JP2007045753A - Composition for prevention and/or treatment of hypertension containing garlic component - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a composition useful for prevention and/or treatment of hypertension. <P>SOLUTION: The composition for the prevention and/or treatment of the hypertension comprises γ-glutamyl-S-allylcysteine and garlic oil. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to a composition for preventing and / or treating hypertension, and uses of the composition as food and medicine.

Hypertension promotes heart and blood vessel lesions and is considered the most important risk factor in heart disease and stroke. Treatment methods for hypertension include diet therapy, non-drug therapy such as moderate exercise, or drug therapy such as β-blockers and calcium antagonists. However, dietary restrictions and exercise therapy often do not improve hypertension, and the effects of antihypertensive drugs are not uniform among cases. Furthermore, since antihypertensive therapy must be continued over a long period of time, there has been a demand for a safe therapy that is free from side effects.
Under such circumstances, attention has been focused on naturally derived components that lower blood pressure.

  For example, Patent Document 1 discloses an antihypertensive agent containing an extract of black ganoderma turf, and Patent Document 2 discloses an eating and drinking composition containing caffeic acid, dietary fiber, and the like useful as an antihypertensive food and an antihypertensive agent. Patent Document 3 discloses a drug for preventing or treating hypertension and a food composition containing collagen and a collagen degradation product, respectively.

Garlic is widely used as a spice, but on the other hand, it is also known as a folk medicine and is widely used for the treatment of arteriosclerosis, pulmonary tuberculosis, and bronchitis. Patent Document 4 describes a composition for improving or preventing discomfort after ingesting alcohol, comprising garlic extract as an active ingredient.
JP 2003-104904 A JP 2002-154977 A JP 2001-267553 A JP-A-10-158183

  The present invention provides compositions useful for the prevention and / or treatment of hypertension.

  The present invention has been obtained in the course of studying the pharmacological action of garlic, and an object of the present invention is to provide a medicine and a food using γ-glutamyl-S-allylcysteine and garlic oil in combination.

As a result of intensive studies, the present inventors have found that a combined use of γ-glutamyl-S-allylcysteine and garlic oil has an excellent blood pressure lowering effect and is useful for the prevention or treatment of hypertension. The present invention has been completed.
That is, the present invention relates to a composition for preventing and / or treating hypertension, which contains γ-glutamyl-S-allylcysteine and garlic oil.

  The composition of the present invention has a lowering effect on hypertension.

  Γ-Glutamyl-S-allylcysteine used in the present invention can be obtained by extraction and purification from garlic by a conventional method, but organic chemical synthesis techniques, biological techniques using enzymes or microorganisms, Or you may synthesize | combine by the method etc. which combined these methods.

The garlic used in the present invention is a plant (Allium sativum L.) belonging to the genus Liliaceae.
In addition to γ-L-glutamyl-S-allyl-L-cysteine, garlic includes alliin, alliamine, scordinin A, citral, geraniol, linalool, α- and β-ferrandolene, propionaldehyde, inulin, arginine, and Contains acid.
Alliin is converted into the stimulating component allicin by the action of the enzyme alliinase contained in garlic. In addition, processing of raw garlic produces allyl sulfides such as diallyl-disulfide, vinyldithiin, ajoene, S-allylcysteine, or S-allylmercaptocysteine.

In the present invention, as garlic, raw garlic may be used as it is or peeled, or processed raw garlic may be used, and is not particularly limited. Examples of the processing method of garlic include, for example, a method of pulverizing after drying, heating, steaming, irradiation with microwaves, soaking in alcohol or alcohol, and aging. You may use it in combination.
In the present invention, two or more of these garlics may be used in combination. In this invention, you may use the thing dried naturally without applying heat, for example, the garlic which water | moisture content reduced about 30% from the time of a harvest.

  One skilled in the art can obtain γ-glutamyl-S-allylcysteine of the present invention by isolating it from garlic in a conventional manner.

