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萘哌地尔治疗良性前列腺增生症患者的尿路症状。

Naftopidil for the treatment of urinary symptoms in patients with benign prostatic hyperplasia.

机构信息

Department of Urology, Sapporo Medical University School of Medicine, Sapporo, Japan.

出版信息

Ther Clin Risk Manag. 2011;7:227-38. doi: 10.2147/TCRM.S13883. Epub 2011 Jun 23.

Abstract

Naftopidil, approved only in Japan, is an α1-adrenergic receptor antagonist (α1-blocker) used to treat lower urinary tract symptoms (LUTS) suggestive of benign prostatic hyperplasia (BPH). Different from tamsulosin hydrochloride and silodosin, in that it has higher and extremely higher affinity respectively, for the α1A-adrenergic receptor subtype than for the α1D type, naftopidil has distinct characteristics because it has a three times greater affinity for the α1D-adrenergic receptor subtype than for the α1A subtype. Although well-designed large-scale randomized controlled studies are lacking and the optimal dosage of naftopidil is not always completely determined, previous reports from Japan have shown that naftopidil has superior efficacy to a placebo and comparable efficacy to other α1-blockers such as tamsulosin. On the other hand, the incidences of ejaculatory disorders and intraoperative floppy iris syndrome induced by naftopidil may be lower than for tamsulosin and silodosin having high affinity for the α1A-adrenergic receptor subtype. However, it remains unknown if the efficacy and safety of naftopidil in Japanese is applicable to white, black and Hispanic men having LUTS/BPH in western countries.

摘要

那夫妥比,仅在日本获准使用,是一种 α1-肾上腺素能受体拮抗剂(α1-阻滞剂),用于治疗下尿路症状(LUTS)提示良性前列腺增生(BPH)。与盐酸坦索罗辛和西洛多辛不同,它对 α1A-肾上腺素能受体亚型的亲和力分别更高、极高,那夫妥比具有独特的特性,因为它对 α1D-肾上腺素能受体亚型的亲和力是 α1A 亚型的三倍。尽管缺乏精心设计的大规模随机对照研究,且那夫妥比的最佳剂量并不总是完全确定,但来自日本的先前报告表明,那夫妥比的疗效优于安慰剂,与其他 α1-阻滞剂(如坦索罗辛)的疗效相当。另一方面,那夫妥比引起的射精障碍和术中软核虹膜综合征的发生率可能低于对 α1A-肾上腺素能受体亚型具有高亲和力的坦索罗辛和西洛多辛。然而,那夫妥比在日本的疗效和安全性是否适用于西方国家有 LUTS/BPH 的白种人、黑人和西班牙裔男性,尚不清楚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b79/3132093/0757fa582f05/tcrm-7-227f1.jpg

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