KR100559495B1 - Composition comprising dineolignan compounds for inhibiting acyl-CoA:cholesterol acyltransferase - Google Patents

Abstract

The present invention relates to a composition for inhibiting acyl coei: cholesterol transferase activity comprising a dyneolignan-based compound as an active ingredient, and in detail, an acyl coei: cholesterol transferase comprising manasanthin A or manasanthin B as an active ingredient. It relates to a composition for inhibiting activity.

The composition of the present invention effectively inhibits the activity on acyl-CoA: cholesterol transferase, thereby preventing cardiovascular diseases such as hyperlipidemia, coronary heart disease, arteriosclerosis and myocardial infarction associated with acyl-CoA: cholesterol transferase and It can be useful for treatment.

Description

Composition comprising dineolignan compounds for inhibiting acyl-CoA: cholesterol acyltransferase}

The present invention relates to a composition for inhibiting acyl-CoA: cholesterol acyltransferase (ACAT) activity, which comprises a dyneolignan-based compound as an active ingredient, and specifically, manasanthin A or manasanthin B is effective. It relates to a composition for inhibiting ACAT activity as a component.

Cardiac circulatory disease is currently the number 1 mortality disease in the world, and in developed countries such as Gumi, more than one-third of all deaths occur in Korea.

Atherosclerosis, a representative disease of the cardiac circulatory system, is one of the major diseases that occur with aging, as the artery thickens and hardens, loses elasticity, and becomes weak. Atherosclerosis is more likely to occur in the cerebral artery or coronary arteries. In the case of cerebral arteriosclerosis, headache, dizziness, and mental disorders are indicated and cause encephalopathy. It is known to be. In addition, this causes high blood pressure, heart disease, cerebral hemorrhage, and diseases caused by arteriosclerosis are emerging as the leading cause of death in modern society, especially among men in their 50s and 60s.

Cardiac circulatory diseases are caused by high plasma cholesterol levels, and research has been actively conducted to develop drugs that can lower plasma total cholesterol levels for the purpose of preventing cardiovascular diseases. As a result, a number of substances that inhibit the biosynthesis of cholesterol in the human body have been developed and commercialized. However, in order to improve the side effects reported by these drugs, research has recently been focused on finding compounds that can only selectively regulate blood cholesterol, and one of them is related to ACAT inhibitors.

ACAT is an enzyme that generally esterifies cholesterol, and its mechanism of action occurs largely in three parts of the body (intestinal, liver, and vascular wall cells).

First, in the intestine, ACAT converts ingested cholesterol into the form of esters to facilitate its absorption into the intestine. Second, cholesterol absorbed from the outside or biosynthesized in the body is accumulated in a carrier called VLDL (very low density lipoprotein) in the liver, and then supplied to each organ through the blood vessels, whereby ACAT converts cholesterol into cholesteryl ester form. This enables the accumulation of cholesterol in the carrier. Third, in the cells that make up the arterial vessel wall, ACAT converts cholesterol into its ester form to promote the accumulation of cholesterol in the cell, which is a direct cause of atherosclerosis.

Therefore, the drug that inhibits the activity of ACAT may first reduce the amount of cholesterol that enters the body by inhibiting the absorption of intestinal cholesterol, and secondly, by inhibiting the release of cholesterol into the blood vessels in the liver to reduce blood cholesterol levels. Third, it is expected to prevent arteriosclerosis by preventing cholesterol from accumulating in blood vessel wall cells.

ACAT activity inhibitors reported to date are activity inhibitors for rat hepatic microsome ACAT or rat hepatic macrophage (J774) ACAT.

