Patent Application
20230381275
This invention relates to an agent for improving muscle function of skeletal muscles that have deteriorated due to aging.
Among sarcopenia, which is the aging of skeletal muscle, treatment for primary sarcopenia mainly caused by aging primarily consists of nutritional therapy such as protein and amino acid intake and exercise therapy (rehabilitation) to prevent muscle weakness, and no effective therapeutic agents have been discovered. Cell migration and cell differentiation originating from the activity of muscle satellite cells, which are progenitor cells, are essential for skeletal muscle regeneration, but it has been reported that in sarcopenia, the cell number of muscle satellite cells decreases with age and the proliferative function of muscle satellite cells declines (Non-Patent Document 1). However, the mechanism and cause of sarcopenia have not yet been clarified. The number of patients with sarcopenia is increasing year by year, and the development of a therapeutic agent that is effective in inhibiting the progression of the disease will lead to improvements in ADL and QOL and will also contribute to the reduction of financial resources of social security and the “extension of healthy life expectancy,” an important national policy, and will have a significant economic impact.
The usefulness of cell therapy, growth factor therapy, and gene therapy using microRNA (miRNA) has been reported as conventional technologies effective for skeletal muscle regeneration (Non-Patent Documents 2-4). However, due to problems such as spontaneous malignant transformation of stem cells, limited administration methods, instability of effective concentration in vivo, immune response, off-target effects of therapeutic miRNA, and high cost in manufacturing and quality control, these technologies have not yet been applied clinically.
The inventors have already shown that a peptide (hereinafter referred to as “SV peptide”) consisting of 7 amino acids (SVVYGLR; SEQ No.1) present in osteopontin (OPN), a type of extracellular matrix, has multiple functions such as promoting angiogenesis, type III collagen secretion, and differentiation of fibroblasts to myofibroblasts (Non-Patent Documents 5, 6, and Patent Documents 1-4). SV peptides have a low molecular weight and low antigenicity, and are safer in biological applications than conventional techniques. Local administration of SV peptide in animal models of injured skeletal muscle promotes muscle tissue regeneration, and morphologically, the diameter of regenerated muscle fibers was significantly higher, proving that SV peptide is a potent substance for the regeneration of skeletal muscle function (Non-Patent Document 7 and Patent Document 5).
[Patent Document 1] WO 2003/030925
[Patent Document 2] WO 2008/026634
[Patent Document 3] WO 2012/172887
[Patent Document 4] WO 2016/084935
[Patent Document 5] WO 2018/230535
[Non-Patent Document 1] Machida, S. and Booth, F W. (2004). “Regrowth of skeletal muscle atrophied from inactivity,” Med Sci Sports Exerc., Jan; 36(1):52-9.
[Non-Patent Document 2] Miyagawa, S. and Sawa, Y. (2018). “Building a new strategy for treating heart failure using Induced Pluripotent Stem Cells” J Cardiol., Dec; 72(6):445-448.
[Non-Patent Document 3] Baoge, L. et al. (2012). “Treatment of Skeletal Muscle Injury: A Review” ISRN Orthop. 689012.
[Non-Patent Document 4] Nakasa, T. et al., (2010). “Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model” J Cell Mol Med., Oct; 14(10):2495-505.
[Non-Patent Document 5] Hamada, Y. (2003). “Angiogenic activity of osteopontin-derived peptide SVVYGLR” Biochem Biophys Res Commun. Oct 10; 310(1):153-7.
[Non-Patent Document 6] Hamada, Y. (2007). “Synthetic osteopontin-derived peptide SVVYGLR can induce neovascularization in artificial bone marrow scaffold biomaterials” Dent Mater J. Jul; 26(4):487-92.
[Non-Patent Document 7] Tanaka, S. (2019) “Osteopontin-derived synthetic peptide SVVYGLR has potent utility in the functional regeneration of oral and maxillofacial skeletal muscles” Peptides. Jun; 116:8-15.
The present invention is to provide a muscle function improving agent that inhibits or improves muscle dysfunction due to aging.
Skeletal muscle is considered to be a highly regenerative tissue by nature, but its regenerative capacity declines with age. One of the causes of sarcopenia is thought to be the inability of muscle regeneration to fully compensate for muscle damage due to injury or other causes.
Activation of muscle satellite cells by muscle injury causes cell proliferation and differentiation into myoblasts. Originally, muscle satellite cells are multipotent, and their activation and expression of the MyoD gene determine their differentiation into myoblasts. Myoblasts proliferate to ensure the number of cells required for muscle regeneration. At the same time, the expression of a downstream gene, Myogenin gene, is induced, which is involved in the differentiation and maintenance of myoblasts into myotubular cells, and then mature muscle cells form. Myoblasts undergo cell fusion with myofibers to promote the regeneration of muscle tissue. Here, some myoblasts reenter the quiescent phase of the cell cycle and revert to muscle satellite cells, which is thought to regulate the number of muscle satellite cells intrinsic to skeletal muscle.
However, muscle satellite cells are thought to decrease cell number and self-renewal capacity due to endogenous changes in the cells with aging and exogenous changes such as a decrease in growth factors. This decreased regenerative muscle capacity is thought to be one of the factors in the development of sarcopenia.
