue plasminogen activator antigen (t-PAAg) in plasma, detection of tissue plasminogen activity (plgA) in plasma, detection of tissue plasminogen antigen (plgAg) in plasma, detection of activity of the inhibitor of tissue plasminogen activators in plasma, detection of inhibitor antigens of tissue plasminogen activators in plasma and detection of plasmin-anti-plasmin (PAP) complex in plasma. The most commonly used detection method is the chromogenic substrate method: streptokinase (SK) and a chromogenic substrate are added to a test plasma, the PLG in the test plasma is converted into PLM by the action of SK, PLM acts on the chromogenic substrate, and then it is determined that the increase in absorbance is directly proportional to plasminogen activity using a spectrophotometer. In addition, plasminogen activity in blood can also be determined by immunochemistry, gel electrophoresis, immunonephelometry, radioimmuno-diffusion and the like.
“Orthologues or orthologs” refer to homologs between different species, including both protein homologs and DNA homologs, and are also known as orthologous homologs and vertical homologs. The term specifically refers to proteins or genes that have evolved from the same ancestral gene in different species. The plasminogen of the present invention includes human natural plasminogen, and also includes orthologues or orthologs of plasminogens derived from different species and having plasminogen activity.
“Conservatively substituted variant” refers to one in which a given amino acid residue is changed without altering the overall conformation and function of the protein or enzyme, including, but not limited to, replacing an amino acid in the amino acid sequence of the parent protein by an amino acid with similar properties (such as acidity, alkalinity and hydrophobicity). Amino acids with similar properties are well known. For example, arginine, histidine and lysine are hydrophilic basic amino acids and are interchangeable. Similarly, isoleucine is a hydrophobic amino acid that can be replaced by leucine, methionine or valine. Therefore, the similarity of two proteins or amino acid sequences with similar functions may be different. For example, the similarity (identity) is 70%-99% based on the MEGALIGN algorithm. “Conservatively substituted variant” also includes a polypeptide or enzyme having amino acid identity of 60% or more, preferably 75% or more, more preferably 85% or more, even more preferably 90% or more as determined by the BLAST or FASTA algorithm, and having the same or substantially similar properties or functions as the natural or parent protein or enzyme.
“Isolated” plasminogen refers to the plasminogen protein that is isolated and/or recovered from its natural environment. In some embodiments, the plasminogen will be purified (1) to a purity of greater than 90%, greater than 95% or greater than 98% (by weight), as determined by the Lowry method, such as more than 99% (by weight); (2) to a degree sufficiently to obtain at least 15 residues of the N-terminal or internal amino acid sequence using a spinning cup sequenator; or (3) to homogeneity, which is determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) under reducing or non-reducing conditions using Coomassie blue or silver staining. Isolated plasminogen also includes plasminogen prepared from recombinant cells by bioengineering techniques and separated by at least one purification step.
The terms “polypeptide”, “peptide” and “protein” are used interchangeably herein and refer to polymeric forms of amino acids of any length, which may include genetically encoded and non-genetically encoded amino acids, chemically or biochemically modified or derivatized amino acids, and polypeptides having modified peptide backbones. The term includes fusion proteins, including, but not limited to, fusion proteins having heterologous amino acid sequences, fusions having heterologous and homologous leader sequences (with or without N-terminal methionine residues), and the like.
The “percent amino acid sequence identity (%)” with respect to the reference polypeptide sequence is defined as the percentage of amino acid residues in the candidate sequence identical to the amino acid residues in the reference polypeptide sequence when a gap is introduced as necessary to achieve maximal percent sequence identity and no conservative substitutions are considered as part of sequence identity. The comparison for purposes of determining percent amino acid sequence identity can be achieved in a variety of ways within the skill in the art, for example using publicly available computer softwares, such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithm needed to achieve the maximum comparison over the full length of the sequences being compared. However, for purposes of the present invention, the percent amino acid sequence identity value is generated using the sequence comparison computer program ALIGN-2.
