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新型胃肠促动力剂KW-5092对犬胃肠运动活性的增强作用。

Enhancement by KW-5092, a novel gastroprokinetic agent, of the gastrointestinal motor activity in dogs.

作者信息

Kishibayashi N, Tomaru A, Ichikawa S, Kitazawa T, Shuto K, Ishii A, Karasawa A

机构信息

Department of Pharmacology, Kyowa Hakko Kogyo Co., Ltd., Shizuoka, Japan.

出版信息

Jpn J Pharmacol. 1994 Jun;65(2):131-42. doi: 10.1254/jjp.65.131.

Abstract

KW-5092 ([1-[2-[[[5-(piperidinomethyl)-2- furanyl]methyl]amino]ethyl]-2-imidazolidinylidene) propanedinitrile fumarate) is a novel gastroprokinetic agent with acetylcholinesterase (AChE) inhibitory activity and acetylcholine (ACh) release facilitatory activity. The present study examined the effects of KW-5092 on gastrointestinal (GI) motor activity in dogs. In anesthetized dogs, KW-5092 at 0.03 to 1 mg/kg, i.v. dose-dependently enhanced the gastric antral and the colonic motor activity. Neostigmine, an AChE inhibitor, enhanced the motor activity at 0.03 and 0.1 mg/kg, i.v. Ranitidine, a histamine H2-receptor antagonist with AChE inhibitory activity and ACh release facilitatory activity, enhanced the motor activity but decreased blood pressure at 1 to 10 mg/kg, i.v. In conscious dogs, KW-5092 at 0.03 to 1 mg/kg, i.v. or 1 to 10 mg/kg, p.o. dose-dependently enhanced the gastric antral, duodenal, ileal and the colonic motor activities. Neostigmine at 0.1 mg/kg, i.v. or 3 mg/kg, p.o. enhanced the duodenal, ileal and colonic motor activities, but induced excitement, slavering, vomiting and diarrhea. Ranitidine at 3 mg/kg, i.v. enhanced the gastric antral and colonic motor activities, but induced collapse or akinesia. The present results suggest that KW-5092 enhances the GI motor activity in a wide range from the gastric antrum to the colon and does not induce behavioral and cardiovascular side effects. KW-5092 may be a useful drug for the treatment of GI motility dysfunctions.

摘要

KW - 5092(富马酸[1 - [2 - [[[5 - (哌啶甲基)-2 - 呋喃基]甲基]氨基]乙基]-2 - 咪唑烷亚基]丙二腈)是一种新型促胃肠动力药物,具有乙酰胆碱酯酶(AChE)抑制活性和乙酰胆碱(ACh)释放促进活性。本研究考察了KW - 5092对犬胃肠道(GI)运动活性的影响。在麻醉犬中,静脉注射0.03至1mg/kg的KW - 5092剂量依赖性地增强胃窦和结肠的运动活性。新斯的明,一种AChE抑制剂,静脉注射0.03和0.1mg/kg时增强运动活性。雷尼替丁,一种具有AChE抑制活性和ACh释放促进活性的组胺H2受体拮抗剂,静脉注射1至10mg/kg时增强运动活性,但降低血压。在清醒犬中,静脉注射0.03至1mg/kg或口服1至10mg/kg的KW - 5092剂量依赖性地增强胃窦、十二指肠、回肠和结肠的运动活性。静脉注射0.1mg/kg或口服3mg/kg的新斯的明增强十二指肠、回肠和结肠的运动活性,但引起兴奋、流涎、呕吐和腹泻。静脉注射3mg/kg的雷尼替丁增强胃窦和结肠的运动活性,但引起虚脱或运动不能。目前的结果表明,KW - 5092在从胃窦到结肠的广泛范围内增强GI运动活性,且不引起行为和心血管副作用。KW - 5092可能是治疗GI运动功能障碍的一种有用药物。

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