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

被引:83
作者
Li, Shu-Yuan [1 ]
Chang, Cui-Qing [1 ]
Ma, Fu-Ying [2 ]
Yu, Chang-Long [1 ]
机构
[1] Peking Univ, Hosp 3, Inst Sports Med, Div Nutr & Biochem, Beijing 100191, Peoples R China
[2] Chinese Peoples Armed Police Forces, Gen Hosp, Dept Pediat, Beijing 100039, Peoples R China
关键词
Chlorogenic acid; Golden hamster; High fat diet; Hypolipidemic effect; Hypoglycemic effect; Lipids clearance; FFA drainage; PPAR-alpha; Insulin sensitivity; INSULIN-RESISTANCE; COFFEE CONSUMPTION; HDL-CHOLESTEROL; PLASMA; TRANSPORT; ENZYMES; PROTEIN; MODEL; RISK; MICE;
D O I
10.1016/S0895-3988(09)60034-9
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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.
引用
收藏
页码:122 / 129
页数:8
相关论文
共 45 条
[1]   Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-α activator [J].
Aasum, E ;
Belke, DD ;
Severson, DL ;
Riemersma, RA ;
Cooper, M ;
Andreassen, M ;
Larsen, TS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (03) :H949-H957
[2]   Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor α (PPARα) [J].
Aoyama, T ;
Peters, JM ;
Iritani, N ;
Nakajima, T ;
Furihata, K ;
Hashimoto, T ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5678-5684
[3]   Chlorogenic acid and hydroxynitrobenzaldehyde: New inhibitors of hepatic glucose 6-phosphatase [J].
Arion, WJ ;
Canfield, WK ;
Ramos, FC ;
Schindler, PW ;
Burger, HJ ;
Hemmerle, H ;
Schubert, G ;
Below, P ;
Herling, AW .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 339 (02) :315-322
[4]   Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-alpha in humans - No alteration in adipose tissue of obese and NIDDM patients [J].
Auboeuf, D ;
Rieusset, J ;
Fajas, L ;
Vallier, P ;
Frering, V ;
Riou, JP ;
Staels, P ;
Auwerx, J ;
Laville, M ;
Vidal, H .
DIABETES, 1997, 46 (08) :1319-1327
[5]   The metabolic syndrome and the hepatic fatty acid drainage hypothesis [J].
Berge, RK ;
Tronstad, KJ ;
Berge, K ;
Rost, TH ;
Wergedahl, H ;
Gudbrandsen, OA ;
Skorve, J .
BIOCHIMIE, 2005, 87 (01) :15-20
[6]  
Boden G, 2001, Endocr Pract, V7, P44
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]  
Chang CuiQing Chang CuiQing, 2004, Acta Nutrimenta Sinica, V26, P280
[9]  
Clifford MN, 1999, J SCI FOOD AGR, V79, P362, DOI 10.1002/(SICI)1097-0010(19990301)79:3<362::AID-JSFA256>3.0.CO
[10]  
2-D