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短链脂肪酸对犬回肠运动的启动作用及药物制剂对其的抑制作用。

Initiation of motility in canine ileum by short chain fatty acids and inhibition by pharmacological agents.

作者信息

Kamath P S, Phillips S F

机构信息

Gastroenterology Unit, Mayo Clinic, Rochester, MN 55905.

出版信息

Gut. 1988 Jul;29(7):941-8. doi: 10.1136/gut.29.7.941.

Abstract

We have previously shown that short chain fatty acids (SCFA) stimulate motility in the canine ileum. Concentrations of SCFA in the ileum are normally low but would be expected to increase after coloileal reflux; thus, this phenomenon could have pathophysiological relevance. The present studies were designed to seek pharmacological means by which this response could be blocked. Four dogs were prepared with isolated, ileocolonic fistulae into which physiological concentrations of SCFA could be instilled so as to stimulate ileal motility. Pretreatment of the ileum with topical lidocaine abolished the response to luminal SCFA but general anaesthesia did not. Indomethacin stimulated ileal motility and prostacyclin abolished the ileal response to SCFA. Naloxone and a calcium channel blocker also negated the response to SCFA; blockage of muscarinic, adrenergic and 5H-T receptors did not. We conclude that the motor response to SCFA is probably a local neural reflex which is sensitive to local anaesthetics, opiates and the prostanoids.

摘要

我们之前已经表明,短链脂肪酸(SCFA)可刺激犬回肠的蠕动。回肠中SCFA的浓度通常较低,但预计在结肠回肠反流后会升高;因此,这种现象可能具有病理生理学意义。本研究旨在寻找能够阻断这种反应的药理学方法。对四只犬制备了孤立的回结肠瘘管,可向其中注入生理浓度的SCFA以刺激回肠蠕动。用局部利多卡因预处理回肠可消除对肠腔SCFA的反应,但全身麻醉则不能。吲哚美辛刺激回肠蠕动,前列环素可消除回肠对SCFA的反应。纳洛酮和一种钙通道阻滞剂也可消除对SCFA的反应;而阻断毒蕈碱、肾上腺素能和5-羟色胺受体则不能。我们得出结论,对SCFA的运动反应可能是一种局部神经反射,对局部麻醉药、阿片类药物和前列腺素敏感。

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