KR20090077611A - Composition comprising orostachys japonicus extract for inhibiting obesity and for preventing or treating hyperlipidemia - Google Patents
Composition comprising orostachys japonicus extract for inhibiting obesity and for preventing or treating hyperlipidemia Download PDFInfo
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- KR20090077611A KR20090077611A KR1020080003650A KR20080003650A KR20090077611A KR 20090077611 A KR20090077611 A KR 20090077611A KR 1020080003650 A KR1020080003650 A KR 1020080003650A KR 20080003650 A KR20080003650 A KR 20080003650A KR 20090077611 A KR20090077611 A KR 20090077611A
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- South Korea
- Prior art keywords
- extract
- composition
- wasong
- obesity
- ethyl acetate
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Abstract
Description
본 발명은 와송 추출물을 포함하는 비만 억제 및 고지혈증 예방 또는 치료용 조성물에 관한 것이다.The present invention relates to a composition for inhibiting obesity and preventing or treating hyperlipidemia, which comprises a Warsong extract.
최근 경제성장과 생활방식의 변화에 따라 식습관에도 많은 변화가 있다. 특히, 바쁜 현대인들은 패스트푸드 등의 고열량 식이와 적은 운동량으로 인하여 체중 과다 및 비만이 증가하고 있다.There are many changes in eating habits due to recent economic growth and lifestyle changes. In particular, busy modern people are gaining weight and obesity due to high calorie diets such as fast food and low exercise.
체중 과다는 체질량 지수(BMI, 체중을 키의 제곱으로 나눈 비만 척도)가 25 이상 30 미만을 의미하며, 비만은 체질량 지수가 30 이상일 때 해당된다.Overweight means a body mass index (BMI, an obesity measure of body weight divided by the square of height) of 25 or more and less than 30. Obesity is applicable when the body mass index is 30 or more.
미국 성인의 3분의 2는 체중 과다이거나 비만이며, 체중 과다는 혈압과 콜레스테롤 수치를 높여 심장 질환 등의 각종 성인병의 발병률을 증가시키고, 비만은 심장병과 당뇨병, 관절염 및 일부 암 위험성을 증가시키고 있다.Two-thirds of American adults are overweight or obese, and overweight increases blood pressure and cholesterol levels, increasing the incidence of various adult diseases such as heart disease, and obesity increases the risk of heart disease, diabetes, arthritis and some cancers .
체중 과다 및 비만은 성인뿐만 아니라 어린이나 청소년들에서도 동맥경화, 고혈압, 고지혈증 또는 심장질환 등의 각종 성인병의 발병률을 증가시키는 한 요인 이 되고 있다.Overweight and obesity have contributed to increasing the incidence of various adult diseases such as arteriosclerosis, hypertension, hyperlipidemia or heart disease in children as well as adolescents.
이와 같이 비만은 모든 연령층에 걸쳐 영향을 주고 있으나, 특히 장년층의 발생빈도가 높다. 동양에서는 채식 위주의 생활습관으로 인해 비만증이 그리 많지 않았던 것으로 알려져 있으나, 현대에 들어서 서양문물의 영향으로 식생활 습관이 바뀌고 주거환경이 바뀌면서 동양인에게서도 점차 비만증이 증가하기 시작하였다.As such, obesity affects all age groups, but the incidence of older adults is high. It is known that obesity was not so much in the East due to the vegetarian-oriented lifestyle, but in modern times, obesity gradually began to increase in Asians as the eating habits and the living environment changed due to the influence of western culture.
또한 현대인은 과로, 과음, 스트레스 등으로 인하여 체력이 저하되며, 약 30~40%가 비만증을 가지고 있고, 그 중 약 10% 정도는 심각하거나 병적인 비만증을 나타낸다고 보고된 바 있다.In addition, modern man has been reported that physical strength is reduced due to overwork, heavy drinking, stress, etc., about 30-40% have obesity, about 10% of them have severe or pathological obesity has been reported.
비만은 체내에 지방이 과도하게 축적되어 있는 상태로 체중에서 지방이 차지하는 비율이 높은 상태를 나타내며, 단순성 비만과 2차성 비만(증후성 비만)으로 분류된다.Obesity refers to a state in which fat is excessively accumulated in the body and a high proportion of fat in the body weight is classified into simple obesity and secondary obesity (symptomatic obesity).
단순성 비만의 원인으로는 과식, 운동부족, 및 기초대사의 저하 등을 들 수 있다. 임상적으로 비만으로 판정되는 경우의 대부분은 단순성 비만이다. 단순성 비만이 발현하여 그 상태가 지속되면, 각종 건강 장해를 일으키는 원인이 된다.The causes of simplicity obesity include overeating, lack of exercise, and decreased metabolism. The majority of cases that are clinically judged as obesity are simplicity obesity. If obesity manifests and the condition persists, it causes various health disorders.
2차성 비만은 임의의 기초질환이 원인이 되어 발생하는 비만으로, 내분비성 비만, 시상하부성 비만, 유전성 비만 또는 약제에 기인한 비만 등을 들 수 있다.Secondary obesity is obesity caused by any underlying disease, and may include endocrine obesity, hypothalamic obesity, hereditary obesity, or obesity due to drugs.
비만의 주요 원인은 지방세포의 과성장에 있으며, 이는 뇌에서 명령하여 분비되는 렙틴(leptin)이라는 호르몬의 결핍으로 일어난다. 이러한 렙틴 호르몬의 결핍은 유전적으로 결핍이 일어난 경우를 제외하고는 과식, 노화로 인한 생체 내 물질대사의 약화, 체내에 과량 축적된 동물성 콜레스테롤에 의해 분비가 줄어든다.The main cause of obesity is overgrowth of fat cells, which is caused by a deficiency of a hormone called leptin, which is ordered and secreted by the brain. The deficiency of leptin hormone is reduced by overeating, weakening of metabolism in vivo due to aging, and animal cholesterol accumulated in the body, except when genetic deficiency occurs.
비만은 그 자체가 고지혈증, 고혈압, 심혈관 질환, 가성 뇌종양(pseudotumor cerebri), 수면 무호흡증(sleep apnea), 암, 폐 고혈압(pulmonary hypertension), 담낭염(cholecystitis) 및 골관절염(osteoarthritis) 등의 각종 질환의 원인이 되거나, 또는 활동성의 저하 등의 문제를 야기한다. 또한, 비만은 여러 가지 질환이 원인이 되어 합병증으로 나타나는 경우도 있다.Obesity itself is the cause of various diseases such as hyperlipidemia, hypertension, cardiovascular disease, pseudotumor cerebri, sleep apnea, cancer, pulmonary hypertension, cholecystitis and osteoarthritis Or cause problems such as deterioration of activity. In addition, obesity may be caused by various diseases and may appear as a complication.
