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5-羟色胺及其衍生物在大鼠离体血液灌注小肠和回肠条中的比较研究。

Comparative studies with 5-hydroxytryptamine and its derivatives in isolated, blood-perfused small intestine and ileum strip of the rat.

作者信息

Sakai K, Akima M, Shiraki Y

出版信息

Jpn J Pharmacol. 1979 Apr;29(2):223-33. doi: 10.1254/jjp.29.223.

Abstract

The mode of actions of 5-hydroxytryptamine (5-HT) and its derivatives, tryptophan (TP), 5-hydroxytryptophan (5-HTP) and 5-hydroxyindole acetic acid (5-HIAA) was studied on the isolated, blood-perfused small intestine and isolated ileum strip of rats. In the isolated, blood-perfused intestinal preparations, 5-HT and 5-HTP injected into the superior mesenteric artery caused a monophasic fast contraction, while TP and 5-HIAA had no effects on the intestine. The contractile responses to 5-HT and 5-HTP were abolished by tetrodotoxin (TTX), hexamethonium (C6) and morphine, but were resistant to blockade of either atropine, methysergide or phentolamine. On the other hand, in the ileum strip preparations, 5-HT contracted the ileum, but its derivatives had no effects on the ileum. TTX, C6, morphine and atropine failed to prevent the contractile response to 5-HT, whereas methysergide effectively antagonized the response. The present results indicate that 5-HT acts by exciting intramural neuronal elements or by directly contracting the smooth muscle of the intestine. 5-HTP seems to act in the same manner as 5-HT.

摘要

研究了5-羟色胺(5-HT)及其衍生物色氨酸(TP)、5-羟色氨酸(5-HTP)和5-羟吲哚乙酸(5-HIAA)对大鼠离体、血液灌注小肠及离体回肠条的作用方式。在离体、血液灌注肠道标本中,注入肠系膜上动脉的5-HT和5-HTP引起单相快速收缩,而TP和5-HIAA对肠道无影响。5-HT和5-HTP引起的收缩反应可被河豚毒素(TTX)、六甲铵(C6)和吗啡消除,但对阿托品、麦角新碱或酚妥拉明的阻断有抗性。另一方面,在回肠条标本中,5-HT使回肠收缩,但其衍生物对回肠无影响。TTX、C6、吗啡和阿托品不能阻止对5-HT的收缩反应,而麦角新碱可有效拮抗该反应。目前的结果表明,5-HT通过兴奋壁内神经元成分或直接收缩肠道平滑肌起作用。5-HTP似乎与5-HT以相同方式起作用。

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