The inventors have confirmed that local injection of SV peptide into the muscles of the lower limbs of aging-accelerated model mice can inhibit or improve the decline in muscle function associated with aging. The present invention was completed based on this finding and includes the following aspects:
One aspect of this invention relates to
[1] a muscle function-improving agent for inhibiting or improving functional decline of skeletal muscles due to aging, comprising the peptide selected from the following (1) to (3) or a salt thereof as an active ingredient:
In one embodiment, the muscle function-improving agent of the present invention is characterized by the following:
[2] the muscle function-improving agent according to [1] above,
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6-X7 (I)
(In the formula, X1, X2, X5, X6, and X7 represent any amino acid residue, identically or differently)
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6 (II)
(In the formula, X1, X2, X5, and X6 represent any amino acid residue, identically or differently)
X2-Val-(Tyr/Phe/Trp)-X5-X6-X7 (III)
(In the formula, X2, X5, X6, and X7 represent any amino acid residue, identically or differently)
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6-X7-X8 (IV)
(In the formula, X1, X2, X5, X6, X7, and X8 represent any amino acid residue, identically or differently).
Another aspect of the invention relates to
[3] a muscle atrophy inhibitor for inhibiting or improving muscle atrophy of fast muscle fibers and/or slow muscle fibers due to aging, comprising at least one peptide selected from the following (1) to (3) or a salt thereof as an active ingredient:
In one embodiment, the muscle atrophy inhibitor of the present invention is characterized by the following:
[4] the muscle atrophy inhibitor according to [3] above,
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6-X7 (I)
(In the formula, X1, X2, X5, X6, and X7 represent any amino acid residue, identically or differently)
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6 (II)
(In the formula, X1, X2, X5, and X6 represent any amino acid residue, identically or differently)
X2-Val-(Tyr/Phe/Trp)-X5-X6-X7 (III)
(In the formula, X2, X5, X6, and X7 represent any amino acid residue, identically or differently)
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6-X7-X8 (IV)
(In the formula, X1, X2, X5, X6, X7, and X8 represent any amino acid residue, identically or differently).
In one embodiment, the muscle function-improving agent of the present invention is characterized by the following:
[5] the muscle function-improving agent according to [1] or [2] above, wherein the agent is for use in conjunction with the loading of stimuli on the skeletal muscle.
In one embodiment, the muscle function-improving agent of the present invention is characterized by the following:
[6] the muscle function-improving agent according to [5] above, wherein the agent is for preventing or improving the functional decline of the skeletal muscle due to sarcopenia or inclusion body myositis
In one embodiment, the muscle function-improving agent of the present invention is characterized by the following:
[7] the muscle function-improving agent according to [6] above, wherein the loading of the stimulus to the skeletal muscles is exercise therapy.
In one embodiment, the muscle function-improving agent of the present invention is characterized by the following:
[8] a muscle-function improving agent for inhibiting or improving the functional decline of the skeletal muscle, wherein the muscle-function improving agent is for use in conjunction with the loading of stimuli and comprise at least one peptide selected from the following (1) to (3) or a salt thereof as an active ingredient:
According to the muscle function-improving agent of the present invention, it can improve the decline function of a skeletal muscle due to aging.
The present invention, in an aspect, provides a muscle function-improving agent for inhibiting or improving the functional decline of a skeletal muscle due to aging,
The term “functional decline of a skeletal muscle due to aging” refers to a decrease in skeletal muscle function resulting from a decline in physiological function. For example, it means a state in which the function to contract or relax muscle fibers declines along with a decrease in skeletal muscle mass caused by a decrease in the regenerative capacity of cells (myocytes, myoblasts, or myocytes) constituting skeletal muscle due to aging. As long as the “functional decline of skeletal muscle due to aging” is caused by a decline in physiological function, it also includes a state in which the skeletal muscle function has declined due to causes other than aging, such as genetic factors, inactivity, diseases such as organ failure, and nutritional status.
The amino acid sequence of human osteopontin includes, but is not limited to, the amino acid sequence shown in SEQ No.: 11. Human osteopontin contains the amino acid sequence shown in SEQ No.: 1 (SVVYGLR), and thrombin cleaves human osteopontin just after SVVYGLR in the amino acid sequence shown in sequence number 11, resulting in a fragment having the sequence of SVVYGLR at the C-terminal end. A “fragment of human osteopontin” herein refers to such a fragment (SEQ No.: 12) or a portion thereof, having the sequence of SVVYGLR at the C-terminus. Proteins having the same structure and function as human osteopontin can be referred to as human osteopontin and their amino acid sequence is the amino acid sequence of human osteopontin.
The length of the fragment of human osteopontin is not particularly limited, but it is preferred that the total number of amino acid residues be about 170 or less, more preferably about 150 or less, and even more preferably about 100 or less. Furthermore, from the viewpoint of simplicity of handling, manufacturing efficiency, and side effects such as antigenicity, it is preferred that the total number of amino acid residues be about 50 or less, about 30 or less is more preferred, about 20 or less is even more preferred, and about 10 or less is especially preferred.
