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川陈皮素可改善高脂饮食诱导肥胖小鼠的肥胖和胰岛素抵抗。

Nobiletin improves obesity and insulin resistance in high-fat diet-induced obese mice.

机构信息

Research Institute for Biological Functions, Chubu University, 1200 Matsumoto, Kasugai, Aichi 487-8501, Japan.

出版信息

J Nutr Biochem. 2013 Jan;24(1):156-62. doi: 10.1016/j.jnutbio.2012.03.014. Epub 2012 Aug 13.

Abstract

Nobiletin (NOB) is a polymethoxylated flavone present in citrus fruits and has been reported to have antitumor and anti-inflammatory effects. However, little is known about the effects of NOB on obesity and insulin resistance. In this study, we examined the effects of NOB on obesity and insulin resistance, and the underlying mechanisms, in high-fat diet (HFD)-induced obese mice. Obese mice were fed a HFD for 8 weeks and then treated without (HFD control group) or with NOB at 10 or 100mg/kg. NOB decreased body weight gain, white adipose tissue (WAT) weight and plasma triglyceride. Plasma glucose levels tended to decrease compared with the HFD group and improved plasma adiponectin levels and glucose tolerance. Furthermore, NOB altered the expression levels of several lipid metabolism-related and adipokine genes. NOB increased the mRNA expression of peroxisome proliferator-activated receptor (PPAR)-γ, sterol regulatory element-binding protein-1c, fatty acid synthase, stearoyl-CoA desaturase-1, PPAR-α, carnitine palmitoyltransferase-1, uncoupling protein-2 and adiponectin, and decreased the mRNA expression of tumor necrosis factor-α and monocyte chemoattractant protein-1 in WAT. NOB also up-regulated glucose transporter-4 protein expression and Akt phosphorylation and suppressed IκBα degradation in WAT. Taken together, these results suggest that NOB improves adiposity, dyslipidemia, hyperglycemia and insulin resistance. These effects may be elicited by regulating the expression of lipid metabolism-related and adipokine genes, and by regulating the expression of inflammatory makers and activity of the insulin signaling pathway.

摘要

川陈皮素(NOB)是一种存在于柑橘类水果中的多甲氧基黄酮,具有抗肿瘤和抗炎作用。然而,关于 NOB 对肥胖和胰岛素抵抗的影响知之甚少。在这项研究中,我们研究了 NOB 对高脂饮食(HFD)诱导肥胖小鼠肥胖和胰岛素抵抗的影响及其潜在机制。肥胖小鼠喂食 HFD 8 周,然后不(HFD 对照组)或用 10 或 100mg/kg 的 NOB 处理。NOB 降低了体重增加、白色脂肪组织(WAT)重量和血浆甘油三酯。与 HFD 组相比,血浆葡萄糖水平有下降趋势,血浆脂联素水平和葡萄糖耐量得到改善。此外,NOB 改变了几种脂质代谢相关和脂肪因子基因的表达水平。NOB 增加了过氧化物酶体增殖物激活受体(PPAR)-γ、固醇调节元件结合蛋白-1c、脂肪酸合酶、硬脂酰辅酶 A 去饱和酶-1、PPAR-α、肉毒碱棕榈酰转移酶-1、解偶联蛋白-2 和脂联素的 mRNA 表达,并降低了 WAT 中肿瘤坏死因子-α和单核细胞趋化蛋白-1 的 mRNA 表达。NOB 还上调了葡萄糖转运蛋白-4 蛋白表达和 Akt 磷酸化,并抑制了 WAT 中 IκBα 的降解。综上所述,这些结果表明,NOB 改善了肥胖、血脂异常、高血糖和胰岛素抵抗。这些作用可能是通过调节脂质代谢相关和脂肪因子基因的表达以及调节炎症标志物的表达和胰岛素信号通路的活性来实现的。

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