Affiliation:
1. Department of Pharmacology, Worsley Medical and Dental Building, University of Leeds, Leeds LS2 9JT, West Yorkshire, UK
Abstract
Abstract
Responses of rat isolated vas deferens to electrical stimulation through field electrodes (400 mA, 1 ms duration, single shocks at 5 min intervals) were potentiated by meptazinol (10 to 300 μM) in whole tissues and also in the separated prostatic and epididymal portions. The effect was fast in onset, reproducible and easily reversed by washing. Prazosin (0·1 μM) practically abolished the response of the epididymal portion to electrical stimulation while the response of the prostatic portion was only slightly reduced (<20%). In the presence of prazosin, meptazinol still produced potentiation of the response of the prostatic portion. Nifedipine (2 μM) practically abolished the response of the prostatic portion to electrical stimulation while the response of the epididymal portion was only slightly reduced (<20%). In the presence of nifedipine, meptazinol no longer produced potentiation of the response of the epididymal portion. Exogenous ATP (5 μM to 1 mM) and phenylephrine (1 to 50 μm) produced a contractile response which was potentiated in the presence of meptazinol (100 μM) but in the presence of meptazinol (100 μM) and nifedipine (5 mM) together, potentiation of phenylephrine no longer occurred. It is suggested that potentiation by meptazinol of electrically induced responses in this tissue is due to a direct action on the smooth muscle.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Reference9 articles.
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2. Separation of adrenergic and non-adrenergic contractions to field stimulation in the rat vas deferens;Brown;Ibid.,1983
3. Pharmacological effects of meptazinol and its enantiomers on guinea-pig ileum and mouse vas deferens;Duchesne;J. Pharm. Pharmacol.,1984
4. On the mechanism involved in the ability of meptazinol to potentiate the effects of sympathetic nerve stimulation;El-Mas;Ibid.,1989
5. Can the effects of meptazinol on the guinea-pig isolated ileum be explained by inhibition of acetylcholinesterase;Ennis;Ibid.,1986