In the case of comparing amino acid sequences using ALIGN-2, the % amino acid sequence identity of a given amino acid sequence A relative to a given amino acid sequence B (or may be expressed as a given amino acid sequence A having or containing a certain % amino acid sequence identity relative to, with or for a given amino acid sequence B) is calculated as follows:
fraction X/Y×100
wherein X is the number of identically matched amino acid residues scored by the sequence alignment program ALIGN-2 in the alignment of A and B using the program, and wherein Y is the total number of amino acid residues in B. It will be appreciated that where the length of amino acid sequence A is not equal to the length of amino acid sequence B, the % amino acid sequence identity of A relative to B will not be equal to the % amino acid sequence identity of B relative to A. Unless specifically stated otherwise, all the % amino acid sequence identity values used herein are obtained using the ALIGN-2 computer program as described in the previous paragraph.
As used herein, the terms “treatment” and “treating” refer to obtaining a desired pharmacological and/or physiologic effect. The effect may be complete or partial prevention of a disease or its symptoms and/or partial or complete cure of the disease and/or its symptoms, and includes: (a) prevention of the disease from developing in a subject that may have a predisposition to the disease but has not been diagnosed as having the disease; (b) suppression of the disease, i.e., blocking its formation; and (c) alleviation of the disease and/or its symptoms, i.e., eliminating the disease and/or its symptoms.
The terms “individual”, “subject” and “patient” are used interchangeably herein and refer to mammals, including, but not limited to, murine (rats and mice), non-human primates, humans, dogs, cats, hoofed animals (e.g., horses, cattle, sheep, pigs, goats) and so on.
“Therapeutically effective amount” or “effective amount” refers to an amount of plasminogen sufficient to achieve the prevention and/or treatment of a disease when administered to a mammal or another subject to treat the disease. The “therapeutically effective amount” will vary depending on the plasminogen used, the severity of the disease and/or its symptoms, as well as the age, body weight of the subject to be treated, and the like.
Preparation of the Plasminogen of the Present Invention
Plasminogen can be isolated and purified from nature for further therapeutic uses, and can also be synthesized by standard chemical peptide synthesis techniques. When chemically synthesized, a polypeptide can be subjected to liquid or solid phase synthesis. Solid phase polypeptide synthesis (SPPS) is a method suitable for chemical synthesis of plasminogen, in which the C-terminal amino acid of a sequence is attached to an insoluble support, followed by the sequential addition of the remaining amino acids in the sequence. Various forms of SPPS, such as Fmoc and Boc, can be used to synthesize plasminogen. Techniques for solid phase synthesis are described in Barany and Solid-Phase Peptide Synthesis; pp. 3-284 in The Peptides: Analysis, Synthesis, Biology. Vol. 2: Special Methods in Peptide Synthesis, Part A., Merrifield et al. J. Am. Chem. Soc., 85: 2149-2156 (1963); Stewart et al. Solid Phase Peptide Synthesis, 2nd ed. Pierce Chem. Co., Rockford, Ill. (1984); and Ganesan A. 2006 Mini Rev. Med Chem. 6:3-10 and Camarero J A et al. 2005 Protein Pept Lett. 12:723-8. Briefly, small insoluble porous beads are treated with a functional unit on which a peptide chain is constructed. After repeated cycles of coupling/deprotection, the attached solid phase free N-terminal amine is coupled to a single N-protected amino acid unit. This unit is then deprotected to expose a new N-terminal amine that can be attached to another amino acid. The peptide remains immobilized on the solid phase before it is cut off.
Standard recombinant methods can be used to produce the plasminogen of the present invention. For example, a nucleic acid encoding plasminogen is inserted into an expression vector, so that it is operably linked to a regulatory sequence in the expression vector. Expression regulatory sequence includes, but is not limited to, promoters (e.g., naturally associated or heterologous promoters), signal sequences, enhancer elements and transcription termination sequences. Expression regulation can be a eukaryotic promoter system in a vector that is capable of transforming or transfecting eukaryotic host cells (e.g., COS or CHO cells). Once the vector is incorporated into a suitable host, the host is maintained under conditions suitable for high-level expression of the nucleotide sequence and collection and purification of plasminogen.
A suitable expression vector is usually replicated in a host organism as an episome or as an integral part of the host chromosomal DNA. In general, an expression vector contains a selective marker (e.g., ampicillin resistance, hygromycin resistance, tetracycline resistance, kanamycin resistance or neomycin resistance) to facilitate detection of those exogenous cells transformed with a desired DNA sequence.
