Presynaptic muscarinic receptors mediating inhibition of neurogenic contractions in rabbit vas deferens are of the ganglionic M1-type
- 1 December 1988
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 158 (3) , 233-242
- https://doi.org/10.1016/0014-2999(88)90072-6
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A pharmacological investigation of the biphasic nature of the contractile response of rabbit and rat vas deferens to field stimulationPublished by Elsevier ,2002
- o-Methoxy-sila-hexocyclium: a new quaternary M1-selective muscarinic antagonistEuropean Journal of Pharmacology, 1988
- MUSCARINIC RECEPTOR SUBTYPES: A CRITIQUE OF THE CURRENT CLASSIFICATION AND A PROPOSAL FOR A WORKING NOMENCLATUREJournal of Autonomic Pharmacology, 1986
- Dicyclomine- and pirenzepine-sensitive muscarinic receptors mediate inhibition of [3H]serotonin release in different rat brain areasEuropean Journal of Pharmacology, 1986
- Muscarinic ganglionic stimulants: conformationally restrained analogs related to [4-[[N-(3-chlorophenyl)carbamoyl]oxy]-2-butynyl]trimethylammonium chlorideJournal of Medicinal Chemistry, 1986
- A comparison of the antimuscarinic effects of pirenzepine and N-methylatropine on ganglionic and vascular muscarinic receptors in the ratLife Sciences, 1984
- [3H]Pirenzepine identifies putative M1 muscarinic receptors in human stellate gangliaBrain Research, 1984
- Muscarinic receptor subtypes: M1 and M2 biochemical and functional characterizationLife Sciences, 1982
- Stereochemical analogs of a muscarinic, ganglionic stimulant. cis- and trans-4-[N-(3-Chlorophenyl)carbamoyloxy]-2-butenyltrimethylammonium iodidesJournal of Medicinal Chemistry, 1973
- Tertiary Carbinols of the Piperazine Series. IJournal of the American Chemical Society, 1958