Andersson Karl-Erik
Department of Clinical Pharmacology, Lund University Hospital, Lund, Sweden.
Urology. 2004 Mar;63(3 Suppl 1):32-41. doi: 10.1016/j.urology.2003.10.005.
Although currently available antimuscarinic agents are the standard of care for overactive bladder (OAB), they are limited by certain side effects, particularly dry mouth and constipation. Research aimed at discovering new therapies for OAB has resulted in the identification of some promising drugs. Investigations of pharmacologic targets in the central nervous system (CNS) have yielded encouraging results with several agents, including tramadol and gabapentin. Further investigation may show that drugs acting at serotonergic and noradrenergic CNS sites are clinically useful as therapies for OAB. Some peripherally acting drugs, such as resiniferatoxin and botulinum toxin, have already been proved to be of clinical value. However, development of other agents that block afferent or efferent nerve impulses in the bladder through activity at vanilloid, purinergic, or opioid-like receptor sites may result in clinically useful drugs.
尽管目前可用的抗毒蕈碱药物是治疗膀胱过度活动症(OAB)的标准疗法,但它们受到某些副作用的限制,尤其是口干和便秘。旨在发现OAB新疗法的研究已确定了一些有前景的药物。对中枢神经系统(CNS)药理靶点的研究已在几种药物(包括曲马多和加巴喷丁)上取得了令人鼓舞的结果。进一步的研究可能表明,作用于CNS中血清素能和去甲肾上腺素能位点的药物作为OAB的治疗方法在临床上是有用的。一些外周作用药物,如树脂毒素和肉毒杆菌毒素,已被证明具有临床价值。然而,开发其他通过作用于香草酸、嘌呤能或阿片样受体位点来阻断膀胱传入或传出神经冲动的药物可能会产生临床上有用的药物。