Human ACAT includes human ACAT-1 and human ACAT-2. Human ACAT-1 (50 kDa) acts mainly on the liver, adrenal glands, macrophages and kidneys of adults. Human ACAT-2 (46 kDa) is a small intestine. (Rudel, LL et al ., Curr. Opin. Lipidol 12 , 121-127, 2001). Substances that inhibit human ACAT activity are targets for the prevention and treatment of hypercholesterolemia, cholesterol stones or atherosclerosis through mechanisms that inhibit the absorption of cholesterol from food and the accumulation of cholesteryl esters in the blood vessel walls. (Buhman, KK et al. , Nature Medicine 6 , 1341-1347, 2000).

On the other hand, three hundred herb (Sarurus chinensis Baill) is a perennial herb of over three hundred, and has been used in China since ancient times as an analgesic, diuretic and anti-inflammatory medicine. Since it was first found out in Korea that three hundred seconds lived in Jeju Island about ten years ago, it has been used for the prevention and treatment of various adult diseases such as constipation, detoxification, diuresis, liver disease, diabetes, cancer, women's diseases and kidney disease.

Therefore, the inventors of the present invention, while studying a substance that inhibits ACAT activity, found that there is an action of inhibiting ACAT activity in manasanthin A and manasanthin B isolated and purified from 300 seconds extract, and completed the present invention.

The present invention aims to provide a composition for inhibiting ACAT activity, which is a dyneolignan-based compound.

The present invention provides a composition for inhibiting ACAT activity, which comprises a dyneolignan-based compound.

Compositions of the present invention include pharmaceutical and health food compositions useful for inhibiting ACAT activity.

Hereinafter, the present invention will be described in detail.

The present invention provides a composition for inhibiting ACAT activity comprising as an active ingredient manasantin A represented by formula 1 or manasantin B represented by formula 2 below.

Dyneolignan compound (manasanthin A, B) as an active ingredient in the composition of the present invention can be used in the form of a pharmaceutically acceptable salt, and includes all salts, hydrates and solvates prepared by conventional methods. .

In the present invention, dyneiolignan-based compounds (manasanthin A, B) were extracted, separated and purified from 300 seconds, and can be obtained by all usual methods, and commercially available reagents can be used.

Extraction, separation and purification methods of dyneolignan compound (manasanthin A, B) from three hundred seconds according to the present invention are as follows.

The dried triticale root powder was extracted with methanol, concentrated, extracted with water and n-hexane, and separated into hexane and water layers. The water layer is extracted with chloroform and separated into a chloroform layer and a water layer. The chloroform layer is concentrated to give a dark brown oily substance (extract 1).

In addition, the dried three hundred sec root powder is extracted with ethyl acetate and concentrated to obtain a dark brown oily substance (extract 2).

As a result of measuring the ACAT activity of the obtained extract 1 and extract 2, the ACAT activity of the ethyl acetate layer shows a greater inhibitory effect than the chloroform layer.

The ethyl acetate layer is separated by silica gel column chromatography using a mixed solvent of chloroform and methanol. At this time, it is preferable to use a solvent of chloroform: methanol = 100-0: 0-100 (v / v), and the active substance is most effectively separated when a solvent having 100% of chloroform is used.

The active fraction is separated by silica gel column chromatography using a mixed solvent of n-hexane and ethyl acetate. At this time, it is preferable to use a solvent having n-hexane: ethyl acetate = 100-50: 0-50 (v / v), and a solvent having n-hexane: ethyl acetate = 1: 1 (v / v) is used. In this case, the active substance is most effectively separated.

The active fraction is separated again by silica gel column chromatography using a mixed solvent of n-hexane ethyl acetate. At this time, it is preferable to use a solvent having n-hexane: ethyl acetate = 100-50: 0-50 (v / v), and a solvent having n-hexane: ethyl acetate = 1: 2 (v / v) is used. In this case, the active substance is most effectively separated.

By the above method, 300 mg or more of manasanthin A, B per kg of dried root of 300 seconds can be obtained.

