ROLE OF M1 MUSCARINIC RECEPTORS IN THE PARASYMPATHETIC CONTROL OF COLONIC MOTILITY IN CATS AND RABBITS

被引:9
作者
BLANQUET, F [1 ]
GONELLA, J [1 ]
机构
[1] LAB NEUROBIOL CELLULAIRE,CNRS,F-13402 MARSEILLE 9,FRANCE
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1992年 / 458卷
关键词
D O I
10.1113/jphysiol.1992.sp019439
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. The effects of pirenzepine (a selective blocking agent of M1 muscarinic receptors) were studied on excitatory junction potentials (EJPs) and inhibitory junction potentials (IJPs) elicited on colonic smooth muscle by stimulation of efferent parasympathetic nerve fibres in anaesthetized cats and rabbits. 2. Pirenzepine (25 mug kg-1 to 0.2 mg kg-1, i.v.) decreased the amplitude of EJPs or abolished them. In pirenzepine, parasympathetic stimulation elicited IJPs in most cases. 3.. In both species, pirenzepine initiated spontaneous IJPs, indicating an increase in the activity of the non-adrenergic, non-cholinergic (NANC) inhibitory neurones. 4. The results suggest that M1 muscarinic receptors are involved in synaptic transmission within intramural plexuses, at interneuronal synapses in the parasympathetic excitatory pathway to colonic smooth muscle, but are not involved in the pathway to the NANC inhibitory neurones. The facilitation of IJPs by pirenzepine suggests that, under normal physiological conditions, NANC neurones are tonically inhibited by an intramural nervous circuit involving M1 muscarinic receptors.
引用
收藏
页码:655 / 666
页数:12
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