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压力会导致衰老过程中中枢胰岛素抵抗的发展:对阿尔茨海默病的影响。

Stress contributes to the development of central insulin resistance during aging: implications for Alzheimer's disease.

作者信息

Solas Maite, Aisa Bárbara, Tordera Rosa M, Mugueta María C, Ramírez María J

机构信息

Department of Pharmacology, University of Navarra, 31008 Pamplona, Spain.

出版信息

Biochim Biophys Acta. 2013 Dec;1832(12):2332-9. doi: 10.1016/j.bbadis.2013.09.013. Epub 2013 Oct 1.

DOI:10.1016/j.bbadis.2013.09.013
PMID:24090692
Abstract

It is becoming evident that chronic exposure to stress not only might result in insulin resistance or cognitive deficits, but may also be considered a risk factor for pathologies such as depression or Alzheimer's disease (AD). There is great interest in determining the molecular mechanisms underlying interactions between stress, aging, memory and Alzheimer's disease (AD). We have used the chronic mild stress (CMS) model to study the effects of chronic stress on the aging process and the development of central insulin resistance and AD pathology. CMS aged mice showed cognitive impairments in the novel object recognition test. In addition, CMS aged mice displayed both peripheral insulin resistance, as shown by HOMA index, and decreased hippocampal levels of pIRS and downstream intracellular signaling (pAKT, pGSK and pERK1/2). Interestingly, there was a significant increase in both C99:C83 ratio and BACE1 levels in the hippocampus of CMS aged mice. Increased expression of the AD marker pTau was also found in stressed aged mice. Increased expression of the stress-activated protein kinase JNK was found in CMS aged mice, accompanied by significant decreases in glucocorticoid receptor (GR) expression and increases in mineralocorticoid receptor (MR) expression. It is suggested that the interaction of stress with aging should be considered when studying determinants of the onset and progression of AD.

摘要

越来越明显的是,长期暴露于应激不仅可能导致胰岛素抵抗或认知缺陷,还可能被视为抑郁症或阿尔茨海默病(AD)等疾病的危险因素。人们对确定应激、衰老、记忆和阿尔茨海默病(AD)之间相互作用的分子机制非常感兴趣。我们使用慢性轻度应激(CMS)模型来研究慢性应激对衰老过程以及中枢胰岛素抵抗和AD病理发展的影响。CMS老龄小鼠在新物体识别测试中表现出认知障碍。此外,如HOMA指数所示,CMS老龄小鼠表现出外周胰岛素抵抗,且海马体中pIRS水平及下游细胞内信号传导(pAKT、pGSK和pERK1/2)降低。有趣的是,CMS老龄小鼠海马体中C99:C83比值和BACE1水平均显著升高。在应激老龄小鼠中还发现AD标志物pTau的表达增加。在CMS老龄小鼠中发现应激激活蛋白激酶JNK的表达增加,同时糖皮质激素受体(GR)表达显著降低,盐皮质激素受体(MR)表达增加。建议在研究AD发病和进展的决定因素时应考虑应激与衰老的相互作用。

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