4.5 Article

Modulating Effects of Chlorogenic Acid on Lipids and Glucose Metabolism and Expression of Hepatic Peroxisome Proliferator-activated Receptor-α in Golden Hamsters Fed on High Fat Diet

期刊

BIOMEDICAL AND ENVIRONMENTAL SCIENCES
卷 22, 期 2, 页码 122-129

出版社

CHINESE CENTER DISEASE CONTROL & PREVENTION
DOI: 10.1016/S0895-3988(09)60034-9

关键词

Chlorogenic acid; Golden hamster; High fat diet; Hypolipidemic effect; Hypoglycemic effect; Lipids clearance; FFA drainage; PPAR-alpha; Insulin sensitivity

资金

  1. Chinese Nutrition Society
  2. Department of Health Technology and Informatics
  3. The Hong Kong Polytechnic University

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Objective To examine the effects of chlorogenic acid (CGA) on lipid and glucose metabolism under a high dietary fat burden and to explore the possible role of peroxisome proliferator-activated receptor-a (PPAR-a) in these effects. Methods Twenty male golden hamsters were randomly divided into CGA treatment group (n=10, given peritoneal injection of CGA solution prepared with PBS, 80 mg CGA/kg body weight daily), and control group (n=10, given PBS i.p. at the average volume of the treatment group). Animals in both groups were given 15% high fat diet. Eight weeks after treatment with CGA, the level of biochemical parameters in fasting serum and tissues and the expression of hepatic mRNA and protein PPAR-a were determined. Results Eight weeks after treatment with CGA, the levels of fasting serum triglyceride (TG), free fatty acid (FFA), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose (FSG), and insulin (FSI) were significantly lower in the GGA treatment group than in the control group. CGA also led to higher activity of hepatic lipase (HL), lower contents of TG and FFA in liver, and lower activity of lipoprotein lipase (LPL) in skeletal muscle. Furthermore, CGA significantly elevated significantly elevated the expression level of mRNA and protein expression in hepatic PPAR-a. Conclusion CGA can modify lipids and glucose metabolism, which may be attributed to PPAR-a facilitated lipid clearance in liver and improved insulin sensitivity.

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