In this specification, “amino acid sequence that one to several amino acids are deleted, substituted, or added” means an amino acid sequence in which a sufficient number (preferably 10 or less, more preferably 7 or less, more preferably 5, 4, 3, 2, or 1) of amino acids are deleted, substituted (preferably conservative substitution), or added by known methods of producing mutant peptides, such as site-directed mutagenesis. An “amino acid sequence that is at least 80% identical” includes an amino acid sequence that is at least 85%, 90%, 92%, 95%, 96%, 97%, 98% or 99% identical.
Amino acids that are functionally similar to a particular amino acid as a conservative substitution are well known in the art. Examples of properties of amino acid side chains are hydrophobic amino acids (A, I, L, M, F, P, W, Y, V), hydrophilic amino acids (R, D, N, C, E, Q, G, H, K, S, T), and side chains having the following common functional groups or features: aliphatic side chains (G, A, V, L, I, P); hydroxyl group containing side chains (S, T Y); sulfur atom-containing side chains (C, M); carboxylic acid and amide-containing side chains (D, N, E, Q); base-containing side chains (R, K, H); and aromatic-containing side chains (H, F, Y, W). The following eight groups also contain amino acids that are each mutually conservative substitutions: 1) alanine (A), glycine (G); 2) aspartic acid (D), glutamic acid (E); 3) asparagine (N), glutamine (Q); 4) arginine (R), lysine (K); 5) isoleucine (I), leucine (L), methionine (M), valine (V); 6) phenylalanine (F), tyrosine (Y), tryptophan (W); 7) serine (S), threonine (T); and 8) cysteine (C), methionine (M) (see for example Creighton, Proteins 1984).
In one embodiment, a peptide consisting of the amino acid sequence of any of the following (I) to (IV) can be listed as a peptide consisting of an amino acid sequence in which one to several amino acids are substituted, added, or deleted in the amino acid sequence of a peptide consisting of the amino acid sequence shown in SEQ ID No.: 1 and having an effect of inhibiting or improving the functional decline of skeletal muscle due to aging:
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6-X7 (I)
(In the formula, X1, X2, X5, X6, and X7 represent any amino acid residue, identically or differently)
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6 (II)
(In the formula, X1, X2, X5, and X6 represent any amino acid residue, identically or differently)
X2-Val-(Tyr/Phe/Trp)-X5-X6-X7 (III)
(In the formula, X2, X5, X6, and X7 represent any amino acid residue, identically or differently)
X1-X2-Val-(Tyr/Phe/Trp)-X5-X6-X7-X8 (IV)
(In the formula, X1, X2, X5, X6, X7, and X8 represent any amino acid residue, identically or differently).
In the preferred embodiment, Xi in the amino acid sequence of any of (I) to (IV) above is serine or a conservatively substituted amino acid thereof, X2 and X3 are valine or a conservatively substituted amino acid thereof, X5 is glycine or a conservatively substituted amino acid thereof, X6 is leucine or a conservatively substituted amino acid thereof, or X7 is arginine or a conservatively substituted amino acid thereof.
A peptide consisting of any of the amino acid sequences (I) to (IV) above may also have several more amino acids at its N-terminus or C-terminus, as long as it acts to inhibit or improve the functional decline of skeletal muscle due to aging.
In another embodiment, a peptide consisting of the amino acids shown in (V) below can be listed as a peptide comprising one to several amino acid substitutions, additions, or deletions in the amino acid sequence of the peptide consisting of the amino acid sequence shown in SEQ ID NO.: 1 and having the effect of inhibiting or improving the functional decline of skeletal muscle due to aging:
X1-Val-Val-(Tyr/Phe/Trp)-X5X6-X7 (V)
In another embodiment, peptides consisting of the amino acids shown in SEQ ID NOs.: 2-10 below can be listed as a peptide comprising one to several amino acid substitutions, additions, or deletions in the amino acid sequence of the peptide consisting of the amino acid sequence shown in SEQ ID NO.: 1 and having the effect of inhibiting or improving the functional decline of skeletal muscle due to aging.
The inventors have confirmed that the angiogenic effect of SVVYGLR (SEQ ID NO.: 1) is maintained in the peptide in which R at the C-terminal of SVVYGLR (SEQ ID NO.: 1) is deleted (SEQ ID NO.: 4), the peptide in which S at the N-terminal is deleted (SEQ ID NO.: 5), and the peptide in which an amino acid is added to the C terminus of SVVYGLR (SEQ ID NO.: 10). The inventors have also confirmed that the angiogenic effect of SVVYGLR (SEQ ID NO.: 1) is maintained in the peptides in which each amino acid other than the fourth tyrosine (Y) in SEQ ID No.: 1 is replaced by an alanine (e.g., SEQ ID Nos.: 2, 3, and 4). The inventors have also confirmed that a fragment of osteopontin having SVVYGLR (SEQ ID No.: 1) at the C-terminus has an effect equivalent to type III collagen production-promoting effect of SVVYGLR (SEQ ID No.: 1) on fibroblasts (see Patent Document 1). It is reasonably analogous that all of the above peptides (1) to (3) have muscle function-improving agent effects.
