JPH1045573A - Hsp47 synthesis suppressor containing magnolol - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain the subject medicine capable of suppressing synthesis of a specific heat shock protein in a cell, suppressing synthesis of collagen in organs and effectively treating hepatocirrhosis, interstitial lung disease, etc., by including magnolol as an active ingredient. SOLUTION: This medicine contains magnolol as an active ingredient. Magnolol is included in a crude medicine such as Magnoliae Cortex. Magnoliae Cortex extract containing magnolol can be obtained by extracting Magnoliae Cortex with water (e.g. cold water, warm water or hot water) or an organic solvent. Magnolol specifically suppresses synthesis of a heat shock protein having 47K dalton molecular weight in a cell and suppresses biosynthesis of collagen. Thereby, the medicine can be used for preventing or treating diseases exhibiting a morbid state accelerating production of extracellular matrix accompanying increase of collagen.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION The present invention relates to a process for producing magnolol as an active ingredient having a molecular weight of 47 kilodaltons (k
D) a heat shock protein (hereinafter referred to as HSP47) synthesis inhibitor. The HSP47 synthesis inhibitor of the present invention particularly suppresses the synthesis of collagen in organs, thereby increasing cirrhosis, interstitial lung disease, chronic renal failure (or disease causing chronic renal failure), cardiac hypertrophy, and postoperative Physiology of patients with diseases that show pathological conditions of extracellular matrix (extracellular matrix) production such as keloids and hypertrophic scars, scleroderma, arteriosclerosis, or rheumatoid arthritis that occur after scars, burn scars, traffic accidents, etc. Effectively improve the condition, cirrhosis, interstitial lung disease, chronic renal failure (or chronic renal failure), cardiac hypertrophy, postoperative scars and burn scars, keloids and thickening after traffic accidents, etc. Diseases showing a pathology of extracellular matrix production enhancement such as sexual scar, scleroderma, arteriosclerosis, or rheumatoid arthritis can be effectively treated.

[0002]

2. Description of the Related Art In recent years, diseases showing a pathological condition of enhanced production of extracellular matrix such as collagen have become a serious problem. As used herein, diseases that exhibit the pathology of increased extracellular matrix production include, for example, liver cirrhosis, interstitial lung disease, chronic renal failure (or diseases that cause chronic renal failure), cardiac hypertrophy, postoperative scarring and burn injury. Includes scars, keloids and hypertrophic scars that occur after traffic accidents, etc., scleroderma, arteriosclerosis, or rheumatoid arthritis.

For example, the number of fatalities in Japan alone is about 2 per year.
Cirrhosis, which is said to be common to all people, is a general term for diseases in which the liver becomes stiff due to the proliferation of connective tissue.It is said that it is the terminal image of various chronic liver diseases, and it is a diffuse liver fibrosis that spreads throughout the liver. is there. In other words, in chronic hepatitis in which liver injury such as inflammation lasts for a long time, the liver fibrosis is accompanied by markedly enhanced production of extracellular matrix (particularly type I collagen) such as fibroblasts and Ito cells. As liver fibrosis progresses chronically, more and more normal liver regeneration is disturbed and replaced by hepatocytes, and extracellular matrix composed mainly of fibroblasts and type I collagen occupies a significant part of liver tissue,
It leads to cirrhosis consisting of many colobules. As cirrhosis progresses, the fibrous septum extends throughout the liver, and the resulting abnormal blood flow also contributes to further degeneration of hepatic parenchymal cells, leading to a vicious cycle in cirrhosis, and alcohol. , Viruses, autoimmunity, etc.
A large amount of collagen fibers are produced in the liver, resulting in necrosis and loss of function of hepatocytes, and patients with cirrhosis eventually die. Type I collagen accounts for about 2% of the total protein in normal liver, but accounts for 10 to 30% in cirrhosis.

Interstitial lung disease is a chronic inflammation of the lower respiratory tract (alveolitis) involving the respiratory bronchioles and terminal bronchi, as well as the alveoli and alveolar ducts, and the resulting interstitial disease. A group of diseases characterized by fibrosis and intraalveolar fibrosis. The interstitial lung disease referred to here includes, for example, interstitial pneumonia, diffuse interstitial lung disease such as pulmonary fibrosis, idiopathic pulmonary fibrosis, permeable pulmonary edema, collagen disease lung, sarcoidosis, etc. . In interstitial lung disease, excessive production and accumulation of extracellular matrix has been observed in fibrotic tissues. That is, in the fibrotic tissue of interstitial lung disease, marked accumulation of type I and type III collagen was observed in the enlarged interstitium, and type III collagen was particularly prominent in the thickened lung in the early stage of fibrosis. Accumulate in the alveolar septum, the stage progresses,
Type collagen increases and becomes the main collagen. The basement membrane is destroyed early, and the infiltration of collagen fibers to the alveolar cavity side is observed.

