Shimatani T
First Department of Internal Medicine, Hiroshima University School of Medicine, Japan.
J Smooth Muscle Res. 1997 Aug-Oct;33(4-5):145-62. doi: 10.1540/jsmr.33.145.
To clarify the exact mechanisms of the pharmacological effects of glucagon on gastrointestinal motility, the following experiments were performed on the conscious and anesthetized dogs. 1) During phase I of interdigestive migrating contractions (IMC), glucagon (5 approximately 50 microg/kg, drip infusion for 5 minutes) induced phasic contractions in the duodenum, jejunum and ileum, but not in the antrum. These excitatory responses were also observed in the truncal vagotomized dogs. These contractions were abolished by atropine or hexamethonium in the conscious dogs, and also by tetrodotoxin in the anesthetized dogs. 2) Glucagon inhibited cisapride-induced contractions only in the antrum in the conscious dogs. After pre treatment with hexamethonium, glucagon inhibited these contractions in the duodenum, jejunum and ileum as well as in the antrum. After pre treatment with tetrodotoxin in the anesthetized dogs, glucagon did not affect acetylcholine induced contractions in any region. 3) Glucagon inhibited spontaneous phase III contractions and erythromycin induced phase III like contractions in the antrum, but did not inhibit either contractions in the other regions in the conscious dogs. These paradoxical effects of glucagon between the antrum and intestine were similar to those involved in the blockade of 5-hydroxytryptamine 3 receptors. After pre-treatment with hexamethonium, glucagon inhibited these contractions in the duodenum, jejunum and ileum as well as in the antrum.
为阐明胰高血糖素对胃肠动力药理作用的确切机制,在清醒和麻醉犬身上进行了以下实验。1)在消化间期移行性收缩(IMC)的I期,胰高血糖素(5~50微克/千克,静脉滴注5分钟)可引起十二指肠、空肠和回肠的阶段性收缩,但胃窦部未出现。在切断迷走神经干的犬身上也观察到了这些兴奋反应。在清醒犬中,这些收缩可被阿托品或六甲铵阻断,在麻醉犬中可被河豚毒素阻断。2)胰高血糖素仅在清醒犬的胃窦部抑制西沙必利诱导的收缩。用六甲铵预处理后,胰高血糖素在十二指肠、空肠、回肠以及胃窦部均抑制这些收缩。在麻醉犬中用河豚毒素预处理后,胰高血糖素对任何区域的乙酰胆碱诱导的收缩均无影响。3)胰高血糖素抑制清醒犬胃窦部的自发性III期收缩和红霉素诱导的III期样收缩,但不抑制其他区域的收缩。胰高血糖素在胃窦部和肠道之间的这些矛盾作用类似于5-羟色胺3受体阻断所涉及的作用。用六甲铵预处理后,胰高血糖素在十二指肠、空肠、回肠以及胃窦部均抑制这些收缩。
1)胰高血糖素并非直接通过与平滑肌细胞上的任何受体结合,而是通过节后胆碱能神经元并可能通过5-羟色胺神经元潜在地抑制胃窦部和肠道的胆碱能运动活动。2)另一方面,在肠道中,通过涉及烟碱和毒蕈碱受体的节前胆碱能神经元产生的相反作用更强。3)因此,在清醒状态下,胰高血糖素抑制胃窦部收缩而不影响肠道收缩。