In one embodiment, a fragment of human osteopontin, comprising one to several amino acid substitutions, additions, or deletions in the amino acid sequence of the peptide whose C-terminal amino acid sequence is the amino acid sequence shown in SEQ ID No.: 1, and having the effect of inhibiting or improving the functional decline of skeletal muscle due to aging include fragments of human osteopontin in which one to several amino acids are substituted, added, or deleted in the C-terminal portion of the amino acid sequence, in the amino acid sequence portion other than the C-terminal portion, or in both thereof amino acid sequence portions.
Amino acids constituting the peptide used as the active ingredient of the muscle function-improving agent of the present invention may have their side chains modified by any substituent. The substituent is not limited but includes, for example, a fluorine atom, a chlorine atom, a cyano group, a hydroxyl group, a nitro group, an alkyl group, a cycloalkyl group, an alkoxy group, and an amino group. Preferably, the benzene ring of tryptophan or phenylalanine is modified by a substituent.
The peptide used as the active ingredient of the muscle function-improving agent of the present invention may have a carboxyl group (—COOH), a carboxylate (—COO—), an amide (—CONH2) or an ester (—COOR) at the C-terminus. Examples of the R moiety in the ester include C1-6 alkyl groups such as methyl, ethyl, n-propyl, isopropyl, and n-butyl; C3-8 cycloalkyl groups such as cyclopentyl and cyclohexyl; C6-12 aryl groups such as phenyl and α-naphthyl; and C7-14 aralkyl groups such as phenyl-C1-2 alkyl groups including benzyl and phenethyl, and α-naphthyl-C1-2 alkyl groups including α-naphthylmethyl. Also included is a pivaloyloxymethyl group, which is widely used in an ester for oral use. Examples of the amide moiety include amides; amides substituted with one or two C1-6 alkyl groups; amides substituted with one or two C1-6 alkyl groups substituted with a phenyl group; and amides in which a 5- to 7-membered azacyclo alkane containing the nitrogen atom of the amide group is formed. When the peptide of the present invention has a carboxyl group or a carboxylate group at a site other than the C-terminus, these groups may be amidated or esterified. Such modified peptides are encompassed in the scope of the peptide of the present invention.
In the peptide used as the active ingredient of the muscle function-improving agent of the present invention, the N-terminal amino group may be protected by a protecting group (e.g., C1-6 acyl groups including a formyl group and a C2-6 alkanoyl group such as acetyl, etc.). In said peptide, the substituent in the side chain of an intramolecular amino acid may be protected by an appropriate protecting group (e.g., C1-6 acyl groups including a formyl group, and a C2-6 alkanoyl group such as acetyl, etc.). Such modified peptides are encompassed in the scope of the peptide of the present invention.
The peptide used as the active ingredient of the muscle function-improving agent of the present invention may be in the form of a salt, and the salt is preferably a pharmaceutically acceptable salt. Examples of the pharmaceutically acceptable salt include salts with acids such as hydrochloric acid, sulfuric acid, phosphoric acid, lactic acid, tartaric acid, maleic acid, fumaric acid, oxalic acid, malic acid, citric acid, oleic acid, palmitic acid, etc.; salts with alkali metals such as sodium and potassium, salts with alkaline earth metals such as calcium, and salts with aluminum hydroxide or carbonate; and salts with triethylamine, benzylamine, diethanolamine, t-butylamine, dicyclohexylamine, arginine, etc.
The peptide used as the active ingredient of the muscle function-improving agent of the present invention or a salt thereof can be produced by a solid phase synthesis method (e.g., the Fmoc method and the Boc method) or a liquid phase synthesis method according to a known ordinary peptide synthesis protocol. Alternatively, a transformant with an expression vector containing a DNA encoding the peptide can be used to produce the peptide. Also, the peptide can be produced by in vitro coupled transcription-translation system.
Subjects of aging skeletal muscles that can be functionally improved by the muscle function-improving agent of the present invention include, for example, skeletal muscles that have developed sarcopenia and/or age-related muscle atrophy or degeneration, skeletal muscles that have developed inclusion body myositis, and muscle atrophy promoted by postoperative bed-ridden conditions such as hip fracture surgery.
Sarcopenia is defined as a decrease in skeletal muscle mass and a decrease in muscle strength or physical function due to aging and other factors. There are several reports on the criteria for determining sarcopenia, which is summarized, for example, in the 2017 edition of the Guidelines for the Treatment of Sarcopenia (published by the Japanese Association on Sarcopenia and Frailty, National Center for Geriatrics and Gerontology). Sarcopenia is classified into primary sarcopenia associated with aging and secondary sarcopenia associated with causes other than aging (including sarcopenia associated with activity such as inactivity; sarcopenia associated with diseases such as organ failure, inflammatory diseases, malignancy, and endocrine disorders; sarcopenia associated with nutrition such as malnutrition). The muscle function-improving agent can be used to treat both primary sarcopenia and secondary sarcopenia.
