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针对磷酸二酯酶的药物疗法用于物质依赖治疗

Targeting Phosphodiesterases in Pharmacotherapy for Substance Dependence.

作者信息

Wen Rui-Ting, Liang Jian-Hui, Zhang Han-Ting

机构信息

Department of Pharmacy, Peking University People's Hospital, Beijing, 100044, China.

Department of Molecular and Cellular Pharmacology, Peking University School of Pharmaceutical Sciences, Beijing, 100191, China.

出版信息

Adv Neurobiol. 2017;17:413-444. doi: 10.1007/978-3-319-58811-7_15.

Abstract

Substance dependence is a chronic relapsing brain disorder associated with adaptational changes in synaptic plasticity and neuronal functions. The high levels of substance consumption and relapse rate suggest more reliable medications are in need to better address the underlying causes of this disease. It has been well established that the intracellular second messengers cyclic AMP (cAMP) and cyclic GMP (cGMP) and their signaling systems play an important role in the molecular mechanisms of substance taking behaviors. On this basis, the phosphodiesterase (PDE) superfamily, which crucially controls cyclic nucleotide levels by catalyzing their hydrolysis, has been proposed as a novel class of therapeutic targets for substance use disorders. This chapter reviews the expression patterns of PDEs in the brain with regard to neural structures underlying the dependent process and highlights available evidence for a modulatory role of PDEs in substance dependence.

摘要

物质依赖是一种慢性复发性脑部疾病,与突触可塑性和神经元功能的适应性变化相关。物质的高消耗量和复发率表明,需要更可靠的药物来更好地解决该疾病的根本原因。众所周知,细胞内第二信使环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)及其信号系统在物质摄取行为的分子机制中起重要作用。在此基础上,磷酸二酯酶(PDE)超家族通过催化环核苷酸水解来关键地控制其水平,已被提议作为物质使用障碍的一类新型治疗靶点。本章回顾了PDEs在大脑中的表达模式,涉及依赖过程背后的神经结构,并强调了PDEs在物质依赖中起调节作用的现有证据。

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