비만에 의해 유발되는 성인병 중 가장 많이 발병되는 질환으로 고지혈증이 있다. 고지혈증(hyperlipidemia)은 동맥경화증의 지수로서, 소장에서 중성지질의 합성과 킬로마이크론(chylomicron)의 분비증가, 간장에서 중성지방의 합성 증가, 초저밀도 지질단백질-트리글리세라이드(Very low density lipoprotein-Triglyceride; VLDL), 저밀도 지질단백질(low density lipoprotein; LDL)-콜레스테롤 합성 및 분비증가, 고밀도 지질단백질(high density lipoprotein; HDL)-콜레스테롤의 합성 감소 및 리파제의 활성 감소로 인한 말초조직에서의 중성지방의 제거 감소에 기인한 것이다(Miller, N.E. 1978. The evidence for the antiatherogenicity of high density lipoprotein in man. Lipid ., 13, 914~919.). 고지혈증은 일반적으로 혈중 콜레스테롤이 240 ㎎/㎗ 이상인 경우를 말하며, 정상 수치인 200 ㎎/㎗ 이하로 낮추어야 한다고 권장하고 있다. 고지혈증의 원인으로는 유전, 알콜의 섭취, 고지방 및 고칼로리 식사, 비만, 당뇨병, 간기능 장애, 갑상선 기능 장애 및 신증후군 등이 알려져 있다.Hyperlipidemia is one of the most common diseases caused by obesity. Hyperlipidemia is an index of arteriosclerosis, which increases the synthesis of triglycerides and secretion of chylomicrons in the small intestine, increases the synthesis of triglycerides in the liver, and very low density lipoprotein-triglycerides (VLDL). ), Increased low density lipoprotein (LDL) -cholesterol synthesis and secretion, decreased synthesis of high density lipoprotein (HDL) -cholesterol, and reduced elimination of triglycerides in peripheral tissues due to decreased lipase activity. (Miller, NE 1978. The evidence for the antiatherogenicity of high density lipoprotein in man. Lipid ., 13 , 914--919.). Hyperlipidemia generally refers to the case where the blood cholesterol level is 240 mg / dl or more, and is recommended to be lowered below the normal level of 200 mg / dL. The causes of hyperlipidemia are heredity, alcohol consumption, high fat and high calorie meals, obesity, diabetes, liver dysfunction, thyroid dysfunction and nephrotic syndrome.
현재 사용되고 있는 비만증을 치료하기 위한 약물요법으로는 식욕억제제, 소화흡수 저해제, 비만축적 방해제 또는 대사촉진제 등이 있으나, 이들 비만 치료제 는 약물 의존성 등의 부작용을 일으킬 위험성이 있다. 또한, 투여한 환자에게 단기간에 내성이 생겨버리는 경우도 있기 때문에, 장기간 연속하여 사용할 수 없다는 문제점도 있다.Drug therapy for the treatment of obesity currently being used include an appetite suppressant, digestive absorption inhibitors, obesity-inhibiting inhibitors or metabolic accelerators, these obesity drugs have a risk of causing side effects such as drug dependence. In addition, there is a problem in that resistance can be developed in a short period of time to a patient to be administered, so that it cannot be used continuously for a long time.
또한, 고지혈증을 치료하기 위해 일반적으로 사용되는 치료방법으로는 식이요법을 통한 치료가 우선되고 있으나, 이로 인해 개선되지 않을 경우 담즙산 결합수지, 니코틴산(nicotinic acid) 유도체류, 피브린산(fibric acid) 유도체류, 프로부콜(probucol) 등의 약제가 사용되고 있다. 최근 들어 가장 많이 사용되고 있는 HMG CoA 환원제 억제제(3-hydroxyl-3-methylglutaryl-coenzyme A reductase inhibitor) 등이 치료제로 사용되고 있으나, 이러한 약제들은 아직까지 임상적으로 만족할만한 효과를 얻지 못하고 있다.In addition, as a treatment method commonly used to treat hyperlipidemia, treatment through diet is preferred, but if it is not improved, bile acid-binding resins, nicotinic acid derivatives, and fibric acid induction Pharmaceuticals such as retention and probucol are used. Recently, the most widely used HMG CoA reducing agent inhibitor (3-hydroxyl-3-methylglutaryl-coenzyme A reductase inhibitor) and the like have been used as a therapeutic agent, but these drugs have not yet obtained a clinically satisfactory effect.
따라서, 많은 연구자들은 장기간 사용하여도 인체에 독성이 없고 부작용이 적은 비만 억제제 및 고지혈증 치료제를 개발하기 위하여 생약재를 이용한 연구를 수행하고 있다.Therefore, many researchers are conducting research using herbal medicines to develop anti-obesity inhibitors and hyperlipidemia drugs that are not toxic to humans even after long-term use and have fewer side effects.
한편, 와송(瓦松, Orostachys japonicus)은 일명 바위솔로 불리는 쌍떡잎식물 장미목 돌나물과의 다년생 초본식물로, 한방고서에 항암효과, 해열, 지열, 간염, 습진, 화상 등에 특효가 있다고 기록되어 있다. 특히 간암, 유방암, 췌장암, 골수암, 식도암, 자궁암, 임파선암, 위암, 대장암, 고혈압, 저혈압, 혈액순환, 당뇨병, 중풍, 관절염, 위장병, 팔 다리 아프고, 손발 저림, 변비, 구토, 각종 성인병 등에 특효가 있다고 알려져 있다. 지금까지 분리·보고된 와송의 성분으로는 프리델린(friedelin), 에피-프리델라놀(epi-friedelanol), 글루티논(glutinone), 글 루티놀(glutinol)과 같은 트리테르페노이드(triterpenoid)류; β-시토스테롤(β-sitosterol), 캄페스테롤(campesterol) 등의 스테롤(sterol) 계열 물질; 지방산 에스테르류 및 캠프페롤(kaempferol), 퀘르세틴과 같은 플라보노이드; 4-히드록시벤조산, 3,4-디히드록시벤조산, 갈릭산(gallic acid) 등의 방향족산(aromatic acid) 등이 있다. Orostachys japonicus is a perennial herbaceous plant with the dicotyledonous rosewood snails, also known as rock brush, and has been reported to have anticancer effects, antipyretic, geothermal, hepatitis, eczema, and burns in oriental medicine. In particular, liver cancer, breast cancer, pancreatic cancer, bone marrow cancer, esophageal cancer, uterine cancer, lymph gland cancer, stomach cancer, colon cancer, hypertension, hypotension, blood circulation, diabetes, stroke, arthritis, gastrointestinal disease, limb pain, hand and foot numbness, constipation, vomiting, various adult diseases It is known that there is effect. Soluble components reported so far are triterpenoids such as friedelin, epi-friedelanol, glutinone, and glutinol. Ryu; sterol-based materials such as β-sitosterol and campesterol; Fatty acid esters and flavonoids such as kaempferol and quercetin; And aromatic acids such as 4-hydroxybenzoic acid, 3,4-dihydroxybenzoic acid, and gallic acid.
상기한 바와 같이, 와송에 대해 다양한 약리학적 효과가 알려져 있지만, 항비만 및 항고지혈 효과에 대해서는 아직까지 알려져 있지 않으며 연구도 전무한 상태이다.As mentioned above, various pharmacological effects are known for vortex, but the anti-obesity and antihyperlipidemic effects are not yet known and there is no research.