Examples of skeletal muscle atrophy include, but are not limited to, lower limb muscle atrophy, lower limb muscle disuse atrophy, muscle atrophy, scapulohumeral atrophy, limb muscle atrophy, upper limb muscle atrophy, generalized muscle atrophy, trapezius muscle partial muscle atrophy, degenerative muscle atrophy, disuse syndrome, disuse muscle atrophy, and thenar muscle atrophy.
The muscle function-improving agent of the present invention can be implemented as a pharmaceutical, cosmetic, or food product for improving the function of skeletal muscles that have deteriorated due to aging. In other words, as other aspects of this invention, pharmaceutical compositions, cosmetics, and food and beverage compositions containing the muscle function-improving agent of the present invention can be provided. When implemented as a pharmaceutical or cosmetic product, the present muscle function-improving agent can be formulated by blending a pharmaceutically acceptable carrier or additive agent as appropriate. Specific examples of the dosage form include oral preparations such as tablets, coated tablets, pills, powders, granules, capsules, solutions, suspensions, and emulsions; and parenteral preparations such as injections, microneedle, infusions, suppositories, ointments, and patches. The amount of the carrier or the additive to be used is determined as appropriate based on the range of amount conventionally used in the pharmaceutical field. The carrier or the additive that can be used is not particularly limited, and examples include various carriers such as water, physiological saline, other aqueous solvents, and aqueous or oily bases; and various additives such as excipients, binders, pH adjusters, disintegrants, absorption enhancers, lubricants, colorants, corrigents, and fragrances. When implemented as a food and beverage composition, it can be prepared by appropriately blending with carriers and additives normally used in the food and beverage field.
Examples of the additive that can be blended into tablets, capsules, and the like include binders such as gelatin, cornstarch, tragacanth, and gum arabic; fillers such as crystalline cellulose; bulking agents such as cornstarch, gelatin, and alginic acid; lubricants such as magnesium stearate; sweeteners such as sucrose, lactose, and saccharin; and flavors such as peppermint, Gaultheria adenothrix oil, and cherry. In the case where the unit dosage form is a capsule, a liquid carrier such as fats and oils can be further contained in addition to the above-mentioned ingredients. A sterile composition for injection can be prepared according to the usual pharmaceutical formulation practice, for example, by dissolving or suspending an active substance in a vehicle such as water for injection and a natural vegetable oil such as sesame oil and coconut oil. As an aqueous liquid for injection, for example, physiological saline, an isotonic solution containing glucose and an auxiliary substance (e.g., D-sorbitol, D-mannitol, sodium chloride, etc.), or the like can be used, optionally together with a suitable solubilizer such as alcohols (e.g., ethanol etc.), polyalcohols (e.g., propylene glycol, polyethylene glycol, etc.), and nonionic surfactants (e.g., polysorbate 80™, HCO-50, etc.). As an oily liquid, for example, sesame oil, soybean oil, or the like can be used, optionally together with a solubilizer such as benzyl benzoate and benzyl alcohol. Further, a buffering agent (e.g., phosphate buffer, sodium acetate buffer, etc.), a soothing agent (e.g., benzalkonium chloride, procaine hydrochloride, etc.), a stabilizer (e.g., human serum albumin, polyethylene glycol, etc.), a preservative (e.g., benzyl alcohol, phenol, etc.), an antioxidant, and/or the like may also be added.
The muscle function-improving agent may be implemented as an injection or microneedle for direct administration to the target skeletal muscle or surrounding muscle (skeletal muscle), or as an ointment or patch for application or affixing to the skeletal muscle or surrounding muscle. Microneedle technology is a transdermal formulation in patch form that contains the drug at the tip of a microscopic needle and is applied to the skin to administer the drug to the body. The muscle function-improving agent can be used in combination with known microneedle technology. When provided as an ointment or patch formulation for application or affixing to the skin, it can also be used in combination with known transdermal absorption enhancers or methods for enhancing transdermal absorption (such as transdermal absorption formulations using microemulsion gel or bioabsorbable gel). The muscle function-improving agent may also be in a form in which the active ingredient, peptide, is bound to a carrier. The carrier is not particularly limited, and examples include resins for use in artificial organs etc., and biopolymers such as proteins. In a particularly preferable embodiment, the agent of the present invention is in the form of a bioabsorbable gel entrapping the active ingredient peptide.
Known bioabsorbable hydrogels are preferably used as the bioabsorbable gel. Specific examples include “MedGEL (trade name)”, a hydrogel for sustained-release manufactured by MedGEL Corporation. This product is a water-insoluble material formed by cross-linking of gelatin and can entrap a peptide via intermolecular interaction including electrostatic interaction between the peptide and the gelatin. When the active ingredient peptide is entrapped in such a gelatin hydrogel and applied to a living body, the gelatin hydrogel is degraded by degrading enzymes such as collagenase secreted from cells. Upon hydrogel degradation, the peptide is gradually released, and the degradation product is absorbed into the living body. The shape of the bioabsorbable gel is not particularly limited, and various shapes may be employed such as a sheet, a disk, a tube, and a particle. The bioabsorbable gel can be applied or affixed to the site of skeletal muscle injury.
