Interplay Between Hippocampal Glutathione Depletion and pH Increment in Alzheimer's Disease.

P. Mandal, D. Dwivedi, D. Shukla, Avantika Samkaria, Rimil Guha Roy, Yashika Arora, Komal Jindal
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引用次数: 1

Abstract

Oxidative stress (OS) is a critical factor in the pathogenesis of Alzheimer's disease (AD). Elevated OS in AD lowers the level of glutathione (GSH), a brain antioxidant. Currently, GSH is under examination in the clinical population for understanding its association with oxidative load in AD research. Significant depletion in hippocampal GSH, as observed using in vivo magnetic resonance spectroscopy (MRS), reportedly correlates with cognitive impairment in AD. Alterations in cellular-energy metabolism and increased hippocampal pH have also been reported in AD. Hence, this combined molecular interplay between hippocampal GSH and pH must be studied longitudinally for advancing AD research. Herein, we propose a schematic model depicting the molecular events in AD pathogenesis and provide a possible link between OS, GSH depletion, and pH alterations in the hippocampus. The model would further potentiate the need for in vivo longitudinal studies to confirm the interlinked mechanism between OS, hippocampal GSH depletion, and pH increment in an AD patient brain.
阿尔茨海默病海马谷胱甘肽耗竭与pH值升高的相互作用
氧化应激(OS)是阿尔茨海默病(AD)发病的关键因素。AD患者的OS升高会降低谷胱甘肽(GSH)水平,GSH是一种大脑抗氧化剂。目前,谷胱甘肽正在临床人群中进行研究,以了解其与AD研究中氧化负荷的关系。据报道,体内磁共振波谱(MRS)观察到海马谷胱甘肽的显著减少与AD患者的认知障碍有关。细胞能量代谢的改变和海马pH值的升高也被报道为AD患者。因此,必须纵向研究海马GSH和pH之间的这种联合分子相互作用,以推进AD的研究。在此,我们提出了一个描述AD发病机制中的分子事件的示意图模型,并提供了海马中OS、GSH消耗和pH改变之间的可能联系。该模型将进一步加强对体内纵向研究的需求,以确认AD患者大脑中OS、海马GSH消耗和pH增加之间的相互关联机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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