이에, 본 발명자들은 와송 추출물의 항비만 및 항고지혈 효과에 대해 연구하던 중, 와송 추출물을 고지방 식이로 사육된 흰쥐에 투여한 결과 음식섭취량과 체중을 감소시키며, 지방조직의 무게를 감소시키고, 혈청 및 간조직 중의 지질 및 총콜레스테롤을 감소시키며, 저밀도 지질단백질 콜레스테롤을 유의적으로 감소시키고, 고밀도 지질단백질 콜레스테롤을 유의적으로 증가시키며, 동맥경화 위험지수(A.I.)도 유의적으로 감소시키고, 분변 중의 지방 함량을 높이는 것을 확인하고, 본 발명을 완성하였다.Therefore, the present inventors while studying the anti-obesity and anti-hyperlipidemic effect of the hawthorn extract, the administration of the hawsong extract in rats reared in a high-fat diet reduced food intake and weight, reduced the weight of fat tissue, serum And decreases lipid and total cholesterol in liver tissue, significantly decreases low-density lipoprotein cholesterol, significantly increases high-density lipoprotein cholesterol, significantly reduces arteriosclerosis risk index (AI), It was confirmed that the fat content was increased, and the present invention was completed.
본 발명은 와송 추출물을 포함하는 비만 억제 및 고지혈증 예방 또는 치료용 조성물을 제공하고자 한다.The present invention is to provide a composition for inhibiting obesity and preventing or treating hyperlipidemia, including the pine fruit extract.
본 발명은 와송 추출물을 포함하는 비만 억제 및 고지혈증 예방 또는 치료용 조성물을 제공한다.The present invention provides a composition for inhibiting obesity and preventing or treating hyperlipidemia, including a vortex extract.
본 발명에 따른 조성물은 약학 조성물 및 식품 조성물을 포함한다.Compositions according to the present invention include pharmaceutical compositions and food compositions.
이하, 본 발명에 대해 상세히 설명한다.Hereinafter, the present invention will be described in detail.
본 발명에 따른 와송 추출물은 하기와 같은 방법으로 추출·분리하여 제조된다. 먼저 와송을 물, 알콜 또는 물과 알콜의 혼합용매에 첨가하여 환류추출한다(3회 반복). 추출액을 여과한 후 감압농축하여 와송 조추출물을 얻는다. 상기 물과 알콜의 혼합용매는 10 내지 100%의 메탄올 또는 10 내지 100%의 에탄올 중에서 선택될 수 있으며, 바람직하게는 10 내지 100%의 메탄올이다.Wasong extract according to the present invention is prepared by extraction and separation in the following manner. First, vortex is added to water, alcohol or a mixed solvent of water and alcohol to extract reflux (3 times). The extract was filtered and concentrated under reduced pressure to obtain a vortex crude extract. The mixed solvent of water and alcohol may be selected from 10 to 100% methanol or 10 to 100% ethanol, preferably 10 to 100% methanol.
상기 와송 조추출물을 증류수에 현탁시키고, 클로로포름으로 3회 용매분획하여 와송 클로로포름 분획물을 얻는다. 그 다음 남은 수층을 에틸아세테이트로 3회 용매분획하여 와송 에틸아세테이트 분획물을 얻고, 남은 수층을 n-부탄올로 3회 용매분획하여 와송 부탄올 분획물을 얻는다. 남은 수층을 농축하여 물 분획물을 얻는다.The crude feed extract is suspended in distilled water and solvent fractionated three times with chloroform to obtain a feed chloroform fraction. Then, the remaining aqueous layer was solvent fractionated three times with ethyl acetate to obtain a Warson ethyl acetate fraction, and the remaining aqueous layer was solvent fractionated three times with n-butanol to obtain a Warson butanol fraction. The remaining aqueous layer is concentrated to give a water fraction.
본 발명에 따른 와송 추출물, 특히 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물은 고지방 식이로 사육된 흰쥐의 음식섭취량과 체중을 감소시키며, 지방조직의 무게를 감소시키고, 혈청 및 간조직 중의 지질 및 총콜레스테롤을 감소시키며, 저밀도 지질단백질 콜레스테롤을 유의적으로 감소시키고, 고밀도 지질단백질 콜레스테롤을 유의적으로 증가시키며, 동맥경화 위험지수(A.I.)도 유의적으로 감소시키고, 분변 중의 지방 함량을 높인다. 따라서, 본 발명에 따른 와송 추출물은 비만 억제 및 고지혈증 예방 또는 치료에 유용한 의약품 및 건강식품으로 사용될 수 있다.Whey extracts, in particular, Whey extract butanol fraction and Whey ethyl acetate fraction, reduced the food intake and body weight of the rats reared in a high fat diet, reduced the weight of adipose tissue, lipid and total cholesterol in serum and liver tissue Decreases, significantly reduces low density lipoprotein cholesterol, significantly increases high density lipoprotein cholesterol, significantly reduces arteriosclerosis risk index (AI), and increases fecal fat content. Therefore, the extracts according to the present invention can be used as medicines and health foods useful for inhibiting obesity and preventing or treating hyperlipidemia.
본 발명의 조성물은 와송 추출물과 함께 비만 억제 및 고지혈증의 예방 또는 치료 효과를 갖는 공지의 유효성분을 1종 이상 함유할 수 있다.The composition of the present invention may contain one or more known active ingredients having an effect of inhibiting obesity and preventing or treating hyperlipidemia together with the vortex extract.
본 발명의 조성물은, 투여를 위해서 상기 기재한 유효성분 이외에 추가로 약학적으로 허용가능한 담체를 1종 이상 포함하여 제조할 수 있다. 약학적으로 허용 가능한 담체는 식염수, 멸균수, 링거액, 완충 식염수, 덱스트로오스 용액, 말토 덱 스트린 용액, 글리세롤, 에탄올 및 이들 성분 중 1 성분 이상을 혼합하여 사용할 수 있으며, 필요에 따라 항산화제, 완충액, 정균제 등 다른 통상의 첨가제를 첨가할 수 있다. 또한 희석제, 분산제, 계면활성제, 결합제 및 윤활제를 부가적으로 첨가하여 수용액, 현탁액, 유탁액 등과 같은 주사용 제형, 환약, 캡슐, 과립 또는 정제로 제제화할 수 있다. 더 나아가 당분야의 적정한 방법으로 또는 Remington's Pharmaceutical Science(최근판), Mack Publishing Company, Easton PA에 개시되어 있는 방법을 이용하여 각 질환에 따라 또는 성분에 따라 바람직하게 제제화할 수 있다.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, as necessary. And other conventional additives such as buffers and bacteriostatic agents can be added. Diluents, dispersants, surfactants, binders and lubricants may also be added in addition to formulate into 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.
