Pak Raymond W, Petrou Steven P, Staskin David R
Department of Urology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL 32224, USA.
Curr Urol Rep. 2003 Dec;4(6):436-40. doi: 10.1007/s11934-003-0023-1.
The mainstay of pharmacologic treatment of overactive bladder is anticholinergic therapy. Cholinergic blockade is efficacious in decreasing the symptoms of urgency, frequency, and urge incontinence, but also is associated with undesirable side effects such as dry mouth, blurred vision, constipation, and central nervous system side effects. The property of anticholinergic agents that has been associated with increased efficacy and tolerability is receptor specificity. The safety of anticholinergic agents has been associated with the pharmacokinetics, metabolism, protein binding, and ability to penetrate the blood brain barrier. Trospium chloride, available in Europe for more than 20 years and under review by the US Food and Drug Administration for the treatment of overactive bladder, is a quaternary amine that is minimally metabolized, not highly protein-bound, and theoretically should not cross the blood brain barrier. Some of the characteristics of this unique anticholinergic agent are reviewed in this article and the relative contributions of these factors are discussed.
膀胱过度活动症药物治疗的主要方法是抗胆碱能疗法。胆碱能阻滞在减轻尿急、尿频和急迫性尿失禁症状方面有效,但也会伴有如口干、视物模糊、便秘和中枢神经系统副作用等不良副作用。与疗效增加和耐受性提高相关的抗胆碱能药物特性是受体特异性。抗胆碱能药物的安全性与药代动力学、代谢、蛋白结合以及穿透血脑屏障的能力有关。氯化托烷司琼在欧洲已上市20多年,美国食品药品监督管理局正在对其用于治疗膀胱过度活动症进行审查,它是一种季铵盐,代谢极少,蛋白结合率不高,理论上不应穿过血脑屏障。本文对这种独特抗胆碱能药物的一些特性进行了综述,并讨论了这些因素的相对作用。