Please use this identifier to cite or link to this item: https://doi.org/10.1016/0014-2999(89)90879-0
Title: Atropine- and scopolamine-resistant subtypes of muscarinic receptors in the rabbit aorta
Authors: Manjeet, S.
Sim, M.K. 
Keywords: Acetylchoine
Aorta (rabbit)
Atropine
Endothelium
Muscarinic receptor subtypes
Scopolamine
Smooth muscle (vascular)
Issue Date: 1989
Source: Manjeet, S., Sim, M.K. (1989). Atropine- and scopolamine-resistant subtypes of muscarinic receptors in the rabbit aorta. European Journal of Pharmacology 174 (1) : 99-105. ScholarBank@NUS Repository. https://doi.org/10.1016/0014-2999(89)90879-0
Abstract: Tritiated acetylcholine ([3H]ACh) binds specifically to different muscarinic binding sites in the rabbit aorta. The binding of [3H]ACh to endothelial membranes was displacable by nanomolar concentrations of scopolamine but only by micromolar concentrations of atropine and homatropine. The reverse was true for smooth muscle membranes, i.e. [3H]ACh binding was displacable by nanomolar concentrations of atropine and homatropine but only by micromolar concentrations of scopolamine. Pirenzepine, AF-DX 116 and 4-phenyl-acetoxy-N-methylpiperidine methobromide (4-DAMP) displaced the binding of [3H]ACh from both tissues in the nano- to micromolar range. Our findings indicate that endothelial receptors are characterised by a high affinity for scopolamine, which possesses a scopine base, and that muscle binding sites have a high affinity for antagonists possessing a tropine base (atropine, homatropine). Both the endothelial and smooth muscle binding sites have a low affinity for AF-DX 116, indicating that they are not of the cardiac type.
Source Title: European Journal of Pharmacology
URI: http://scholarbank.nus.edu.sg/handle/10635/32114
ISSN: 00142999
DOI: 10.1016/0014-2999(89)90879-0
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