Escherichia coli is an example of prokaryotic host cells that can be used to clone a polynucleotide encoding the subject antibody. Other microbial hosts suitable for use include Bacillus, for example, Bacillus subtilis and other species of Enterobacteriaceae (such as Salmonella spp. and Serratia spp.), and various Pseudomonas spp. In these prokaryotic hosts, expression vectors can also be generated which will typically contain an expression control sequence (e.g., origin of replication) that is compatible with the host cell. In addition, there will be many well-known promoters, such as the lactose promoter system, the tryptophan (trp) promoter system, the beta-lactamase promoter system or the promoter system from phage lambda. Optionally in the case of manipulation of a gene sequence, a promoter will usually control expression, and has a ribosome binding site sequence and the like to initiate and complete transcription and translation.
Other microorganisms, such as yeast, can also be used for expression. Saccharomyces (e.g., S. cerevisiae) and Pichia are examples of suitable yeast host cells, in which a suitable vector has an expression control sequence (e.g., promoter), an origin of replication, a termination sequence and the like, as required. A typical promoter comprises 3-phosphoglycerate kinase and other glycolytic enzymes. Inducible yeast promoters specifically include promoters derived from alcohol dehydrogenase, isocytochrome C, and enzymes responsible for maltose and galactose utilization.
In addition to microorganisms, mammalian cells (eg, mammalian cells cultured in in vitro cell culture) can also be used to express and produce the protein of the invention (eg, polynucleotides encoding the subject protein). See Winnacker, From Genes to Clones, VCH Publishers, N.Y., N.Y. (1987). Suitable mammalian host cells include CHO cell lines, various Cos cell lines, HeLa cells, myeloma cell lines and transformed B cells or hybridomas. Expression vectors for these cells may comprise an expression control sequence, such as an origin of replication, promoter and enhancer (Queen et al. Immunol. Rev. 89:49 (1986)), as well as necessary processing information sites, such as a ribosome binding site, RNA splice site, polyadenylation site and transcription terminator sequence. Examples of suitable expression control sequences are promoters derived from white immunoglobulin gene, SV40, adenovirus, bovine papilloma virus, cytomegalovirus and the like. See Co et al. J. Immunol. 148:1149 (1992).
Once synthesized (chemically or recombinantly), the plasminogen of the present invention can be purified according to standard procedures in the art, including ammonium sulfate precipitation, affinity column, column chromatography, high performance liquid chromatography (HPLC), gel electrophoresis and the like. The plasminogen is substantially pure, e.g., at least about 80% to 85% pure, at least about 85% to 90% pure, at least about 90% to 95% pure, or 98% to 99% pure or purer, for example free of contaminants such as cell debris, macromolecules other than the plasminogen and the like.
Pharmaceutical Formulations
A therapeutic formulation can be prepared by mixing plasminogen of a desired purity with an optional pharmaceutical carrier, excipient or stabilizer (Remington's Pharmaceutical Sciences, 16th edition, Osol, A. ed. (1980)) to form a lyophilized preparation or an aqueous solution. Acceptable carriers, excipients and stabilizers are non-toxic to the recipient at the dosages and concentrations employed, and include buffers, such as phosphates, citrates and other organic acids; antioxidants, including ascorbic acid and methionine; preservatives (e.g., octadecyl dimethyl benzyl ammonium chloride; hexane chloride diamine; benzalkonium chloride and benzethonium chloride; phenol, butanol or benzyl alcohol; alkyl p-hydroxybenzoates, such as methyl or propyl p-hydroxybenzoate; catechol; resorcinol; cyclohexanol; 3-pentanol; and m-cresol); low molecular weight polypeptides (less than about 10 residues); proteins, such as serum albumin, gelatin or immunoglobulins; hydrophilic polymers, such as polyvinylpyrrolidone; amino acids, such as glycine, glutamine, asparagine, histidine, arginine or lysine; monosaccharides, disaccharides and other carbohydrates, including glucose, mannose or dextrins; chelating agents, such as EDTA; sugars, such as sucrose, mannitol, fucose or sorbitol; salt-forming counterions, such as sodium; metal complexes (e.g., zinc-protein complexes); and/or non-ionic surfactants, such as TWEEN™, PLURONICS™ or polyethylene glycol (PEG).
The formulations of the invention may also comprise one or more active compounds required for the particular disorder to be treated, preferably those that are complementary in activity and have no side effects with one another, for example anti-hypertensive drugs, anti-arrhythmic drugs, drugs for treating diabetes mellitus, and the like.