본 발명의 조성물은 목적하는 방법에 따라 경구 투여하거나 비경구 투여(예를 들어, 정맥 내, 피하, 복강 내 또는 국소에 적용)할 수 있으며, 투여량은 환자의 체중, 연령, 성별, 건강상태, 식이, 투여시간, 투여방법, 배설율 및 질환의 중증도 등에 따라 그 범위가 다양하다. 상기 와송 추출물의 일일 투여량은 약 1~1,000 ㎎/㎏, 바람직하게는 약 10~500 ㎎/㎏이며, 하루 일회 내지 수회에 나누어 투여하는 것이 더욱 바람직하다.The composition of the present invention can be administered orally or parenterally (eg, applied intravenously, subcutaneously, intraperitoneally or topically) according to the desired method, and the dosage is based on the weight, age, sex and health of the patient. The range varies depending on the diet, the time of administration, the method of administration, the rate of excretion and the severity of the disease. The daily dosage of the Wasong extract is about 1 to 1,000 mg / kg, preferably about 10 to 500 mg / kg, and more preferably, divided once to several times a day.
본 발명의 조성물은 비만 억제 및 고지혈증의 예방 또는 치료를 위하여 단독으로, 또는 수술, 호르몬 치료, 약물 치료 및 생물학적 반응 조절제를 사용하는 방법들과 병용하여 사용할 수 있다.The composition of the present invention can be used alone or in combination with methods using surgery, hormonal therapy, drug treatment and biological response modifiers for the inhibition of obesity and the prevention or treatment of hyperlipidemia.
본 발명의 조성물은 비만 억제 및 고지혈증의 개선을 목적으로 건강식품에 첨가될 수 있다. 본 발명의 와송 추출물을 식품 첨가물로 사용할 경우, 상기 와송 추출물을 그대로 첨가하거나 다른 식품 또는 식품 성분과 함께 사용할 수 있고, 통 상적인 방법에 따라 적절하게 사용할 수 있다. 유효 성분의 혼합양은 사용 목적(예방, 건강 또는 치료적 처치)에 따라 적합하게 결정될 수 있다. 일반적으로, 식품 또는 음료의 제조시에는 본 발명의 와송 추출물은 원료에 대하여 15 중량% 이하, 바람직하게는 10 중량% 이하의 양으로 첨가된다. 그러나, 건강 및 위생을 목적으로 하거나 또는 건강 조절을 목적으로 하는 장기간의 섭취의 경우에는 상기 양은 상기 범위 이하일 수 있으며, 안전성 면에서 아무런 문제가 없기 때문에 유효성분은 상기 범위 이상의 양으로도 사용될 수 있다.The composition of the present invention can be added to health food for the purpose of inhibiting obesity and improving hyperlipidemia. When using the walrus extract of the present invention as a food additive, the walrus extract can be added as it is or used with other foods or food ingredients, and can be suitably 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 beverages, the extract of the present invention is added in an amount of up to 15% by weight, preferably up 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. .
상기 식품의 종류에는 특별한 제한은 없다. 상기 물질을 첨가할 수 있는 식품의 예로는 육류, 소세지, 빵, 쵸코렛, 캔디류, 스넥류, 과자류, 피자, 라면, 기타 면류, 껌류, 아이스크림류를 포함한 낙농제품, 각종 스프, 음료수, 차, 드링크제, 알콜 음료 및 비타민 복합제 등이 있으며, 통상적인 의미에서의 건강식품을 모두 포함한다.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.
본 발명의 건강음료 조성물은 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다. 상술한 천연 탄수화물은 포도당, 과당과 같은 모노사카라이드, 말토오스, 수크로오스와 같은 디사카라이드, 및 덱스트린, 시클로덱스트린과 같은 폴리사카라이드, 자일리톨, 소르비톨, 에리트리톨 등의 당알콜이다. 감미제로서는 타우마틴, 스테비아 추출물과 같은 천연 감미제나, 사카린, 아스파르탐과 같은 합성 감미제 등을 사용할 수 있다. 상기 천연 탄수화물의 비율은 본 발명의 조성물 100㎖당 일반적으로 약 0.01~0.04g, 바람직하게는 약 0.02~0.03g 이다.The health beverage composition of the present invention may contain various flavors or natural carbohydrates, etc. as additional components, as in the general beverage. Natural carbohydrates described above are glucose, monosaccharides such as fructose, malsaccharides, disaccharides such as sucrose, and polysaccharides such as dextrin, 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.
상기 외에 본 발명의 조성물은 여러 가지 영양제, 비타민, 전해질, 풍미제, 착색제, 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알콜, 탄산 음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 본 발명의 조성물은 천연 과일쥬스, 과일쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 이러한 첨가제의 비율은 크게 중요하진 않지만 본 발명의 조성물 100 중량부 당 0.01~0.1 중량부의 범위에서 선택되는 것이 일반적이다.In addition to the above, the composition of the present invention includes various nutrients, vitamins, electrolytes, flavors, coloring agents, pectic acid and salts thereof, alginic acid and salts thereof, organic acids, protective colloidal thickeners, pH adjusting agents, stabilizers, preservatives, glycerin, alcohols, And a carbonation agent used for the carbonated beverage. In addition, the composition of the present invention may contain a pulp for the production of natural fruit juices, fruit juice drinks and vegetable drinks. 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.
이하, 본 발명의 이해를 돕기 위하여 바람직한 실시예를 제시한다. 그러나 하기의 실시예는 본 발명을 보다 쉽게 이해하기 위하여 제공되는 것일 뿐, 실시예에 의해 본 발명의 내용이 한정되는 것은 아니다.Hereinafter, preferred examples are provided to aid in understanding the present invention. However, the following examples are merely provided to more easily understand the present invention, and the contents of the present invention are not limited by the examples.
실시예Example 1 One : 와송 추출물의 제조 : Preparation of Wasong Extract
와송 3.6㎏을 5ℓ 둥근 바닥 플라스크에 넣고, 메탄올 3ℓ를 가한 후 환류 하에 5시간씩 3회 추출하였다. 추출액을 여과하고 진공농축기로 감압 하에 농축하여 와송 메탄올 추출물 268g을 얻었다. 상기 와송 메탄올 추출물을 2ℓ의 증류수에 현탁시킨 후, 0.8ℓ의 클로로포름으로 용매분획하여 클로로포름 분획물을 얻었다(3회 반복). 상기 클로로포름 분획물을 모은 다음 진공농축하여 클로로포름 분획물 112g을 얻었다. 그 다음 남은 수층을 0.8ℓ의 에틸아세테이트로 용매분획하여 에틸아세테이트 분획물 17g을 얻었다(3회 반복). 남은 수층을 0.8ℓ의 n-부탄올로 용매분획하여 부탄올 분획물 65g을 얻었다(3회 반복). 남은 수층을 농축하여 물 분획물 96g을 얻었다.3.6 kg of vortex was placed in a 5 L round bottom flask, and 3 L of methanol was added thereto, followed by extraction three times for 5 hours under reflux. The extract was filtered and concentrated under reduced pressure with a vacuum concentrator to give 268 g of Wasong methanol extract. The turmeric methanol extract was suspended in 2 L of distilled water, and then solvent fractioned with 0.8 L of chloroform to obtain a chloroform fraction (repeat three times). The chloroform fractions were collected and concentrated in vacuo to give 112 g of chloroform fractions. Then, the remaining aqueous layer was solvent fractionated with 0.8 L of ethyl acetate to obtain 17 g of ethyl acetate fraction (repeated three times). The remaining aqueous layer was solvent fractionated with 0.8 L of n-butanol to obtain 65 g of butanol fraction (repeat 3 times). The remaining aqueous layer was concentrated to give 96 g of water fractions.