[0005] Chronic renal failure is a condition in which homeostasis in the body cannot be maintained due to deterioration of renal function as a result of chronic nephritis syndrome. A pathological view of the progression of chronic renal failure is the progression of glomerulosclerosis and interstitial fibrosis. Glomerulosclerosis is an increase in extracellular matrix centered on the mesangial region. Compared to normal, the component of mesangial sclerosis markedly increased the component of glomerular basement membrane such as type IV collagen, and the type I collagen, which is a stromal component, grew in line with the site of sclerosis . That is, the promotion of extracellular matrix production is a major factor in chronic glomerulosclerosis. Here, the disease falling into chronic renal failure includes, for example, IgA nephropathy, focal glomerulosclerosis, membranous proliferative nephritis, diabetic nephropathy, chronic interstitial nephritis, chronic glomerulonephritis and the like.

[0006] Cardiomyocytes are highly differentiated cells.
Does not have the ability to divide and proliferate. Therefore, when a certain load is applied to the heart, each of the myocardial cells enlarges to increase the contractile force and try to maintain the heart function. Furthermore, if the load lasts for a long time, various obstacles are accumulated, mainly due to the cause of ischemia, and the compensation mechanism for the load breaks down, the contractile force of the myocardium rapidly decreases, and the heart's pump function is impaired. It is known that heart failure occurs, and cardiac hypertrophy is the largest cause of heart failure in Japan. Moreover, the formation of cardiac hypertrophy is not only the greatest risk factor for the development of heart failure, but also the complication rate of ischemic heart disease and severe ventricular arrhythmia is significantly increased, and it is an independent factor that determines the prognosis of life. Has become. When cardiac hypertrophy progresses, not only individual cardiomyocytes are remarkably enlarged, but also because the cardiomyocytes are tightly bundled, fibrosis of the interstitium is promoted and collagen which is an extracellular matrix increases. When myocardial cells are lost due to myocarditis, myocardial ischemia, etc., collagen is biosynthesized and replaces the gap. If the interstitial fibrosis progresses excessively, the result is a hardened myocardium,
Extensions fail. In addition, muscular body function is reduced and diastolic relaxation of the myocardium is also impaired. In addition, post-operative scars and burn scars, or diseases showing the pathophysiology of extracellular matrix production enhancement such as scleroderma and arteriosclerosis, due to some reason, abnormally increased collagen synthesis, which promotes fibrosis and promotes tissue formation. It is believed that a change in cure is a major cause.

It has been pointed out that the basement membrane and collagen synthesis in the basement membrane also play an important role in angiogenesis (Maragoudakis, E., Sarmonika, M., and
Panoutsacopoulous, M., "J. Pharmacol. Exp. The
r. ", 244 : 729, 1988; Ingber, DE, Madri, J.
A., and Folkman, J., "Endocrinology", 119 : 1768,
1986). Examples of diseases caused by angiogenesis include diabetic retinopathy, posterior lens fibroplasia, angiogenesis associated with corneal transplantation, glaucoma, eye tumor, trachoma, stem gland, suppurative granuloma, hemangiomas, fibrous blood vessels Tumors, hypertrophic scars, granulation, rheumatoid arthritis, edema sclerosis, atherosclerosis, various tumors and the like are known. In spite of the fact that diseases that show the pathological condition of enhanced production of extracellular matrix such as collagen have become a major problem, the suppression of extracellular matrix synthesis that has been satisfactory in various aspects such as side effects and pharmacological effects has been conventionally performed. Agents (eg, collagen synthesis inhibitors) have not yet been developed.

On the other hand, heat shock proteins (heat shock proteins)
protein; HSP, also called stress protein)
A group of proteins expressed in cells by stimulating the cells with some stress, such as heat, heavy metals, drugs, amino acid analogs, or hypoxia (low oxygen concentration). Heat shock proteins are ubiquitous in nature and are produced by bacteria, yeast, plants, insects, and higher animals including humans. HSPs vary in their types, but due to their large molecular weight, the HSP90 family (eg, 90 kD or 110 kD HSPs), HSP
SP70 family (eg, 70-73 kD HSP
Etc.), HSP60 family (for example, 57 to 68k)
D HSP), the small HSP family (eg,
20kD, 25-28kD, or 47kD HSP). In this specification, HSP having a specific molecular weight is referred to as HS
Shall be indicated by P and the number immediately following it,
For example, an HSP having a molecular weight of 47 kD is referred to as “HSP47”. As described above, there are many kinds of HSPs, but they differ not only in molecular weight but also in structure, function, or property. In addition to stress response, some of these proteins are constitutively synthesized and, under normal circumstances, are involved in protein folding, unfolding, protein subunit association, and protein membrane transport. It has been shown to play an essential physiological role. These functions as heat shock proteins are called molecular chaperones.