The plasminogen of the present invention may be encapsulated in microcapsules prepared by techniques such as coacervation or interfacial polymerization, for example, it may be incorporated in a colloid drug delivery system (e.g., liposomes, albumin microspheres, microemulsions, nanoparticles and nanocapsules), or incorporated in hydroxymethylcellulose or gel-microcapsules and poly-(methyl methacrylate) microcapsules in macroemulsions. These techniques are disclosed in Remington's Pharmaceutical Sciences, 16th edition, Osol, A. Ed. (1980).
The plasminogen of the present invention for in vivo administration must be sterile. This can be easily achieved by filtration through a sterile filtration membrane before or after freeze drying and reconstitution.
The plasminogen of the present invention can be prepared into a sustained-release preparation. Suitable examples of sustained-release preparations include solid hydrophobic polymer semi-permeable matrices having a shape and containing glycoproteins, such as films or microcapsules. Examples of sustained-release matrices include polyesters, hydrogels (e.g., poly(2-hydroxyethyl-methacrylate)) (Langer et al. J. Biomed. Mater. Res., 15: 167-277 (1981); and Langer, Chem. Tech., 12:98-105 (1982)), or poly(vinyl alcohol), polylactides (U.S. Pat. No. 3,773,919, and EP 58, 481), copolymer of L-glutamic acid and γ ethyl-L-glutamic acid (Sidman et al. Biopolymers 22:547 (1983)), nondegradable ethylene-vinyl acetate (Langer et al. supra), or degradable lactic acid-glycolic acid copolymers such as Lupron Depot™ (injectable microspheres composed of lactic acid-glycolic acid copolymer and leuprolide acetate), and poly D-(−)-3-hydroxybutyric acid. Polymers, such as ethylene-vinyl acetate and lactic acid-glycolic acid, are able to persistently release molecules for 100 days or longer, while some hydrogels release proteins for a shorter period of time. A rational strategy for protein stabilization can be designed based on relevant mechanisms. For example, if the aggregation mechanism is discovered to be formation of an intermolecular S—S bond through thio-disulfide interchange, stability is achieved by modifying sulfhydryl residues, lyophilizing from acidic solutions, controlling moisture content, using appropriate additives, and developing specific polymer matrix compositions.
Administration and Dosage
The pharmaceutical composition of the present invention can be administered in different ways, for example by intravenous, intraperitoneal, subcutaneous, intracranial, intrathecal, intraarterial (e.g., via carotid), intramuscular, intranasal, topical or intradermal administration or spinal cord or brain delivery. An aerosol preparation, such as a nasal spray preparation, comprises purified aqueous or other solutions of the active agent along with a preservative and isotonic agent. Such preparations are adjusted to a pH and isotonic state compatible with the nasal mucosa.
Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, and alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, or fixed oils. Intravenous vehicles include liquid and nutrient supplements, electrolyte supplements and the like. Preservatives and other additives may also be present, for example, such as antimicrobial agents, antioxidants, chelating agents and inert gases.
The medical staff will determine the dosage regimen based on various clinical factors. As is well known in the medical field, the dosage of any patient depends on a variety of factors, including the patient's size, body surface area, age, the specific compound to be administered, sex, frequency and route of administration, overall health and other drugs administered simultaneously. The dosage range of the pharmaceutical composition comprising plasminogen of the present invention may be, for example, about 0.0001 to 2000 mg/kg, or about 0.001 to 500 mg/kg (such as 0.02 mg/kg, 0.25 mg/kg, 0.5 mg/kg, 0.75 mg/kg, 10 mg/kg and 50 mg/kg) of the subject's body weight daily. For example, the dosage may be 1 mg/kg body weight or 50 mg/kg body weight, or in the range of 1 mg/kg-50 mg/kg, or at least 1 mg/kg. Dosages above or below this exemplary range are also contemplated, especially considering the above factors. The intermediate dosages in the above range are also included in the scope of the present invention. A subject may be administered with such dosages daily, every other day, weekly or based on any other schedule determined by empirical analysis. An exemplary dosage schedule includes 1-10 mg/kg for consecutive days. During administration of the drug of the present invention, the therapeutic effect and safety of diabetic hepatopathy and its related disorders are required to be assessed real-timely and regularly.
