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丁酸钠通过促进 GSK-3β/Nrf2 信号通路和线粒体功能来防止高脂肪饮食诱导的肥胖大鼠的氧化应激。

Sodium butyrate protects against oxidative stress in high-fat-diet-induced obese rats by promoting GSK-3β/Nrf2 signaling pathway and mitochondrial function.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, China.

School of Food Science and Technology, Jiangnan University, Wuxi, China.

出版信息

J Food Biochem. 2022 Oct;46(10):e14334. doi: 10.1111/jfbc.14334. Epub 2022 Jul 18.

Abstract

Sodium butyrate (NaB), obtained by fermenting dietary fiber via intestinal microflora, was recently shown to improve the activity of some antioxidant enzymes in vivo. This study aims to investigate the term changes of mitochondrial energy metabolism and redox homeostasis in skeletal muscles and clarify the regulatory mechanism and dose effect of NaB on skeletal muscle. Male Sprague-Dawley rats were divided into the control group, obesity-prone (OP) group and obesity-resistant (OR) group based on the gain of body weight after 8 weeks' of feeding high-fat diet (HFD), followed by sacrificing rats at the end of 20th week. NaB intervention (12 weeks) could effectively reduce the body weight of rats in the OP and OR groups. NaB also mediated upregulation of antioxidant enzyme activity and GSH/GSSG ratio, while reducing reactive oxygen species (ROS) levels and malondialdehyde (MDA) content. At the molecular level, NaB upregulated Pi3k, Nrf2, Nqo-1, and Ho-1, but downregulated Gsk-3β mRNA expression by regulating the Nrf2 antioxidant pathway to enhance tissue antioxidant capacity. At the same time, NaB intervention significantly upregulated Glut4, Irs-1, Pdx1, and MafA, expression in gastrocnemius muscles of OP and OR rats, and elevated insulin secretion and muscle insulin sensitivity. Thus, NaB activates antioxidant pathway, improves the antioxidant capacity of obese rat tissues and promotes glucose metabolism. PRACTICAL APPLICATIONS: This study found that obesity-prone and obesity-resistant rats have differences in mitochondrial redox homeostasis and energy metabolism in tissues. Meanwhile, sodium butyrate can effectively promote muscle protein synthesis, increase insulin sensitivity, and promote glucose metabolism in obesity rats. Thus, sodium butyrate supplementation or increasing intestinal butyrate production (e.g., by consuming foods rich in dietary fiber) is a potential means of improving the body's glucose metabolism and obesity profile.

摘要

丁酸钠(NaB)通过肠道微生物发酵膳食纤维获得,最近研究表明,其可提高体内某些抗氧化酶的活性。本研究旨在探讨骨骼肌中线粒体能量代谢和氧化还原平衡的变化,并阐明 NaB 对骨骼肌的调节机制和剂量效应。雄性 Sprague-Dawley 大鼠根据 8 周高脂饮食(HFD)喂养后体重增加情况分为对照组、肥胖易感(OP)组和肥胖抵抗(OR)组,然后在第 20 周末处死大鼠。NaB 干预(12 周)可有效降低 OP 和 OR 组大鼠的体重。NaB 还介导抗氧化酶活性和 GSH/GSSG 比值升高,同时降低活性氧(ROS)水平和丙二醛(MDA)含量。在分子水平上,NaB 通过调节 Nrf2 抗氧化途径上调 Pi3k、Nrf2、Nqo-1 和 Ho-1 的表达,同时下调 Gsk-3βmRNA 表达,增强组织抗氧化能力。同时,NaB 干预可显著上调 OP 和 OR 大鼠腓肠肌中 Glut4、Irs-1、Pdx1 和 MafA 的表达,提高胰岛素分泌和肌肉胰岛素敏感性。因此,NaB 激活抗氧化途径,提高肥胖大鼠组织的抗氧化能力,促进葡萄糖代谢。实际应用:本研究发现肥胖易感和肥胖抵抗大鼠组织中线粒体氧化还原平衡和能量代谢存在差异。同时,丁酸钠能有效促进肥胖大鼠肌肉蛋白合成,提高胰岛素敏感性,促进葡萄糖代谢。因此,丁酸钠补充或增加肠道丁酸生成(例如,通过食用富含膳食纤维的食物)可能是改善机体葡萄糖代谢和肥胖表型的一种潜在手段。

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