Gregersen H, Dall F H, Jørgensen C S, Jensen S L, Ahrén B
Department of Surgical Gastroenterology L, Aarhus University Hospital, Denmark.
Regul Pept. 1992 Jun 11;39(2-3):157-67. doi: 10.1016/0167-0115(92)90537-5.
The influence of neurotransmitters on gastrointestinal motility is different in different segments of the gastrointestinal tract. To clarify the regulation of duodenal motility, the aim of the present study was to investigate the effects of alpha-adrenoceptor agonism and blockade and of galanin on duodenal motility. The study was undertaken in the isolated perfused porcine pancreatico-duodenal block. The agents under investigation were administered arterially. Duodenal motility was measured by means of a low-compliance perfusion system using an intraluminal catheter. In addition the concentration of galanin was measured in the portal effluent. We found that spontaneous motility was abolished by noradrenaline by an effect that was counteracted by the alpha 2-adrenoceptor antagonist idazoxan. In contrast, the selective alpha 1-adrenoceptor antagonist prazosin did not influence the effect of noradrenaline. Galanin, like noradrenaline, abolished duodenal motility. Furthermore, the concentration of galanin in the portal effluent was decreased by noradrenaline by an alpha 2-adrenoceptor mediated mechanism. We conclude that alpha 2-adrenoceptor activation and galanin inhibit duodenal motility and that the release of galanin from the pancreatico-duodenal preparation is reduced by alpha 2-adrenoceptors.
神经递质对胃肠道不同节段的蠕动影响各异。为阐明十二指肠蠕动的调节机制,本研究旨在探究α-肾上腺素能受体激动与阻断以及甘丙肽对十二指肠蠕动的影响。研究在离体灌注的猪胰十二指肠块上进行。所研究的药物通过动脉给药。十二指肠蠕动通过使用腔内导管的低顺应性灌注系统进行测量。此外,还测量了门静脉流出液中甘丙肽的浓度。我们发现,去甲肾上腺素可消除自发性蠕动,而α2-肾上腺素能受体拮抗剂咪唑克生可抵消该效应。相反,选择性α1-肾上腺素能受体拮抗剂哌唑嗪不影响去甲肾上腺素的作用。甘丙肽与去甲肾上腺素一样,可消除十二指肠蠕动。此外,去甲肾上腺素通过α2-肾上腺素能受体介导的机制降低门静脉流出液中甘丙肽的浓度。我们得出结论,α2-肾上腺素能受体激活和甘丙肽可抑制十二指肠蠕动,且α2-肾上腺素能受体可减少胰十二指肠制剂中甘丙肽的释放。