In order to investigate the effect on the ACAT activity of manasanthin A and B isolated and purified from the extract of Trichophytium according to the present invention, the human body ACAT-1 and human ACAT-2 were used as enzyme sources (1- ¹⁴ C) The radiation dose of cholesteryl oleate produced by the reaction of the oleyl-CoA solution was measured. As a result, the Mana xanthine A of hACAT-1, and are each 11 μM, 5 μM value IC ₅₀ for hACAT-2, Mana xanthine B of each as a 29 μM, 160 μM value IC ₅₀ for hACAT-1 and hACAT-2 It effectively inhibits ACAT activity.

Therefore, manasanthin A, B according to the present invention effectively inhibits activity against ACAT, and thus can be usefully used for the prevention and treatment of cardiovascular diseases such as hyperlipidemia, coronary heart disease, arteriosclerosis, and myocardial infarction associated with ACAT. .

The composition of the present invention may further contain at least one active ingredient exhibiting the same or similar function in addition to the dyneiolignan-based compound (manasanthin A, B).

The composition of the present invention may be prepared by including one or more pharmaceutically acceptable carriers in addition to the above-described active ingredients for administration. Pharmaceutically acceptable carriers may be used in combination with saline, sterile water, Ringer's solution, buffered saline, dextrose solution, maltodextrin solution, glycerol, ethanol and one or more of these components, if necessary, as antioxidants, buffers And other conventional additives such as bacteriostatic agents can be added. In addition, diluents, dispersants, surfactants, binders and lubricants may be additionally added to formulate injectable formulations, pills, capsules, granules or tablets such as aqueous solutions, suspensions, emulsions and the like. Furthermore, it may be preferably formulated according to each disease or component by a suitable method in the art or using a method disclosed in Remington's Pharmaceutical Science (Recent Edition), Mack Publishing Company, Easton PA.

The compositions of the present invention may be administered parenterally (eg, intravenously, subcutaneously, intraperitoneally or topically) or orally, depending on the desired method, and the dosage may be based on the weight, age, sex, health status, The range varies depending on diet, administration time, administration method, excretion rate and severity of disease. The daily dosage is about 0.1 to 10 mg / kg of manasanthin A or manasanthin B, preferably 0.1 to 5.0 mg / kg, and more preferably administered once to several times a day.

Toxicity test by oral administration of the manasanthin A, manasanthin B and three hundred seconds extract of the present invention to the mouse, 50% lethal dose (LD ₅₀ ) of manasanthin A, B was found to be 200 ~ 400mg / kg , The extract of three hundred seconds was found to be more than 1g / kg.

The composition of the present invention can be used alone or in combination with methods using surgery, hormonal therapy, drug therapy and biological response modifiers for the prevention and treatment of cardiovascular diseases.

The composition of the present invention can be added to health foods for the purpose of improving cardiovascular disease. When the manasanthin A or manasanthin B of the present invention is used as a food additive, the manasanthin A or manasanthin B may be added as it is or used with other foods or food ingredients, and may be appropriately used according to a conventional method. . The mixed amount of the active ingredient may be suitably determined depending on the purpose of use (prevention, health or therapeutic treatment). In general, in the preparation of food or beverage, manasanthin A or manasanthin B of the present invention is added in an amount of 1 to 20% by weight, preferably 5 to 10% by weight based on the raw materials. However, in the case of long-term intake for health and hygiene or health control, the amount may be below the above range, and the active ingredient may be used in an amount above the above range because there is no problem in terms of safety. .

There is no particular limitation on the kind of food. Examples of the food to which the substance can be added include dairy products including meat, sausage, bread, chocolate, candy, snacks, confectionery, pizza, ramen, other noodles, gums, ice cream, various soups, drinks, tea, drinks, Alcoholic beverages and vitamin complexes, and the like and include all of the health foods in the conventional sense.

