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硫辛酸对高脂肪饮食诱导的突触可塑性和脑葡萄糖代谢改变的影响:PET/CT 和 C-NMR 研究。

Effects of Lipoic Acid on High-Fat Diet-Induced Alteration of Synaptic Plasticity and Brain Glucose Metabolism: A PET/CT and C-NMR Study.

机构信息

College of Food Science and Engineering, Northwest A&F University, Yangling, Shaanxi, 712100, China.

Pharmacology & Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA, 90089-9121, USA.

出版信息

Sci Rep. 2017 Jul 14;7(1):5391. doi: 10.1038/s41598-017-05217-z.

Abstract

High-fat diet (HFD)-induced obesity is accompanied by insulin resistance and compromised brain synaptic plasticity through the impairment of insulin-sensitive pathways regulating neuronal survival, learning, and memory. Lipoic acid is known to modulate the redox status of the cell and has insulin mimetic effects. This study was aimed at determining the effects of dietary administration of lipoic acid on a HFD-induced obesity model in terms of (a) insulin signaling, (b) brain glucose uptake and neuronal- and astrocytic metabolism, and (c) synaptic plasticity. 3-Month old C57BL/6J mice were divided into 4 groups exposed to their respective treatments for 9 weeks: (1) normal diet, (2) normal diet plus lipoic acid, (3) HFD, and (4) HFD plus lipoic acid. HFD resulted in higher body weight, development of insulin resistance, lower brain glucose uptake and glucose transporters, alterations in glycolytic and acetate metabolism in neurons and astrocytes, and ultimately synaptic plasticity loss evident by a decreased long-term potentiation (LTP). Lipoic acid treatment in mice on HFD prevented several HFD-induced metabolic changes and preserved synaptic plasticity. The metabolic and physiological changes in HFD-fed mice, including insulin resistance, brain glucose uptake and metabolism, and synaptic function, could be preserved by the insulin-like effect of lipoic acid.

摘要

高脂肪饮食(HFD)诱导的肥胖伴随着胰岛素抵抗,并通过损害调节神经元存活、学习和记忆的胰岛素敏感途径来损害大脑突触可塑性。已知硫辛酸可调节细胞的氧化还原状态,并具有胰岛素模拟作用。本研究旨在确定膳食中硫辛酸对高脂肪饮食诱导肥胖模型的影响,具体涉及:(a)胰岛素信号;(b)脑葡萄糖摄取以及神经元和星形胶质细胞代谢;(c)突触可塑性。3 个月大的 C57BL/6J 小鼠被分为 4 组,分别接受 9 周的相应处理:(1)正常饮食;(2)正常饮食加硫辛酸;(3)高脂肪饮食;(4)高脂肪饮食加硫辛酸。高脂肪饮食导致体重增加、胰岛素抵抗发展、脑葡萄糖摄取和葡萄糖转运蛋白减少、神经元和星形胶质细胞糖酵解和乙酸盐代谢改变,以及最终突触可塑性丧失,表现为长时程增强(LTP)减少。高脂肪饮食喂养的小鼠中硫辛酸的治疗预防了几种高脂肪饮食诱导的代谢变化,并保留了突触可塑性。硫辛酸的胰岛素样作用可以维持高脂肪饮食喂养的小鼠的代谢和生理变化,包括胰岛素抵抗、脑葡萄糖摄取和代谢以及突触功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b43e/5511189/da066e0b93ab/41598_2017_5217_Fig1_HTML.jpg

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