The peptide used as the active ingredient of the muscle function-improving agent of the present invention or a salt thereof is safe and less toxic, and therefore can be administered to, for example, humans and other mammals (rats, mice, rabbits, sheep, pigs, cows, cats, dogs, monkeys, etc.).
The dosage varies depending on the site of dysfunction, route of administration, etc. For example, when injected intramuscularly around dysfunctional skeletal muscles in adults, the daily dosage of the active ingredient may be from about 0.00001 to 100 mg, from about to 90 mg, from about 0.00005 to 80 mg, from about 0.0001 to 50 mg, from about to 30 mg, from about 0.1 to 20 mg, or from about 0.1 to 10 mg.
The muscle function-improving agent can be administered, for example, daily (once per day, twice per day, three times per day, four times per day, five times per day, six times per day), every two days, every three days, every four days, every five days, every six days, weekly, twice per week, every other week, every three weeks, once per four weeks, monthly, every two months, once every three months, once every four months, once every five months or once every six months.
In one embodiment, the muscle function-improving agent of the present invention can be provided as a muscle function-improving agent for use in combination with a stimulus load to a skeletal muscle functionally declined.
When used in combination with a stimulus load to skeletal muscles, the muscle function-improving agent of the present invention can suppress the functional decline of skeletal muscles more than when the muscle function-improving agent is used alone or when a stimulus load to skeletal muscles is applied alone. In a preferred embodiment, the muscle function-improving agent of the present invention can have an excellent muscle function-improving effect that cannot be obtained when the muscle function-improving agent is used alone or when the stimulation load to skeletal muscles is applied alone.
“Stimulus loading to skeletal muscles” is not limited as long as it is a stimulus loading that elicits muscle contraction and/or relaxation of skeletal muscles. Known stimulus-loading methods can be employed as stimulus loading to skeletal muscles. These include, but are not limited to, stimulus loading by exercise therapy, etc., loading by physiological muscle stimulation methods (e.g., electrical stimulation methods (neuromuscular electrical stimulation: NMES) (Jpn J Rehabil Med 2017; 54:764-767), stimulus loading by vibration (see, for example, U.S. Pat. No. 6,886,559), etc.)
The “exercise load to skeletal muscles with functional decline” is not limited as long as it can suppress or improve the functional decline of skeletal muscles when used in combination with the muscle function-improving agent of the present invention, and is not limited to the following, for example, when targeting patients suffering from sarcopenia, known exercise therapies used for the treatment of sarcopenia can be employed. The preferred exercise loading method can be set as appropriate depending on the age and health status of the subject, the targeted skeletal muscle, and the amount of skeletal muscle.
Specific examples of exercise loading methods include squatting, knee extension, knee raising, etc. for the quadriceps muscle, one-leg standing exercise, etc. for the gluteus medius muscle, and heel raising exercise, etc. for the gastrocnemius muscle. The above are only examples, and those skilled in the art can adopt an appropriate exercise load method and set the number of times and number of sets according to the target skeletal muscles.
The “physiological muscle stimulation to skeletal muscles” and “vibration stimulation to skeletal muscles” are not limited as long as they can suppress or improve the functional decline of skeletal muscles when used in combination with the muscle function-improving agent of the present invention, and known stimulation means and methods normally used in clinical practice can be employed. A person skilled in the art can set the preferred stimulation load method according to the age and health condition of the subject, the target skeletal muscle, and the amount of skeletal muscle.
The “loading of stimuli to the skeletal muscles with functional decline” may be performed before administration (e.g., 30 minutes before administration, 1 hour before administration, 2 hours before administration, 6 hours before administration, 12 hours before administration, 1 day before administration, etc.), during administration, or after administration (e.g., 30 minutes after administration, 1 hour after administration, 2 hours after administration, 6 hours after administration, 12 hours after administration, 1 day after administration, etc.) of the muscle function-improving agent, as long as the functional decline of skeletal muscle due to aging is suppressed or improved. In the preferable embodiment, the muscle function-improving agent of the present invention can be administered after or simultaneously with stimulus loading to skeletal muscle.
In another aspect, the present invention can be provided as a muscle function-improving agent for suppressing or improving the functional decline of skeletal muscles or for repairing muscle damage of skeletal muscles. In this aspect, the muscle function-improving agent is used in combination with the loading of stimuli to skeletal muscles and contains at least one peptide selected from the following (1) to (3) or a salt thereof as an active ingredient:
In this aspect, the muscle function-improving agent is used in combination with stimulus loading on skeletal muscles to repair skeletal muscle damage, such as muscle tears, muscle atrophy, and muscle degeneration, or to improve skeletal muscle function that is reduced due to such damage, in addition to skeletal muscle with the functional decline due to aging. Skeletal muscle injuries include, for example, muscle tears, muscle atrophy, and muscle degeneration. Specifically, muscle tears associated with major trauma, muscle tears associated with surgery, muscle tears associated with trauma such as fractures, contusions, and separated muscles, muscle injuries in athletes, muscle tears or muscle atrophy after ligament surgery, muscle tears or muscle atrophy after hip replacement surgery, disuse muscle atrophy due to reduced exercise units after head and neck surgery requiring long-term closed mouth conditions, muscle atrophy associated with cancer cachexia, progressive muscle atrophy in inherited neuromuscular diseases such as muscular dystrophy, muscle atrophy associated with erector spinae disorders, muscle atrophy associated with lumbar disc herniation, muscle atrophy associated with dropped head syndrome, inclusion body myositis, fibrosis and scar contracture after surgery involving extensive myectomy, and scar contracture with motor dysfunction after plastic surgery for congenital abnormal muscle morphology such as cleft palate. Scar contractures with motor dysfunction after plastic surgery for congenital muscle morphology abnormalities such as cleft palate, etc. are examples. For example, the muscle function-improving agent can be used in conjunction with exercise loading, such as post-surgical rehabilitation.