One skilled in the art can also obtain the γ-glutamyl-S-allylcysteine of the present invention according to conventional organic chemical synthesis techniques. Or it can also obtain by the method shown below.
N- (tert-butoxycarbonyl) -glutamic acid 1-tert-butyl ester and S-allylcysteine are reacted at room temperature in a solvent such as N, N-dimethylformamide (DMF) in the presence of a water-soluble carbodiimide reagent. Let The reaction mixture is partitioned by adding water and ether, and the water-ether layer is separated. The water-ether layer is evaporated to obtain a residue, which is deprotected with trifluoroacetic acid (TFA) to obtain γ-glutamyl-S-allylcysteine of the present invention.
The starting materials N- (tert-butoxycarbonyl) -glutamic acid 1-tert-butyl ester and S-allylcysteine are commercially available or can be easily produced by those skilled in the art using conventional techniques.

The γ-glutamyl-S-allylcysteine of the present invention includes individual stereoisomers of γ-glutamyl-S-allylcysteine, such as optical isomers (enantiomers or enantiomers) or diastereoisomers (diastereomers). Or mixtures of these stereoisomers.
As optical isomers, γ-DL-glutamyl-S-allyl-L-cysteine, γ-DL-glutamyl-S-allyl-D-cysteine, γ-D-glutamyl-S-allyl-DL-cysteine, and γ- Examples include L-glutamyl-S-allyl-DL-cysteine, and γ-L-glutamyl-S-allyl-L-cysteine, γ-L-glutamyl-S-allyl-D-cysteine, γ-D-glutamyl. Examples include -S-allyl-D-cysteine and γ-D-glutamyl-S-allyl-L-cysteine.
Examples of the mixture of stereoisomers include racemates such as γ-DL-glutamyl-S-allyl-DL-cysteine.
These stereoisomers can be obtained by conventional means such as chiral synthesis or optical resolution.
Since γ-L-glutamyl-S-allyl-L-cysteine is a component usually contained in garlic, it can be obtained by extraction from garlic and purification.

The γ-glutamyl-S-allylcysteine of the present invention includes a salt of γ-glutamyl-S-allylcysteine. Examples of the salt of γ-glutamyl-S-allylcysteine are shown below.
(1) An acid addition salt of γ-glutamyl-S-allylcysteine formed with an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, or phosphoric acid;
(2) Formic acid, acetic acid, benzenesulfonic acid, benzoic acid, camphor sulfonic acid, citric acid, ethanesulfonic acid, fumaric acid, glycoheptanoic acid, gluconic acid, glutamic acid, glycolic acid, hydroxynaphthoic acid, 2-hydroxyethanesulfonic acid , Lactic acid, maleic acid, malic acid, malonic acid, mandelic acid, methanesulfonic acid, benzenesulfonic acid, muconic acid, 2-naphthalenesulfonic acid, propionic acid, salicylic acid, succinic acid, tartaric acid, p-toluenesulfonic acid, trimethylacetic acid Or an acid addition salt of γ-glutamyl-S-allylcysteine formed with an organic acid such as trifluoroacetic acid;
(3) The dissociable hydrogen ion in at least one of the carboxyl groups of γ-glutamyl-S-allylcysteine is a metal ion, for example, an alkali metal ion such as lithium, sodium, or potassium, or magnesium, calcium, or the like A base addition salt of γ-glutamyl-S-allylcysteine formed by replacing an alkaline earth metal ion;
(4) A base addition salt of γ-glutamyl-S-allylcysteine formed when coordinated with an organic base or inorganic base.
Examples of the organic base include diethanolamine, ethanolamine, N-methylglucamine, triethanolamine, and tromethamine. Examples of the inorganic base include aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, and sodium hydroxide.

The γ-glutamyl-S-allylcysteine of the present invention includes esters of γ-glutamyl-S-allylcysteine.
As esters of γ-glutamyl-S-allylcysteine, those in which a hydrogen atom in at least one carboxyl group of γ-glutamyl-S-allylcysteine is replaced by a hydrocarbon group, such as methyl ester, ethyl ester, propyl Examples thereof include esters and morpholinoethanol esters.

