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过氧化物酶体增殖物激活受体γ激动剂在阿尔茨海默病中的抗炎作用

Anti-inflammatory actions of peroxisome proliferator-activated receptor gamma agonists in Alzheimer's disease.

作者信息

Landreth G E, Heneka M T

机构信息

Department of Neurosciences, Alzheimer Research Laboratory, Case Western Reserve University, School of Medicine, Cleveland, OH 44106, USA.

出版信息

Neurobiol Aging. 2001 Nov-Dec;22(6):937-44. doi: 10.1016/s0197-4580(01)00296-2.

Abstract

The role of inflammatory processes in the brains of Alzheimer's Disease (AD) patients has recently attracted considerable interest. Indeed, the only demonstrated effective therapy for AD patients is long-term treatment with non-steroidal anti-inflammatory drugs (NSAIDs). The mechanistic basis of the efficacy of NSAIDs in AD remains unclear. However, the recent recognition that NSAIDs can bind to and activate the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARgamma), has offered an explanation for the action of these drugs in AD. PPARgamma activation leads to the inhibition of microglial activation and the expression of a broad range of proinflammatory molecules. The newly appreciated anti-inflammatory actions of PPARgamma agonists may allow novel therapies for AD and other CNS indications with an inflammatory component.

摘要

炎症过程在阿尔茨海默病(AD)患者大脑中的作用最近引起了广泛关注。事实上,目前唯一被证明对AD患者有效的治疗方法是长期使用非甾体抗炎药(NSAIDs)。NSAIDs在AD中发挥疗效的机制基础仍不清楚。然而,最近人们认识到NSAIDs可以结合并激活核受体过氧化物酶体增殖物激活受体γ(PPARγ),这为这些药物在AD中的作用提供了一种解释。PPARγ激活会导致小胶质细胞活化受到抑制以及多种促炎分子的表达受到抑制。PPARγ激动剂新发现的抗炎作用可能为AD和其他具有炎症成分的中枢神经系统疾病带来新的治疗方法。

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