The health beverage composition of the present invention may contain various flavors or natural carbohydrates, etc. as additional components, as in the general beverage. The above-mentioned natural carbohydrates are glucose, monosaccharides such as fructose, disaccharides such as maltose and sucrose, and polysaccharides such as dextrin and cyclodextrin, sugar alcohols such as xylitol, sorbitol and erythritol. As the sweetening agent, natural sweetening agents such as tautin and stevia extract, synthetic sweetening agents such as saccharin and aspartame, and the like can be used. The ratio of the natural carbohydrate is generally about 0.01 to 0.04 g, preferably about 0.02 to 0.03 g per 100 ml of the composition of the present invention.

In addition to the above, the composition of the present invention includes various nutrients, vitamins, electrolytes, flavoring agents, coloring agents, pectic acid and salts thereof, alginic acid and salts thereof, organic acids, protective colloidal thickeners, pH regulators, stabilizers, preservatives, glycerin, alcohols, carbonic acid. Carbonating agents and the like used in beverages. In addition, the composition of the present invention may contain a flesh for preparing natural fruit juice, fruit juice beverage and vegetable beverage. These components can be used independently or in combination. The proportion of such additives is not critical but is generally selected in the range of 0.01 to 0.1 parts by weight per 100 parts by weight of the composition of the present invention.

Hereinafter, preferred examples and experimental examples are presented to help understand the present invention. However, the following Examples and Experimental Examples are provided only to more easily understand the present invention, and the contents of the present invention are not limited by the Examples.

Example: extraction, separation and purification of lignan compound Neo die (mana Santin A, B) from three hundred seconds

1. Extract from 300 seconds

500 g of dried three hundred sec roots purchased from Geochang, Gyeongsangnam-do, Korea were washed and dried, and then pulverized using a grinder to make a powder.

1) Chloroform Fraction

After adding 300 liters of powder to 1.5 L of methanol and standing at room temperature for 24 hours, the methanol solution was stirred and filtered through a filter paper to separate the liquid phase. The above extraction process was repeated twice to collect only the liquid phase and concentrated under reduced pressure.

The methanol extract obtained above was suspended in 500 ml of water, and 500 ml of n-hexane was further added thereto. The separatory funnel was separated into a hexane layer and a water layer.

The water layer was extracted again by adding chloroform and separated into a chloroform layer and a water layer using a separatory funnel.

As a result of measuring the ACAT activity of the hexane layer, the chloroform layer and the water layer obtained in the above process, the ACAT activity was strongly inhibited in the chloroform layer.

Thus, the chloroform layer was concentrated and dried under reduced pressure to give a dark brown oily substance.

2) ethyl acetate fraction

The white powder was added to 1.5 liter of ethyl acetate and left at room temperature for 24 hours. Then, the ethyl acetate solution was stirred and filtered through a filter paper to separate the liquid phase. The above extraction process was repeated two times to collect only the liquid phase, and concentrated and dried under reduced pressure to obtain a dark brown oily material.

As a result of measuring the ACAT activity of the ethyl acetate layer obtained in the above process, the ACAT activity was strongly inhibited.

In addition, the ACAT activity of the ethyl acetate layer showed a greater inhibitory effect than that of the chloroform layer.

2. Isolation and Purification of Ethyl Acetate Extract

The ethyl acetate extract obtained in step 1 was separated using silica gel column chromatography (silica gel; Merck, Art 9385, column size: φ 7.5 x 21.5 cm) by varying the ratio of chloroform and methanol. When the solvent with 100% chloroform was used, the active substance was most effectively separated, and an active fraction of 4.1 g was obtained.

The active fraction was separated using silica gel column chromatography (silica gel; Merck, Art 9385, column size: Φ 3.5 x 19.0 cm) with varying ratios of n-hexane and ethyl acetate solution. In the case of using a solvent of n-hexane: ethyl acetate = 1: 1 (v / v), the active substance was most effectively separated, and 2 g of an active fraction was obtained.

The active fractions were separated using silica gel column chromatography (silica gel; Merck, Art 9385, column size: Φ2.0 x 19.0 cm) while varying the ratio of n-hexane and ethyl acetate solution. In the case of using a solvent of n-hexane: ethyl acetate = 1: 2 (v / v), the active substance was most effectively separated. At this time, 150 mg of the pure active substance manasanthin A and B were obtained.

