Patent Application
20130150598
The present invention relates to use of 25-hydroxyvitamin D3 (calcifediol, 25-OH D3) to increase muscle strength, muscle function, or both. Vitamin D (cholecalciferol and/or ergocalciferol) may optionally be used together with 25-OH D3.
Vitamin D (e.g., ergocalciferol and cholecalciferol) is a group of fat-soluble compounds defined by their biological activity. A deficiency of vitamin D causes rickets in children and osteomalacia in adults. But toxicity can occur after chronic intake of more than 100 times the recommended daily allowance (i.e., 5-15 μg or 200-600 IU vitamin D) for several months. For vitamin D, “The threshold for toxicity is 500 to 600 mcg/kg body weight per day. In general, adults should not consume more than three times the RDA for extended period of time” (Garrison & Somer, The Nutrition Desk Reference, Third Ed., McGraw-Hill, pg. 82, 1997). Hypercalcemia may occur at a blood concentration of 25-hydroxyvitamin D greater than 375 nmol/L. More recently, a safe upper level of Vitamin D was identified to be at least 250 μg/day (10'000 IU) (Hathcock et al. Am. J. Clin. Nutr. 85:6-18, 2007). Ingestion of such as a dietary supplement has been shown to result in a blood concentration of about 200 nmol/L 25-hydroxyvitamin D.
Vitamin D is a prohormone which has to be hydroxylated in the liver to produce 25-hydroxyvitamin D (calcifediol; 25-OH vitamin D; 25-OH D), which then undergoes another hydroxylation in the kidney and other tissues to produce 1,25-dihydroxyvitamin D, the active hormone form of vitamin D. 1,25-dihydroxyvitamin D is released into the blood, binds to vitamin D binding protein (DBP), and is transported to target tissues. Binding between 1,25-dihydroxyvitamin D and vitamin D receptor allows the complex to act as a transcription factor in the cell's nucleus.
Vitamin D deficiency may promote resorption of bone. It may also modulate function of the cardiovascular, immune, and muscular systems. Epidemiological studies find associations between vitamin D intake and its effect on blood pressure or glucose metabolism. The activity of vitamin D is under negative feedback control by parathyroid hormone.
Both Vitamin D and 25-OH D3 have been administered as pharmaceuticals in the past. Vitamin D, is of course widely available; 25-OH D3 was previously sold in the USA by Organon USA under the name “CALDEROL”, but is currently on the FDA's list of discontinued drugs. It was a gelatine capsule containing corn oil and 25-OH D3.
A liquid form of 25-OH D3 is currently sold in Spain by FAES Farma under the name “HIDROFEROL” in an oil solution.
The combination of vitamin D and 25-OH D3 has been used in animal feed. 25-OH D3 for use in feed is commercially available from DSM under the name “ROVIMIX HY-D”.
Tritsch et al. (US 2003/0170324) disclose a feed premix composition of at least 25-OH D3 in an amount between 5% and 50% (wt/wt) dissolved in oil and an antioxidant, an agent encapsulating droplets of 25-OH D3 and oil, and a nutritional additive (e.g., Vitamin D3). The premix may be added to poultry, swine, canine, or feline food. This composition stabilizes 25-OH D3 against oxidation.
Simoes-Nunes et al. (US 2005/0064018) discloses adding a combination of 25-OH Vitamin D3 and Vitamin D3 to animal feed. In particular, about 10 μg/kg to about 100 μg/kg of 25-OH Vitamin D3 and about 200 IU/kg to about 4,000 IU/kg of Vitamin D3 are added to swine feed. This addition improves the pig's bone strength.
Stark et al. (U.S. Pat. No. 5,695,794) disclose adding a combination of 25-OH Vitamin D3 and Vitamin D3 to poultry feed to ameliorate the effects of tibial dyschondroplasia.
Borenstein et al U.S. Pat. No. 5,043,170 discloses the combination of Vitamin D3 and either 1-alpha-hydroxycholecalciferol or 1alpha, 25-dihydroxycholecalciferol to improve egg strength and leg strength in laying hens and older hens.
Chung et al, WO 2007/059960 discloses that sows fed a diet containing both Vitamin D3 and 25-hydroxVitamin D3 had improved general health status, body frame, litter size and health, and other production parameters. Also a 25-OH D3 human food supplement is disclosed, but its dosage range, 5-15 micrograms per kg body weight, which equals to an extremely high daily dosage of 300-900 micrograms per human is very high.
PCT/EP08/006,357 discloses that prenatal exposure of piglets to 25-OH D3 (by feeding the pregant sow) enhances muscle development in the offspring.
To our knowledge the prior art does not teach or suggest use of 25-OH vitamin D3 or the combination of 25-OH D3 and vitamin D as a medicament for humans to increase muscle strength, muscle function, or both. Other advantages and improvements are described below or would be apparent from the disclosure herein.
It has been found, in accordance with this invention, that daily or weekly treatment with 25-OH D3 surprisingly results in improvements of muscle strength and/or function compared to consumption of identical dosages of Vitamin D.
Thus, one aspect of this invention is to use 25-OH D3 as a medicament to increase muscle strength and/or function in a human. The medicament may optionally further comprise vitamin D. The human may be any age, including children and juveniles, starting from birth to adulthood, and from 18 years to 80 years of age, or more than 80 years of age. Forms and dosages of a pharmaceutical composition, as well as processes for manufacturing medicaments, are also disclosed.
