首页> 外文期刊>European urology >Antimuscarinic mechanisms and the overactive detrusor: an update.
【24h】

Antimuscarinic mechanisms and the overactive detrusor: an update.

机译:抗毒蕈碱机制和逼尿肌过度活跃:更新。

获取原文
获取原文并翻译 | 示例
           

摘要

CONTEXT: Antimuscarinics are the drugs of choice for the treatment of detrusor overactivity (DO) and overactive bladder (OAB) syndrome. However, the mechanisms for their beneficial effects have not yet been definitely established. OBJECTIVE: Literature available on the pathophysiologic aspects of storage symptoms and of antimuscarinic actions on the bladder was reviewed. EVIDENCE ACQUISITION: Medline was searched for the period ending October 2010 and included studies on human and animal tissues and animal models. Clinical studies exploring mechanisms involved in the effects of antimuscarinics were included. Searches were limited to the English language. EVIDENCE SYNTHESIS: Evidence for release of acetylcholine (ACh) from non-neuronal as well as neuronal sources during bladder filling has been demonstrated in isolated animal bladders as well as the human bladder. Urothelially derived ACh, probably via release of adenosine triphosphate, may stimulate afferent activity ("afferent noise") from the bladder contributing to OAB and DO. Afferent noise may also be generated by local ACh release within the detrusor muscle. This afferent activity can be inhibited by antimuscarinics at the low concentrations obtained with doses recommended for clinical use in OAB/DO. Within this therapeutic window, antimuscarinics may decrease OAB symptoms and DO without affecting the voiding contraction. Changes in muscarinic receptor functions have been demonstrated with aging and in different disorders associated with OAB/DO. CONCLUSIONS: ACh, derived from non-neuronal as well as neuronal sources and during bladder filling, directly or indirectly stimulates afferent activity from the bladder, contributing to OAB and DO. By inhibiting this effect, antimuscarinics may decrease OAB symptoms and DO without affecting the voiding contraction. Even if changes in muscarinic receptor functions may occur with aging and in different disorders associated with OAB/DO, such changes have not been shown convincingly to modify the beneficial effect of antimuscarinics in OAB/DO.
机译:背景:抗毒蕈碱类药物是治疗逼尿肌过度活动症(DO)和膀胱过度活动症(OAB)综合征的首选药物。但是,尚未明确确定其有益作用的机制。目的:综述了有关贮藏症状和膀胱抗毒蕈碱作用的病理生理方面的文献。证据获取:对Medline进行了截至2010年10月的搜索,其中包括有关人类和动物组织及动物模型的研究。临床研究探讨了抗毒蕈碱作用的机制。搜索仅限于英语。证据综合:在孤立的动物膀胱以及人膀胱中,已经证明了在膀胱充盈期间从非神经源以及神经元来源释放乙酰胆碱(ACh)的证据。尿嘧啶衍生的乙酰胆碱可能通过释放三磷酸腺苷来刺激膀胱的传入活动(“喧闹声”),从而导致OAB和DO。逼尿肌内局部乙酰胆碱释放也可能产生传入噪声。在推荐用于OAB / DO的临床剂量下,低浓度的抗毒蕈碱药物可以抑制这种传入活性。在此治疗范围内,抗毒蕈碱药可以减轻OAB症状和DO,而不会影响排尿收缩。毒蕈碱受体功能的变化已随着衰老以及与OAB / DO相关的各种疾病而得到证明。结论:ACh来源于非神经源以及神经元,在膀胱充盈过程中直接或间接刺激了膀胱的传入活动,从而促进了OAB和DO。通过抑制这种作用,抗毒蕈碱药可以减轻OAB症状和DO,而不会影响排尿收缩。即使毒蕈碱受体功能的变化可能随年龄增长以及与OAB / DO相关的不同疾病而发生,也没有令人信服地显示出这种变化能改变抗毒蕈碱剂在OAB / DO中的有益作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号