Physiology Laboratory of College of Life Sciences, Anhui Normal University, Wuhu, China.
Neurobiology Laboratory of College of Life Sciences, Anhui Normal University, Wuhu, China.
Life Sci. 2018 Aug 15;207:23-29. doi: 10.1016/j.lfs.2018.05.040. Epub 2018 May 23.
Little is known regarding whether the NFE2/miR-423-5p and FAM3A-ATP-Akt pathway in liver mediates exercise allured alleviation of insulin resistance connected with diet-induced obesity. This research inquired the influence of exercise on liver insulin sensitivity and whole body insulin resistance in high-fat diet fed rats.
Forty male Sprague-Dawley rats at seven-week-old were assigned to four groups at random: standard diet as normal control group (NC, n = 10), high-fat diet group (HFD, n = 10), high-fat diet with chronic exercise intervention group (HFD-CE, n = 10) and high-fat diet with acute exercise intervention group (HFD-AE, n = 10).
Compared with rats fed with a standard diet, eight-week high-fat diet feeding lead to elevated body weight, visceral fat content and serum FFAs, and decreased insulin sensitivity index. Moreover, high-fat diet enhanced NFE2 protein expression and miR-423-5p level, decreased FAM3A mRNA and protein expression, ATP level and Akt phosphorylation in liver. In contrast, physical exercise, both chronic and acute exercise alleviated whole body insulin resistance, reduced hepatic NFE2 and miR-423-5p expression, and serum FFAs level, meanwhile enhanced FAM3A mRNA and protein expression, ATP level and Akt phosphorylation in liver. The current findings indicated that exercise in diet-induced obesity, both chronic and acute, induce a momentous regulation in NFE2/miR-423-5p and FAM3A-ATP-Akt pathway in liver, and improve hepatic insulin sensitivity and whole body insulin resistance.
All these results supply crucial evidence in our comprehending of the molecular mechanism that connected exercise to an alleviation of insulin resistance.
关于 NFE2/miR-423-5p 和 FAM3A-ATP-Akt 通路在肝脏中是否介导运动诱导的饮食诱导肥胖相关胰岛素抵抗的改善,目前知之甚少。本研究探讨了运动对高脂肪饮食喂养大鼠肝脏胰岛素敏感性和全身胰岛素抵抗的影响。
将 40 只 7 周龄雄性 Sprague-Dawley 大鼠随机分为 4 组:标准饮食正常对照组(NC,n=10)、高脂肪饮食组(HFD,n=10)、高脂肪饮食合并慢性运动干预组(HFD-CE,n=10)和高脂肪饮食合并急性运动干预组(HFD-AE,n=10)。
与标准饮食喂养的大鼠相比,8 周高脂肪饮食喂养导致体重、内脏脂肪含量和血清游离脂肪酸升高,胰岛素敏感性指数降低。此外,高脂肪饮食增强了 NFE2 蛋白表达和 miR-423-5p 水平,降低了 FAM3A mRNA 和蛋白表达、肝脏 ATP 水平和 Akt 磷酸化。相比之下,慢性和急性运动均能改善全身胰岛素抵抗,降低肝脏 NFE2 和 miR-423-5p 表达及血清游离脂肪酸水平,同时增强 FAM3A mRNA 和蛋白表达、肝脏 ATP 水平和 Akt 磷酸化。本研究结果表明,在饮食诱导肥胖中,慢性和急性运动均能显著调节肝脏中的 NFE2/miR-423-5p 和 FAM3A-ATP-Akt 通路,并改善肝脏胰岛素敏感性和全身胰岛素抵抗。
这些结果为我们理解运动与胰岛素抵抗改善相关的分子机制提供了重要依据。