In another aspect of this invention, is the use of a combination of 25-OH D3 and Vitamin D to enhance muscle strength and function in a human.
Optionally, vitamin D3 may be administered together with or separately from 25-OH D3. They may be administered once per day, once per week, or once per month. Generally, the administration period is at least for one month, preferably for more than two months, and more preferably for at least four months so that changes in muscle strength can be clearly observed. Strength may be measured using art-recognized tests, such as knee flexor and extensor strength tests.
In another aspect, a method of increasing muscle function by administering an effective amount of 25-OH D3 is provided. Optionally, vitamin D may be administered together with or separately from 25-OH D3. They may be administered once per day, once per week, or once per month. Muscle function may be assessed by art-recognized tests, such as the repeated sit-to-stand test, and the timed up and go test.
In another aspect, a pharmaceutical composition suitable for human use is provided which comprises vitamin D3, 25-OH D3, and a pharmaceutically acceptable carrier in muscle strengthening amounts.
Further, it has been found, in accordance with this invention that the combination of 25-OH D3 and Vitamin D synergistically regulates (either up-regulates or down-regulates) a synergistic number of Vitamin D responsive skeletal muscle genes, including a high number of genes which are not responsive to the presence of either Vitamin D nor 25-OH D3 alone. This is a surprising result, as it is not explained by the current model of Vitamin D metabolism, which postulates that virtually all Vitamin D is first metabolized into 25-OH D.
The combination, in accordance with this invention, provides two significant advantages:
1) It results in a rapid and synergistic plasma response of 25-OH D
2) It leads to an unexpectedly pronounced and long plateau of plasma 25-OH D levels. These are especially important goals of treatment of muscular disorders which are the consequence of a Vitamin D deficiency: a rapid correction of suboptimal Vitamin D status and a long and stable plasma concentration to ensure sufficient supply of 25-OH to muscle tissue.
Another aspect of this invention is a food, functional food, food supplement or nutraceutical suitable maintaining muscle strength and function for human consumption containing 25-OH D3, and preferably a combination of Vitamin D and 25-OH D3.
As used throughout the specification and claims, the following definitions apply:
“Vitamin D” means either Vitamin D3 (cholecalciferol) and/or Vitamin D2 (ergocaciferol). Humans are unable to make Vitamin D2 (ergocalciferol), but are able to use it as a source of Vitamin D. Vitamin D2 can be synthesized by various plants and is often used in Vitamin D in supplements as an equivalent to Vitamin D.
“Vitamin D metabolite” means any metabolite of Vitamin D other than 25-hydroxy vitamin D3.
“25-OH D3” refers specifically to 25-hydroxyvitamin D3
“25-OH D” refers to the 25-hydroxylated metabolite of either Vitamin D2 or Vitamin D3 which is the major circulating form found in plasma.
“Prevent” is meant to include amelioration of the disease, lessening of the severity of the symptoms, early intervention, and lengthening the duration of onset of the disease, and not intended to be limited to a situation where the patient is no longer able to contract the disease nor experience any symptoms.
In another embodiment, a kit is provided which is comprised of multiple, separate dosages of Vitamin D or Vitamin D3 along with a dosage of 25-OH D3. They may be enclosed in a container: e.g., bottle, blister pack, or vial rack. Further, instructions for administering the composition as a dosage to a human are provided within the kit.
In another embodiment, the 25-OH D3, alone or in combination with Vitamin D is the active ingredient to preserve healthy muscle strength or function in a food, functional food, food supplement or nutraceutical suitable for human consumption. The dosages of the 25-OH and/or D3 may be the same as those present in the pharmaceutical product, but preferably will tend towards the lower ranges. The food supplements and nutraceuticals may be in the form of tablets, capsules or other convenient dosage forms. The food may be a beverage or food, and if desired, may also contain other nutritionally effective compounds such as other vitamins, minerals, and the like.
Vitamin D deficiency is an especially prevalent condition in the elderly population and those who suffer chronic immobility regardless of age. This may be due to the general lack of exposure to sunlight, a lessened ability of the body to manufacture vitamin D or metabolize it efficiently, or a number of other causes. One consequence of Vitamin D deficiency is a loss of muscle strength and/or function. Thus one aspect of this invention is the use of the combination of Vitamin D and 25-OH D3 in an elderly population to maintain, prevent the loss of, and/or restore healthy muscle strength and function. As used throughout, the term “elderly” is meant to encompass those individuals who are over 65 years of age, preferably over 70, and even over 80.
In another embodiment, this combination of 25-OH D3 and Vitamin D is suitable to maintain, prevent the loss of, and/or restore healthy muscle strength and function in people who are at risk of developing muscle strength and or function conditions characterized by Vitamin D deficiency or insufficiency. This would include especially adults, including post-menopausal women (i.e. about age 45 and older) and men who are about age 45 and older. It is especially suitable for individuals who do not receive a great deal of natural sunlight exposure, such as for people who traditionally wear long clothing, do not go out of doors regularly, or who use sunscreens when they are exposed to sunlight, or live in geographical areas significantly north or south of the equator, where sunlight is less intense.
Another aspect of this invention is a method to maintain, prevent the loss of, and/or restore healthy muscle strength and function in a human with a malabsorption syndrome (e.g., affected by celiac disease, sprue, or short bowel syndrome), and it thereby at risk of Vitamin D deficiency by administering the combination of Vitamin D and 25-OH D3.
