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Positive modulators of the alpha 7 nicotinic receptor against neuroinflammation and cognitive impairment in Alzheimer's disease

机译:α7烟碱样受体的正调节剂,可抵抗阿尔茨海默氏病的神经炎症和认知障碍

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Evidence so far indicates that therapies targeting a single aspect of Alzheimer's disease (AD) have no sufficient efficacy in diminishing long-term the progression of AD. Neuroinflammation is an early event during the development of the disease and it is thought to exacerbate the abnormal aggregation of the amyloid beta peptide (AP) and the microtubule associated protein Tau. Inhibition of gliosis is considered fundamental to reduce neuroinflammation, oxidative stress, apoptosis and synaptic dysfunction driving the progression of AD. Drugs that are able to target more than one aspect of the pathology may have higher chances of success. Modulators of alpha 7 nicotinic acetylcholine receptors (alpha 7nAChRs) such as nicotine and some of its derivatives have this potential because of their anti-inflammatory, antiapoptotic, pro-cognitive and anti-protein aggregation effects. However, the rapid desensitization of alpha 7nAChRs is considered an important factor limiting its potential therapeutic use. In here, in light of current evidence, the objective of this review is to discuss the advantages and potential therapeutic value of positive allosteric modulators (PAMs) of the nAChRs in halting or delaying the progression of AD by diminishing neuroinflammation, abnormal protein aggregation and synaptic dysfunction. Published by Elsevier Ltd.
机译:迄今为止的证据表明,针对阿尔茨海默氏病(AD)单一方面的疗法在减少AD的长期进展方面没有足够的疗效。神经炎症是疾病发展过程中的早期事件,被认为会加剧淀粉样β肽(AP)和微管相关蛋白Tau的异常聚集。抑制神经胶质增生被认为是减少神经炎症,氧化应激,细胞凋亡和突触功能障碍的基础,这些神经驱动AD进展。能够靶向病理学多个方面的药物可能具有更高的成功机会。 α7烟碱乙酰胆碱受体(α7nAChRs)的调节剂,例如尼古丁及其某些衍生物,由于其抗炎,抗凋亡,促认知和抗蛋白质聚集作用而具有这种潜力。但是,α7nAChRs的快速脱敏被认为是限制其潜在治疗用途的重要因素。在此,根据当前证据,本综述的目的是讨论nAChRs的正变构调节剂(PAM)在通过减少神经炎症,异常蛋白质聚集和突触来中止或延迟AD进程中的优势和潜在治疗价值。功能障碍。由Elsevier Ltd.发布

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