Effects of Taraxacum mongolicum Extract on Blood Glucose Levels and Lipid Profiles in Streptozotocin-Induced Diabetic Rats
(주)코리아스칼라
- 최초 등록일
- 2023.04.03
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- 2023.02
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서지정보
ㆍ발행기관 : 한국식품영양학회
ㆍ수록지정보 : 한국식품영양학회지 / 36권 / 1호
ㆍ저자명 : Hye Kyoung Han, Eun Young Choi
목차
Abstract
Introduction
Materials and Methods
1. Experimental materials and extraction methods
2. Animal care and experimental diet
3. Induction of diabetes
4. Sample collection and biochemical analysis
5. Statistical analysis
Results and Discussion
1. Effects of T.m. ethanol extract on body weight, foodintake, and food efficiency ratio
2. Effects of T.m. ethanol extract on hematocrit andplasma aminotransferase activity
3. Effects of T.m. ethanol extract on blood glucose levels
4. Effects of T.m. ethanol extract on lipid profiles
Conclusion
References
영어 초록
This study was designed to evaluate antihyperglycemic and antihyperlipidemic effects of ethanol extracts of Taraxacum mongolicum (T.m.) on streptozotocin (STZ)-induced diabetic rats. Sprague-Dawley rats were randomly assigned to five groups: normal (NC), STZ-control (DC), and three experimental groups. Diabetes was induced in Sprague-Dawley rats with a single intravenous injection [45 mg/kg body weight (b.w.)] of STZ. An ethanol extract of T.m. was orally given to diabetic rats for 14 days. Three experimental groups were additionally treated with T.m. extract at doses of 1 g/kg b.w./day for T.m.-1, 2 g/kg b.w./day for T.m.-2, and 3 g/kg b.w./day for T.m.-3. Oral administration of T.m.-2 significantly increased their body weights. T.m.-1 and T.m.-2 significantly decreased aspartate aminotransferase (AST) levels than DC. T.m.-1 and T.m.-2 group significantly decreased blood glucose levels. Total cholesterol, triglycerides, and free fatty acids were significantly decreased whereas high-density lipoprotein cholesterol was significantly increased in groups treated with T.m. extract than those in the DC group. These results support the fact that administration of T.m. extract can reduce hyperglycemia and hyperlipidemia risk in diabetic rats.
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