Another aspect of this invention is a method to maintain, prevent the loss of, and/or restore healthy muscle strength and function in a human with impared liver function, wherein the human cannot process Vitamin D into 25-hydroxyvitamin D efficiently, by providing the human with a combination of Vitamin D and 25-hydroxyvitamin D3.
The compositions of this invention are also beneficial for the retention of muscle mass in the elderly (up to 80 years old) and the very elderly (80 or above years old), particularly those who are in institutionalized care facilities (e.g., hospital, nursing home, rehabilitation clinic, elder assisted living), or those with muscle atrophy.
Another embodiment of this invention is the use of 25-OH D3 to maintain or prevent loss of muscle strength in the elderly. Loss of muscle strength is also a major cause of falls in the elderly and may contribute to the high number of falls that take place in the hospital. For an older person who has diminished physiologic reserves but still can perform daily activities (such as walking, bathing and toileting functions), the accelerated losses of muscle strength after even a few days bed rest may result in a prolonged loss if independent function. Even if this loss is eventually reversed, rehabilitation requires extensive and expensive intervention because reconditioning of muscles takes considerably longer than the deconditioning process.
The compositions of this invention are also beneficial for the retention and/or increase of muscle mass in people who may not be elderly, but who lose muscle mass because they are immobilized due to another condition. As explained by the Merck Manual of Geriatrics, 2nd Ed: (p316-318): with complete inactivity, muscle strength decreases by 5% per day. Even young men on bed rest lose muscle strength at a rate of 1.0% to 1.5% per day (or about 10% per week).
Thus the compositions of this invention are beneficial for people who are subject to loss of muscle mass due to decreased mobility, or who are even immobile. The cause of the decreased mobility does not matter in the practice of this invention, as the goal here is to protect against loss of muscle mass. For example, the loss of mobility may be from trauma, stroke, being in a cast, Parkinson's disease, multiple sclerosis, myasthenia gravis, or even Creutzfeldt-Jacobs disease. Thus another aspect of this invention is to administer the compounds of this invention to a paraplegic, or a quadriplegic individual.
The compositions of this invention are also beneficial for those suffering from cachexia or sarcopenia. Cachexia is a “body-wasting” syndrome that is a co-morbidity with cancers and AIDS. Other syndromes or conditions which can induce skeletal muscle atrophy are congestive heart disease, chronic obstructive pulmonary disease, liver disease, starvation, burns, etc. Sarcopenia is another condition (distinct from cachexia and atrophy) which relates to an age-related decrease in muscle function. The exact cause is unknown.
This invention also relates to benefiting those with muscle weakness. Muscle weakness is the physical part of fatigue (medical). Locations for muscle weakness are central, neural and peripheral. Central muscle weakness is an overall exhaustion of the whole body, while peripheral weakness is an exhaustion of individual muscles. Neural weakness is somewhere between.
Muscle weakness may be due to problems with the nerve supply or problems with muscle itself. The latter category includes polymyositis and other muscle disorders e.g. amyotrophic lateral sclerosis, botulism, centronuclear myopathy, myotubular myopathy, dysautonomia, Charcot-Marie-Tooth, hypokalemia, motor neurone disease, muscular dystrophy, myotonic dystrophy, myasthenia gravis, progressive muscular atrophy, spinal muscular atrophy, cerebral palsy, infectious mononucleosis, herpes zoster, vitamin D deficiency, fibromyalgia, celiac disease, hypercortisolism (Cushing's syndrome), hypocortisolism (Addison's disease), primary hyperaldosteronism (Conn's syndrome), and diarrhea.
Vitamin D and 25-OH D3 may be obtained from any source, and a composition thereof may be prepared using convenient technology. In general, crystals of vitamin D3, 25-OH D3, or both (separately or together) are dissolved in an oil with heating and agitation. Preferably, the oil is transferred into a vessel and heated. Thereafter, vitamin D3, 25-OH D3, or both are added to the vessel, while maintaining the temperature of the oil or increasing it over time. The composition is agitated to dissolve the crystals of vitamin D3, 25-OH D3, or both. Prior to addition to the oil, the crystals may be reduced in size by milling and/or sieving, to enhance dissolving. The composition may be agitated by stifling, vessel rotation, mixing, homogenization, recirculation, or ultrasonication. Preferably, the oil may be heated in the vessel to a temperature from about 80° C. to about 85° C., sized crystals are introduced into the vessel, and the contents are stirred to dissolve the crystals into the oil.
The “oil” may be any edible oil, lipid, or fat: e.g., babassu oil, coconut oil, cohune oil, murumyru tallow, palm kernel oil, or tucum oil. The oil may be natural, synthetic, semisynthetic, or any combination thereof. Natural oil may be derived from any source (e.g., animal, plant, fungal, marine); synthetic or semisynthetic oil may be produced by convenient technology. Preferably, the oil is a mixture of plant medium chain triglycerides, mainly caprylic and capric acids. The composition may optionally contain one or more other suitable ingredients such as, for example, and a pharmaceutically acceptable antioxidant, preservatives, dissolution agents, surfactants, pH adjusting agents or buffers, humectants, and any combination thereof. The foregoing are examples of pharmaceutically acceptable carriers.
