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[膀胱过度活动症的新药理学治疗理念]

[New pharmacological treatment concepts for overactive bladder].

作者信息

Michel M C

机构信息

Abteilung Pharmakologie und Pharmakotherapie, Universität, Amsterdam, Netherlands.

出版信息

Urologe A. 2003 Jun;42(6):807-11. doi: 10.1007/s00120-003-0365-9. Epub 2003 Apr 25.

Abstract

Muscarinic receptor antagonists such as oxybutynin, propiverine, tolterodine, or trospium are the basis of medical treatment for overactive bladder. While they are moderately efficacious, their use can be limited by adverse effects such as dry mouth. This has sparked the search for new treatment options. Vanilloid receptor agonists, tachykinin receptor antagonists, potassium channel openers, and beta(3)-adrenoceptor agonists are currently under investigation, but are unlikely to become clinically available in the next few years. Therefore, current attempts to optimize treatment focus on improvement of existing drugs by new pharmaceutical formulations. Indeed, extended release formulations of oxybutynin (not available in Germany) or tolterodine have demonstrated an improved tolerability in clinical studies which was accompanied by an efficacy at least equal to that of their standard formulations.

摘要

毒蕈碱受体拮抗剂,如奥昔布宁、丙哌维林、托特罗定或曲司氯铵,是治疗膀胱过度活动症的药物基础。虽然它们疗效中等,但使用时可能会受到如口干等不良反应的限制。这引发了对新治疗方案的探索。目前,香草酸受体激动剂、速激肽受体拮抗剂、钾通道开放剂和β(3) -肾上腺素能受体激动剂正在研究中,但在未来几年内不太可能用于临床。因此,目前优化治疗的尝试集中在通过新的药物制剂改进现有药物。事实上,奥昔布宁(德国未上市)或托特罗定的缓释制剂在临床研究中已显示出耐受性改善,同时疗效至少与标准制剂相当。

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