HSP47 is a protein discovered by Nagata et al. In 1986 and is a basic protein (pI = 9.0) having a molecular weight of 47 kilodaltons. HSP47
Increased collagen expression has been shown to increase collagen synthesis in various cells ("J. Biol. Che.
m. ", 261 : 7531, 1986;" Eur. J. Biochem. ", 206 :
323, 1992; "J. Biol. Chem.", 265 : 992, 1990;
"J. Clin. Invest.", 94 : 2481, 1994). That is, H
SP47 functions as a collagen-specific molecular chaperone in the process of intracellular processing of procollagen in the endoplasmic reticulum, formation of triple-stranded helix, or transport / secretion of procollagen from the endoplasmic reticulum to the Golgi apparatus. As such, increased HSP47 expression stimulates the accumulation of collagen molecules in the extracellular matrix. Thus, HSP47, a collagen-bound heat shock protein, is a heat shock protein closely related to collagen, which is an extracellular matrix protein, in terms of function as well as expression.

[0010]

In view of the above circumstances, the present inventors have considered that cirrhosis, interstitial lung disease, chronic renal failure (or a disease that causes chronic renal failure), cardiac hypertrophy, postoperative scarring, and Keloids and hypertrophic scars that occur after burn scars, traffic accidents, etc.
Effectively improve the physiological status of patients with scleroderma, arteriosclerosis, or diseases exhibiting extracellular matrix production enhancement such as rheumatoid arthritis, and improve cirrhosis, interstitial lung disease, chronic renal failure (or chronic renal failure) Disease), cardiac hypertrophy, postoperative scars and burn scars, keloids and hypertrophic scars that occur after traffic accidents, scleroderma, arteriosclerosis, or enhanced extracellular matrix production such as rheumatoid arthritis. Various studies have been made in order to provide an extracellular matrix synthesis inhibitor capable of effectively treating the indicated disease.

As described above, cirrhosis, interstitial lung disease,
Chronic renal failure (or a disease that leads to chronic renal failure), cardiac hypertrophy,
Fibrosis such as keloids and hypertrophic scars, scleroderma, arteriosclerosis, and rheumatoid arthritis that occur after postoperative scars and burn scars, traffic accidents, etc. are mainly lesions with markedly increased extracellular matrix in organs. Is understood. Cirrhosis, interstitial lung disease, chronic renal failure (or a disease that leads to chronic renal failure), cardiac hypertrophy, postoperative scar or burn scar, keloid or hypertrophic scar after traffic accident, scleroderma, Arteriosclerosis,
Alternatively, fibrosis accompanying a disease showing a pathological condition of enhanced extracellular matrix production such as rheumatoid arthritis is considered to be caused by an increase in collagen biosynthesis or a decrease in collagen degradability. For example, in liver fibrosis, synthetic activation of type I, type III, and type IV collagen occurs, and in particular, synthetic activation of type I collagen, which is a main component, has an important meaning.

Under these circumstances, the present inventors have surprisingly found that magnolol, a component of Aspergillus niger, specifically suppresses the synthesis of HSP47 in cells of a tissue exhibiting a pathological condition. That is, administration of magnolol suppresses the synthesis of HSP47 in cells, suppresses the synthesis of collagen in organs, and eventually leads to cirrhosis, interstitial lung disease, chronic renal failure (or chronic renal failure). Disease), cardiac hypertrophy, postoperative scars and burn scars, keloids and hypertrophic scars after traffic accidents, scleroderma, arteriosclerosis,
It has also been discovered that it is possible to treat diseases that exhibit pathological conditions of increased extracellular matrix production, such as rheumatoid arthritis. The present invention is based on these findings, and after cirrhosis, interstitial lung disease, chronic renal failure (or a disease that causes chronic renal failure), cardiac hypertrophy, postoperative scars and burn scars, traffic accidents, etc. An HSP47 synthesis inhibitor capable of effectively treating a disease showing a pathological condition of enhanced extracellular matrix production, such as a resulting keloid or hypertrophic scar, scleroderma, arteriosclerosis, or rheumatoid arthritis, An object of the present invention is to provide an inhibitor of synthesis of HSP47, a collagen-specific molecular chaperone that plays an important role in the process of maturation and transport of collagen.

[0013]

Accordingly, the present invention is characterized by containing magnolol as an active ingredient,
It relates to a heat shock protein synthesis inhibitor having a molecular weight of 47 kilodaltons.

[0014]

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The synthesis inhibitor of the present invention contains magnolol as an active ingredient. Magnolol which can be used as an active ingredient in the synthetic inhibitor of the present invention has the formula (I):

Embedded image The compound is represented by the formula (1), and is contained in crude drugs such as red pearls.

