Suppr超能文献

高脂饮食诱导的空间记忆改变、海马 JNK、P38、ERK 和 Akt 活性的时程研究。

Time-course study of high fat diet induced alterations in spatial memory, hippocampal JNK, P38, ERK and Akt activity.

机构信息

Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Physiology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Metab Brain Dis. 2019 Apr;34(2):659-673. doi: 10.1007/s11011-018-0369-1. Epub 2018 Dec 14.

Abstract

Consumption of high fat diet (HFD) is a health concern in modern societies, which participate in wide range of diseases. One underlying mechanism in the HFD mediated pathologies is disruption of insulin signaling activity. It is believed that HFD activates several stress signaling molecules such as MAPKs signaling pathway and these molecules participate in harmful effects in different cell populations including hippocampal cells. However, the activity of MAPKs signaling molecules are time dependent, even causing some opposing effects. Given that, MAPKs activity fluctuate with time of stress, there is less cleared how different lengths of HFD consumption can affect hippocampal MAPK. To test how duration of HFD consumption affect hippocampal MAPKs and insulin signaling activity and animal's cognitive function, rats were fed with HFD for different lengths (up to 6 months) and after each point spatial memory performances of animals was tested, then the peripheral indices of insulin resistance and hippocampal MAPKs and insulin signaling activity was evaluated. Results showed that while different time courses of HFD, up to 6 months, did not bring about significant spatial memory impairment, meanwhile the peripheral insulin sensitivity as well as hippocampal insulin and MAPKs signaling showed significant fluctuations during the different time courses of high fat diet regime. These results showed that neuronal responses to HFD is not constant and differ in a time-dependent manner, it seems that in acute phase molecular responses aimed to compensate the HFD stress but in chronic states these responses failed and devastating effects of stress began.

摘要

高脂肪饮食(HFD)的摄入是现代社会的一个健康关注点,它与多种疾病有关。HFD 介导的病理学中的一个潜在机制是胰岛素信号活性的破坏。人们认为,HFD 会激活几种应激信号分子,如 MAPK 信号通路,这些分子参与包括海马细胞在内的不同细胞群体的有害作用。然而,MAPK 信号分子的活性是时间依赖性的,甚至会产生一些相反的影响。鉴于此,MAPK 的活性随应激时间而波动,因此尚不清楚不同时间长度的 HFD 摄入如何影响海马体中的 MAPK。为了测试 HFD 摄入时间长短如何影响海马体中的 MAPK 和胰岛素信号活性以及动物的认知功能,研究人员让大鼠摄入 HFD 不同时间(长达 6 个月),并在每个时间点测试动物的空间记忆表现,然后评估动物的外周胰岛素抵抗指数以及海马体中的 MAPK 和胰岛素信号活性。结果表明,虽然 HFD 的不同时间进程(长达 6 个月)并没有导致明显的空间记忆障碍,但同时外周胰岛素敏感性以及海马体中的胰岛素和 MAPK 信号在不同时间进程的高脂肪饮食期间表现出明显的波动。这些结果表明,神经元对 HFD 的反应不是一成不变的,而是随时间而变化,在急性阶段,分子反应旨在补偿 HFD 应激,但在慢性状态下,这些反应失败,应激的破坏性影响开始显现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验