실험예Experimental Example 1 One : : 항비만Anti-obesity 및 항고지혈 효과 측정 And antihyperlipidemic effects
본 발명에 따른 와송 추출물이 항비만 및 항고지혈 효과에 미치는 영향을 알아보기 위하여, 하기와 같은 실험을 수행하였다.In order to determine the effect of the hawsong extract according to the present invention on the anti-obesity and anti-hyperlipidemic effect, the following experiment was performed.
1. 실험동물1. Experimental Animal
실험동물은 체중 150±10g의 Sprague-Dawley계 웅성 흰쥐를 효창사이언스로부터 분양받아 동물사의 일정한 조건(온도: 20±2℃, 습도: 40~60%, 명암: 12시간 낮과 밤의 명암 주기(light/dark cycle)) 하에서 2주 정도 충분하게 적응시켜 사육하였다. 실험 시작 전 24시간 동안 물만 주고 절식하였다. 이때 효소 활성의 일중 변동을 고려하여 실험동물을 일정시간(오전 10:00~12:00) 내에서 처치하였다. 실험동물은 7개의 군으로 나누어 1군당 6마리씩 할당하였다.The experimental animals were supplied with Sprague-Dawley male rats weighing 150 ± 10g from Hyochang Science, and were subjected to constant conditions (temperature: 20 ± 2 ℃, humidity: 40-60%, contrast: 12 hours day and night contrast cycles). 2 weeks under light / dark cycle). 24 hours before the start of the experiment only watered and fasted. At this time, the experimental animals were treated within a certain time (10:00 AM ~ 12:00 AM) in consideration of the daily variation of enzyme activity. The experimental animals were divided into seven groups and 6 animals were allocated to each group.
2. 고지혈증 유발 및 시료 투여2. Induce hyperlipidemia and sample administration
실험동물의 1주일간의 적응기간을 거친 후, 1개의 군은 정상군으로 하여 일반식이 사료를 공급하였으며, 6개의 실험군에는 우지를 첨가한 조제 시료를 6주간 자유 공급하여 고지혈증을 유발하였다. 조제 시료는 표 1에 나타내었다.After one week of adaptation of the experimental animals, one group was fed a normal diet as a normal group, and six experimental groups were freely fed a preparation sample containing wedges for 6 weeks to induce hyperlipidemia. The preparation sample is shown in Table 1.
정상군 및 1개의 고지방 식이군에는 각각 1㎖의 생리식염수를 투여하였고, 5개의 고지방 식이군에는 상기 실시예 1에서 제조한 와송 메탄올 추출물, 와송 클로로포름 분획물, 와송 에틸아세테이트 분획물, 와송 부탄올 분획물 및 와송 물 분획물을 생리식염수에 용해한 4% 트윈 80을 사용하여 각각 100 ㎎/㎏씩 경구 존데 (oral jonde)를 사용하여 실험동물에 4주간 경구투여하였다.The normal group and one high-fat diet group were administered 1 ml of physiological saline, respectively, and the five high-fat diet groups were Wahsong methanol extract, Wahsong chloroform fraction, Wahsong ethyl acetate fraction, Wahson butanol fraction and Wahsong prepared in Example 1 above. Water fractions were orally administered to experimental animals for 4 weeks using oral jonde at 100 mg / kg each using 4% Tween 80 dissolved in saline.
실험에서 얻어진 결과의 통계처리는 평균치±표준편차로 표시하였으며, 통계적 유의성 검증은 Duncan's multiple range test를 이용하여 그 유의성을 나타내었다.The statistical results of the experimental results were expressed as mean ± standard deviation, and statistical significance verification was shown by Duncan's multiple range test.
※ 1) AIN-미네랄 혼합물(g/㎏ 식이) : 제2인산칼슘(calcium phosphate dibasic) 500.0, NaCl 74.0, 구연산칼륨(potassium citrate monohydrate) 220.0, 황산칼륨(potassium sulfate) 52.0, 산화마그네슘(magnesium oxide) 24.0, 탄산마그네슘(magnesium carbonate) 3.5, 구연산철(ferric citrate) 6.0, 탄산아연(zinc carbonate) 1.6, 탄산구리(cupuric carbonate) 0.3, 요오드화칼륨(potassium iodate) 0.01, 황산크롬칼륨(chromium potassium sulfate) 0.55, 수크로오스, 미세 분말로 하여 1,000이 되게 함.※ 1) AIN-mineral mixture (g / kg dietary): dicalcium phosphate dibasic 500.0, NaCl 74.0, potassium citrate monohydrate 220.0, potassium sulfate 52.0, magnesium oxide ) 24.0, magnesium carbonate 3.5, ferric citrate 6.0, zinc carbonate 1.6, cupuric carbonate 0.3, potassium iodate 0.01, chromium potassium sulfate ) 0.55, sucrose, fine powder to 1,000.
2) AIN-비타민 혼합물(g/㎏ 식이) : 티아민 HCl 0.6, 비오틴 0.02, 리보플라빈 0.6, 시아노코발아민(cyanocobalamine) 0.001, 피리독신(pyridoxine) HCl 0.7, 레티닐 아세테이트(retinyl acetate) 0.8, 티코틴산 3.0, DL-토코페롤 3.8, Ca-판토테네이트 1.6, 7- 데히드로콜레스테롤(7-dehydrocholesterol) 0.0025, 엽산 (folic acid) 0.2, 메티오닌 0.005, 수크로오스, 미세 분말로 하여 1,000이 되게 함.2) AIN-vitamin mixture (g / kg diet): Thiamine HCl 0.6, Biotin 0.02, Riboflavin 0.6, Cyanocobalamine 0.001, Pyridoxine HCl 0.7, Retinyl acetate 0.8, Ticotinic acid 3.0, DL-tocopherol 3.8, Ca-pantothenate 1.6, 7-dehydrocholesterol 0.0025, folic acid 0.2, methionine 0.005, sucrose, fine powder to 1,000.
3. 음식섭취량, 체중변화 및 지방조직의 무게 측정3. Measurement of food intake, weight change and adipose tissue weight
3-1. 음식섭취량 및 체중변화 측정3-1. Measurement of food intake and weight change
고지방 식이로 사육된 흰쥐의 음식섭취량과 체중변화는 실험개시일로부터 1주일마다 측정하였다. 음식섭취량 및 체중변화는 표 2에 나타내었다. Changes in food intake and body weight of rats fed a high-fat diet were measured weekly from the start of the experiment. Food intake and body weight change are shown in Table 2.
