Abstract:
본 발명은 디오스민(diosmin)을 포함하는 동맥경화증 및 고지혈증의 예방 및 치료용 조성물에 관한 것으로, 디오스민은 동물에게 투여되었을 때 동맥내피에 대식세포-지질 복합체가 침착되는 것을 강력히 억제할 뿐만 아니라, ACAT 및 HMG-CoA 환원효소의 활성을 억제하고, 혈중 콜레스테롤 및 중성지질의 농도를 감소시키므로, 동맥경화증 및 고지혈증의 예방 및 치료제로서 유용하게 사용될 수 있다.
Abstract:
PURPOSE: Food composites including tannin or tannin-derived phenolics are provided to prevent and treat arteriosclerosis, hyperlipidemia and hepatic steatosis by dosing tannin, gallic acid or/and ellagic acid. CONSTITUTION: Tannin, gallic acid or/and ellagic acid is/are added to a food or a drink to prevent and treat arteriosclerosis. Tannin(C76H52O46) is extracted from acorns, persimmons and walnut shells. Gallic acid(C7H6O5) and ellagic acid(C14H6O8) are the decomposition products of tannin and have anticancer activities. The amount of the tannin-derived phenolics is from 0.01wt.% to 20wt.% according to the weight, age, gender, health status, diet, dosage time and method, excretory rate and disease level of patients.
Abstract:
PURPOSE: A composition containing tannin, gallic acid or ellagic acid is provided for preventing and treating arteriosclerosis, hyperlipemia and liver diseases. CONSTITUTION: When tannin, gallic acid or ellagic acid are administrated into an animal body, they prevent the deposition of macrophage-lipid complex within the inner surface of arterial duct, decrease the concentration of GOT(glutamate-oxaloacetate transaminase), GPT(glutamate-pyruvate transaminase), gammaGTP(gamma-glutamyl transpeptidase), and lipid in serum, and strongly inhibit the damage of liver cells and the progress of fatty liver. The composition contains an effective of ellagic acid displaying an anticancer activity, that is 0.1 mg to 500 mg/weight kg a day. The composition is preferably administrated into an animal body 5 times a day in a dosage of 1 mg to 100 mg/weight kg.
Abstract:
PURPOSE: A pharmaceutical composition containing one of rutin and Quercetin or the mixture is provided to prevent and treat hyperlipidemia, arteriosclerosis and liver diseases. CONSTITUTION: The rutin is extracted from buckwheat or leaves, stems and flowers of the buckwheat by leaving the materials at a base of pH10-12 by using calcium hydroxide, neutralizing and settling the materials, or by using 20-97% alcohol or water at a high temperature and pressure. The buckwheat and the leaves, stems and flowers also can be dried and pulverized to get powdered buckwheat. The resulting buckwheat flour or buckwheat extract containing 0.01-10wt% of the rutin, quercetin or the mixture of them is added to tomato ketchup, sauce and juice, ramen, noodle, bread, cookies and cracker, soup and gravies, ground beef, or dairy products to get functional foods.
Abstract:
PURPOSE: A microorganism, Penicillium griseofulvum, producing pyripyropene A and a method for producing cholesterol metabolism inhibitor are provided, wherein pyripyropene A inhibits the activity of cholesterol acyltransferase(ACAT) which adsorbs cholesterol into blood, and is thus used in decreasing the blood cholesterol concentration. CONSTITUTION: Penicillium griseofulvum F1959 separated from soil by Samson method produces pyripyropene A which inhibits the activity of cholesterol acyltransferase(ACAT) and its inhibition concentration IC50 is about 35 ng/ml which is calculated by the equation. The ACAT inhibitor pyripyropene A is produced by the steps of: incubating Penicillium griseofulvum F1959 in a spawn medium containing 0.5% of glucose, 0.2% of yeast extract, 0.5% of polypeptone, 0.1% of potassium phosphate and 0.05% of magnesium sulfate at 29 deg. C for 18 hours; and incubating the microorganism in a growth medium containing 2% of starch, 0.4% of soytone, 0.3% of pama media, 0.1% of potassium phosphate, 0.05% of magnesium sulfate, 0.3% of calcium carbonate and 0.2% of sodium chloride at 29 deg. C for 120 hours.
Abstract translation:目的:提供微生物青霉菌青霉菌,产生吡柔比星A和生产胆固醇代谢抑制剂的方法,其中吡哆灵A抑制胆固醇酰基转移酶(ACAT)的活性,胆固醇酰基转移酶(ACAT)将胆固醇吸附到血液中,因此用于降低血液胆固醇浓度 。 构成:通过Samson方法从土壤中分离的灰黄霉菌F1959产生抑制胆固醇酰基转移酶(ACAT)活性的白藜芦醇A,其抑制浓度IC50为约35ng / ml,其通过该方程式计算。 通过以下步骤制备ACAT抑制剂pyripyropene A:在含有0.5%葡萄糖,0.2%酵母提取物,0.5%多聚蛋白胨,0.1%磷酸钾和0.05%硫酸镁的产卵培养基中将灰黄青霉F1959温育于29℃ 度。 C 18小时; 并在29℃下将微生物培养在含有2%淀粉,0.4%大豆油,0.3%帕马培养基,0.1%磷酸钾,0.05%硫酸镁,0.3%碳酸钙和0.2%氯化钠的生长培养基中 度。 C 120小时。
Abstract:
본 발명은 담배풀(Carpesium adrotanoides L)로부터 신생혈관 유도현상(angiogenesis)을 억제하는 활성을 갖는 세스큐터핀 락톤(sesquiterpene lacton)계 화합물의 제조 방법 및 이를 포함하는 조성물에 관한 것으로, 상기 화합물은 신생혈관 유도현상을 억제할 수 있으므로, 각막이식시 실명, 암전이 및 당뇨병성 망막증의 예방 및 치료에 유용하게 사용할 수 있다.
Abstract:
본 발명은 담배로부터 유도 발현되는 메탈로티오네인(metallotionein) 단백질에 관한 것으로, 식물의 병원체 또는 물리적인 상처에 의해서 야생종 담배로부터 발현 유도되는 메탈로티오네인 단백질은 식물체의 병저항성 유도물질 탐색으로 식물체의 병저항성 발현을 확인할 수 있고, 식물체에 가해지는 상처에 대한 방어기작을 조사할 수 있는 표지로서 이용되어 식물체의 스트레스에 대한 저항성 식물의 개발 및 이의 생물학적 치료도 가능하리라 본다.