The magnolol contained in the synthesis inhibitor of the present invention can be prepared by chemical synthesis or by extracting and purifying from natural products. Alternatively, a commercially available product may be used. When magnolol used as an active ingredient in the synthesis inhibitor of the present invention is extracted from a natural product, for example, whole or a part of a plant containing magnolol (for example, whole plant, leaf, root, rhizome, stem,
Root bark, flower, or fruit) can be used as is or simply processed (eg, dried, cut, blanched, steam heated,
Or powdered) (for example, a crude drug). The extraction conditions are not particularly limited as long as they are generally used for plant extraction. Examples of the plant containing magnolol include, but are not limited to, Magnolia obovata Thumb.
erg), Magnolia biroba [Magnolia b
iloba (Rehd. et Wils.) Chen
g], Calla hoo (Magnolia Magnolia o)
ficinalis Rehd. et Wil
s. ) Or Magnolia splengeri (Magnol)
ia sprengeriPamp. ) Etc. can be used.

When magnolol in the present invention is extracted from a crude drug, it is not limited to this, but for example,
It is preferable to extract from pearl oysters. Koboku (Makol; Magnoliae Cortex; Magnol)
ia Bark is the bark of Japanese cypress (Wakoboku;
Japanese bark) or bark of Karahoo (Karakoboku; Karako)
And these parts can be used alone or in any combination.

The Komoku extract which can be used as an active ingredient in the synthesis inhibitor according to the present invention only needs to contain the above-mentioned magnolol, and therefore, the crude extract of Komoku can be used. As a method for producing an extract of Asparagus which can be used in the present invention, Aspergillus oryzae is extracted with water (for example, cold water, hot water or hot water) or by extraction with an organic solvent,
Obtainable. Examples of the organic solvent include alcohols having 1 to 6 carbon atoms (eg, methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, or butyl alcohol), esters (eg, methyl acetate, ethyl acetate, propyl acetate, or Butyl acetate), ketones (eg, acetone or methyl isobutyl ketone), ethers, petroleum ethers, n-hexane, cyclohexane, toluene, benzene, halogen derivatives of hydrocarbons (eg, carbon tetrachloride,
Dichloromethane or chloroform), pyridine,
Glycol (eg, propylene glycol or butylene glycol), polyethylene glycol, or acetonitrile can be used, and these organic solvents can be used alone or in an appropriate combination, mixed at a certain ratio, and further used in an anhydrous or water-containing state. be able to. As a method of water extraction or an organic solvent extraction, a method used for a usual herbal medicine extraction can be used.
It is desirable to use 0 parts by weight and heat and reflux at a temperature not higher than the boiling point while stirring and to perform ultrasonic extraction or cold immersion at room temperature. The extraction step is usually carried out for 5 minutes to 7 days, preferably 10 minutes to 60 hours, and the extraction time can be shortened by adding an auxiliary means such as stirring if necessary.

After completion of the extraction step, the insoluble matter can be separated from the water or organic solvent extract by a suitable method such as filtration or centrifugation to obtain a crude extract. In the synthesis inhibitor of the present invention, when magnolol extracted and fractionated from a natural product is used, the crude extract may be used as it is without further purification. In addition to the water extract or organic solvent extract by a conventional method, a purified extract obtained by further treating the above crude extract with various organic solvents or adsorbents is also used as an active ingredient of the synthesis inhibitor of the present invention. You can As for the red pearl extract containing these crude extracts and purified extracts that have undergone various purification treatments, the solution as extracted may be used, or an extract obtained by concentrating the solvent may be used, or the solvent is distilled off. A dry powder, a crystallized and purified product, or a viscous substance may be used, or a diluted solution thereof may be used. The kelp extract thus obtained contains magnolol contained in kelp, and at the same time, contains impurities derived from kelp as a raw material.

The synthesis inhibitor of the present invention is a magnolol or an extract of a plant containing magnolol, for example, an extract of a herbal medicine containing magnolol (in particular, an extract of magnolia) alone, Or preferably with a conventional carrier which is pharmaceutically or veterinarily acceptable,
It can be administered to animals, preferably mammals (especially humans). The dosage form is not particularly limited. For example, oral preparations such as powders, fine granules, granules, tablets, capsules, suspensions, emulsions, syrups, extracts, or pills, or injections And parenteral agents such as topical solutions, topical solutions, ointments, suppositories, creams for topical administration, and eye drops. These oral agents are, for example,
Gelatin, sodium alginate, starch, corn starch, sucrose, lactose, glucose, mannitol, carboxymethylcellulose, dextrin, polyvinylpyrrolidone, crystalline cellulose, soy lecithin, sucrose, fatty acid ester, talc, magnesium stearate, polyethylene glycol, magnesium silicate. Excipients such as silica, anhydrous silicic acid or synthetic aluminum silicate, binders, disintegrants, surfactants, lubricants, fluidity promoters, diluents, preservatives, coloring agents, flavors, flavoring agents, stabilizing agents. It can be produced according to a conventional method using an agent, a humectant, a preservative, an antioxidant, or the like. For example, 1 part by weight of magnolol and 9 lactose
And 9 parts by weight of a capsule.