The γ-glutamyl-S-allylcysteine of the present invention includes a solvate of γ-glutamyl-S-allylcysteine. For example, a solvate of the aforementioned salt of γ-glutamyl-S-allylcysteine.
Examples of solvates of γ-glutamyl-S-allylcysteine include hydrates of γ-glutamyl-S-allylcysteine.

  The γ-glutamyl-S-allylcysteine of the present invention includes a prodrug of γ-glutamyl-S-allylcysteine. As prodrugs of γ-glutamyl-S-allylcysteine, esters of carboxyl groups (for example, ethyl esters, morpholinoethanol esters, etc.); N-acyl derivatives of amino groups (for example, N-acetyl), N-mannich bases, Schiff Examples include bases and enaminones; ketone group oximes, acetals, ketals, and enol esters.

  The γ-glutamyl-S-allylcysteine of the present invention includes a glycoside of γ-glutamyl-S-allylcysteine. Examples of sugars that form glycosides with γ-glutamyl-S-allylcysteine include monosaccharides such as fructose, glucose, and xylose; disaccharides such as sucrose and gentiobiose; and oligosaccharides in which several types of monosaccharides are combined Is exemplified.

The garlic oil (also referred to as garlic oil) used in the present invention can be obtained from garlic by a conventional method. For example, from garlic bulbs, steam distillation method; pressing method; solvent extraction method with organic solvent such as petroleum ether or alcohol; oil and fat adsorption method by adsorption of fats and oils; liquefied gas extraction method by liquefied gas such as propane or butane; It can be obtained by a critical extraction method or the like. An example is shown below.
Garlic bulbs are ground with a mixer together with water to obtain a homogenate. For example, the homogenate is allowed to stand at room temperature for 1 hour and then subjected to steam distillation to obtain a distillate containing an oily component. An extraction solvent such as hexane is added to the distillate, and the solvent is separated into an aqueous layer and a solvent layer, and the solvent layer is separated. Anhydrous sodium sulfate is added to the solvent layer for dehydration, and then the solvent is evaporated to obtain a residual oily substance as garlic oil.

  The mixing ratio of γ-glutamyl-S-allylcysteine and garlic oil in the composition of the present invention is not particularly limited, but in order to obtain an excellent blood pressure lowering effect, 1 part by weight of γ-glutamyl-S-allylcysteine is used. On the other hand, the garlic oil is preferably contained in an amount of 1 to 10 parts by weight, particularly 0.5 to 5 parts by weight, particularly 0.1 to 1 part by weight.

In addition to γ-glutamyl-S-allylcysteine, the composition of the present invention may contain other components such as substances useful for the prevention and / or treatment of hypertension. For example, red yeast, turmeric, chitosan, Ganoderma lucidum, black beans, and a coenzyme _{Q 10,} preferably Monascus, turmeric, chitosan, and coenzyme _{Q 10.}

  The composition of the present invention may contain additives such as excipients, sweeteners, acidulants, thickeners, fragrances, pigments, or emulsifiers as long as the effects of the present invention are not impaired.

  The composition according to the present invention can be used as a food, particularly as a health food, a functional food, a health supplement, or a food for specified health use. These foods may be in the form of drinking water such as tea and juice; jelly, candy, chocolate, chewing gum and the like. Moreover, the foodstuff which concerns on this invention may be manufactured in the form of a liquid agent, a powder agent, a granule, a capsule, and a tablet as a dietary supplement (supplement).

  The composition according to the present invention can also be used as a medicine. These medicaments can be administered orally, for example in the form of tablets, coated tablets, dragees, hard or soft gelatin capsules, solutions, emulsions or suspensions, eg rectally in the form of suppositories; It can also be administered locally or transdermally in the form of an agent, cream, gel or solution; for example, parenterally in the form of an injection or infusion; and intranasally in the form of a nasal drop.

  The amount of intake of the composition according to the present invention is not particularly limited, but can be appropriately selected according to the administration route, the type of disease, the dosage form, and the age, weight, and symptoms of the intaker. For example, when ingesting the composition of the present invention, the amount of active ingredient per day for an adult weighing 60 kg is 25 to 250 g, particularly 0.25 to 2.5 g, especially 25 to 25 g of γ-glutamyl-S-allylcysteine. It is preferable to obtain 250 mg and garlic oil in an amount of 0.1 to 1 g, particularly 50 to 500 mg, particularly 25 to 250 mg, in order to obtain a good blood pressure improving effect. The intake period can be arbitrarily determined according to the age and symptoms of the intake person.

