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高脂肪饮食与慢性应激相结合会加重雄性Wistar大鼠的胰岛素抵抗。

The combination of a high-fat diet and chronic stress aggravates insulin resistance in Wistar male rats.

作者信息

Fu J-h, Xie S-r, Kong S-j, Wang Y, Wei W, Shan Y, Luo Y-m

机构信息

Department of Physiology, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing, P.R. China.

出版信息

Exp Clin Endocrinol Diabetes. 2009 Jul;117(7):354-60. doi: 10.1055/s-0028-1119406. Epub 2009 Apr 8.

Abstract

We observed the effects of the combination of a high-fat diet and chronic stress on insulin resistance. Male Wistar rats were fed on either a control or a high-fat diet and given chronic stress with the electric foot shock or not for 10 weeks. After checking the glucose infusion rate (GIR) and the HOMA-IR index, the results showed that the three groups all revealed insulin resistance with increased free fatty acid (FFA), adrenocorticotropic hormone (ACTH) and corticosterone in the serum, in addition to increased tumour necrosis factor alpha (TNF-alpha) in the serum and adipose tissue, and decreased density of high affinity receptors (R1) and expression of peroxisome proliferator-activated receptor-alpha (PPARalpha) mRNA in the hepatocytes as compared with the control, but the highest alteration on aforementioned parameters revealed in the chronic stress fed with a high-fat diet. Significant interactions between high-fat diet and chronic stress were revealed on GIR, HOMA-IR index, FFA, ACTH, corticosterone, TNF-alpha (in adipose tissue) and R1. These observations strongly suggest that a combination of a high-fat diet and chronic stress can produce a synergic effect on aggravating insulin resistance associated with the abnormal hypothalamic-pituitary-adrenocortical axis, endocrine abnormality of the adipose tissue, and pathological changes of the liver.

摘要

我们观察了高脂饮食与慢性应激联合作用对胰岛素抵抗的影响。将雄性Wistar大鼠分为两组,分别给予对照饮食或高脂饮食,并对其中一组施加电足电击进行慢性应激处理,持续10周。检测葡萄糖输注率(GIR)和稳态模型胰岛素抵抗指数(HOMA-IR)后,结果显示,与对照组相比,三组均出现胰岛素抵抗,血清中游离脂肪酸(FFA)、促肾上腺皮质激素(ACTH)和皮质酮水平升高,血清及脂肪组织中肿瘤坏死因子α(TNF-α)增加,肝细胞中高亲和力受体(R1)密度降低,过氧化物酶体增殖物激活受体α(PPARα)mRNA表达减少,但高脂饮食合并慢性应激组上述参数的变化最为显著。高脂饮食与慢性应激在GIR、HOMA-IR指数、FFA、ACTH、皮质酮、TNF-α(脂肪组织中)和R1方面存在显著交互作用。这些观察结果强烈表明,高脂饮食与慢性应激联合作用可通过下丘脑-垂体-肾上腺皮质轴异常、脂肪组织内分泌异常以及肝脏病理改变,对加重胰岛素抵抗产生协同效应。

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