Li Wenbang, Fu Xinyan, Lin Dai, Li Tong, Zhang Nan, Huo Yanzi, Zhu Pingping, Guo Fuchuan, Huang Fang
Department of Nutrition and Food Safety, School of Public Health, Fujian Medical University, No.1 Xuefu North Road, University Town, FuZhou 350122, Fujian Province, P.R. China.
Food Funct. 2023 Feb 6;14(3):1685-1698. doi: 10.1039/d2fo03760b.
Although conjugated linoleic acid (CLA) has been shown to have anti-obesity properties, the effect and mechanism of CLA in alleviating glycolipid metabolism disorders remains unclear. In this work, it was observed that rats fed a high-fat diet (HFD) had lower body weight and body fat levels after 9 weeks of low-dose and high-dose CLA interventions. The results of blood biochemical indices showed that CLA significantly reduced the levels of total cholesterol, triglycerides, fasting blood glucose and insulin. Additionally, high-dose CLA could restore the intestinal microbiota composition, including increasing the relative abundances of short-chain fatty acid (SCFA)-producing microbiota, such as , and ; decreasing the relative abundances of and _2; and increasing the content of SCFAs in feces and serum. Further analysis showed that high-dose CLA could increase the expression levels of , , and in the liver tissue of HFD-induced obese rats. Consistently, high dose of CLA could reversibly improve the downregulation of INSR, AKT, PI3K and GLUT4 protein expression caused by HFD and reverse the decline in AKT phosphorylation levels. Correlation clustering analysis with a heatmap showed that the changes in specific microbiota induced by high-dose CLA were correlated with changes in obesity-related indices and gene expression. The molecular docking analysis showed that the molecular docking of SCFAs with the IRS-2, AKT and GLUT4 proteins had high linking activity. The results supported that CLA can alleviate glycolipid metabolic imbalances associated with obesity by altering the intestinal microbiota to induce the production of SCFAs and thereby activate the INSR/IRS-2/AKT/GLUT4 pathway. This study supports CLA may be preferentially used by the intestinal microbiota of the host to promote its health.
尽管共轭亚油酸(CLA)已被证明具有抗肥胖特性,但其在缓解糖脂代谢紊乱方面的作用及机制仍不清楚。在本研究中,观察到高脂饮食(HFD)喂养的大鼠在低剂量和高剂量CLA干预9周后体重和体脂水平降低。血液生化指标结果显示,CLA显著降低了总胆固醇、甘油三酯、空腹血糖和胰岛素水平。此外,高剂量CLA可恢复肠道微生物群组成,包括增加产生短链脂肪酸(SCFA)的微生物群的相对丰度,如 、 和 ;降低 和_2的相对丰度;并增加粪便和血清中SCFAs的含量。进一步分析表明,高剂量CLA可增加HFD诱导的肥胖大鼠肝脏组织中 、 、 和 的表达水平。同样,高剂量CLA可逆转HFD引起的INSR、AKT、PI3K和GLUT4蛋白表达下调,并逆转AKT磷酸化水平的下降。热图相关性聚类分析表明,高剂量CLA诱导的特定微生物群变化与肥胖相关指标和基因表达变化相关。分子对接分析表明,SCFAs与IRS-2、AKT和GLUT4蛋白的分子对接具有高连接活性。结果支持CLA可通过改变肠道微生物群诱导SCFAs产生从而激活INSR/IRS-2/AKT/GLUT4途径来缓解与肥胖相关的糖脂代谢失衡。本研究支持CLA可能被宿主肠道微生物群优先利用以促进其健康。