3. Structural Analysis of Dyneolignan Compounds (Manasanthin A, B)

The material obtained through the above example was determined using a VG high resolution GC / MS spectrometer, Election Ionization MS, Autospec-Ultima, and the molecular weight and molecular formula were determined by using a polarizer (Jasco DIP-). 181 digital polarimeter). Nuclear Magnetic Resonance (NMR) analysis (Bruker AMX 300) also revealed ¹ H NMR, ¹³ C NMR, Homo-Cozy (HOMO-COSY), 1M-Detected heteronuclear Multiple-Quantum Coherence (HMQC), and Heteronuclear Multiple-Bond (HMBC). Coherence) and DEPT (Distortionless Enhancement by Polarization) spectra were obtained and molecular structure was determined.

The measurement results are as follows, and the results of comparative analysis showed that the compounds of the formulas (1) and (2) were manasanthin A, B (Koppaka V. Rao and Francisco M. Alvarez, Tetrahedron Letters, 24 (45) 4947- 4950, 1983).

[Manaxanthine A]

1) Physical property: amorphous powder

2) Linearity: [α] _D -100

3) Molecular Weight: 732

4) Molecular formula: C ₄₂ H ₅₂ O ₁₁

5) ¹ H-NMR (CDCl ₃ , 300 MHz) δ 0.67, 0.78 (d, J = 6 Hz, 2 CH-C H ₃ ), 1.10, 1.20 (d, J = 6 Hz, 2 C H ₃ -CH-O) , 2.3 (m, 2 C H -CH ₃ ), 3.86 (s, 6 OCH ₃ ), 4.10 (m, 2 CH ₃ -C H -O), 4.57, 4.70 (d, J = 8 Hz, 2 Ar-C H -OH), 5.40, 5.50 (d, J = 6 Hz, 2 Ar-C H -O-), 6.70-7.05 (m, 12 atom H)

6) ¹³ C-NMR (CDCl ₃ , 75 MHz) δ 150.4, 148.9, 148.7, 146.3, 136.2, 132.6 (Aromatic C), 119.8, 118.6, 118.4, 111.8, 110.1 (Aromatic CH), 83.6, 83.2 (-O- C H-Ar, HO- C H-Ar), 78.1 (O- C H-CH ₃ ), 55.7 (O-CH ₃ ), 44.0 (CH-CH ₃ ), 16.8 (O-CH- C H ₃ ) , 14.7 (CH-CH ₃ )

7) EIMS (rel. Int.) M / z [M] + 732

[Manaxanthine B]

1) Physical property: amorphous white powder

2) Linearity: [α] _D -99

3) Molecular Weight: 716

4) Molecular formula: C ₄₁ H ₄₈ O ₁₁

5) ¹ H-NMR (CDCl ₃ , 500 MHz) δ 6.77-7.00 (m, 12 atom.H), 5.94 (s, OC H ₂ -O), 5.46 (d, 2 Ar-C H -O), 4.63 (t, 2Ar-C H -OH), 4.16 (m, 2 Ar-OC H -CH ₃ ), 3.90 (s, 2 OC H ₃ ), 2.29 (s, -OC H ₃ ). 2.16 (s, OC H ₃ ), 1.72 (s), 1.16 (m, 2 O-CH-C H -CH ₃ ), 0.72 (d, 2 CH-C H ₃ ),

6) ¹³ C-NMR (CDCl ₃ , 125 MHz) δ 150.5, 150.5, 148.9, 148.8, 147.7, 147.3, 146.4, 146.2, 136.5, 136.4, 133.9, 132.5 (aromatic C), 121.0, 119.9, 118.8, 118.6, 118.6 , 118.6, 110.8, 110.0, 110.0, 108.0, 107.5 (aromatic CH), 101.0 (O-CH2-O), 83.9, 83.8, 83.3, 83.2 (-O-CH-Ar, HO-CH-Ar), 78.3 ( O- C H-CH ₃ ), 55.8, 55.8, 55.8 (-O- C H ₃ ), 44.1 (O-CH- C H-CH ₃ ), 16.9, 16.8, 14.8 (-CH- C H ₃ )