  Hereinafter, the present invention will be described in more detail by way of examples. The present invention is not limited by the examples. In the examples,% means% by weight unless otherwise specified.

1. Production Example (1) Production of Garlic Oil 300 ml of pure water was added to 100 g of garlic bulbs and then ground with a mixer to obtain a homogenate. This was left at room temperature for 1 hour and then steam distilled for 3-5 hours. Hexane was added to the resulting distillate containing the oily component and the aqueous layer and the hexane layer were partitioned. The hexane layer was separated, and anhydrous sodium sulfate was added thereto for dehydration. Next, the solvent was evaporated using a rotary evaporator in a water bath at about 10 ° C. to obtain garlic oil as an oily substance.

(2) Production of γ-L-glutamyl-S-allyl-L-cysteine N- (tert-butoxycarbonyl) -L-glutamic acid 1-tert-butyl ester (Boc-Glu-OtBu, manufactured by Kokusan Chemical Co., Ltd.) 6 g , 3 g of S-allyl-L-cysteine (deoxy alliin, manufactured by Wako Pure Chemical Industries, Ltd.) and 4.6 g of a water-soluble carbodiimide reagent (HOSu, manufactured by Dojin Chemical Laboratories Co., Ltd.) are mixed in 50 ml of DMF and brought to room temperature. Stir all day and night. To this mixture, 25 ml of water and 25 ml of ether were added, and the mixture was partitioned into a DMF layer and a water-ether layer. The water-ether layer was separated and dried to obtain a residue. To this residue, 10 ml of 80% TFA aqueous solution was added and stirred at room temperature for 3 hours. The solvent was evaporated with a rotary evaporator, an appropriate amount of toluene was added, and the solvent was continuously evaporated with the rotary evaporator. The residue was subjected to high performance liquid chromatography [column: YMC Pack ODS-A, eluent: 10 mM potassium phosphate buffer (pH 2.6) +50 mM sodium sulfate, gradient: acetonitrile 0 to 45% (25 minutes), flow rate: 1. 0 ml / min, detection: 210 nm] to obtain γ-L-glutamyl-S-allyl-L-cysteine (hereinafter referred to as “GSAC”).
Analysis purity 98.4%
Elemental analysis Experimental values: C, 43.03; H, 6.35; N, 8.56% (N recovery rate = 88.7%)
Calculated values: C, 43.03; H, 6.59; N, 8.52%
Mass spectrometry value 291.0 (ESI-MS, calculated value [M + H] _mono = 291.101)
Structural formula ¹ Confirmed by H-NMR (in D ₂ O) test

2. Test Example (1) Preparation of Test Solution An example of preparing a test solution is shown below. In addition, the water for injection used the commercial item (made by Otsuka Pharmaceutical Factory Co., Ltd.). In addition, each test solution was prepared at the time of use, and after preparation, the test solution was stored at room temperature, protected from light until use.
(I) Garlic egg yolk powder test solution 6.768 g of commercially available garlic egg yolk powder (trade name: Traditional garlic egg yolk, manufactured by Kenko Family Co., Ltd.) was precisely weighed using an upper pan balance (METTLER, AE200) for high-precision analysis. One drop of Tween 80 was added thereto, and then dissolved in water for injection to make a total volume of 20 mL, thereby preparing a 338.4 mg / mL garlic egg yolk powder test solution.
(Ii) GSAC test solution 42 mg of the GSAC produced as described above was precisely weighed using a high precision analytical top balance (METTLER, AE200). One drop of Tween 80 was added to this, and then dissolved in water for injection to make a total volume of 10 mL to prepare a 4.2 mg / mL GSAC test solution. This 4.2 mg / mL test solution was diluted 10-fold with water for injection to prepare a 0.42 mg / mL GSAC test solution.
(Iii) Garlic oil test solution 65 mg of the garlic oil produced above was precisely weighed using a high precision analytical top pan balance (METTLER, AE200). A 6.5 mg / mL garlic oil test solution was prepared by adding 1 drop of Tween 80 to this and then dissolving in water for injection to make a total volume of 10 mL. This 6.5 mg / mL test solution was diluted 10-fold with water for injection to prepare a 0.65 mg / mL garlic oil test solution.
(Iv) Mixed test solution of GSAC and garlic oil The 4.2 mg / mL GSAC test solution and 6.5 mg / mL garlic oil test solution prepared above were diluted 5 times with water for injection, respectively, A mixed test solution of GSAC and garlic oil containing GSAC 0.42 mg / mL and garlic oil 0.65 mg / mL was prepared.

