翻訳と辞書
Words near each other
・ PRTG Network Monitor
・ Prthudakasvami
・ PRTM
・ Prtovč
・ PRTP
・ Pru
・ Pru (band)
・ Pru (Ghana parliament constituency)
・ Pru District
・ Pru Goward
・ PRU Inter-Department Rugby Championship
・ PRU Inter-Department Sevens Rugby Championship
・ Pru River
・ PRU-70
・ Prubi railway station
Prucalopride
・ Prucheńsko Duże
・ Prucheńsko Małe
・ Pruchna
・ Pruchnik
・ Pruchnowo, Greater Poland Voivodeship
・ Pruchnowo, Kuyavian-Pomeranian Voivodeship
・ Pruchten
・ Pruchya Isarow
・ Prucol
・ Prud
・ Prud Agreement
・ Prud'homme, Saskatchewan
・ Prud, Bosnia and Herzegovina
・ Prudden-Whitehead monoplane


Dictionary Lists
翻訳と辞書 辞書検索 [ 開発暫定版 ]
スポンサード リンク

Prucalopride : ウィキペディア英語版
Prucalopride

Prucalopride (brand name Resolor, developed by Johnson & Johnson and licensed to Movetis) is a drug acting as a selective, high affinity 5-HT4 receptor agonist which targets the impaired motility associated with chronic constipation, thus normalising bowel movements. Prucalopride was approved for use in Europe in 2009,〔(European Medicines Agency -EPAR )〕 in Canada (named Resotran) on December 7, 2011〔(Health Canada, Notice of Decision for Resotran )〕 and in Israel in 2014〔( Digestive Remedies in Israel )〕 but it has not been approved by the Food and Drug Administration for use in the United States. The drug has also been tested for the treatment of chronic intestinal pseudo-obstruction.
== Mechanism of action ==
Prucalopride, a first in class dihydro-benzofuran-carboxamide, is a selective, high affinity serotonin (5-HT4) receptor agonist with enterokinetic activities.〔SmPC. Summary of product characteristics Resolor (prucalopride) October, 2009: 1-9.〕 Prucalopride alters colonic motility patterns via serotonin 5-HT4 receptor stimulation: it stimulates colonic mass movements, which provide the main propulsive force for defecation.
The observed effects are exerted via highly selective action on 5-HT4 receptors:〔 prucalopride has >150-fold higher affinity for 5-HT4 receptors than for other receptors.〔 Prucalopride differs from other 5-HT4 agonists such as tegaserod and cisapride, which at therapeutic concentrations also interact with other receptors (5-HT1B/D and the cardiac human ether-a-go-go K+ or hERG channel respectively) and this may account for the adverse cardiovascular events that have resulted in the restricted availability of these drugs.〔 Clinical trials evaluating the effect of prucalopride on QT interval and related adverse events have not demonstrated significant differences compared with placebo.〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Prucalopride」の詳細全文を読む



スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース

Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.