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噻唑烷二酮类药物、过氧化物酶体增殖物激活受体-γ 与神经保护

Glitazones, PPAR-γ and Neuroprotection.

机构信息

Department of Pharmacology, JSS College of Pharmacy, Ooty-643001, Tamilnadu, India.

Department of Pharmaceutical Chemistry, JSS College of Pharmacy, Mysuru-570015, India.

出版信息

Mini Rev Med Chem. 2021;21(12):1457-1464. doi: 10.2174/1389557521666210304112403.

Abstract

The transcriptional factor PPAR-γ belongs to the nuclear receptor family, which has become a potential therapeutic target for several neurodegenerative diseases and metabolic disorders. Interestingly, PPAR-γ has been reported to have beneficial effects in various chronic neurological conditions via upregulation of its transcriptional co-activator PGC-1α and followed by regulation of multiple molecular events. Although several factors contribute to the progression of neurodegeneration, the dysfunction of PGC-1α expression is primarily interlinked with the pathogenesis of major neurodegenerative diseases. This review gives an insight that ligand-dependent activation of PPAR-γ by glitazones could initiate the structural conformational changes of the secondary proteins, thus recruiting the PGC-1α to form a stable regulatory complex that hampers the various molecular pathways contributing to neurodegeneration. The promising outcomes of the preliminary in silico studies included in this review support that PPAR-γ dependent activation of central PGC-1α signaling by novel glitazones is an encouraging strategy to enhance the oxy-radicals detoxifying system, antiinflammatory responses, and mitochondrial biogenesis required for neuroprotection in various neurodegenerative conditions.

摘要

转录因子 PPAR-γ 属于核受体家族,已成为多种神经退行性疾病和代谢紊乱的潜在治疗靶点。有趣的是,PPAR-γ 通过上调其转录共激活因子 PGC-1α 并随后调节多种分子事件,已被报道对各种慢性神经疾病具有有益作用。尽管有几个因素导致神经退行性变的进展,但 PGC-1α 表达的功能障碍主要与主要神经退行性疾病的发病机制有关。本综述表明,通过格列酮激活 PPAR-γ 的配体依赖性可引发二级蛋白的结构构象变化,从而募集 PGC-1α 形成稳定的调节复合物,阻止导致神经退行性变的各种分子途径。本综述中包含的初步计算机模拟研究的有希望的结果支持,通过新型格列酮激活中枢 PGC-1α 信号的 PPAR-γ 依赖性是增强各种神经退行性疾病中所需的氧自由基解毒系统、抗炎反应和线粒体生物发生的有希望的策略。

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