7) EIMS (rel. Int.) M / z [M] + 716 (33), 538 (11), 522 (14), 370 (29), 192 (100), 164 (59)

Experimental Example 1 : Effect on the ACAT activity of dyneolignan compound (manasanthin A, B)

In order to determine the effect on the ACAT activity of manasanthin A, B extracted, separated and purified from three hundred seconds according to the present invention, the following experiment was performed.

1. Preparation of ACAT Enzyme Source

Human ACAT-1 and ACAT-2 proteins were obtained using baculovirus expression system to investigate the effects on human ACAT-1 and ACAT-2 activity.

First, cDNAs of hACAT-1 and hACAT-2 obtained through human cDNA library screening were inserted into baculovirus delivery vectors and introduced into sf9 cells, which are insect cells, to prepare viruses. Subsequently, the recombinant viruses of hACAT-1 and hACAT-2 were isolated by plaque purification, and the titer of the viral stock was increased through three amplification processes. Recombinant virus was infected to Hi5 insect cells having good protein expression efficiency to 1 (Mutiplicity of Infection), and then cultured for one day at 27 ° C.

The cultured hACAT-1 and hACAT-2 were collected by centrifugation at 500xg for 15 minutes to separate microsomal fractions from overexpressed Hi5 cells, and then quenched by rapid freeze thawing in hypotonic buffer. After breaking the ultracentrifugation for 100,000 hours at 100,000xg.

The obtained microsomal fractions were suspended in storage buffer so that the protein concentration was 8 mg / ml and stored in a deep freezer until use.

2. ACAT activity measurement

6.67 μl of a cholesterol solution dissolved in acetone at a concentration of 1 mg / ml was mixed with 6 μl of 10% triton WR-1339 (Sigma Co.) in acetone, and acetone was removed by evaporation using nitrogen gas. It was. Distilled water was added to the obtained mixture to adjust the concentration of cholesterol to 30 mg / ml.

10 μl of aqueous solution of cholesterol, 10 μl of 1M KH ₂ PO ₄ (pH 7.4), 5 μl of 0.6 mM bovine serum albumin (BSA), 10 μl of microsome solution obtained in 1, 10 μl Samples (manasanthin A, manasanthin B) and 45 μl of distilled water were added (90 μl total). The mixture was pre-reacted for 30 minutes in a 37 ° C. water bath.

10 μl of (1- ¹⁴ C) oleyl-CoA solution (0.05 μCi, final concentration: 10 μM) was added to the pre-reacted mixture and the resulting mixture was reacted for 30 minutes in a 37 ° C. water bath. To this was added 500 μl isopropanol: heptane mixture (4: 1 (v / v)), 300 μl heptane and 200 μl 0.1 M KH ₂ PO ₄ (pH 7.4) and the mixture was vigorously vortexed. After mixing, the mixture was left at room temperature for 2 minutes.

200 μl of supernatant was placed in a scintillation bottle, and 4 ml of scintillation solution (Lumac) was added. The radiation dose of this mixture was measured with a 1450 Microbeta liquid scintillation counter, Wallacoy, Finland.

ACAT activity was calculated from cholesteryl oleate picolol (picomol / min / mg protein) synthesized per mg of protein for 1 minute by calculating the radiation dose per hour from the measured radiation dose.

The results are shown in Table 1 and Table 2.