Suitable antioxidants include tocopherol, mixed tocopherols, tocopherols from natural or synthetic sources, butylated hydroxy toluene (BHT), butylated hydroxy anisole (BHA), natural antioxidants like rosemary extract, propyl galate, and any others used in the manufacture of pharmaceuticals for humans. Preferably, the antioxidant is tocopherol. Suitable preservatives include methyl paraben, propyl paraben, potassium sorbate, sodium benzoate, benzoic acid, and any combination thereof. Suitable dissolution agents include inorganic or organic solvents: e.g., alcohols, chlorinated hydrocarbons, and any combination thereof. Suitable surfactants may be anionic, cationic, or nonionic: e.g., ascorbyl palmitate, polysorbates, polyethylene glycols, and any combination thereof. Suitable pH adjusting agents or buffers include citric acid-sodium citrate, phosphoric acid-sodium phosphate, acetic acid-sodium acetate, and any combination thereof. Suitable humectants include glycerol, sorbitol, polyethylene glycol, propylene glycol, and any combination thereof.
Once formed, the oil composition may be incorporated in various other useful compositions, some of which are discussed below. For example, emulsions may be formed, which may be optionally encapsulated or spray dried. A variety of emulsions may be prepared by combining the nonaqueous compositions described above with an aqueous composition. The emulsion may be of any type. Suitable emulsions include oil-in-water emulsions, water-in-oil emulsions, anhydrous emulsions, solid emulsions, and microemulsions. The emulsions may be prepared by any convenient technology. The emulsion contains an aqueous composition and a nonaqueous (e.g., oil) composition, wherein the latter comprises vitamin D3, 25-OH D3, or both (separately or together) dissolved in an oil in an amount of between about 3% and about 50% by weight based on the total weight of the oil composition. As used herein, “aqueous composition” and “aqueous phase” are used interchangeably. Generally, the emulsion may contain from about 20% to about 95% of an aqueous composition, and from about 5% to about 80% of a nonaqueous composition. Preferably, however, the emulsion contains from about 85% to about 95% (vol/vol) of an aqueous composition, and from about 5% to about 15% (vol/vol) of a nonaqueous composition. Conveniently, the nonaqueous composition may be dispersed as droplets in the aqueous composition. For example, the droplets may have a mean diameter of less than about 500 nm in the aqueous composition. Conveniently, the droplets have a mean diameter of between about 150 nm and about 300 nm.
In a particularly advantageous embodiment, the emulsion contains an encapsulating agent, which facilitates encapsulating the oil composition upon further processing of the emulsion (e.g., by spray drying). The encapsulating agent may be any edible substance capable of encapsulating the oil composition. Preferably, the encapsulation agent is predominantly a colloidal material. Such materials include starches, proteins from animal sources (including gelatins), proteins from plant sources, casein, pectin, alginate, agar, maltodextrins, lignin sulfonates, cellulose derivatives, sugars, saccharides, sorbitols, gums, and any combination thereof.
Suitable starches include: plant starches (e.g., CAPSUL® or HI-CAP® from National Starch & Chemical Corp., New York, N.Y.), other modified food starches, and any combination thereof. Preferably, the starch is CAPSUL® modified plant starch. Suitable proteins from animal sources include: gelatins (e.g., bovine gelatins, porcine gelatins (Type A or B) with different Bloom numbers, fish gelatins), skim milk protein, caseinate, and any combination thereof. Preferably, the animal protein is a gelatin. Suitable proteins from plant sources include: potato protein (e.g., ALBUREX® from Roquette Preres Societe Anonyme, Lestrem, France), pea protein, soy protein, and any combination thereof. Preferably, the plant protein is ALBUREX® potato protein. Suitable maltodextrins with a different dextrose equivalent include: maltodextrin 5, maltodextrin 10, maltodextrin 15, maltodextrin 20, maltodextrin 25, and any combination thereof. Preferably, the maltodextrin is maltodextrin 15. Suitable cellulose derivatives include: ethyl cellulose, methylethyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, carboxymethylcellulose, and any combination thereof. Suitable saccharides include lactose, sucrose, or any combination thereof. Preferably, the saccharide is sucrose. Suitable gums include: acacia, locust bean, carragean, and any combination thereof. Preferably, the gum is gum acacia.
When the emulsion contains an encapsulating agent, the encapsulating agent may be dispersed in water by any convenient technology to form an aqueous phase. The aqueous phase may be a solution or a mixture depending on the properties of the components selected. The selected components may be dispersed by any convenient technology including: homogenizing, mixing, emulsifying, recirculating, static mixing, ultrasonication, stirring, heating, or any combination thereof. The viscosity of the resulting aqueous phase may then be adjusted, as desired, by the addition of water. The aqueous composition of the emulsion may optionally contain any other suitable material including but not limited to, those discussed above in reference to the nonaqueous composition. Preferably, the aqueous composition may include, an encapsulating agent, a film-forming agent, a plasticizer, a preservative, an antioxidant, or any combination thereof. Suitable preservatives include methyl paraben, propyl paraben, sorbic acid, potassium sorbate, sodium benzoate, and any combination thereof. Suitable antioxidants include sodium ascorbate, ascorbic acid, citric acid, and any combination thereof.