Examples of the parenteral administration method include injection (subcutaneous, intravenous, etc.), rectal administration and the like. Among these, the injection is most preferably used. For example, in the preparation of injectables, magnolol as an active ingredient, or a plant extract containing magnolol, for example, in addition to a crude drug extract containing magnolol (particularly, kokuboku extract), For example, water-soluble solvents such as physiological saline or Ringer's solution, non-water-soluble solvents such as vegetable oils or fatty acid esters, isotonic agents such as glucose or sodium chloride, solubilizing agents, stabilizers, preservatives, suspending agents. , Or an emulsifier can be optionally used. In addition, the synthetic inhibitor of the present invention may be administered by the method of sustained release preparation using a sustained release polymer or the like. For example, the synthetic inhibitors of the present invention can be incorporated into a pellet of ethylene vinyl acetate polymer and the pellet can be surgically implanted into the tissue to be treated.

The synthesis inhibitor of the present invention can contain, but is not limited to, magnolol in an amount of 0.01 to 99% by weight, preferably 0.1 to 80% by weight. . Further, a plant extract containing magnolol, for example, a synthetic inhibitor of the present invention containing an extract of a herbal medicine containing magnolol (particularly, an extract of magnolia) as an active ingredient is included therein. Magnolol can be prepared by appropriately adjusting the amount of magnolol to fall within the above range. Incidentally, a plant extract containing magnolol,
For example, when a synthetic inhibitor containing an extract of a crude drug containing magnolol (especially an extract of Asparagus) as an active ingredient is used as a formulation for oral administration, a pharmaceutically acceptable carrier can be used. It is preferable to formulate the compound using The dose when the synthetic inhibitor of the present invention is used is
There is no particular limitation, depending on the type of illness, age, sex, weight of the patient, degree of symptoms, administration method, etc., but there is no particular limitation, but the amount of magnolol is usually 1 mg to 10 g per adult 1 to 4 times a day. It is orally or parenterally administered to some extent. Furthermore, the application is not limited to pharmaceuticals, and various applications such as functional foods and health foods can be given in the form of food and drink.

[0022]

As described above, magnolol contained in the synthesis inhibitor of the present invention has an action of specifically inhibiting HSP47 synthesis in cells. Therefore, administration of the aforementioned magnolol causes production of HSP47 in cells. The synthesis is specifically reduced, and the biosynthesis of collagen is suppressed. As a result, extracellular matrix production is also suppressed. Therefore, the magnolol is a disease showing a pathological condition of extracellular matrix production accompanied by an increase in collagen, such as cirrhosis, interstitial lung disease, chronic renal failure (or a disease causing chronic renal failure),
It can be used for the prevention and treatment of cardiac hypertrophy, postoperative scars and burn scars, keloids and hypertrophic scars generated after traffic accidents, scleroderma, arteriosclerosis, rheumatoid arthritis and the like. That is, the synthesis inhibitor of the present invention inhibits the synthesis of collagen by inhibiting the synthesis of HSP47 which is a collagen-specific chaperone.

As described above, it has been pointed out that the basement membrane and collagen synthesis in the basement membrane also play an important role in angiogenesis. It is extremely useful as a prophylactic / therapeutic drug for many diseases based on proliferation, and each of the above-mentioned diseases, namely diabetic retinopathy, posterior lens fibroplasia, neovascularization associated with corneal transplantation, glaucoma, eye tumors. , Trachoma,
It can be used for psoriasis, suppurative granulomas, hemangiomas, fibrous hemangiomas, hypertrophic scars, granulation, rheumatoid arthritis, edema sclerosis, atherosclerosis and various tumors. Furthermore, it has been clarified that an interstitial stroma having type I collagen and fibronectin as a basic skeleton plays a role of guiding a detached cancer cell into invading neighboring vessels in cancer metastasis. So ["B
IOTHERAPY ", 7 (8): 1181, 1993], and it is also possible to suppress cancer metastasis by administering the synthetic inhibitor of the present invention.

[0024]

The present invention will be described in detail below with reference to examples, but these do not limit the scope of the present invention. Example 1: Preparation of anti-HSP47 polyclonal antibody (1) Preparation of anti-HSP47 polyclonal antibody A peptide consisting of 15 amino acids corresponding to the amino acid sequence of the 2nd to 16th amino acids from the N-terminal of human HSP47 [hereinafter,
Human HSP47 peptide (2-16)] was prepared using an automatic peptide synthesizer (PSSM-8 system, Shimadzu Corporation), and succinimidyl 4- (p-maleimidophenyl) butyrate [SMPB: Succinimidyl 4
-(p-maleimidophenyl) butyrate] as a cross-linking agent,
A sensitizing antigen was prepared by binding with lactoglobulin by a conventional method ("Biochemistry", 18 : 690, 1979). Phosphate buffered saline containing 150 μg of this sensitizing antigen [composition: KC
l = 0.2 g / l, KH ₂ PO ₄ = 0.2 g / l, Na
Cl = 8 g / l, Na ₂ HPO ₄ (anhydrous) = 1.15 g
/ L: hereinafter referred to as PBS (-): Cosmo Bio, Catalog No. 320-01] 0.2 ml and an equal volume of Freund's complete adjuvant (Jatron, Catalog No. RM606-1) are mixed, and the resulting mixture is obtained. 0.2 ml was subcutaneously administered to a rat (6 weeks old, female: CLEA Japan, Inc.) for immunization. After the second and third immunizations were repeated in the same manner, 6 times immunization was performed using an adjuvant (Hunter's TiterMax; CytRx Corporation, Georgia, USA). Blood was collected from the sensitized animals, serum was separated and collected by a conventional method, and the antibody titer in the serum was measured by the enzyme antibody method (ELISA method) and the Western blot method described below.