※ - FER(Food Efficiency Ratio) = 체중증가/음식섭취량※-FER (Food Efficiency Ratio) = weight gain / food intake
- 같은 활자가 뒤이어 오는 값은 유의적으로 차이가 없다(p<0.05). -Values that follow the same letter are not significantly different (p <0.05).
표 2에 나타난 바와 같이, 본 발명에 따른 와송 추출물, 특히 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물 투여군에서는 타 실험군에 비하여 음식섭취량이 적었으며, 현저한 체중감소 효과를 나타내었다. 또한, 음식섭취량에 의한 체중증가율도 현저히 낮은 것으로 나타났다.As shown in Table 2, in the administration group of the Songsong extract, in particular the Wasong butanol fraction and Wasong ethyl acetate fraction according to the present invention was less food intake than other experimental groups, and showed a significant weight loss effect. In addition, the weight gain rate by food intake was also significantly lower.
3-2. 지방조직의 무게 측정3-2. Weight measurement of adipose tissue
고지방 식이로 사육된 흰쥐의 지방조직의 무게는 후복강(Retroperitoneal) 지방조직 및 부고환(Epididymal) 지방조직을 절개한 후 측정하였다.The weight of adipose tissue in rats fed with a high fat diet was measured after incision of Retroperitoneal adipose tissue and Epididymal adipose tissue.
지방조직의 무게는 표 3에 나타내었다.The weight of adipose tissue is shown in Table 3.
※ 같은 활자가 뒤이어 오는 값은 유의적으로 차이가 없다(p<0.05).※ There is no significant difference between the values following the same letter (p <0.05).
표 3에 나타난 바와 같이, 본 발명에 따른 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물은 후복강 지방조직 및 부고환 지방조직의 무게를 유의적으로 감소시켰다.As shown in Table 3, the Warson butanol fraction and Warsong ethyl acetate fraction according to the present invention significantly reduced the weight of the celiac adipose tissue and epididymal adipose tissue.
4. 혈청 지질 함량 측정4. Determination of Serum Lipid Content
상기 시료 투여가 끝난 고지방 식이로 사육된 흰쥐에 나트륨 페노바르비탈 (sodium phenobarbital) 200㎎/㎏을 복강주사하여 마취시킨 후 복부 대동맥으로부터 혈액을 채취하였다. 채취한 혈액을 원심분리하여 상등액을 사용하였다.Rats bred in a high-fat diet after the administration of the sample were intraperitoneally injected with sodium phenobarbital 200 mg / kg and anesthetized, and blood was collected from the abdominal aorta. The collected blood was centrifuged to use a supernatant.
4-1. 혈청 총지질 함량 측정4-1. Measurement of Serum Total Lipid Content
혈청 총지질은 Richmond 등의 효소법에 의해 조제된 kit(AM 202-K, Asan)를 사용하여 측정하였다.Serum total lipid was measured using a kit (AM 202-K, Asan) prepared by enzyme method of Richmond et al.
4-2. 혈청 인지질 함량 측정4-2. Determination of Serum Phospholipid Content
혈청 인지질은 Chen 등의 효소법에 의해 조제된 kit(Iatron Chem. Co.)를 사용하여 측정하였다. 즉, 빙냉상에서 효소시약(phospholipase 3.9U, choline oxidase 5.6U, peroxidase 3.6U, 4-aminoantipyrine 0.3252㎎ 함유)을 효소시약 용해액[tris(hydroxy-methyl)-aminomethane 6.057㎎ 함유]에 용해한 후 시료 20㎕에 조제한 효소시액 3.0㎖를 첨가한 후, 37℃에서 20분간 배양하여 파장 500㎚에서 흡광도를 측정하였다. 표준 검량선에 준해 그 함량을 ㎎/㎗로 표시하였다.Serum phospholipid was measured using a kit (Iatron Chem. Co.) prepared by the enzyme method of Chen et al. In other words, the enzyme reagent (containing phospholipase 3.9U, choline oxidase 5.6U, peroxidase 3.6U, 4-aminoantipyrine 0.3252 mg) was dissolved in enzyme reagent solution [containing tris (hydroxy-methyl) -aminomethane 6.057 mg] in an ice-cold phase. 3.0 ml of the prepared enzyme solution was added to 20 µl, followed by incubation at 37 ° C. for 20 minutes to measure absorbance at a wavelength of 500 nm. The content was expressed in mg / dl according to the standard calibration curve.
4-3. 혈청 중성지방 함량 측정4-3. Determination of Serum Triglyceride Content
혈청 중성지방은 McGown 등의 방법에 준하여 조제된 kit(AM 157S-K, Asan)를 사용하여 측정하였다. 즉, 빙냉상에서 효소시약(lipoprotein lipase 10800U, glycerol kinase 5.4U, peroxidase 135000U, L-α-glycero phosphooxidase 160U 함유)을 효소시약 용해액[N,N-bis(2-hydroxyethyl)-2-aminomethane sulfonic acid 0.427g/㎗ 함유]에 용해한 후 시료 20㎕에 조제한 효소시액 3.0㎖를 첨가한 후 37℃에서 10분간 배양하여 파장 550㎚에서 흡광도를 측정하였다. 표준 검량선에 준해 혈중 함량은 ㎎/㎗로 표시하였다.Serum triglycerides were measured using a kit (AM 157S-K, Asan) prepared according to McGown et al. In other words, the enzyme reagent (containing lipoprotein lipase 10800U, glycerol kinase 5.4U, peroxidase 135000U, L-α-glycero phosphooxidase 160U) was dissolved in an enzyme reagent [N, N-bis (2-hydroxyethyl) -2-aminomethane sulfonic acid dissolved in 0.427 g /]], 3.0 ml of the enzyme solution prepared in 20 μl of the sample was added thereto, and the resultant was incubated at 37 ° C. for 10 minutes to measure absorbance at a wavelength of 550 nm. The blood content was expressed in mg / dl according to the standard calibration curve.
결과는 표 4에 나타내었다.The results are shown in Table 4.
※ 같은 활자가 뒤이어 오는 값은 유의적으로 차이가 없다(p<0.05).※ There is no significant difference between the values following the same letter (p <0.05).
표 4에 나타난 바와 같이, 본 발명에 따른 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물은 혈청 총지질 함량, 인지질 함량 및 중성지방 함량을 유의적으로 감소시켰다.As shown in Table 4, the Warson butanol fraction and Warsong ethyl acetate fraction according to the present invention significantly reduced serum total lipid content, phospholipid content and triglyceride content.
