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5-羟色胺对从豚鼠小肠分离出的肠肌间神经节中环磷酸腺苷形成的刺激作用。

Stimulation of formation of cAMP by 5-hydroxytryptamine in myenteric ganglia isolated from guinea pig small intestine.

作者信息

Xia Y, Fertel R H, Wood J D

机构信息

Department of Physiology, College of Medicine, Ohio State University Columbus 43210.

出版信息

Life Sci. 1994;55(9):685-92. doi: 10.1016/0024-3205(94)00675-x.

Abstract

Effects of 5-hydroxytryptamine (5-HT) and related agonists and antagonists on formation of cAMP were determined for enzymatically dissociated ganglia from the myenteric plexus of the guinea-pig small intestine. Formation of cAMP was stimulated by 5-HT in both dose- and time- dependent manners. The stimulatory action of 5-HT was suppressed by the 5-HT1P antagonist, renzapride, but not by the 5-HT3 antagonist, tropisetron (formerly ICS 205-930). Neither renzapride nor cisapride increased the levels of cAMP. Levels of cAMP were suppressed by concentrations of tropisetron greater than 1.0 microM. Levels of cAMP were unaffected by the 5-HT3 agonist, 2-methyl-5-hydroxytryptamine. A putative 5-HT4 receptor agonist, 5-methoxytryptamine, stimulated formation of cAMP, but to a lesser extent than 5-HT. We conclude that 5-HT acts to stimulate adenylate cyclase and the formation of cAMP in myenteric ganglia. The 5-HT1P receptor is the most likely subtype involved in 5-HT action on cAMP formation.

摘要

针对豚鼠小肠肌间神经丛经酶解离的神经节,测定了5-羟色胺(5-HT)及相关激动剂和拮抗剂对环磷酸腺苷(cAMP)形成的影响。5-HT以剂量和时间依赖性方式刺激cAMP的形成。5-HT1P拮抗剂伦扎必利可抑制5-HT的刺激作用,但5-HT3拮抗剂托烷司琼(原ICS 205-930)则无此作用。伦扎必利和西沙必利均未增加cAMP水平。浓度大于1.0微摩尔的托烷司琼可抑制cAMP水平。5-HT3激动剂2-甲基-5-羟色胺对cAMP水平无影响。一种假定的5-HT4受体激动剂5-甲氧基色胺可刺激cAMP的形成,但程度低于5-HT。我们得出结论,5-HT可刺激肌间神经节中的腺苷酸环化酶和cAMP的形成。5-HT1P受体最有可能是参与5-HT对cAMP形成作用的亚型。

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