The Challenge of the Overactive Bladder: From Laboratory to New Drugs

Massimo Lazzeri , Massimo Porena
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引用次数: 4

Abstract

Antimuscarinic agents are currently the first-line therapy for overactive bladder (OAB). Many urologists believe the pharmacologic management of OAB is not altogether satisfactory. Pharmacologic research is trying to provide answers to the issues of efficacy, tolerability, and convenience of new drugs. This paper discusses the rationale underlying the development of new compounds, provides an update of progress in the search for new therapies for OAB, and tracks their translation into clinical practice. It offers an insight into the mechanism of action, efficacy, side-effects, and “market status” of several drug categories targeting the central nervous system (adrenoceptor modulators, serotonin/norepinephrine reuptake inhibitors, tachykinin modulators, opioids), neuromuscular blocking agents (botulinum toxin A), selective modulators of the afferent branch of micturition reflex (vanilloid, nociceptin/orphanin FQ), autonomic nervous system modulators (β3-agonists), potassium and calcium channel openers, and nonsteroidal anti-inflammatory drugs.

膀胱过度活动的挑战:从实验室到新药
抗毒蕈碱类药物是目前治疗膀胱过动症(OAB)的一线药物。许多泌尿科医生认为,OAB的药物治疗并不完全令人满意。药理学研究正试图为新药的疗效、耐受性和便利性等问题提供答案。本文讨论了开发新化合物的基本原理,提供了寻找OAB新疗法的最新进展,并跟踪了它们在临床实践中的转化。它提供了针对中枢神经系统的几种药物(肾上腺素能受体调节剂,血清素/去甲肾上腺素再摄取抑制剂,速激肽调节剂,阿片类药物),神经肌肉阻滞剂(肉毒杆菌毒素A),排尿反射传入分支的选择性调节剂(香兰素,痛觉肽/孤啡肽FQ),自主神经系统调节剂(β3激动剂)的作用机制,功效,副作用和“市场状况”的见解。钾和钙通道打开剂,以及非甾体抗炎药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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