Graf S, Sarna S K
Department of Surgery, Medical College of Wisconsin, Milwaukee 53226, USA.
Am J Physiol. 1996 Jun;270(6 Pt 1):G992-1000. doi: 10.1152/ajpgi.1996.270.6.G992.
The role of 5-hydroxytryptamine (5-HT), its enteric locus of action, and receptor subtypes involved in the regulation of jejunal contractions were investigated by close intra-arterial infusions in conscious dogs. Close intra-arterial infusions of 5-HT in short segments of the jejunum stimulated phasic contractions that were blocked completely by atropine, partially by tetrodotoxin, and not affected by hexamethonium. This response was also blocked significantly by 5-HT2A and 5-HT2C receptor antagonists but was not affected by 5-HT1A/5-HT1B, 5-HT3, and 5-HT4 receptor antagonists. Spontaneous phase III contractions were inhibited significantly by 5-HT2A and 5-HT2C receptor antagonists, not affected by 5-HT1A/5-HT1B and 5-HT3 receptor antagonists, and enhanced by 5-HT4 receptor antagonists. Repeated close intra-arterial infusions of 5-HT over several days stimulated giant migrating contractions. We conclude that in the conscious state, 5-HT acts on 5-HT2A and 5-HT2C receptors located on postsynaptic cholinergic neurons in the canine jejunum to stimulate phasic contractions and phase III activity. The 5-HT4 receptors in the canine small intestine may be localized on nonadrenergic, noncholinergic inhibitory neurons; these receptors suppress the amplitude and duration of phase III activity.
通过对清醒犬进行近距离动脉内输注,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空肠收缩调节的受体亚型。在空肠短节段内近距离动脉内输注5-HT可刺激相性收缩,该收缩可被阿托品完全阻断,被河豚毒素部分阻断,而不受六甲铵影响。5-HT2A和5-HT2C受体拮抗剂也可显著阻断此反应,但5-HT1A/5-HT1B、5-HT3和5-HT4受体拮抗剂对此反应无影响。5-HT2A和5-HT2C受体拮抗剂可显著抑制自发性III相收缩,5-HT1A/5-HT1B和5-HT3受体拮抗剂对此无影响,而5-HT4受体拮抗剂可增强该收缩。连续数天重复进行近距离动脉内输注5-HT可刺激巨大移行性收缩。我们得出结论,在清醒状态下,5-HT作用于犬空肠突触后胆碱能神经元上的5-HT2A和5-HT2C受体,以刺激相性收缩和III相活动。犬小肠中的5-HT4受体可能位于非肾上腺素能、非胆碱能抑制性神经元上;这些受体可抑制III相活动的幅度和持续时间。