噻唑烷二酮类药物与缺血性卒中(文献综述及新治疗途径的论证)

N. Lytvynenko, M. Delva
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引用次数: 0

摘要

中风是成年人死亡和残疾的主要原因。包括炎症、氧化应激和细胞凋亡在内的许多病理事件可导致脑卒中后继发性神经元死亡。本综述的目的是讨论噻唑烷二酮类药物(过氧化物酶体增殖物激活受体-γ激动剂)在缺血性卒中中的治疗潜力和可能的神经保护作用机制。噻唑烷二酮具有胰岛素增敏和其他额外的多效性。噻唑烷二酮类药物具有抗炎、抗氧化、抗细胞凋亡、内皮功能和修复等保护作用。噻唑烷二酮类药物的这些新作用可能对腹部肥胖和胰岛素抵抗患者脑缺血的潜在增强损伤提供一定的保护,并可能为卒中治疗开辟新的令人兴奋的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiazolidinediones and ischemic stroke (literature review and reasoning for the new potential treatment approaches)
Stroke is a leading cause of death and disability among adult population. Many pathological events including inflammation, oxidative stress, and apoptosis contribute to the secondary neuronal death after stroke. The goal of this review is to discuss the therapeutic potential and putative mechanisms of neuroprotective properties of thiazolidinediones (peroxisome proliferator-activated receptors-γ agonists) at ischemic stroke. Thiazolidinediones have insulin-sensitizing and other additional pleiotropic properties. Ischemic neuroprotection afforded by thiazolidinediones has been involved anti-inflammatory, anti-oxidant, anti-apoptotic properties, as well as effects on endothelial function and repair. These novel actions of thiazolidinediones could offer some protection against the potentially enhanced damage of brain ischemia in patients with abdominal obesity and insulin resistance and may open new exciting lines of investigation on stroke treatment.
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