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2型糖尿病中的脑代谢改变:我们从饮食诱导的糖尿病模型中学到了什么?

Brain Metabolism Alterations in Type 2 Diabetes: What Did We Learn From Diet-Induced Diabetes Models?

作者信息

Garcia-Serrano Alba M, Duarte João M N

机构信息

Department of Experimental Medical Science, Faculty of Medicine, Lund University, Lund, Sweden.

Wallenberg Centre for Molecular Medicine, Faculty of Medicine, Lund University, Lund, Sweden.

出版信息

Front Neurosci. 2020 Mar 20;14:229. doi: 10.3389/fnins.2020.00229. eCollection 2020.

Abstract

Type 2 diabetes (T2D) is a metabolic disease with impact on brain function through mechanisms that include glucose toxicity, vascular damage and blood-brain barrier (BBB) impairments, mitochondrial dysfunction, oxidative stress, brain insulin resistance, synaptic failure, neuroinflammation, and gliosis. Rodent models have been developed for investigating T2D, and have contributed to our understanding of mechanisms involved in T2D-induced brain dysfunction. Namely, mice or rats exposed to diabetogenic diets that are rich in fat and/or sugar have been widely used since they develop memory impairment, especially in tasks that depend on hippocampal processing. Here we summarize main findings on brain energy metabolism alterations underlying dysfunction of neuronal and glial cells promoted by diet-induced metabolic syndrome that progresses to a T2D phenotype.

摘要

2型糖尿病(T2D)是一种代谢性疾病,通过葡萄糖毒性、血管损伤和血脑屏障(BBB)损伤、线粒体功能障碍、氧化应激、脑胰岛素抵抗、突触功能障碍、神经炎症和胶质增生等机制影响脑功能。已经开发出啮齿动物模型来研究T2D,并有助于我们理解T2D诱导的脑功能障碍所涉及的机制。也就是说,暴露于富含脂肪和/或糖的致糖尿病饮食的小鼠或大鼠已被广泛使用,因为它们会出现记忆障碍,尤其是在依赖海马体处理的任务中。在这里,我们总结了关于饮食诱导的代谢综合征发展为T2D表型所促进的神经元和神经胶质细胞功能障碍背后的脑能量代谢改变的主要发现。

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