收缩胆囊素诱导的胆囊收缩受烟碱受体和毒蕈碱受体的影响。

M J Pozo, G M Salido, J A Madrid
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引用次数: 15

摘要

以阿托品和六甲溴铵为对照,研究了哌嗪(一种毒蕈碱受体拮抗剂)对胆囊收缩素(CCK)引起的犬胆囊收缩的影响。采用原位麻醉犬腔内胆囊压模型研究胆囊运动。静脉给药哌renzepine (0.75 mg/kg b.wt.)、阿托品(3 mg/kg b.wt.)或六甲溴铵(5 mg/kg b.wt.),可显著降低静脉注射CCK (0.25-2 Ivy dog单位/kg b.wt.)和持续输注CCK (0.025-0.4 Ivy dog单位/kg b.wt./min)引起的腔内胆囊压升高。由此可见,CCK诱导的胆囊收缩同时受到烟碱受体和毒蕈碱受体的影响。
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Cholecystokinin induced gallbladder contraction is influenced by nicotinic and muscarinic receptors.

Effects of pirenzepine, known as a muscarinic receptor antagonist, on the contraction of dog gallbladder elicited by cholecystokinin (CCK) were examined in comparison with atropine and hexamethonium ones. Intraluminal gallbladder pressure in an in situ anaesthetized dog model was chosen for studying gallbladder motility. The intravenous administration of pirenzepine (0.75 mg/kg b.wt.), atropine (3 mg/kg b.wt.) or hexamethonium (5 mg/kg b.wt.) elicited a marked decrease in the increase of intraluminal gallbladder pressure induced by intravenous bolus injections of CCK (0.25-2 Ivy dog unit/kg b.wt.) and by continuous infusion of CCK (0.025-0.4 Ivy dog unit/kg b.wt./min). It was concluded that CCK induced gallbladder contractions were influenced by both nicotinic and muscarinic receptors.

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