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针对中枢神经系统中一氧化氮/环磷酸鸟苷信号通路治疗神经退行性疾病和阿尔茨海默病

Targeting NO/cGMP Signaling in the CNS for Neurodegeneration and Alzheimer's Disease.

作者信息

Ben Aissa Manel, Lee Sue H, Bennett Brian M, Thatcher Gregory R J

机构信息

Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, Chicago, USA.

出版信息

Curr Med Chem. 2016;23(24):2770-2788. doi: 10.2174/0929867323666160812145454.

Abstract

cAMP-response element-binding protein (CREB) plays a central role in various aspects of central nervous system (CNS) function, ranging from the developmental stages to neuronal plasticity and survival in adult brain. Activation of CREB plays a crucial role in learning and memory and is at the convergence of multiple intracellular signaling cascades including CAMKII and MAPK. This review focuses on the important functions of nitric oxide (NO) in activating CREB via the NO receptor, soluble guanylyl cyclase (sGC), and production of the second messenger, cGMP. The involvement of the NO/cGMP signaling pathway in synaptic plasticity suggests several avenues for therapeutic intervention, and targeting early synaptic degeneration could be an attractive approach for the development of novel disease-modifying approaches to treat cognition and memory dysfunction in neurodegenerative diseases.

摘要

环磷酸腺苷反应元件结合蛋白(CREB)在中枢神经系统(CNS)功能的各个方面都发挥着核心作用,从发育阶段到成年大脑中的神经元可塑性和存活。CREB的激活在学习和记忆中起着关键作用,并且处于包括钙/钙调蛋白依赖性蛋白激酶II(CAMKII)和丝裂原活化蛋白激酶(MAPK)在内的多个细胞内信号级联反应的交汇点。本综述重点关注一氧化氮(NO)通过NO受体、可溶性鸟苷酸环化酶(sGC)激活CREB以及第二信使环磷酸鸟苷(cGMP)产生的重要功能。NO/cGMP信号通路参与突触可塑性提示了几种治疗干预途径,针对早期突触退变可能是开发新型疾病修饰方法以治疗神经退行性疾病中认知和记忆功能障碍的一种有吸引力的方法。

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