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离子通道作为勃起功能障碍的潜在治疗靶点:综述

Ionic Channels as Potential Therapeutic Targets for Erectile Dysfunction: A Review.

作者信息

Diniz Anderson Fellyp Avelino, Ferreira Rafael Carlos, de Souza Iara Leão Luna, da Silva Bagnólia Araújo

机构信息

Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos, Universidade Federal da Paraíba, João Pessoa, Brazil.

Departamento de Ciências Biológicas e da Saúde, Universidade Estadual de Roraima, Boa Vista, Brazil.

出版信息

Front Pharmacol. 2020 Jul 24;11:1120. doi: 10.3389/fphar.2020.01120. eCollection 2020.

Abstract

Erectile dysfunction (ED) is a prevalent condition, especially in men over 40 years old, characterized by the inability to obtain and/or maintain penile erection sufficient for satisfactory sexual intercourse. Several psychological and/or organic factors are involved in the etiopathogenesis of ED. In this context, we gathered evidence of the involvement of Large-conductance, Ca-activated K channels (BK), Small-conductance, Ca-activated K channels (SK), KCNQ-encoded voltage-dependent K channels (K7), Transient Receptor Potential channels (TRP), and Calcium-activated Chloride channels (CaCC) dysfunctions on ED. In addition, the use of modulating agents of these channels are involved in relaxation of the cavernous smooth muscle cell and, consequent penile erection, suggesting that these channels are promising therapeutic targets for the treatment of erectile dysfunction.

摘要

勃起功能障碍(ED)是一种常见病症,尤其在40岁以上男性中较为普遍,其特征为无法获得和/或维持足以进行满意性交的阴茎勃起。ED的发病机制涉及多种心理和/或器质性因素。在此背景下,我们收集了证据,证明大电导钙激活钾通道(BK)、小电导钙激活钾通道(SK)、KCNQ编码的电压依赖性钾通道(K7)、瞬时受体电位通道(TRP)以及钙激活氯通道(CaCC)功能障碍与ED有关。此外,这些通道调节剂的使用参与海绵体平滑肌细胞的舒张以及随之而来的阴茎勃起,这表明这些通道是治疗勃起功能障碍的有前景的治疗靶点。

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