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Cholecystokinin induced gallbladder contraction is influenced by nicotinic and muscarinic receptors.

作者信息

Pozo M J, Salido G M, Madrid J A

机构信息

Department of Physiology, Faculty of Veterinary Sciences, University of Extremadura, Caceres, Spain.

出版信息

Arch Int Physiol Biochim. 1989 Oct;97(5):403-8. doi: 10.3109/13813458909104553.

DOI:10.3109/13813458909104553
PMID:2480096
Abstract

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.

摘要

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