Preferably, the aqueous phase contains a modified food starch, such as octenyl succinyl starch (CAPSUL®), maltodextrin, and sodium ascorbate. Another preferred aqueous phase contains potato protein (ALBUREX®), maltodextrin 20, and sodium ascorbate. The selected components may be dissolved in water by any convenient technology, preferably stirring. The mixture is preferably homogenized until it is uniform and lump free. Preferably, the homogenization is carried out at a temperature between about 50° C. and about 75° C. The final viscosity of the resulting aqueous phase may then be adjusted to the desired viscosity, preferably about 250 cp to about 450 cp, more preferably about 300 cp to about 400 cp, even more preferably about 385 cp.
The emulsion may be formed by emulsifying the nonaqueous composition and the aqueous phase by any means, including homogenization, rotor-stator shear, high pressure shear and cavitation, high speed “cowles” or shear agitation, and any combination thereof. The volume and viscosity of the emulsion may preferably be adjusted by the addition of water after emulsification. Preferably, the nonaqueous and aqueous compositions are emulsified by homogenization. Preferably, the emulsion should not contain any mineral, transition metal, or peroxide.
As noted above, the emulsion may be incorporated or employed in producing other useful compositions, especially encapsulated oils, e.g., spray-dried powders. Generally, the encapsulated oil comprises an oil composition and an encapsulation agent encapsulating the oil composition, wherein the oil composition contains vitamin D3, 25-OH D3, or both dissolved in the oil in an amount between about 3% and about 50% by weight based on the total weight of the oil composition. The encapsulated oil may be produced by any convenient technology: e.g., drying an emulsion described above by any conventional technology, including spray drying, freeze drying, fluid bed drying, tray drying, adsorbtion, and any combination thereof. Preferably, the encapsulated oil is produced by spray drying an emulsion having an aqueous phase above containing an encapsulation agent; spray drying parameters are dictated by the physical characteristics desired in the final encapsulated oil. Such physical parameters include particle size, powder shape and flow, and water content. Preferably, the oil is in an amount less than about 30%, less than about 20%, less than about 10%, or less than about 5% by weight based on the total weight of the encapsulated oil. The encapsulated oil should have good flowability and the vitamin D3 and/or 25-OH D3 should be distributed homogeneously throughout the composition. Conveniently, the encapsulated oil is a powder. Any other suitable additive may be added to the encapsulated oil. One such additive may be a flow agent such as silicon dioxide, to increase the flowability of the encapsulated oil.
The composition may be provided in the form of a tablet, capsule (e.g., hard or soft), or injection (e.g., oil or emulsion). They may be packaged in a single daily dosage.
Daily. A composition according to this invention where the two active ingredients are to be administered separately, contains Vitamin D or 25-OH D3 in an amount from about 1 μg to about 50 μg, preferably about 5 μg and 25 μg. Alternatively, a single daily dosage having both Vitamin D and 25-OH D3 contains each active ingredient in an amount from about 1 μg to about 50 μg, preferably about 5 μg and 25 μg.
The dosage ratio of Vitamin D to 25-OH D3 may be from about 50:1 to about 1:50, more preferably from about 25:1 to about 1:25, and even more preferably from about 6:1 to about 1:6.
Multiple, separate dosages may be packaged in a single kit (or container). For example, the kit may be comprised of thirty separate daily dosages of both actives separately (i.e. 60 separate dosages), or combined (i.e. 30 dosages containing both active ingredients). Instructions for administering the dosages to a human may be included in the kit.
Weekly. A single weekly dosage contains Vitamin D or 25-OH D3 in an amount from about 7 μg to about 350 μg, and preferably from about 35 to 175 μg. Alternatively, a single weekly dosage may contain both Vitamin D and 25-OH D3 each in an amount from about 7 μg to about 350 μg, and preferably from about 35 to 175 μg. The dosage ratio of Vitamin D to 25-OH D3 may be from about 50:1 to about 1:50, more preferably from about 25:1 to about 1:25, and even more preferably from about 6:1 to about 1:6.
Monthly. A single monthly dosage contains Vitamin D or 25-OH D3 in an amount from 30 μg to about 1500 μg, preferably about 75 μg to about 500 μg. Alternatively, a single monthly dosage may contain both Vitamin D and 25-OH D3 each in an amount from 30 μg to about 1500 μg, preferably about 75 μg to about 500 μg. A kit may be comprised of one, two, three, four, five, six, seven, eight, nine, ten, eleven, or twelve weekly or monthly dosages.
Dosage ratios of Vitamin D to 25-OH D3 should range between 50:1 to about 1:50, more preferably from about 25:1 to about 1:25, and even more preferably from about 6:1 to about 1:6.
To demonstrate increased bioactivity of the combination, a gene chip analysis of muscle tissue exposed to Vitamin D, 25-OH D3 and the combination was performed. Details are given in Example 2, using a murine hind-leg suspension model. As can be seen, there is a dramatic increase in the number of genes activated or regulated (either up-regulated or down-regulated) when the combination of the two are delivered as compared to individual administration. As it is currently believed that the vast majority of Vitamin D is converted into 25-OH D upon ingestion and processing in the liver, this is a surprising result.
Thus, another aspect of this invention is a process of activating or regulating Vitamin D and 25-OH D responsive human muscle-related genes comprising administering to a person a combination of Vitamin D and 25-OH D3.
The following non-limiting Examples are presented to better illustrate the invention.