The present invention comprises, in another aspect, a muscle fiber hypertrophy-stimulating agent for hypertrophy of fast and/or slow muscle fibers that have atrophied due to aging, comprising at least one peptide selected from the following (1) to (3), or a salt thereof, as an active ingredient:
In another aspect, the present invention provides a muscle regenerative ability-improving agent for improving the decline of muscle regenerative ability of skeletal muscles due to aging, comprising at least one peptide selected from (1) through (3) above or a salt thereof.
The muscle fiber hypertrophy-stimulating agent and the muscle regenerative ability-improving agent of the present invention can be implemented in the same manner as the above-mentioned muscle function-improving agent of the present invention.
The present invention further comprises the following inventions.
In this example, a peptide consisting of the amino acid sequence of SVVYGLR (SEQ ID No.: 1) (SV peptide) was administered to aging-accelerated model mice, and their effects on restoring muscle function were confirmed.
SV peptide was synthesized by the Fmoc method using a multi-species solid-phase automated peptide synthesizer (PSSM-8; Shimadzu Corp.) SV peptide was added to PBS and adjusted to 20 ng/ml to prepare an injection formulation.
Aging-accelerated model mice (SAMP10 21 weeks old) were used to perform training on a treadmill (MK-680; Muromachi Kikai Co., Ltd.) and subsequent SV peptide administration according to the schedule in the following table.
exercise 17 m/min (35 minutes)
cool down 7 m/min
exercise 18 m/min (35 minutes)
cool dowa 10 m/min (5 degree angle)
exercise 18 m/min (35 minutes)
cool down 10 m/min (5 degree angle)
exercise 18 m/min (36 minutes)
cool down 10 m/min (5 degree angle)
exercise 18 m/min (90 minutes)
cool down 10 m/min (5 degree angle)
exercise 18 m/min (35 minutes)
cool down 10 m/min (5 degree angle)
exercise 20 m/min (90 minutes)
cool down 10 m/min (5 minutes)
indicates data missing or illegible when filed
At 30-35 weeks of age, mice underwent the first basic training session and the second to fourth training sessions at 12, 24, and 72 h after the first training session.
Once a week, the mice were tested on a treadmill to measure the number of collisions. After SV peptide injection, the mice have trained on the treadmill again (18 m/min×90 min), and the number of times the mice collided with the treadmill wall due to being unable to run at a speed equal to or faster than that of the belt was measured during treadmill training. Treadmill running, peptide injection, and weekly collision measurements were continued until the mice reached 35 weeks of age. In the control group, after training on the treadmill in the same manner as the experimental group, PBS was injected into the bilateral lower limb muscles instead of SV peptide, and the number of collisions was measured once a week.
As a result, although the number of collisions showed an increasing trend over time in the control group after 30 weeks of age, the experimental group showed significant suppression of the increase in the number of collisions compared to the control group (
In this example, SV peptide was administered to aging-accelerated model mice, and the recovery effect of muscle function after a certain period of time by the administration was confirmed.
Treadmill running was performed using aging-accelerated model mice (SAMP10 36 weeks old) under the same conditions as the first basic training of 35-week-old mice in Example 1, and SV peptide (total 40 ng) was injected into the bilateral lower limb muscles immediately after treadmill running (experimental group).
SV peptide was administered at the same site and dose as in the 35-week-old mice of Example 1. The number of collisions was evaluated by retesting treadmill running (18 m/min×90 min) at 12, 24, or 72 hours after local injection. In the control group, after treadmill running as in the experimental group, PBS was injected into the bilateral leg muscles instead of SV peptide, and the number of collisions on the treadmill was measured 12, 24, or 72 hours after the injection.
As a result, the number of collisions in the experimental group was significantly reduced at 12, 24, and 72 hours after localization compared to the control group. This result suggests that SV peptide administration promoted the recovery of muscle function after exercise (
In this example, we evaluated muscle fibers in aging-accelerated model mice after continuous administration of SV peptide.
