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姜黄素通过激活 FNDC5/鸢尾素增加高脂肪饮食诱导肥胖小鼠的胰岛素敏感性和能量消耗。

Curcumin improves insulin sensitivity and increases energy expenditure in high-fat-diet-induced obese mice associated with activation of FNDC5/irisin.

机构信息

Jiangxi Province Key Laboratory of Animal Nutrition, Jiangxi Agricultural University, Jiangxi, China.

State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University, Beijing, China.

出版信息

Nutrition. 2021 Oct;90:111263. doi: 10.1016/j.nut.2021.111263. Epub 2021 Apr 7.

DOI:10.1016/j.nut.2021.111263
PMID:33975064
Abstract

OBJECTIVE

Curcumin (Cur) has a beneficial role in preventing metabolic dysfunctions; however, the underlying mechanism are not yet fully understood. The aim of this study was to evaluate whether the beneficial metabolic effects of curcumin are associated with the regulation of energy metabolism and activation of fibronectin type 3 domain-containing protein 5 (FNDC5)/irisin.

METHODS

We used cellular and molecular techniques to investigate the effects of Cur on C57 BL/6 mice that were fed either a control diet or a high-fat diet (HFD) with or without 0.2% Cur for 10 wk. Factors involved in energy metabolism, inflammatory responses, and insulin signaling, as well as the involvement of FNDC5/irisin pathway, were assessed.

RESULTS

Cur alleviated adiposity and suppressed inflammatory response in white adipose tissue (WAT) of HFD mice. Meanwhile, Cur administration increased plasma irisin concentration and improved insulin sensitivity of HFD mice. Cur increased the oxygen consumption and heat production and reduced respiratory exchange ratio (RES) in HFD mice, which were accompanied by the enhancement of metabolic activity in brown fat and inguinal WAT. Additionally, the improvement of basal metabolic rate by Cur may be partly regulated by the FNDC5/ p38 mitogen-activated protein kinase (p38 MAPK)/extracellular signal-related kinase (ERK) 1/2 pathway.

CONCLUSIONS

These findings demonstrated that dietary Cur alleviated diet-induced adiposity by improving insulin sensitivity and whole body energy metabolism via the FNDC5/p38 MAPK/ERK pathways.

摘要

目的

姜黄素(Cur)在预防代谢功能障碍方面具有有益作用;然而,其潜在机制尚未完全阐明。本研究旨在评估姜黄素的有益代谢作用是否与能量代谢调节和纤连蛋白结构域蛋白 3 型包含蛋白 5(FNDC5)/鸢尾素的激活有关。

方法

我们使用细胞和分子技术研究了姜黄素对喂食对照饮食或高脂肪饮食(HFD)的 C57BL/6 小鼠的影响,HFD 组同时给予或不给予 0.2%姜黄素 10 周。评估了能量代谢、炎症反应和胰岛素信号转导中涉及的因素,以及 FNDC5/鸢尾素途径的参与情况。

结果

姜黄素减轻了 HFD 小鼠的肥胖和白色脂肪组织(WAT)中的炎症反应。同时,姜黄素给药增加了血浆鸢尾素浓度并改善了 HFD 小鼠的胰岛素敏感性。姜黄素增加了 HFD 小鼠的耗氧量和产热量,并降低了呼吸交换率(RES),同时还增强了棕色脂肪和腹股沟 WAT 的代谢活性。此外,姜黄素对基础代谢率的改善可能部分受到 FNDC5/p38 丝裂原活化蛋白激酶(p38 MAPK)/细胞外信号调节激酶(ERK)1/2 途径的调节。

结论

这些发现表明,膳食姜黄素通过 FNDC5/p38 MAPK/ERK 途径改善胰岛素敏感性和全身能量代谢,从而减轻饮食引起的肥胖。

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