Spray-dried formulation of 25-OH D3 was provided as a powder. In summary, 25-OH D3 and DL-α-tocopherol were dissolved in an oil of medium chain triglycerides, then emulsified into an aqueous solution of modified starch, sucrose, and sodium ascorbate. The emulsion was atomized in a spray dryer in the presence of silicon dioxide. The resulting powder was collected when water content (LDO) was less than 4% and sieved through 400 μm. It was packed and sealed in alu-bags, then stored in a dry area below 15° C. and used within 12 months of its manufacture.
Three separate lots were manufactured. In detail, a matrix was produced by mixing for 120 min in a FRYMIX processing unit with an anchor stirrer at 70° C. under vacuum and consisting of:
For each of the three lots of 25-OH D3, an average of 8.4 kg of spray-dried powder with about 0.25% content of 25-OH D3 was obtained. The other components of the formulation are: 73.2% modified food starch, 17.6% sucrose, 4.0% sodium ascorbate, 3.0% medium chain triglycerides, 1.0% silicon dioxide, and 1.0% DL-α-tocopherol.
Spray-dried formulation of vitamin D3 was provided as a powder. In summary, vitamin D3 and DL-α-tocopherol were dissolved in an oil of medium chain triglycerides, then emulsified into an aqueous solution of modified starch, sucrose, and sodium ascorbate. The emulsion was atomized in a spray dryer in the presence of silicon dioxide. The resulting powder was collected when water content (LOD) was less than 4% and sieved to remove big lumps. It was stored in a dry area below 15° C. and used within 12 months of its manufacture.
Healthy, postmenopausal women (50 to 70 years of age) were recruited using informed consent and screened using the following criteria: serum 25-OH D3 between 20 nmol/L and 50 nmol/L, body mass index between 18 kg/m2 and 27 kg/m2, blood pressure less than 146/95 mm Hg, serum calcium less than 2.6 nmol/L, fasting glucose less than 100 mg/dl, no high-intensity exercise more than three times per week, no treatment for hypertension, no use of high-dose vitamin D or calcium supplement or drug affecting bone metabolism (e.g., biphosphonate, calcitonin, estrogen receptor modulator, hormone replacement therapy, parathyroid hormone), and not visiting a “sunny” location during the study.
Subjects were randomly assigned to one of seven treatment groups (i.e., daily, weekly, bolus as single dose, and bolus as combination dose). Each group included five subjects. They are followed for four months in Zurich, Switzerland during the winter.
The objective was studying and comparing the pharmacokinetic characteristics of vitamin D3 and 25-OH D3 administered to humans. Equimolar quantities of both substances were investigated. The regimen is based on 20 μg/day (or its equivalent on a weekly basis) of 25-OH D3. As the maximum pre-existing baseline concentration of 25-OH D3 will be 50 nmol/L, it is not anticipated that subjects will approach the range where disturbance in Ca2+ homeostasis has been observed. For comparative purposes, it is necessary to administer equimolar quantities of either vitamin D3 or 25-OH D3. In respect to administration of vitamin D3, the dose is considered to be sufficient to overcome background variability and provide and efficacious dose to the participants.
Hard gel capsules, which are packaged in bottles, contain either 20 μg or 140 μg of either spray-dried vitamin D3 or 25-OH D3 per capsule. Each dosage is consumed orally at breakfast. The duration of the study is four months for the “Daily” and “Weekly” groups. Subjects enrolled in the “Bolus” group consume orally a single dosage at the second study visit.
Plasma concentrations of 25-OH D3 (e.g., peak and steady state) are determined by obtaining samples from the subjects at various times after the dosage is ingested. For screening purposes and to establish baseline values, a blood sample is obtained prior to enrollment into the study and the clinical laboratory measures vitamin D3, 25-OH D3, calcium, creatinine, albumin, and fasting glucose in the serum. On Monday of Week 1 of the study, pharmacokinetics of serum vitamin D3, 25-OH D3, and 1,25-dihydroxy vitamin D3; serum markers (i.e., vitamin D3, 25-OH D3, calcium, creatinine, albumin, PTH, GOT, GPT, ALP, triglycerides, HDL, LDL, total cholesterol, bALP, and fasting glucose); and urine markers (i.e., calcium, creatinine, and DPD) are assessed over 24 hours. Daily samples for the remaining days of Week 1 and Monday of Week 2 are taken to assess serum vitamin D3 and 25-OH D3, serum markers (i.e., calcium, creatinine, albumin), and urine markers (i.e., calcium, creatinine). The assessments continue on Monday of Weeks 3, 5, 7, 9, 11, 13 and 15. On Monday of Week 16, samples are taken to assess pharmacokinetics of serum vitamin D3, 25-OH D3, and 1,25-dihydroxy vitamin D3; serum markers (i.e., vitamin D3, 25-OH D3, calcium, creatinine, albumin, PTH, GOT, GPT, ALP, triglycerides, HDL, LDL, total cholesterol, bALP, and fasting glucose); and urine markers (i.e., calcium, creatinine, and DPD).
Muscle strength and function were assessed by the following standard performance tests: knee flexor and extensor strength, repeated sit-to-stand test and timed up & go (TUG) in Week 1 on visit 2 (baseline) and at study end on visit 15. Muscle strength was measured as knee extensor and flexor in Newtons (kiloponds). TUG is a measure of functional mobility including muscle strength, gait speed, and balance and is assessed in seconds. The repeated sit-to-stand is a functional test and measured in seconds.