Aging-accelerated model mice (SAMP10 21 weeks old) were trained on a treadmill (MK-680; Muromachi Kikai Co., Ltd.) (18 m/min×90 min) and subsequent SV peptide administration was performed according to the same schedule as in Example 1. After 36 weeks of age, training on the treadmill and subsequent SV peptide administration were conducted under the same conditions as at 35 weeks of age, and continued until the aging-accelerated model mice reached 40 weeks of age. In the control group, after training under the same conditions as the experimental group, PBS was injected into the bilateral lower limb muscles instead of SV peptide.
The gastrocnemius and soleus muscles of the lower limbs were then removed from 40-week-old aging-accelerated model mice, sections were prepared according to the standard method, and HE staining was performed.
In this example, we evaluated exercise in aging-accelerated model mice when SV peptide was administered continuously.
Aging-accelerated model mice (SAMP10 28 weeks old) were trained on a treadmill (MK-680; Muromachi Kikai Co., Ltd.) (18 m/min×90 min) and subsequent SV peptide administration was performed according to the schedule in the following table. After 30 weeks of age, training was performed continuously from Monday to Friday of each week. SV peptides were added to PBS to adjust to a concentration of 1 μg/ml or 20 ng/ml for injection formulation. Localized injections were made into the bilateral leg muscles of each mouse anesthetized by inhalation with sevoflurane immediately after training on Tuesday and Friday (SV group). Exercise evaluations were performed after SV peptide localization on Friday.
Exercise evaluations were conducted for endurance evaluation, in which the belt speed on the treadmill was increased incrementally at regular intervals, and for slope-up evaluation, in which the belt incline was increased incrementally at regular intervals.
exercise 17 m/min (35 minutes)
cool down 7 m/min
exercise 18 m/min (35 minutes)
cool down 10 m/min
indicates data missing or illegible when filed
The results of the endurance evaluation test are shown in
The mean workload was calculated as the mean value of workload calculated by multiplying body weight, running time, slope (grade), running speed, and gravitational acceleration g(9.8 m/s2) for each mouse in each group by body weight, running time, slope (grade), running speed, and gravitational acceleration g(9.8 m/s2). As shown in
In this example, the training schedule and SV peptide administration concentration were changed from Example 4, and exercise evaluation (endurance evaluation) was conducted in aging-accelerated model mice when SV peptide was continuously administered. In addition, the cross-sectional area of muscle fibers (gastrocnemius (type I, type IIa, type IIb), extensor digitorum longus, and tibialis anterior muscles) were evaluated in mice that continued training and SV peptide administration until 51 weeks of age.
Aging-accelerated model mice were trained on a treadmill (MK-680; Muromachi Kikai Co., Ltd.) (18 m/min×90 min) and subsequent SV peptide administration was performed according to the schedule in the following table. 30 weeks of age and thereafter, training was performed continuously from Monday to Friday of each week. SV peptide was added to PBS to adjust to a concentration of 1 μg/ml for an injection formulation and localized to the bilateral leg muscles of each mouse anesthetized by inhalation with sevoflurane immediately after training on Tuesday and Friday (SV group; twice weekly administration). Exercise evaluations were performed every other Friday.
Exercise evaluation was performed by endurance assessment, in which the belt speed on the treadmill was increased stepwise at regular intervals. The elapsed time and belt speed increase used for the endurance evaluation test were the same as in Example 4. In the PBS group as a control group, PBS was injected into the bilateral leg muscles instead of SV peptide after training on the treadmill in the same manner as in the SV group.
6
exercise 17 m/min (35 minutes)
cool down 7 m/min
exercise 18 m/min (35 minutes)
cool down 10 m/min
indicates data missing or illegible when filed
7
The results of the endurance evaluation test are shown in
The results of the endurance evaluation test are also shown in
The gastrocnemius, extensor digitorum longus, and tibialis anterior muscles of the lower limbs were removed from 51-week-old aging-accelerated model mice, and after sections were prepared according to the standard method, the cross-sectional area of muscle fibers was measured by HE staining.
In this example, the number of SV peptide doses and dosage in Example 4 was changed as shown in the following table, and exercise evaluation (endurance evaluation) was performed when SV peptide was continuously administered to aging-accelerated model mice. The conditions other than the number of SV peptide doses and dosage were the same as in Example 4.
Specifically, SV peptide was added to PBS to adjust to a concentration of 2 μg/ml for the injectable formulation, and localized to the bilateral lower limb muscles of each mouse anesthetized by inhalation with sevoflurane immediately after training on Friday every other week (even weeks) (SV group; one dose every other week).
8
The results of the endurance evaluation test are shown in
In this example, the number of SV peptide doses and dosage in Example 4 were changed as shown in the following table, and exercise evaluation (endurance evaluation) was performed when SV peptide was continuously administered to aging-accelerated model mice. The conditions other than the number of SV peptide doses and dosage were the same as in Example 4.
Specifically, SV peptide was added to PBS to adjust to a concentration of 20 μg/ml for the injectable formulation, and localized to the bilateral lower limb muscles of each mouse anesthetized by inhalation with sevoflurane immediately after training once every 4 weeks (Friday) (SV group; once every 4 weeks).
The results of the endurance evaluation test are shown in
The change over time in the mean maximum speed in each group is shown in
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-178486 | Oct 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/039133 | 10/22/2021 | WO |
