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基于下尿路功能障碍病理生理学的新型治疗药物的前沿:琥珀酸索利那新(卫喜康),一种膀胱选择性抗毒蕈碱药物,对膀胱过度活动症症状,特别是尿急发作的改善作用。

The forefront for novel therapeutic agents based on the pathophysiology of lower urinary tract dysfunction: ameliorative effect of solifenacin succinate (Vesicare), a bladder-selective antimuscarinic agent, on overactive bladder symptoms, especially urgency episodes.

机构信息

Applied Pharmacology Research Laboratories, Drug Discovery Research, Astellas Pharma Inc., Tsukuba-shi, Ibaraki 305-8585, Japan.

出版信息

J Pharmacol Sci. 2010;112(2):135-41. doi: 10.1254/jphs.09r13fm. Epub 2010 Feb 4.

DOI:10.1254/jphs.09r13fm
PMID:20134114
Abstract

Overactive bladder (OAB) syndrome is a common condition that is most often observed in the elderly. Pharmacological treatment with muscarinic receptor antagonists has been most widely used for OAB. An antimuscarinic agent, solifenacin, showed the highest affinity for the muscarinic M(3) receptor, which mediates urinary bladder contraction. In preclinical studies, solifenacin exhibited a highly bladder-selective profile compared with other antimuscarinic agents. Solifenacin was also shown to increase bladder capacity without affecting residual urine in an OAB model of rats. Urgency is now considered to result from overactivation of afferent nerves from the urinary bladder. It has been reported that afferent nerves are located adjacent to the urothelium, and stimulation of muscarinic receptors expressed on the urothelium may contribute to the activation of afferent nerves via non-neuronal ATP release. Solifenacin produces its inhibitory effect on bladder afferent activity partly via the suppression of non-neuronal ATP release. Clinically, solifenacin ameliorates all symptoms in OAB patients; and in particular, it produces a significant decrease in urgency episodes, which is the principal symptom of OAB. The pharmacological profile of solifenacin is therefore considered to contribute to its beneficial effects of high efficacy against OAB symptoms with good tolerability.

摘要

膀胱过度活动症(OAB)是一种常见病症,多见于老年人。目前,使用毒蕈碱受体拮抗剂进行药物治疗是 OAB 的主要治疗方法。作为一种抗毒蕈碱药物,索利那新对介导膀胱收缩的毒蕈碱 M(3)受体具有最高亲和力。在临床前研究中,与其他抗毒蕈碱药物相比,索利那新表现出高度的膀胱选择性。在大鼠 OAB 模型中,索利那新可增加膀胱容量,而不影响残余尿量。目前认为,急迫性尿失禁是由于膀胱传入神经过度兴奋引起的。有报道称,传入神经位于尿路上皮附近,刺激尿路上皮表达的毒蕈碱受体可能通过非神经元 ATP 释放来激活传入神经。索利那新通过抑制非神经元 ATP 释放来部分发挥其对膀胱传入活动的抑制作用。在临床上,索利那新可改善 OAB 患者的所有症状;特别是,它可显著减少急迫性尿失禁的发作次数,这是 OAB 的主要症状。因此,索利那新的药理学特征被认为有助于其发挥高效治疗 OAB 症状的作用,且具有良好的耐受性。

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