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前列腺素对术后肠梗阻大鼠胃肠道转运的刺激作用。

Prostaglandin stimulation of gastrointestinal transit in post-operative ileus rats.

作者信息

Ruwart M J, Klepper M S, Rush B D

出版信息

Prostaglandins. 1980 Mar;19(3):415-26. doi: 10.1016/0090-6980(80)90075-1.

Abstract

The prostaglandins PGF2 alpha, PGE2 and 16,16-dimethyl PGE2, when administered intravenously, orally, subcutaneously or intraduodenally to laparotomized rats, decreased gastric emptying, small intestinal transit and colonic transit as compared to unoperated controls. All three prostaglandins increased colonic transit above that found with unoperated controls. This activity was independent of small intestinal fluid accumulation (i.e., enteropooling) since ligating the ileal-cecal junction had no effect on colonic transit. Small intestinal transit was increased, but not normalized, by PGE2 and 16,16-dimethyl PGE2. 16,16-Dimethyl PGE2 completely restored gastric emptying when given intravenously to laparotomized rats of doses greater than 5.0 microgram/kg. This effect on gastric emptying lasted approximately 4 hrs. Thus, 16,16-dimethyl PGE2, when given intravenously, normalized gastric emptying, significantly increased small intestinal transit, and made the colon hypermotile. Prostaglandins may be beneficial in the treatment of postoperative ileus and other conditions of sluggish gastrointestinal propulsion.

摘要

将前列腺素PGF2α、PGE2和16,16-二甲基PGE2经静脉、口服、皮下或十二指肠内给予开腹大鼠后,与未做手术的对照组相比,胃排空、小肠转运和结肠转运均减慢。所有这三种前列腺素均使结肠转运加快,超过未做手术的对照组。该活性与小肠液积聚(即肠内积液)无关,因为结扎回盲部对结肠转运没有影响。PGE2和16,16-二甲基PGE2可使小肠转运加快,但未恢复正常。当以大于5.0微克/千克的剂量静脉给予开腹大鼠时,16,16-二甲基PGE2可完全恢复胃排空。这种对胃排空的作用持续约4小时。因此,静脉给予16,16-二甲基PGE2可使胃排空恢复正常,显著加快小肠转运,并使结肠运动亢进。前列腺素可能有益于治疗术后肠梗阻及其他胃肠推进迟缓的病症。

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