Graf S, Sarna S K
Department of Surgery, Medical College of Wisconsin, Milwaukee 53226, USA.
Am J Physiol. 1997 Jul;273(1 Pt 1):G68-74. doi: 10.1152/ajpgi.1997.273.1.G68.
The role of 5-hydroxytryptamine (5-HT), its enteric locus of action, and the receptor subtypes involved in the stimulation of in vivo phasic contractions in the colon were investigated by close intra-arterial infusions in conscious dogs. The contractile response to 5-HT was blocked completely by prior close intra-arterial infusion of atropine and reduced significantly by prior close intra-arterial infusions of tetrodotoxin and hexamethonium. The contractile response was, however, enhanced by the inhibition of nitric oxide (NO) synthase by a prior close intra-arterial infusion of N omega-nitro-L-arginine methyl ester. Prior close intra-arterial infusions of 5-HT1A/5-HT1B, 5-HT2A, 5-HT2C, and 5-HT4 receptor antagonists had no significant effect on the contractile response to 5-HT. By contrast, 5-HT3 receptor antagonist significantly and dose dependently inhibited the contractile response to 5-HT. We conclude that the in vivo phasic contractile response to 5-HT in the colon is mediated mainly by 5-HT3 receptors located on pre- and postsynaptic cholinergic enteric neurons. 5-HT receptors may also be localized on nonadrenergic, noncholinergic inhibitory motoneurons that use NO as a neurotransmitter.
通过对清醒犬进行动脉内近距离输注,研究了5-羟色胺(5-HT)的作用、其在肠道的作用位点以及参与刺激结肠体内阶段性收缩的受体亚型。预先动脉内近距离输注阿托品可完全阻断对5-HT的收缩反应,而预先动脉内近距离输注河豚毒素和六甲铵可使其显著降低。然而,预先动脉内近距离输注Nω-硝基-L-精氨酸甲酯抑制一氧化氮(NO)合酶可增强收缩反应。预先动脉内近距离输注5-HT1A/5-HT1B、5-HT2A、5-HT2C和5-HT4受体拮抗剂对5-HT的收缩反应无显著影响。相比之下,5-HT3受体拮抗剂可显著且剂量依赖性地抑制对5-HT的收缩反应。我们得出结论,结肠对5-HT的体内阶段性收缩反应主要由位于突触前和突触后胆碱能肠神经元上的5-HT3受体介导。5-HT受体也可能定位于以NO作为神经递质的非肾上腺素能、非胆碱能抑制性运动神经元上。