Treatment Efficacy and Treatment Safety
One embodiment of the present invention relates to the judgment of treatment efficacy and treatment safety after treating a subject with plasminogen. The methods for judging the treatment efficacy include, but are not limited to: 1) examining the liver function of a subject, for example, enzymatic levels in the patient, such as levels of serum aspartate aminotransferase (AST), alanine transaminase (ALT), total bilirubin, direct bilirubin, indirect bilirubin, albumin, globulin, cholinesterase, alkaline phosphatase and transpeptidase, are examined to determine whether they are in the normal value ranges or not, and after treating the subject with plasminogen of the present invention, it is expected that the above liver function indexes will return to normal value or be improved, such as alanine transaminase (ALT) at 0-40μ/L, aspartate transaminase (AST) at 0-40 μL, gamma glutamyl transferase (GGT) of less than 40 units and total bilirubin at 3.4-20.5 μmol/L; 2) examining the prothrombin time (PT) and prothrombin activity (PTA) of the subject: PT is an important index reflecting the function of hepatic coagulation factor synthesis; PTA is a commonly used expression method for PT measurement value and of great value in judging the progression and prognosis of hepatopathy, in which the progressive decrease of PTA to less than 40% is an important diagnostic criterion for hepatic failure, and to less than 20% indicates hepatic dysfunction; and after treating the subject with plasminogen and its variants of the present invention, the decrease in PTA of the patient is expected to be remarkably improved; 3) imageological examination: including abdominal color ultrasonography of the liver, gallbladder and spleen, CT or MRI to learn the degree of recovery of hepatic injury; 4) examining tumor markers, such as alpha fetal protein (AFP), CA199 and AFU; and 5) hepatic biopsy to determine the degree of recovery of fibrosis and other injuries. In addition, the present invention also relates to the judgment of the safety of the therapeutic regimen during and after treating a subject with plasminogen and its variants, including, but not limited to, statistics of serum half-life, half-life of treatment, median toxic dose (TD50) and median lethal dose (LD50) in the subject, or observing various adverse events such as sensitization that occur during or after treatment.
Articles or Kits
One embodiment of the present invention relates to an article or kit comprising plasminogen of the present invention useful in the treatment of the hepatic injury and its related disorders caused by diabetes mellitus. The article preferably includes a container, label or package insert. Suitable containers include bottles, vials, syringes and the like. The container can be made of various materials, such as glass or plastic. The container contains a composition that is effective to treat the disease or disorder of the present invention and has a sterile access (for example, the container may be an intravenous solution bag or vial containing a plug that can be pierced by a hypodermic injection needle). At least one active agent in the composition is plasminogen/plasmin. The label on or attached to the container indicates that the composition is used to treat the hepatic injury and its related disorders caused by diabetes mellitus according to the present invention. The article may further comprise a second container containing a pharmaceutically acceptable buffer, such as phosphate buffered saline, Ringer's solution and glucose solution. It may further comprise other substances required from a commercial and user perspective, including other buffers, diluents, filters, needles and syringes. In addition, the article comprises a package insert with instructions for use, including, for example, instructions to a user of the composition to administer the plasminogen composition and other drugs to treat an accompanying disease to a patient.
Ten male db/db mice aged 24-25 weeks were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 15 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. The mice were weighed on days 0, 4, 7, 11 and 16 after administration of plasminogen, respectively. The results showed that there was no significant difference in body weight between mice in the group administered with plasminogen and those in the control group administered with vehicle PBS on days 0, 4, 7, 11 and 16 (
Ten male db/db mice aged 24-25 weeks were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 15 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Mice were sacrificed on day 16, and liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were sealed after dehydration with alcohol gradient.
The HE staining results showed that in mice in the control group administered with vehicle PBS, the hepatocytes showed severe steatosis and lipid deposition, cell nuclei were squeezed to the edge, the cells showed mild hydropic degeneration, and the hepatic cord was disordered; and compared with mice in the control group administered with vehicle, in mice in the group administered with plasminogen, hepatocytes showed relieved steatosis, mild steatosis and mainly moderate hydropic degeneration. This indicated that plasminogen can promote the repair of diabetic hepatic injury.