(2) Evaluation of anti-HSP47 polyclonal antibody properties by enzyme-linked immunosorbent assay (ELISA) Human HSP47 peptide (2-1) prepared in (1) above
6) was dissolved in PBS (-) to prepare a peptide solution having a concentration of 10 µg / ml, and the peptide solution was dropped in 50 µl portions to each well of a rigid assay plate (Falcon, catalog number 3910). P on the outermost well
After adding only 50 μl of BS (−) and leaving it at 4 ° C. overnight under humid condition, the peptide solution was discarded, and each well was washed with PBS (−), and then 1% bovine serum albumin (hereinafter, PBS (-) 100 containing BSA)
μl was placed in each well and left at room temperature for 1 hour. PB
After washing 3 times with S (-), 50 μl of the rat rat serum obtained in the above (1) was put into each well and left at room temperature for 1 hour. After washing 3 times with PBS (-), a peroxidase-labeled anti-rat IgG5 was added to each well as a secondary antibody.
After adding 0 μl, the mixture was left at room temperature for 1 hour. PBS (-)
After washing twice with 0.1%, 4 μl of a hydrogen peroxide solution was added.
100 μl of substrate solution prepared by dissolving one o-phenylenediamine (OPD) tablet (Sigma, catalog number P8287) (10 mg) in 10 ml of M citrate buffer (pH 4.5) was added dropwise to each well, and the mixture was allowed to come to room temperature. After being left for 30 minutes under light shielding, the absorbance at 492 nm of each well was measured using a microplate reader (Tosoh, MPR-A4).
i-type). The serum in which an increase in the antibody titer was confirmed was used as an anti-human HSP47 polyclonal antibody in the following Examples.

(3) Anti-HS by Western blotting
Evaluation of P47 polyclonal antibody properties Laemmli buffer system (Laemmli, NK, "Nat
ure ", 283 : pp. 249-256, 1970), HeLa cell lysates were subjected to sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis according to the following method. The concentrated gel was prepared as follows. 6.1 ml of distilled water, 2.5 ml of 0.5 M Tris (Bio-Rad, Cat. No. 161-0716) -HCl (pH 6.8),
10% SDS (Bio-Rad, Catalog No. 161-030)
1) 100 μl and 30% acrylamide (Bio
Rad, Catalog No. 161-1001) / N, N'-Methylenebisacrylamide (Bio-Rad, Catalog No. 16)
1-0201) Mix 1.3 ml, degas for 15 minutes,
% Ammonium persulfate (Bio-Rad, catalog number
161-0700) 50 μl and N, N, N ′, N′-tetramethylethylenediamine (hereinafter abbreviated as TEMED)
(Bio-Rad, catalog number 161-0800) 10 μl was added to prepare a concentrated gel. Separation gels were prepared as follows. 4.045 ml of distilled water, 2.5 ml of 1.5 M Tris-HCl (pH 8.8), 10% SDS
100 μl and 3.3 ml of 30% acrylamide / N, N′-methylenebisacrylamide were slowly mixed, degassed with an aspirator for 15 minutes, and 50 μl of 10% ammonium persulfate and 5 μl of TEMED were added. As the running buffer, tris 9.0 g, glycine (Bio-Rad, catalog number 161-0717) 43.2 g, and SDS 3.0 g were added with distilled water to make 600 ml, which was diluted 5 times with distilled water. Using. The sample buffer was 2 ml of distilled water, 2M Tris-HCl (pH
6.8) 500 μl, SDS 0.32 g, β-mercaptoethanol 800 μl, and 0.05% (w / v) bromophenol blue (Bio-Rad, catalog number).
161-0404) A mixture of 400 μl was used.

