論文

査読有り 国際誌
2017年5月

Synergic Suppressive Effect of Silodosin and Imidafenacin on Non-Voiding Bladder Contractions in Male Rats with Subacute Bladder Outlet Obstruction.

Lower urinary tract symptoms
  • Rino Sugiyama
  • ,
  • Naoki Aizawa
  • ,
  • Hiroki Ito
  • ,
  • Tetsuya Fujimura
  • ,
  • Motofumi Suzuki
  • ,
  • Tohru Nakagawa
  • ,
  • Hiroshi Fukuhara
  • ,
  • Haruki Kume
  • ,
  • Yukio Homma
  • ,
  • Yasuhiko Igawa

9
2
開始ページ
94
終了ページ
101
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/luts.12109
出版者・発行元
WILEY

OBJECTIVES: To investigate single or combined effect of silodosin, an α1A-adrenoceptor antagonist, and imidafenacin, an antimuscarinic agent, on bladder function in a subacute bladder outlet obstruction (BOO) model of male rats. METHODS: Partial BOO was created in male Wistar rats by ligating the urethra with a steel rod. On day 10 after surgery, when frequent voiding was most remarkable on voiding behavior measurement in a metabolic cage, cystometric investigations in a conscious restrained condition were conducted with cumulative intravenous administration of silodosin alone (0.1, 1, 10, and 100 µg/kg), imidafenacin alone (1, 3, and 10 µg/kg), or a combination of the two drugs. RESULTS: When compared with the Sham rats, the BOO rats showed an increase in bladder capacity, residual volume, mean amplitude and the number of non-voiding contractions (NVCs), accompanied with an increase in bladder weight. In the BOO rats, silodosin alone at 100 µg/kg significantly decreased the number of NVCs, whereas imidafenacin alone at 3 and 10 µg/kg significantly decreased both the number and mean amplitude of NVCs. The combination administration with lower doses (silodosin at 10 µg/kg and imidafenacin at 1 µg/kg) significantly suppressed both the number and mean amplitude of NVCs. CONCLUSIONS: The present results indicate a suppressive effect of silodosin or imidafenacin alone and a synergic effect of the combination of these two drugs on NVCs in a subacute BOO model of male rats.

リンク情報
DOI
https://doi.org/10.1111/luts.12109
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28394493
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000398862500005&DestApp=WOS_CPL
ID情報
  • DOI : 10.1111/luts.12109
  • ISSN : 1757-5664
  • eISSN : 1757-5672
  • PubMed ID : 28394493
  • Web of Science ID : WOS:000398862500005

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