Table 1 shows the change in muscle strength after daily and weekly treatment with 25-OH D3 (20 μg per day; 140 μg per week, respectively) or daily and weekly treatment with Vitamin D3 (20 μg per day; 140 μg per week, respectively). Treatment duration was 4 months. Values are given as change after 4 months versus baseline (before start of treatment).
Table 2 shows the relative change in muscle strength after daily and weekly treatment with 25-OH D3 (20 μg per day; 140 μg per week, respectively) compared to daily and weekly treatment with Vitamin D3 (20 μg per day; 140 μg per week, respectively). Treatment duration was 4 months. Values are GLM (general linear model) least square means given as % improvement adjusted for baseline strength, age and body mass index for 25-OH D3 versus Vitamin D3.
Table 3 shows the change in muscle function after daily and weekly treatment with 25-OH D3 (20 μg per day; 140 μg per week, respectively) or daily and weekly treatment with Vitamin D3 (20 μg per day; 140 μg per week, respectively). Treatment duration was 4 months. Values are given as time (in seconds) needed to complete the task after 4 months versus baseline (before start of treatment).
Table 4 shows the relative change in muscle function after daily and weekly treatment with 25-OH D3 (20 μg per day; 140 μg per week, respectively) compared to daily and weekly treatment with Vitamin D3 (20 μg per day; 140 μg per week, respectively). Treatment duration was 4 months. Values are GLM (general linear model) least square means given as % time needed to complete the task adjusted for baseline function, age and body mass index for 25-OH D3 versus Vitamin D3.
These data demonstrate that daily or weekly treatment with 25-OH D3 surprisingly results in much stronger improvements of muscle strength and function compared to consumption of identical dosages of Vitamin D3. After treatment with 25-OH D3, subjects were able to perform stronger knee extension and flexion compared to before treatment and compared to treatment with Vitamin D3. The relative improvement of muscle strength in subjects treated with 25-OH D3 versus Vitamin D3 was between 3 to 18%, an effect size that is clinically relevant and represents a significant benefit for subjects in all age groups and especially for postmenopausal females.
Muscle function determined by standard performance tests (repeated sit-to-stand, timed-up-and-go) was better in subjects treated with 25-OH D3 compared to treatment with identical dosages of Vitamin D3. After treatment with 25-OH D3, subjects treated completed the performance tests faster compared to before treatment and compared to treatment with Vitamin D3. Relative improvements of muscle function after treatment with 25-OH D3 versus Vitamin D3 was between 8 to 14%, an effect size that is clinically relevant and represents a significant benefit for subjects in all age groups and especially for postmenopausal females.
Furthermore, an unadjusted analysis across the four lower extremity tests (knee extension, knee flexion, timed-up-and-go, and repeated-sit-to-stand) revealed that subjects treated with 25-OH D3 have a 2.8-fold higher likelihood of maintaining or improving lower extremity strength and function compared to subjects treated with identical dosages of Vitamin D3. This effect is statistically significant and clinically relevant and indicates that 25-OH D3 is suitable for treatments aimed at maintaining or improving skeletal muscle strength and function.
The objective of this study was to test the effects of Vitamin D3, 25-OH D3, and the combination of Vitamin D3 and 25-OH D3 in a skeletal muscle atrophy model using BalbC mice where tail suspension leads to skeletal muscle atrophy in the unloaded hindlimbs of the animals. Initially this model was established in rats for simulating spaceflight in humans and is commonly used in other scientific fields to study the loss of skeletal muscle mass or bone. The results are considered indicative of human conditions such as sarcopenia (degenerative loss of skeletal muscle mass and strength during the process of ageing) or immobilization of skeletal muscle (e.g. after prolonged bed rest due to fractures, surgery or trauma).
Methods For our study, nine month old BalbC female mice were randomized at the beginning of the study into four groups with 10 animals per group
The animals were placed in special cages for duration of seven days; all mice were housed separately and had free access to feed and water ad libidum. All animals were treated twice by gavage at the beginning of the experiment and 3 hours before the section:
At the end of the study the gastrocnemius muscle was taken out and directly frozen in liquid nitrogen for further analysis. To identify changes in gene expression and analyse shifts in mRNA levels in the gastrocnemius muscle we used Affymetrix Mouse 430-2 microarrays together with the version 27 (December 2008) annotation files from Affymetrix for this array type. The array contains “45,000 probe sets to analyze the expression level of more than 39,000 transcripts and variants from more than 34,000 well-characterized mouse genes and UniGene clusters” (Affymetrix, 2009).
Total RNA was isolated using the commonly used Trizol protocol. The RNA was quantified by using spectrophotometric analysis. The integrity of total RNA samples was also assessed qualitatively on an Agilent 2100 Bioanalyzer. RNA was then prepared for the one cycle cDNA synthesis. A poly-A RNA control is used for this step to provide exogenous positive controls to monitor the entire eukaryotic target labelling process. The first cDNA synthesis is done, and after the second strand cDNA synthesis the cDNA is cleaned up of double-stranded cDNA. A biotin labelled cRNA is then synthesised, cleaned up and quantified using a spectrophotometer at 260/280 nm. It is important that cRNA target is fragmented before hybridization onto a GeneChip probe arrays to obtain optimal assay sensitivity. After fragmentation the probes are hybridized on the chips (Affymetrix Mouse 430-2 chips). The chips are washed and stained in the fluidics station of Affymetrix and scanned in the gene chip scanner. The data is then transferred from the scanner for further analysis using software from Genedata (Expressionist 5.0: Refiner Array and Analyst). Data interpretation and pathway analysis was done with the online version of the GeneGo Metacore package (V5.2 build 17389).
