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止泻剂洛哌丁胺的药理学研究。II. 对豚鼠小肠和结肠蠕动的影响(作者译)

[Pharmacological studies of loperamide, an anti-diarrheal agent. II. Effects on peristalsis of the small intestine and colon in guinea pigs (author's transl)].

作者信息

Sohji Y, Kawashima K, Shimizu M

出版信息

Nihon Yakurigaku Zasshi. 1978 Jan;74(1):155-63. doi: 10.1254/fpj.74.155.

DOI:10.1254/fpj.74.155
PMID:640534
Abstract

Effects of loperamide on peristalsis in the guinea pig intestines were investigated in comparison with those of morphine and atropine. The following results were obtained. The ejection of intraluminal fluid produced by the peristaltic contraction of the isolated ileum was suppressed by loperamide at a concentration of 10(-8) or 2 X 10(-8) g/ml. Peristalsis in the intestinal loop of anesthetized guinea pigs was inhibited by i.v. administration of loperamide at a dose of 0.03 mg/kg. Morphine (0.03 mg/kg i.v.) and atropine (0.05 mg/kg i.v.) also inhibited the peristaltic contraction. The effect of loperamide continued longer than that of morphine. Peristalsis in the colonic loop of anesthetized guinea pigs was inhibited by i.v. administration of loperamide at a dose of 0.01 or 0.03 mg/kg. Morphine (0.1 mg/kg i.v.) and atropine (0.03 mg/kg i.v.) also inhibited the peristaltic contraction of the colonic loop. Loperamide (0.01 or 0.03 mg/kg i.v.) and morphine (0.1 mg/kg i.v.) caused a slight and temporary increase of resting level of intraluminal pressure with inhibition of peristalsis in the colonic loop. These results suggest that loperamide suppresses the peristaltic contraction caused by distension of the intestinal lumen.

摘要

将洛哌丁胺与吗啡和阿托品相比较,研究了其对豚鼠肠道蠕动的影响。获得了以下结果。洛哌丁胺在浓度为10(-8)或2×10(-8)克/毫升时,可抑制离体回肠蠕动收缩产生的肠腔内液体排出。静脉注射剂量为0.03毫克/千克的洛哌丁胺可抑制麻醉豚鼠肠袢的蠕动。吗啡(静脉注射0.03毫克/千克)和阿托品(静脉注射0.05毫克/千克)也抑制蠕动收缩。洛哌丁胺的作用持续时间比吗啡长。静脉注射剂量为0.01或0.03毫克/千克的洛哌丁胺可抑制麻醉豚鼠结肠袢的蠕动。吗啡(静脉注射0.1毫克/千克)和阿托品(静脉注射0.03毫克/千克)也抑制结肠袢的蠕动收缩。洛哌丁胺(静脉注射0.01或0.03毫克/千克)和吗啡(静脉注射0.1毫克/千克)在抑制结肠袢蠕动的同时,使肠腔内压力的静息水平略有短暂升高。这些结果表明,洛哌丁胺可抑制肠腔扩张引起的蠕动收缩。

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