10% at 37 ° C. under 5% carbon dioxide conditions
HeLa cells were cultured in a MEM medium containing% inactivated fetal bovine serum (hereinafter abbreviated as FBS) to prepare a lysate. SD of the obtained HeLa cell lysate
After performing S-polyacrylamide gel electrophoresis, 0.1%
45 μm nitrocellulose membrane (Schleicher & Schuell,
Attach the gel to the catalog number 401196) and use a protein transfer device (Trans-Blot Electrophoretic Transfer Cell:
Blotting was performed for 3 hours at 100 V at room temperature using Bio-Rad. As a blotting buffer, Tris Gly Running and Blotting Buffer (Enprot), which was made of 0.025 M Tris and 0.192 M glycine and adjusted to pH 8.5.
ech, Massachusetts, USA, catalog number SA100034)
A buffer prepared by adding methyl alcohol to a concentration of 20% was used. After blotting, the nitrocellulose membrane was immersed in a PBS (-) solution containing 5% skim milk (Snow Brand Milk Products) at room temperature for 30 minutes to perform blocking. After blocking, a primary antibody reaction was carried out using a Lurat serum obtained in the above section (1) as a primary antibody using a screener blotter (SAMPLATEC). The primary antibody reaction is PB containing 2% skim milk (Snow Brand Milk Products)
The rat rat serum 200 diluted 10-fold with S (-)
Performed in μl at room temperature for 120 minutes. After completion of the primary antibody reaction, use a slow rocking shaker to add PBS
Shake for 5 minutes twice with (-), 0.1% Tween20
PB including (Bio-Rad, Catalog No. 170-6531)
Shake for 15 minutes 4 times with S (-) solution, then PBS
The nitrocellulose membrane was washed by shaking twice for 5 minutes at (-). After washing, peroxidase-labeled goat anti-rat IgG antibody (Southern Biotechnolog
y, Catalog No. 3030-05) was subjected to a secondary antibody reaction for 2 hours using 5 ml of a 5000-fold diluted solution of PBS (-) containing 2% skim milk. After the reaction,
BS (-) solution and P containing 0.1% Tween 20
The nitrocellulose membrane was washed with the BS (-) solution under the same conditions as those after the primary antibody reaction.

After removing the excess PBS (-) solution, a Western blotting detection reagent (ECL Western blotti
ng detection reagent; Amersham, Catalog number RP
N2106) was sprinkled on the nitrocellulose membrane, allowed to stand at room temperature for 1 minute, excess detection reagent was removed, the nitrocellulose membrane was wrapped in a wrap, and the reaction surface was coated with an X-ray film (Kodak X-OMAT, AR, It was exposed by contacting it to the catalog number 165 1454). After development, a molecular weight of 47 corresponding to HSP47
The reactivity of the anti-HSP47 polyclonal antibody was examined by measuring the band near the kilodalton. Sera confirmed to have increased antibody titers were treated with anti-human HSP4
7 polyclonal antibodies were used in the following examples.

Example 2: HSP expression level in cultured human cancer cells
Measurement (1) Culture of human cultured cancer cells The following various human cultured cancer cells were cultured at 37 ° C. under 5% carbon dioxide conditions except during heat shock treatment. Lung cancer cell line H69 (ATCC HTB 119) is 10%
The cells were cultured in RPMI1640 medium containing inactivated FBS.
Uterine cancer cell line HeLa S3 (ATCC CCL 2.
2) was cultured in a MEM medium containing 10% inactivated FBS.

(2) Magnolol treatment and heat shock treatment Two days after seeding, in the culture medium of the lung cancer cell line H69, the magnolol represented by the above formula (I) was adjusted to a final concentration of 100 μM (Matsuura Pharmaceutical) Was added and cultured for 24 hours. Magnolol (Matsuura Pharmaceutical Co., Ltd.) represented by the above formula (I) was added to the medium of the uterine cancer cell line HeLa S3 two days after the seeding so as to have a final concentration of 20 μM, and the cells were cultured for 24 hours. Then, after heat shock treatment at 45 ° C. for 15 minutes, the cells were cultured at 37 ° C. overnight. The control test was performed as described above except that no magnolol was added.

(3) Measurement of HSP Expression Level in Cultured Human Cancer Cells Each cell treated in (2) above was homogenized by the following method, and the HSP expression level was measured by Western blotting. That is, the cells treated in the above (2) were washed with PBS (-), and then lysed buffer (ly
sis buffer) [1.0% NP-40, 0.1
5M sodium chloride, 50 mM Tris-HCl (pH
8.0) 5 mM EDTA, 2 mM N-ethylmaleimide, 2 mM phenylmethylsulfonyl fluoride,
2 μg / ml leupeptin and 2 μg / ml pepstatin] were added and left on ice for 20 minutes. afterwards,
Centrifugation was performed at 4 ° C. and 12000 rpm for 20 minutes. 10 μl of the supernatant after centrifugation was added to 790 μl of PBS (−), and a protein assay staining solution (Dye Reagent Co., Ltd.) was added.
ncentrate: Bio-Rad, Catalog No. 500-0006) 2
00 μl was added. After standing at room temperature for 5 minutes, 59
The protein was quantified by measuring the absorbance at 5 nm. Using the protein-quantified sample, SDS polyacrylamide gel electrophoresis of a lysate containing an equal amount of protein was performed in a Laemmli buffer system. After the electrophoresis, blotting and subsequent blocking were performed according to the method described in Example 1. That is,
Protein transfer device (Trans-Blot Electrophoretic Tra
nsfer Cell: Bio-Rad) at room temperature for 10
At 0 V, 0.45 μm nitrocellulose membrane (Schleich
er & Schuell, catalog number 401196), and the gel was blotted for 3 hours. As the blotting buffer, the same buffer as used in Example 1 (3) above was used. After blotting, nitrocellulose membrane was coated with 10% skim milk (Snow Brand Milk Products) -PBS
(-) The solution was incubated at room temperature for 30 minutes to block non-specific binding.