5. 혈청 콜레스테롤 함량 측정5. Determination of Serum Cholesterol Content
5-1. 혈청 총콜레스테롤 함량 측정5-1. Determination of Serum Total Cholesterol Content
혈청 총콜레스테롤 함량은 Richmon의 효소법에 의해 조제된 kit(AM 202-K, Asan)를 사용하여 측정하였다. 즉, 빙냉상에서 효소시약(cholesterol esterase 20.5U/ℓ, cholesterol oxidase 10.7U/ℓ, sodium hydroxide 1.81g/ℓ함유)을 효소시약 용해액(potassium phosphate monobasic 13.6g/ℓ, phenol 1.88g/ℓ 함유)에 용해한 후 시료 20㎕에 조제한 효소시액 3.0㎖를 첨가한 후 37℃에서 5분간 배양하여 파장 500㎚에서 흡광도를 측정하였다. 표준 검량선에 준해 혈중 함량은 ㎎/㎗로 표시하였다.Serum total cholesterol content was measured using a kit prepared by Richmon's enzyme method (AM 202-K, Asan). In other words, it contains enzyme reagents (potassium phosphate monobasic 13.6g / l, phenol 1.88g / l) in an ice-cooled bed with cholesterol esterase 20.5U / l, cholesterol oxidase 10.7U / l and sodium hydroxide 1.81g / l. After dissolving in), 3.0 ml of the prepared enzyme solution was added to 20 µl of the sample, followed by incubation at 37 ° C. for 5 minutes, and the absorbance at 500 nm was measured. The blood content was expressed in mg / dl according to the standard calibration curve.
5-2. 혈청 고밀도 5-2. Serum density 지질단백질Lipoprotein 콜레스테롤 함량 측정 Cholesterol Content Measurement
고밀도 지질단백질 콜레스테롤(HDL-C) 함량은 Noma 등의 효소법에 의해 조제된 kit(AM 203-K, Asan)를 사용하여 측정하였다. 즉, 혈청 20㎕에 침강시약 (dextran sulfate 0.1%, magnesium chloride 0.1M 함유) 0.2㎖를 가하고 잘 혼합한 후 실온에서 10분간 방치하고 3000rpm에서 10분간 원심분리하였다. 그 다음 상층액을 0.1㎖ 취하여 효소시액 3.0㎖와 잘 혼합하여 37℃에서 5분간 배양하여 파장 500㎚에서 흡광도를 측정하였다. 표준 검량선에 준해 그 함량을 ㎎/㎗로 표시하였다.High-density lipoprotein cholesterol (HDL-C) content was measured using a kit (AM 203-K, Asan) prepared by the enzyme method such as Noma. That is, 0.2 ml of sedimentation reagent (containing dextran sulfate 0.1% and magnesium chloride 0.1M) was added to 20 µl of serum, and the mixture was mixed well, and left at room temperature for 10 minutes and centrifuged at 3000 rpm for 10 minutes. Next, 0.1 ml of the supernatant was mixed with 3.0 ml of enzyme solution, incubated at 37 ° C. for 5 minutes, and absorbance was measured at a wavelength of 500 nm. The content was expressed in mg / dl according to the standard calibration curve.
5-3. 혈청 저밀도 5-3. Serum low density 지질단백질Lipoprotein 콜레스테롤 함량 측정 Cholesterol Content Measurement
저밀도 지질단백질 콜레스테롤(LDL-C) 함량은 Fridewald 등의 방법에 따라 하기 수학식 1에 의하여 산출하였다.Low-density lipoprotein cholesterol (LDL-C) content was calculated by Equation 1 according to the method of Fridewald et al.
결과는 표 5에 나타내었다.The results are shown in Table 5.
※ 같은 활자가 뒤이어 오는 값은 유의적으로 차이가 없다(p<0.05).※ There is no significant difference between the values following the same letter (p <0.05).
표 5에 나타난 바와 같이, 본 발명에 따른 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물은 혈청 총콜레스테롤 및 저밀도 지질단백질 콜레스테롤을 유의적으로 감소시켰고, 고밀도 지질단백질 콜레스테롤을 유의적으로 증가시켰으며, 동맥경화 위험지수(artherogenic index, A.I.)도 유의적으로 감소시켰다.As shown in Table 5, the Warson butanol fraction and Warsong ethyl acetate fraction according to the present invention significantly reduced serum total cholesterol and low density lipoprotein cholesterol, significantly increased high density lipoprotein cholesterol, and risk of atherosclerosis. The artherogenic index (AI) was also significantly reduced.
6. 6. 분변의Fecal 중량, 및 Weight, and 분변Feces 및 And 간조직에서In liver tissue 지방 함량 측정 Fat content measurement
각 실험군별로 24시간 배설되는 분변을 수집하여 건조 중량(dry weight)을 측정하였다. 분변 및 간조직 2g을 취하여 Folch와 Stanley의 방법으로 지방을 추출하고, 이를 클로로포름으로 25㎖가 되도록 정확하게 편취하여 분석용 시료로 사용하였다. 콜레스테롤 함량 및 중성지질의 함량은 kit를 사용하여 측정하였으며, 혼탁을 방지하기 위하여 0.5% 트리톤 X-100을 첨가하였다.Fecals excreted in each experimental group for 24 hours were collected to measure the dry weight (dry weight). 2 g of fecal and liver tissues were taken to extract fat using the method of Folch and Stanley, which was precisely decanted to 25 ml with chloroform and used as analytical sample. Cholesterol content and neutral lipid content were measured using a kit, and 0.5% Triton X-100 was added to prevent turbidity.
간조직에서의 총지질, 중성지방 및 콜레스테롤 함량은 표 6에 나타내었고, 분변의 건조 중량 및 분변 중의 중성지방 함량과 총콜레스테롤 함량은 표 7에 나타내었다.The total lipid, triglyceride and cholesterol contents in liver tissue are shown in Table 6, and the dry weight of feces, triglyceride content and total cholesterol content in feces are shown in Table 7.
※ 같은 활자가 뒤이어 오는 값은 유의적으로 차이가 없다(p<0.05).※ There is no significant difference between the values following the same letter (p <0.05).
※ 같은 활자가 뒤이어 오는 값은 유의적으로 차이가 없다(p<0.05).※ There is no significant difference between the values following the same letter (p <0.05).
표 6에 나타난 바와 같이, 본 발명에 따른 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물은 간조직에서 총지질, 중성지방 및 콜레스테롤 함량을 유의적으로 감소시켰다.As shown in Table 6, the Warson butanol fraction and Warsong ethyl acetate fraction according to the present invention significantly reduced the total lipid, triglyceride and cholesterol content in liver tissue.
또한 표 7에 나타난 바와 같이, 본 발명에 따른 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물을 투여한 군의 분변에서 지방함량이 고지방식이군보다 2배 정도 높게 나타났다. 이는 본 발명에 따른 와송 부탄올 분획물 및 와송 에틸아세테이트 분획물이 장에서의 지방 흡수를 감소시키거나 장으로의 배설을 증가시키기 때문인 것으로 판단된다.In addition, as shown in Table 7, fat content in the feces of the group that was administered Waksong butanol fraction and Waksong ethyl acetate fraction according to the present invention was about 2 times higher than the high fat diet group. It is believed that this is because the Warson butanol fraction and the Warson ethyl acetate fraction according to the present invention reduce fat absorption in the intestine or increase excretion into the intestine.
하기에 본 발명의 조성물을 위한 제제예를 예시한다.Examples of preparations for the compositions of the present invention are illustrated below.
