Premium
Two populations of muscarinic binding sites in the chick heart distinguished by affinities for ligands and selective inactivation
Author(s) -
Jakubik Jan,
Tuĉek Stanislav
Publication year - 1994
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1994.tb17170.x
Subject(s) - pirenzepine , methoctramine , muscarinic acetylcholine receptor , affinities , population , binding site , receptor , chemistry , biology , stereochemistry , biochemistry , medicine , environmental health
1 By measuring the binding of N‐[ 3 H‐methyl]‐scopolamine ([ 3 H]‐NMS) and of unlabelled subtype‐specific muscarinic antagonists, two populations of muscarinic binding sites can be distinguished in the membranes of cardiac ventricles taken from 1‐day‐old chicks. One of them, corresponding to approximately 80% of [ 3 H]‐NMS binding sites, has higher affinities for AF‐DX116 (p K i = 6.42) and methoct‐ramine (p K i = 7.33); the rate of [ 3 H]NMS dissociation from these sites is fast. The other population, corresponding to approximately 20% of [ 3 H]‐NMS binding sites, has lower affinities for AF‐DX116 (p K i = 5.00) and methoctramine (p K i = 6.19); the rate of [ 3 H]‐NMS dissociation from these sites is slow. Both populations have high affinities for pirenzepine, but the affinity of the former (major) population is lower (p K i = 7.99) than that of the latter (minor) population (p K i = 10.14). 2 Since it has been shown earlier that two mRNAs for muscarinic receptors are expressed in the chick heart, one of them close to the genetically defined m2 and the other to the m4 subtype, we propose that the major population of binding sites with high affinities for AF‐DX116 and methoctramine and the lower affinity for pirenzepine represents the M 2 ‐like receptors, while the minor population represents the M 4 ‐like receptors. 3 It proved possible to obtain isolated samples of either population by selectively protecting the M 2 ‐like sites with AF‐DX116 and the M 4 ‐like sites with pirenzepine, and by inactivating the unprotected sites with benzilylcholine mustard. The properties of the isolated populations corresponded to those derived from the analysis of [ 3 H]‐NMS binding to the original mixed population. 4 Alcuronium exerted positive allosteric action on the binding of [ 3 H]‐NMS both to the M 2 ‐like and the M 4 ‐like population and severely slowed down [ 3 H]‐NMS dissociation from them; its affinity for the M 2 ‐like sites was 3–10 times higher.