After blocking, a primary antibody reaction was performed on the nitrocellulose membrane using the anti-human HSP47 rat polyclonal antibody prepared in Example 1. afterwards,
The solution was exchanged with PBS (-) for 5 minutes each, and two washes were performed with a slow rocking shaker, and further with PBS (-)-0.1% Tween 20 (Bio-Rad, catalog number 170-6531) solution. The solution was replaced every 15 minutes, and four washes were performed. Finally, PBS
(−) Was washed twice for 5 minutes each. After washing was completed, peroxidase-labeled goat anti-rat IgG antibody (So
uthern Biotechnology, Catalog No. 3030-05), 2%
A secondary antibody reaction was performed for 2 hours using 5 ml of an antibody solution prepared by diluting 5000 times with a PBS (-) solution containing skim milk. After completion of the reaction, change the solution of the nitrocellulose membrane with a PBS (-) solution for 5 minutes each.
Washing was further carried out 5 times with a slow rocking shaker by changing the solution with PBS (-)-0.1% Tween 20 solution for 15 minutes each. Finally, washing was performed twice for 5 minutes each with a PBS (-) solution. Extra PBS
(-) After removing the solution, Western blotting detection reagent (ECL Westernblotting detection reagent; Ame
rsham, catalog number RPN2106), sprinkle onto the nitrocellulose membrane, incubate for 1 minute, remove excess detection reagent, wrap the nitrocellulose membrane in wrap, and cover the reaction surface with X-ray film (Kodak X-OMAT, AR, (Catalog No. 165 1454), exposure, development and HSP47
It was examined whether or not. Table 1 shows the results. In the table,
"↓" indicates that HS is higher due to magnolol treatment than control.
This means that the P47 expression level was decreased.

[0033]

[Table 1] Cancer type Cancer cell Uterus HeLa S3 ↓ Lung H69 ↓

In the control test, the uterine cancer cell line HeLaS3 and the lung cancer cell line H without the addition of magnolol were used.
In 69, one band having a molecular weight of about 47 kD was detected. The molecular weight was determined by molecular weight markers (bovine carbonic anhydrase, egg white ovalbumin, and bovine serum albumin). In the uterine cancer cell line HeLa S3 to which magnolol was added, no band having a molecular weight of about 47 kD was detected. The lung cancer cell line H69 supplemented with magnolol had a molecular weight of about 47 kD compared to the control test.
Band significantly decreased in concentration. That is, it was concluded that magnolol has the activity of a synthetic inhibitor that suppresses the expression of HSP47, and this fact indicates that magnolol acts suppressively on the enhancement of extracellular matrix production.

[0035]

As described in detail above, the synthetic inhibitors of the present invention include, for example, cirrhosis, interstitial lung disease, chronic renal failure (or a disease that results in chronic renal failure), cardiac hypertrophy, post-operative Collagen synthesis in cells affected by diseases such as keloids and hypertrophic scars, scleroderma, arteriosclerosis, or increased extracellular matrix production such as rheumatoid arthritis, which occur after scars or burn scars, traffic accidents, etc. It has the effect of improving acceleration. Therefore, administration of the synthetic inhibitor according to the present invention prevents fibrosis and hardening of organs and tissues, and as a result, effectively improves the physiological condition of patients with the above diseases.
The disease can be effectively treated. Further, the synthetic inhibitor of the present invention is also useful for the preventive treatment of various diseases accompanied by abnormal growth of angiogenesis. Furthermore, it has been clarified that the stroma having the basic skeleton of type I collagen and fibronectin serves as a guide for the cancer cells detached in the metastasis of cancer to enter the nearby blood vessels. It is also possible to suppress cancer metastasis by administering a synthetic inhibitor of

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Claims (3)

[Claims] 1. A synthesis inhibitor of a heat shock protein having a molecular weight of 47 kilodaltons, comprising magnolol as an active ingredient. 2. A molecular weight of 47, which contains a plant extract containing magnolol as an active ingredient.
A kilodalton heat shock protein synthesis inhibitor. 3. A heat shock protein synthesis inhibitor having a molecular weight of 47 kilodaltons, which comprises an extract of Aspergillus niger as an active ingredient.