Refiner Array evaluates microarray data for quality issues and flags problematic measurements. It provides a set of normalization algorithms and validated condensing methods to automatically pre-process and summarize raw microarray data for subsequent statistical analysis.
Analysis of microarray data revealed genes (mRNAs) which were differentially expressed between HU group and HU plus treatment groups (Vitamin D3, 25-OH D3 or combination).
Our key findings are
During one's life span, the skeletal muscles are permanently adapting to different stimuli, such as physical exercise and training, but also to immobilization. The skeletal muscle responds with either hypertrophy or atrophy. The development and adaptation of the skeletal muscle is a complex process. Briefly, satellite cells—the so called stem cells of the skeletal muscle—receive stimuli and form undifferentiated myoblasts which undergo fusion to form myotubes—new muscle fibers.
For the movements and the adaptation of the skeletal muscle, contraction is important. Skeletal muscle contraction is a mutual sliding of the two main skeletal muscle fibers myosin (thick filaments) and actin (thin filaments) which are organized in sarcomeres. They give skeletal muscles its cross striated appearance in the microscope.
Beside the thin and the thick filaments the skeletal muscle is composed of titin and nebulin and also sarcomeric proteins such as tropomyosin. Skeletal muscle function depends on a precise alignment of the actin and myosin filaments and the accessory proteins such as a-actinin, myomesin, M-protein, titin, desmin and myosin binding proteins.
It has been suggested that myomesin and M-protein may connect titin and myosin filament systems and that myomesin plays a role in integrating thick filaments into assembling sarcomeres. Titin, which is a huge protein, forms a continuous filament system in myofibrils. The predominant intermediate filament protein of striated muscle is desmin, and contributes to maintaining the integrity and alignment of myofibrils.
Mutations in several protein components (e.g. myosin heavy chain, actin, tropomyosin etc.) and also sarcomer proteins (e.g. titin, desmin etc.) are associated with muscle diseases/myopathies.
Tropomyosin 1, alpha (Tpm1):
As stated on WIKIPEDIA,
Tropomyosin 1 alpha is a gene which is required for development and muscle function (e.g. muscle contraction). In general the muscle-specific Tropomyosins regulate actin-myosin interactions and hence contraction. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. (NCBI)
Expression pattern (Tpm1):
Titin interacts with many sarcomeric proteins including:
Z line region: telethonin and alpha-actinin
I band region: calpain-3 and obscurin
M line region: myosin-binding protein C, calmodulin 1, CAPN3, and MURF1
The objective of this study was to test the effects of 25-OH D3 in a muscle hypertrophy model and in an endurance exercise capacity test in C57BL/6J mice. It is recognized in the art that removal of the gastrocnemius muscle induces compensatory hypertrophy in the soleus and plantaris muscles by multiple mechanisms leading to improved muscle strength and leg power.
Two groups of 10 animals were anesthetized and the left hindlimb of the animals was fixed. All animals received an analgesic. A small incision was made through the skin over the gastrocnemius muscle. The complete gastrocnemius muscle and the tendons were exposed. Both heads of the gastrocnemius muscle were carefully dissected from the underlying intact muscles and care was taken not to rupture nerves and vessels. The skin was closed with a silk suture and the animals were returned into the cages. After recovering from anesthesia the animals could move directly without problems in their cages. Animals were treated for three weeks by gavage with 25-OH D3 at a daily dosage of 50 μg/kg and the control group received vehicle. At the end of the study endurance exercise capacity of all animals was tested on a rodent treadmill.
The wet weight of the soleus and plantaris muscles were increased in animals treated with 25-OH D3 compared to control animals (Table 8). Furthermore, when muscle weights were normalized to the body weights of in mice compared to the body weight, animals treated with 25-OH D3 demonstrated an increased soleus-plantaris muscle weight/body weight ratio (Table 8). Computer tomography measurements of muscle and total leg area confirmed that 25-OH D3 treatment increases skeletal mass (Table 8). Animals receiving 25-OH D3 displayed increased endurance exercise capacity compared to control mice demonstrated by longer running distance and time (Table 8).
Table 8 shows muscle weights, muscle weight/body weight ratios, total leg and muscle cross-sectional areas, running distance and running time of mice treated with 25-OH D3 at a dosage of 50 μg/kg/day or placebo (control) for 3 weeks.
This application is a divisional of commonly owned U.S. application Ser. No. 12/867,305 filed on Nov. 2, 2010, which in turn is the national phase under application 35 USC §371 of PCT/EP2009/051641, filed Feb. 12, 2009 which designated the US and claims priority benefits from U.S. Provisional Application Ser. Nos. 61/028,510 filed Feb. 13, 2008, 61/031,671 filed Feb. 26, 2008, 61/036,924 filed Mar. 14, 2008, 61/036,928 filed Mar. 15, 2008 and 61/129,139 filed Jun. 6, 2008, the entire contents of each of which are hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61028510 | Feb 2008 | US | |
| 61031671 | Feb 2008 | US | |
| 61036924 | Mar 2008 | US | |
| 61036928 | Mar 2008 | US | |
| 61129139 | Jun 2008 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12867305 | Nov 2010 | US |
| Child | 13467414 | US |
