Supplementation of a High-Fat Diet with Chlorogenic Acid Is Associated with Insulin Resistance and Hepatic Lipid Accumulation in Mice

被引:68
|
作者
Mubarak, Aidilla [1 ,2 ,3 ,4 ]
Hodgson, Jonathan M. [3 ]
Considine, Michael J. [1 ,2 ,5 ]
Croft, Kevin D. [3 ]
Matthews, Vance B. [6 ]
机构
[1] Univ Western Australia, Sch Plant Biol, Crawley, WA 6009, Australia
[2] Univ Western Australia, Inst Agr, Crawley, WA 6009, Australia
[3] Univ Western Australia, Med Res Fdn, Sch Med & Pharmacol, Perth, WA 6000, Australia
[4] Univ Malaysia Terengganu, Fac Agrotechnol & Food Sci, Kuala Terengganu 21030, Malaysia
[5] Dept Agr & Food Western Australia, S Perth, WA 6151, Australia
[6] Med Res Fdn, Western Australian Inst Med Res, UWA Ctr Med Res, Lab Metab Dysfunct, Perth, WA 6000, Australia
基金
澳大利亚研究理事会;
关键词
Chlorogenic acid; glucose tolerance; insulin sensitivity; fatty acid oxidation; mouse; metabolic syndrome; NITRIC-OXIDE STATUS; ENDOTHELIAL FUNCTION; METABOLIC SYNDROME; BLOOD-PRESSURE; CAFFEIC ACID; COFFEE; OBESITY; POLYPHENOLS; MORTALITY; OXIDATION;
D O I
10.1021/jf400920x
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The increasing prevalence of the metabolic syndrome requires a greater need for therapeutic and prevention strategies. Higher coffee consumption is consistently associated with a lower risk of type 2 diabetes in population studies. Dietary polyphenols have been linked to benefits on several features of the metabolic syndrome. Chlorogenic acid (CGA), a major component of coffee, is one of the most consumed polyphenols in the diet. In our study, we conducted a controlled dietary intervention over 12 weeks in male mice. There were three dietary groups: (i) normal diet, (ii) high-fat diet, and (iii) high-fat diet + CGA. We assessed the effect of CGA at a physiologically obtainable dose (1 g/kg of diet) on high-fat-diet-induced obesity, glucose intolerance, insulin resistance, and also fatty acid oxidation and insulin signaling in C57BL/6 male mice. Supplementation of CGA in the high-fat diet did not reduce body weight compared to mice fed the high-fat diet alone (p = 0.32). CGA resulted in increased insulin resistance compared to mice fed a high-fat diet only (p < 0.05). CGA resulted in decreased phosphorylation of AMP-activated protein kinase (AMPK) (p < 0.001) and acetyl carboxylase beta (ACC beta), a downstream target of AMPK (p < 0.05), in liver. The liver of mice fed a high-fat diet supplemented with CGA had a higher lipid content (p < 0.05) and more steatosis relative to mice fed a high-fat diet only, indicating impaired fatty acid oxidation. This study suggests that CGA supplementation in a high-fat diet does not protect against features of the metabolic syndrome in diet-induced obese mice.
引用
收藏
页码:4371 / 4378
页数:8
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