Ten male db/db mice aged 24-25 weeks were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 15 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Mice were sacrificed on day 16, and liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated and washed with water once. The sections were incubated with 3% hydrogen peroxide for 15 minutes and wash with water twice for 5 minutes each time. The sections were blocked with 10% normal goat serum solution (Vector laboratories, Inc., USA) for 1 hour; and after the time was up, the goat serum solution was discarded, and the tissues were circled with a PAP pen. The sections were incubated with rabbit anti-mouse fibrin (fibrinogen) antibody (Abcam) overnight at 4° C. and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds, flushed with running water for 5 minutes, and then washed with TBS once. After gradient dehydration, permeabilization and sealing, the sections were observed under a microscope at 200×.
Fibrinogen is the precursor of fibrin, and in the presence of tissue injury, as a stress response to the body's injury, fibrinogen is hydrolyzed into fibrin[1244]. Therefore, the fibrinogen level can be used as a sign of the degree of injury.
The study found that compared with mice in the control group administered with vehicle PBS (
Twenty male db/db mice aged 24-25 weeks were randomly divided into two groups, ten in the control group administered with vehicle PBS and ten in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 31 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. The mice were weighted on days 0, 4, 7, 11, 16, 21, 26 and 31.
The results showed that there was no significant difference in body weight between mice in the group administered with plasminogen and those in the control group administered with vehicle PBS on days 0, 4, 7, 11, 16, 21, 26 and 31 (
Ten male db/db mice aged 24-25 weeks were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 31 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Mice were sacrificed on day 32, and liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were sealed after dehydration with alcohol gradient.
The HE staining results showed that in mice in the control group administered with vehicle PBS (
and in mice in the group administered with plasminogen (
Ten male db/db mice aged 24-25 weeks were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 31 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Mice were sacrificed on day 32, and liver tissues were fixed in 10% neutral formalin fix solution for 24 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated and washed with water once. The sections were incubated with 3% hydrogen peroxide for 15 minutes and wash with water twice for 5 minutes each time. The sections were blocked with 10% normal goat serum solution (Vector laboratories, Inc., USA) for 1 hour; and after the time was up, the goat serum solution was discarded, and the tissues were circled with a PAP pen. The sections were incubated with rabbit anti-mouse fibrin (fibrinogen) antibody (Abcam) overnight at 4° C. and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After gradient dehydration, permeabilization and sealing, the sections were observed under a microscope at 200×.
Fibrinogen is the precursor of fibrin, and in the presence of tissue injury, as a stress response to the body's injury, fibrinogen is hydrolyzed into fibrin[12-14]. Therefore, the fibrinogen level can be used as a sign of the degree of injury.
The study found that compared with mice in the control group administered with vehicle PBS (
Ten male db/db mice aged 24-25 weeks were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 31 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Mice were sacrificed 31 days after administration of plasminogen, and liver tissues were fixed in 10% neutral formalin fix solution for 24 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated and washed with water once. The sections were incubated with 3% hydrogen peroxide for 15 minutes and wash with water twice for 5 minutes each time. The sections were blocked with 10% normal goat serum for 1 hour, and after the time was up, the serum was thrown away, and the tissues were circled with a PAP pen. The sections were incubated with a rabbit polyclonal antibody against F4/80 (Abcam) overnight at 4° C. and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After gradient dehydration, permeabilization and sealing, the sections were observed under a microscope at 400×.
F4/80 is a macrophage marker that can indicate the extent and stage of an inflammatory response. The results showed that compared with mice in the control group administered with vehicle PBS (
Nine male db/db mice aged 25-28 weeks were randomly divided into two groups, three in the control group administered with vehicle PBS and six in the group administered with plasminogen, respectively. The day when the experiment began was recorded on Day 0, and the mice were weighed and grouped. From the second day of the experiment, plasminogen or PBS was administered to the mice for 31 consecutive days, and the day was recorded as Day 1. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Whole blood was taken from the removed eyeballs 31 days after administration of plasminogen. After the serum was precipitated, it was centrifuged at 3500 r/min for 10 minutes at 4° C., and the supernatant was taken for detection. In this experiment, the content of alanine transaminase (ALT) in serum was detected by Reitman-Frankel colorimetry using an alanine transaminase detection kit (Nanjing Jiancheng Biological Engineering Research Institute, Catalog No. C009-2).
