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通过阻断前列腺素合成的药物对豚鼠离体回肠和结肠蠕动的抑制作用。

Inhibition of peristalsis in guinea-pig isolated ileum and colon by drugs that block prostaglandin synthesis.

作者信息

Bennett A, Eley K G, Stockley H L

出版信息

Br J Pharmacol. 1976 Jul;57(3):335-40.

Abstract

1 Methods of analysing peristaltic activity have been evaluated by the use of recordings of longitudinal and circular muscle activity and of propulsion in whole segments of guinea-pig ileum and colon. 2 Some prostaglandin synthesis inhibitors, and antagonists of prostaglandin action were tested for their suitability for studying the role of prostaglandins in peristalsis. Aspirin was suitable; at 10-200 mug/ml it had little effect on responses of longitudinal muscle strips of the guinea-pig ileum to acetylcholine (ACh), histamine, nicotine or prostaglandin E2. Indomethacin (1-4 mug/ml) reduced responses to nicotine and prostaglandin E2. The prostaglandin antagonists polyphloretin phosphate and SC-19220 reduced contractions of ileal longitudinal muscle caused by nerve excitation with either nicotine or transmural stimulation. 3 Aspirin (20-100 mug/ml) or indomethacin (1-4 mug/ml) applied serosally greatly inhibited all aspects of peristalsis in guinea-pig ileum and colon. Inhibition of peristalsis of the ileum by aspirin was antagonized by prostaglandin E2 and that by indomethacin was removed by prostaglandin F2alpha or ACh. Inhibition of colonic peristalsis by aspirin was antagonized by prostaglandin E2 but rarely by ACh, and that by indomethacin by prostaglandin E1 or E2. Mucosal application of aspirin had little effect on either ileum or colon but indomethacin caused some inhibition. 4 These results support the supposition that prostaglandins contribute to peristaltic activity.

摘要

1 通过记录豚鼠回肠和结肠全段的纵行肌和环行肌活动以及推进情况,对分析蠕动活动的方法进行了评估。2 测试了一些前列腺素合成抑制剂以及前列腺素作用拮抗剂,以确定它们是否适合用于研究前列腺素在蠕动中的作用。阿司匹林是合适的;在10 - 200微克/毫升浓度下,它对豚鼠回肠纵行肌条对乙酰胆碱(ACh)、组胺、尼古丁或前列腺素E2的反应影响很小。吲哚美辛(1 - 4微克/毫升)降低了对尼古丁和前列腺素E2的反应。前列腺素拮抗剂聚磷酸根皮苷和SC - 19220减少了由尼古丁或跨壁刺激引起的神经兴奋所导致的回肠纵行肌收缩。3 经浆膜应用阿司匹林(20 - 100微克/毫升)或吲哚美辛(1 - 4微克/毫升)可极大地抑制豚鼠回肠和结肠蠕动的各个方面。阿司匹林对回肠蠕动的抑制作用可被前列腺素E2拮抗,吲哚美辛所致的抑制作用可被前列腺素F2α或ACh消除。阿司匹林对结肠蠕动的抑制作用可被前列腺素E2拮抗,但很少被ACh拮抗,吲哚美辛所致的抑制作用可被前列腺素E1或E2拮抗。经黏膜应用阿司匹林对回肠或结肠几乎没有影响,但吲哚美辛会引起一些抑制作用。4 这些结果支持了前列腺素有助于蠕动活动的假设。

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