首页> 美国卫生研究院文献>Current Neuropharmacology >Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimers Disease: An Update
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Current Progress on Peroxisome Proliferator-activated Receptor Gamma Agonist as an Emerging Therapeutic Approach for the Treatment of Alzheimers Disease: An Update

机译:过氧化物酶体增殖物激活的受体γ激动剂作为治疗阿尔茨海默氏病的新兴治疗方法的最新进展:更新

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摘要

Alzheimer’s disease (AD) is an age-related progressive neurodegenerative disorder, characterized by the deposition of amyloid-β within the brain parenchyma resulting in a significant decline in cognitive functions. The pathophysiological conditions of the disease are recognized by the perturbation of synaptic function, energy and lipid metabolism. In Addition deposition of amyloid plaques also triggers inflammation upon the induction of microglia. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors known to play important role in the regulation of glucose ab-sorption, homeostasis of lipid metabolism and are further known to involved in repressing the expression of genes related to inflammation. Therefore, agonists of this receptor represent an attractive therapeutic target for AD. Recently, both clinical and preclinical studies showed that use of Peroxisome proliferator-activated receptor gamma (PPARγ) agonist improves both learning and memory along with other AD related pathology. Thus, PPARγ signifies a significant new therapeutic target in treating AD. In this review, we have shed some light on the recent progress of how, PPARγ agonist selectively modulated different cellular targets in AD and its amazing potential in the treatment of AD.
机译:阿尔茨海默氏病(AD)是一种与年龄有关的进行性神经退行性疾病,其特征是淀粉样β沉积在脑实质内,导致认知功能明显下降。该疾病的病理生理状况通过突触功能,能量和脂质代谢的扰动来识别。另外,淀粉样蛋白斑块的沉积还由于诱导小胶质细胞而引发炎症。过氧化物酶体增殖物激活受体(PPAR)是配体激活的转录因子,已知在调节葡萄糖吸收,脂质代谢的稳态方面起重要作用,并且还已知与抑制炎症相关基因的表达有关。因此,该受体的激动剂代表AD的有吸引力的治疗靶标。最近,临床和临床前研究均表明,过氧化物酶体增殖物激活的受体伽玛(PPARγ)激动剂的使用可改善学习和记忆以及其他与AD相关的病理。因此,PPARγ是治疗AD的重要新治疗靶标。在这篇综述中,我们揭示了PPARγ激动剂如何选择性调节AD中不同细胞靶标及其在AD治疗中的惊人潜力的最新进展。

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