Alanine transaminase is an important index of liver health status[15,16], and the normal reference value interval of alanine transaminase is 9-50 U/L. The detection results showed that the ALT content in serum of mice in the control group administered with vehicle PBS was significantly higher than the normal physiological index, whereas the content in mice in the group administered with plasminogen had returned to normal levels in the body; and the content in mice in the group administered with plasminogen was significantly lower than that in mice in the control group administered with vehicle PBS, and there was a statistical difference (
Eighteen male or female 7-8-week-old plg−/− mice were randomly divided into two groups, nine in the control group administered with vehicle PBS and nine in the group administered with plasminogen, respectively. Two groups of mice were administered with carbon tetrachloride via intraperitoneal injection at 0.5 mL/kg body weight for 2 consecutive days to establish an acute hepatic injury model[17,18]. Carbon tetrachloride should be diluted with corn oil before use, and the volume ratio of the former to the latter is 1:7. The day of model establishment was day 0, and plasminogen or PBS was administered to the mice from day 1. Mice in the group administered with plasminogen were administered with plasminogen at a dosage of 1 mg/0.1 mL/mouse/day, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS, both for 7 consecutive days. Three mice from both groups were respectively sacrificed on days 0, 2 and 7, the mice were dissected and the liver conditions were observed and recorded, and then liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were sealed after dehydration with alcohol gradient and observed under a microscope at 200×.
The HE staining results showed that on day 0, the livers of mice in the control group administered with vehicle PBS (
Eighteen male 7-11-week-old plg−/− mice were randomly divided into two groups, nine in the control group administered with vehicle PBS and nine in the group administered with plasminogen, respectively. Two groups of mice were administered with carbon tetrachloride via intraperitoneal injection at 0.5 mL/kg body weight once to establish an acute hepatic injury model[17,18]. Carbon tetrachloride should be diluted with corn oil before use, and the volume ratio of the former to the latter is 1:7. Plasminogen or vehicle PBS was administered to the mice within half an hour after completion of model establishment. Mice in the group administered with plasminogen were injected with plasminogen at a dosage of 1 mg/0.1 mL/mouse/day, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS, both for 2 consecutive days. Three mice from both groups were respectively sacrificed at hours 18, 24 and 48 after administration, the mice were dissected and the liver conditions were observed and recorded, and then liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were sealed after dehydration with alcohol gradient and observed under a microscope at 200×.
The results showed that mice in the control group administered with vehicle PBS (
Eighteen male 7-11-week-old plg−/− mice were randomly divided into two groups, nine in the control group administered with vehicle PBS and nine in the group administered with plasminogen, respectively. Two groups of mice were administered with carbon tetrachloride via intraperitoneal injection at 0.5 mL/kg body weight once to establish an acute hepatic injury model[17,18]. Carbon tetrachloride should be diluted with corn oil before use, and the volume ratio of the former to the latter is 1:7. Plasminogen or vehicle PBS was administered to the mice within half an hour after completion of model establishment. Mice in the group administered with plasminogen were injected with plasminogen at a dosage of 1 mg/0.1 mL/mouse/day, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS, both for 2 consecutive days. Three mice from both groups were respectively sacrificed at hours 18, 24 and 48 after administration, the mice were dissected and the liver conditions were observed and recorded, and then liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated and washed with water once. The sections were incubated with 3% hydrogen peroxide for 15 minutes and wash with water twice for 5 minutes each time. The sections were blocked with 10% normal goat serum solution (Vector laboratories, Inc., USA) for 1 hour; and after the time was up, the goat serum solution was discarded, and the tissues were circled with a PAP pen. The sections were incubated with rabbit anti-mouse fibrin (fibrinogen) antibody (Abcam) overnight at 4° C. and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After gradient dehydration, permeabilization and sealing, the sections were observed under a microscope at 200×.
Fibrinogen is the precursor of fibrin, and in the presence of tissue injury, as a stress response to the body's injury, fibrinogen is hydrolyzed into fibrin[12-14]. Therefore, the fibrinogen level can be used as a sign of the degree of injury.