제제예Formulation example 1 One : 약학적 제제의 제조 : Preparation of Pharmaceutical Formulations
1. 산제의 제조1. Preparation of powder
와송 추출물 2gWasong Extract 2g
유당 1g1g lactose
상기의 성분을 혼합하고 기밀포에 충진하여 산제를 제조하였다.The above ingredients were mixed and filled in airtight cloth to prepare a powder.
2. 정제의 제조2. Preparation of Tablets
와송 추출물 100㎎Wasong Extract 100mg
옥수수전분 100㎎Corn Starch 100mg
유 당 100㎎Lactose 100mg
스테아린산 마그네슘 2㎎2 mg magnesium stearate
상기의 성분을 혼합한 후, 통상의 정제의 제조방법에 따라서 타정하여 정제를 제조하였다.After mixing the above components, tablets were prepared by tableting according to a conventional method for producing tablets.
3. 캡슐제의 제조3. Preparation of Capsule
와송 추출물 100㎎Wasong Extract 100mg
옥수수전분 100㎎Corn Starch 100mg
유 당 100㎎Lactose 100mg
스테아린산 마그네슘 2㎎2 mg magnesium stearate
상기의 성분을 혼합한 후, 통상의 캡슐제의 제조방법에 따라서 젤라틴 캡슐에 충전하여 캡슐제를 제조하였다.After mixing the above components, the capsule was prepared by filling in gelatin capsules according to the conventional method for producing a capsule.
제제예Formulation example 2 2 : 식품의 제조 : Manufacture of food
1. 조리용 양념의 제조1. Preparation of Cooking Seasonings
와송 추출물 20~95 중량%로 건강 증진용 조리용 양념을 제조하였다.Wasong extract 20 to 95% by weight was prepared for health promotion cooking seasoning.
2. 토마토 케찹 및 소스의 제조2. Preparation of Tomato Ketchup and Sauce
와송 추출물 0.2~1.0 중량%를 토마토 케찹 또는 소스에 첨가하여 건강 증진용 토마토 케찹 또는 소스를 제조하였다.Health care tomato ketchup or sauce was prepared by adding 0.2 ~ 1.0% by weight of the quince extract to tomato ketchup or sauce.
3. 밀가루 식품의 제조3. Manufacturing of Flour Foods
와송 추출물 0.5~5.0 중량%를 밀가루에 첨가하고, 이 혼합물을 이용하여 빵, 케이크, 쿠키, 크래커 및 면류를 제조하여 건강 증진용 식품을 제조하였다.0.5-5.0% by weight of pine nuts extract was added to the flour, and the mixture was used to prepare bread, cake, cookies, crackers, and noodles to prepare health-promoting foods.
4. 스프 및 육즙(gravies)의 제조4. Preparation of soups and gravy
와송 추출물 0.1~5.0 중량%를 스프 및 육즙에 첨가하여 건강 증진용 육가공 제품, 면류의 수프 및 육즙을 제조하였다.0.1-5.0% by weight of the quince extract was added to soups and broth to prepare meat products for health promotion, soups and noodles of noodles.
5. 그라운드 비프(ground beef)의 제조5. Preparation of Ground Beef
와송 추출물 10 중량%를 그라운드 비프에 첨가하여 건강 증진용 그라운드 비프를 제조하였다.Health weight ground beef was prepared by adding 10% by weight of the pine nuts extract to the ground beef.
6. 유제품(dairy products)의 제조6. Manufacture of Dairy Products
와송 추출물 5~10 중량%를 우유에 첨가하고, 상기 우유를 이용하여 버터 및 아이스크림과 같은 다양한 유제품을 제조하였다.5-10% by weight of the hawthorn extract was added to milk, and the milk was used to prepare various dairy products such as butter and ice cream.
제제예Formulation example 3 3 : 음료의 제조 : Preparation of Beverages
1. 탄산음료의 제조1. Preparation of carbonated drinks
설탕 5~10%, 구연산 0.05~0.3%, 카라멜 0.005~0.02%, 비타민 C 0.1~1%의 첨가물을 혼합하고, 여기에 79~94%의 정제수를 섞어서 시럽을 만들고, 상기 시럽을 85~98℃에서 20~180초간 살균하여 냉각수와 1:4의 비율로 혼합한 다음 탄산가스를 0.5~0.82%를 주입하여 본 발명의 와송 추출물을 함유하는 탄산음료를 제조하였다.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, and then mixed with cooling water in a ratio of 1: 4, and then injected with 0.5 to 0.82% of carbon dioxide gas to prepare a carbonated beverage containing the Wahsong extract of the present invention.
2. 건강음료의 제조2. Manufacture of health drinks
액상과당(0.5%), 올리고당(2%), 설탕(2%), 식염(0.5%), 물(75%)과 같은 부재료와 와송 추출물을 균질하게 배합하여 순간 살균을 한 후 이를 유리병, 패트병 등 소포장 용기에 포장하여 건강음료를 제조하였다.Homogeneous blending of subsidiary materials such as liquid fructose (0.5%), oligosaccharide (2%), sugar (2%), salt (0.5%), water (75%), and Wongsong extract, and sterilized them immediately Health drinks were prepared by packaging in small packaging containers such as plastic bottles.
3. 야채쥬스의 제조3. Preparation of Vegetable Juice
와송 추출물 5g을 토마토 또는 당근 쥬스 1,000㎖에 가하여 건강 증진용 야채쥬스를 제조하였다.5 g of the quince extract was added to 1,000 ml of tomato or carrot juice to prepare vegetable juice for health promotion.
4. 과일쥬스의 제조4. Preparation of Fruit Juice
와송 추출물 1g을 사과 또는 포도 쥬스 1,000㎖에 가하여 건강 증진용 과일쥬스를 제조하였다.1 g of the pine fruit extract was added to 1,000 ml of apple or grape juice to prepare fruit juice for health promotion.
본 발명에 따른 와송 추출물은 고지방 식이로 사육된 흰쥐의 음식섭취량과 체중을 감소시키며, 지방조직의 무게를 감소시키고, 혈청 및 간조직 중의 지질 및 총콜레스테롤을 감소시키며, 저밀도 지질단백질 콜레스테롤을 유의적으로 감소시키고, 고밀도 지질단백질 콜레스테롤을 유의적으로 증가시키며, 동맥경화 위험지수 (A.I.)도 유의적으로 감소시키고, 분변 중의 지방 함량을 높임으로써, 비만 억제 및 고지혈증 예방 또는 치료에 유용하게 사용될 수 있다.Wahsong extract according to the present invention reduces the food intake and weight of rats reared in a high fat diet, reduce the weight of adipose tissue, reduce the lipid and total cholesterol in serum and liver tissue, and significantly lower lipoprotein cholesterol It can be useful for inhibiting obesity and preventing or treating hyperlipidemia by reducing the amount of fat, increasing high density lipoprotein cholesterol, significantly reducing arteriosclerosis risk index (AI), and increasing fecal fat content. .
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