Activity against ACAT of Manasanthin A Enzyme IC ₅₀ (μM) Person ACAT-1 11 Person ACAT-2 5

Activity against ACAT of Manasanthin B Enzyme IC ₅₀ (μM) Person ACAT-1 29 Person ACAT-2 160

As shown in Table 1 and Table 2, ManaSanthin A, a dyneolignan compound, has an IC ₅₀ value of 11 μM and 5 μM for human ACAT-1 and human ACAT-2, respectively, and manasanthin B represents human ACAT-1. The IC ₅₀ values for human ACAT-2 were 29 μM and 160 μM, respectively.

Therefore, it can be seen that manasanthin A and B effectively inhibit ACAT activity and prevent and treat cardiovascular diseases such as hyperlipidemia, coronary heart disease, arteriosclerosis and myocardial infarction caused by the synthesis and accumulation of cholesteryl esters. This can be useful for.

Experimental Example 2  : Acute Toxicity Test

In order to determine the acute toxicity of the compounds manasanthin A, B, an acute toxicity test was carried out as follows.

Six-week-old SPF mice were used as experimental animals, and three animals were divided per group. The compound (manasanthin A, B) obtained in the above example was suspended in 0.5% Tween 80 solution to prepare a test substance dose of the highest dose group at 100 mg / ml, and the dilution of the test solution of the low dose groups was performed. It prepared. Preparations were made just prior to dosing and were administered once orally to rats.

After administration of the test substance, mortality, clinical symptoms, and changes in body weight were observed. Hematological and hematological examinations were performed. Necropsy was performed to observe abdominal and thoracic organ abnormalities.

As a result of the test, manasanthin A and B showed death of all animals in the 400 mg / kg administration group, and gastric mucosal hemorrhage was observed at necropsy of the dead animals. In weight change, no weight loss was observed in all dose groups. One hundred and thirty seconds extracts were observed in the 1000 mg / kg administration group and three in the 1500 mg / kg administration group, and hemorrhage of gastric mucosa was observed at necropsy of the dead animals.

From the above results, the LD ₅₀ value of single oral administration of the test substance manasanthin A and B mice was estimated to be between 200 and 400 mg / kg, and the LD ₅₀ value of oral administration to the trichophytium extract was 1 g / kg or more. Was judged to exist in.

Examples of preparations for the compositions of the present invention are illustrated below.

Formulation Example 1  : Preparation of Pharmaceutical Formulations

1. Preparation of powder

Manasanthin A or Manasanthin B 2g

1g lactose

The above ingredients were mixed and filled in airtight cloth to prepare a powder.

2. Preparation of Tablets

Manasanthin A or Manasanthin B 100 mg

Corn Starch 100mg

Lactose 100mg

2 mg magnesium stearate

After mixing the above components, tablets were prepared by tableting according to a conventional method for producing tablets.

3. Preparation of Capsule

Manasanthin A or Manasanthin B 100 mg

Corn Starch 100mg

Lactose 100mg

2 mg magnesium stearate

After mixing the above components, the capsule was prepared by filling in gelatin capsules according to the conventional method for producing a capsule.

4. Preparation of Injection Solution

Manasanthin A or Manasanthin B 10 μg / ml

Dilute hydrochloric acid BP until pH 3.5

Injectable sodium chloride BP up to 1 ml

Dissolve manasanthin A or manasanthin B in an appropriate volume of sodium chloride BP for injection, adjust the pH of the resulting solution to pH 3.5 with dilute hydrochloric acid BP, adjust volume with injectable sodium chloride BP and mix well It was. The solution was filled into a 5 ml Type I ampoule of clear glass, dissolved in glass and enclosed under an upper grid of air, sterilized by autoclaving at 120 ° C. for at least 15 minutes to prepare an injection solution.

Formulation Example 2  : Manufacture of food

Foods containing manasanthin A or manasanthin B were prepared as follows.

1. Preparation of Cooking Seasonings

Manasanthin A or manasanthin B 0.2 to 10% by weight for health promotion cooking seasoning was prepared.

2. Preparation of Tomato Ketchup and Sauce

Health promotion tomato ketchup or sauce was prepared by adding 0.2-1.0 wt% of manasanthin A or manasanthin B to tomato ketchup or sauce.