The results showed that at three time points, 18 h, 24 h and 48 h, mice in the group administered with plasminogen (
In this experiment, ten healthy 6-8-week-old male C57 mice were used and randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. After the grouping was completed, a radiation-induced injury model was established by uniformly irradiating the mice with 6 MV X-rays from a linear accelerator at 5.0 Gy once systemically, in which the absorbed dosage rate was 2.0 Gy/min and the absorbed dosage was 5.0 Gy (irradiation for 2.5 minutes). Plasminogen was administered to the mice within 3 hours after the model was established. The day when the experiment began was Day 0, and the mice were weighed and grouped. The mice were treated with radiation and administered with plasminogen or vehicle PBS from day 1. The administration period was 10 days. After the completion of the administration, the medication of animals was discontinued and they were observed for 11 days. The entire experimental period was 21 days. Mice in the group administered with plasminogen were injected with plasminogen at a dosage of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. Mice were sacrificed and dissected on day 21, and livers were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated and washed with water once. The sections were repaired with Tris-EDTA for 30 minutes, and gently rinsed with water after cooling at room temperature for 20 minutes. The sections were incubated with 3% hydrogen peroxide for 15 minutes, and the tissues were circled with a PAP pen. The sections were blocked with 10% normal goat serum (Vector laboratories, Inc., USA) for 1 hour; and after the time was up, the goat serum solution was discarded. The sections were incubated with rabbit anti-mouse F4/80 antibody (Abcam) at 4° C. overnight and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After gradient dehydration, permeabilization and sealing, the sections were observed under a microscope at 200×.
The F4/80 immunohistochemical results showed that after model establishment with 5.0 Gy X-ray irradiation, the expression level of the macrophage marker in mice in the control group administered with vehicle PBS (
Ten healthy 8-9-week-old male C57 mice were used and randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. After the grouping was completed, a chemotherapy-induced injury model was established by single intraperitoneal injection of cisplatin at 10 mg/Kg body weight. After the model was established, mice in the group administered with plasminogen were administered with plasminogen at a dosage of 1 mg/mouse/day via tail vein injection, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS. The day when the experiment began was Day 0, and the mice were weighed and grouped. The mice were injected with cisplatin intraperitoneally from day 1 for model establishment. Plasminogen or vehicle PBS was administered to the mice within 3 hours after completion of model establishment, and the administration period was 7 days. Mice were sacrificed on day 8, and livers were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated and washed with water once. The sections were repaired with citric acid for 30 minutes, and gently rinsed with water after cooling at room temperature for 10 minutes. The sections were incubated with 3% hydrogen peroxide for 15 minutes, and the tissues were circled with a PAP pen. The sections were blocked with 10% normal goat serum (Vector laboratories, Inc., USA) for 1 hour; and after the time was up, the goat serum solution was discarded. The sections were incubated with rabbit anti-mouse fibrin antibody (Abcam) overnight at 4° C. and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After gradient dehydration, permeabilization and sealing, the sections were observed under a microscope at 200×.
Fibrinogen is the precursor of fibrin, and in the presence of tissue injury, as a stress response to the body's injury, fibrinogen is hydrolyzed into fibrin[12-14]. Therefore, the fibrinogen level can be used as a sign of the degree of injury.
The results showed that fibrin-positive staining in the liver tissues of mice in the control group administered with vehicle PBS (
Six male 7-11-week-old plg−/− mice were randomly divided into two groups, three in the control group administered with vehicle PBS and three in the group administered with plasminogen, respectively. Two groups of mice were administered with carbon tetrachloride via intraperitoneal injection at 0.5 mL/kg body weight once to establish an acute hepatic injury model[17,18]. Carbon tetrachloride should be diluted with corn oil before use, and the volume ratio of the former to the latter is 1:7. Plasminogen or vehicle PBS was administered to the mice within half an hour after completion of model establishment. Mice in the group administered with plasminogen were administered with plasminogen at a dosage of 1 mg/0.1 mL/mouse/day, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS, both for 7 consecutive days. Mice were sacrificed and dissected on day 8, the liver conditions were observed and recorded, and then liver tissues were fixed in 10% neutral formalin fix solution for 24-48 hours. The fixed liver tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 5 μm. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were sealed after dehydration with alcohol gradient and observed under a microscope at 200×.
The results showed that in the livers of mice in the control group administered with vehicle PBS (
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2015/097945 | Dec 2015 | CN | national |
| PCT/CN2015/097949 | Dec 2015 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2016/110451 | 12/16/2016 | WO | 00 |