(2) Test animal Seven-week-old male SHR rats (SPF, Nippon SLC Co., Ltd., Hamamatsu City, Shizuoka Prefecture) were used.
Rats were given free access to radiation-sterilized commercial solid feed F-2 (Funabashi Farm, Funabashi, Chiba) and tap water.

(3) Measurement items and measurement procedure (i) Observation of general condition and life and death During the administration period, the general condition and life and death were observed at least once a day for all cases.
(Ii) Measurement of systolic blood pressure The systolic blood pressure of the rat was measured by a tail cuff method using a non-invasive automatic blood pressure monitor (UR-5000, Ueda Seisakusho). The systolic blood pressure was measured three times or more for each individual, and the average value was taken as the systolic blood pressure.

(4) Test procedure The blood pressure of the rats was measured, and 5 rats were divided into 5 groups by a complete random sampling method based on the mean value of systolic blood pressure.
Subsequently, each test solution prepared as described above was administered to each group of rats according to Table 1 by single oral gavage using a disposable syringe and an oral sonde at a dose of 10 mL / kg body weight.
Then, the blood pressure of the rats was measured 90 minutes after administration, 180 minutes after administration, and 240 minutes after administration.
The measured values were expressed as mean ± standard error for each group. Paired t-tests were performed on the measurement values at each measurement time, using the measurement values before administration as control values for the significant difference test with the measurement values before administration in each group. Between 1 and 5 groups, Dunnett's multiple comparison test was used when the variance was found to be uniform by the Bartlett test for one group. If not, a non-parametric Dunnett multiple comparison test was performed. Significance levels are expressed as 5% and 1%.

(5) Test results No death or general abnormalities were observed in all treatment groups.
Regarding blood pressure, a decrease was observed in the group administered with garlic egg yolk powder as compared with the pre-administration group and the water-administered group for injection (hereinafter referred to as “control group”). In particular, significant decreases were observed 90 minutes after administration and 180 minutes after administration, and 90 minutes after administration, compared with the control group (Table 1).
In the GSAC administration group and the garlic oil administration group, a decrease in blood pressure was observed as compared with that before administration and the control group (Table 1).
Even in the GSAC / garlic oil mixed test solution group, blood pressure was reduced compared to the pre-dose and control group, especially after 90 minutes, compared with the pre-dose and control group. (Table 1).

(6) Discussion From the above results, it was confirmed that garlic egg yolk powder, GSAC, garlic oil, and a mixture of GSAC and garlic oil all had a blood pressure lowering effect on hypertension in SHR rats. In particular, a synergistic effect was confirmed by the combined use of GSAC and garlic oil.

According to the present invention, a composition for preventing and / or treating hypertension can be obtained.
These compositions are used to prevent and / or treat hypertension not only in humans, but also in animals such as dogs and cats, as pharmaceuticals or foods such as health foods, health supplements, foods for specified health use, or dietary supplements. Available.

Claims (4)

  A composition for preventing and / or treating hypertension, comprising γ-glutamyl-S-allylcysteine and garlic oil.   A composition for preventing and / or treating hypertension, comprising γ-L-glutamyl-S-allyl-L-cysteine and garlic oil.   The composition according to claim 1 or 2, which is a food.   The composition of Claim 1 or 2 which is a pharmaceutical.