3. Manufacturing of Flour Foods

0.1 to 5.0% by weight of manasanthin A or manasanthin B was added to the flour, and bread, cake, cookies, crackers and noodles were prepared using the mixture to prepare foods for health promotion.

4. Preparation of soups and gravy

Manaxanthin A or manasanthin B 0.1-1.0% by weight was added to the soup and gravy to prepare health products, health soups and gravy.

5. Preparation of Ground Beef

Health promotion ground beef was prepared by adding 10% by weight of manasanthin A or manasanthin B to the ground beef.

6. Manufacture of Dairy Products

0.1-1.0% by weight of manasanthin A or manasanthin B was added to milk and various milk products such as butter and ice cream were prepared using the milk.

7. Manufacture of wire

Brown rice, barley, glutinous rice, and yulmu were alphad by a known method, and then dried and roasted to prepare a powder having a particle size of 60 mesh using a grinder.

Black beans, black sesame seeds, and perilla were also steamed and dried by a known method, and then ground to a powder having a particle size of 60 mesh.

Manasanthin A or manasanthin B was decompressed and concentrated in a vacuum concentrator, and the dried product obtained by drying with spray and hot air dryer was pulverized with a particle size of 60 mesh to obtain a dry powder.

The dry grains of the grains, seeds and manasanthin A (or manastanthin B) prepared above were prepared in the following ratio.

Cereals (30% by weight brown rice, 15% by weight radish, 20% by weight barley),

Seeds (7% by weight perilla, 8% by weight black beans, 7% by weight black sesame),

Dry powder of manasanthin A or manasanthin B (1% by weight),

Ganoderma lucidum (0.5% by weight),

Foxglove (0.5 wt%)

Formulation Example 3  : Preparation of Beverages

1. Preparation of Carbonated Drinks

5-10% of sugar, 0.05-0.3% citric acid, 0.005-0.02% caramel, 0.1-1% of vitamin C are mixed, and 79-94% purified water is mixed to make syrup, and the syrup is 85-98 Sterilizing at 20 ℃ for 180 seconds, mixed with cooling water in a ratio of 1: 4, and then injected with 0.5 to 0.82% carbon dioxide gas to prepare a carbonated beverage containing manasanthin A or manasanthin B.

2. Manufacture of health drinks

Instant sterilization by homogeneously combining manasanthin A or manasanthin B with liquids such as liquid fructose (0.5%), oligosaccharide (2%), sugar (2%), salt (0.5%) and water (75%). After that, it was packaged in small packaging containers such as glass bottles and plastic bottles to prepare a healthy beverage.

3. Preparation of Vegetable Juice

Health supplement vegetable juice was prepared by adding 0.5 g of manasanthin A or manasanthin B to 1,000 ml of tomato or carrot juice.

4. Preparation of Fruit Juice

0.1 g of manasanthin A or manasanthin B was added to 1,000 ml of apple or grape juice to prepare fruit juice for health promotion.

Manasanthin A or manasanthin B as an active ingredient in the composition of the present invention effectively inhibits the activity of acyl-CoA: cholesterol transferase, and thus, hyperlipidemia associated with acyl-CoA: cholesterol transferase, coronary heart disease, and arteriosclerosis. And it can be usefully used for the prevention and treatment of cardiovascular diseases such as myocardial infarction.

Claims (2)

Hyperlipidemia, coronary heart disease, arteriosclerosis, and myocardial infarction, which are the active ingredients of dynalignan-based compounds of manasantin A represented by the following formula (1) or manasantin B (manassantin B) represented by the following formula: Food composition for preventing the same cardiovascular disease. <Formula 1>

<Formula 2>

The food composition for preventing cardiovascular diseases such as hyperlipidemia, coronary heart disease, arteriosclerosis and myocardial infarction according to claim 1, wherein the manasanthin A or manasanthin B is obtained by extraction, separation and purification from three hundred seconds.