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• W1860217984 abstract "17,21-Dimethyl-19-nor-pregn-4,9-diene-3,20-dione (promegestone) was used to characterize the mechanism of inhibition of nicotinic acetylcholine (ACh) receptors (AChR) by progestin steroids. Promegestone reversibly inhibited ACh-induced currents of<i>Torpedo</i> AChRs expressed in <i>Xenopus</i>oocytes. Between 1–30 μM promegestone produced a concentration-dependent enhancement of the equilibrium binding affinity of [³H]ACh to <i>Torpedo</i> AChR-rich membranes. For AChRs in the presence of agonist (desensitized state) promegestone was a more potent inhibitor of the binding of the noncompetitive antagonist [³H]phencyclidine (IC₅₀ = 9 μM) than of [³H]histrionicotoxin (IC₅₀ ∼ 100 μM). To identify AChR domains in contact with the steroid, AChR-rich membranes equilibrated with [³H]promegestone were irradiated at 312 nm, and ³H-labeled amino acids were identified by amino-terminal sequencing of fragments isolated from subunit proteolytic digests. Within AChR α-subunit, 70% of³H was covalently incorporated in a 10-kDa fragment beginning at Asn-339 and containing the M4 membrane spanning segment, and 30% was in a 20-kDa fragment beginning at Ser-173 and containing the M1–M3 segments. Fragments containing the M2 channel domains as well as the M4 segments were isolated from proteolytic digests of AChR subunits and subjected to amino-terminal sequence analysis. No evidence of [³H]promegestone incorporation was detected in any of the M2 segments. The amino acids in the M4 segments labeled by [³H]promegestone were among those previously shown to be in contact with the lipid bilayer (Blanton and Cohen, 1994). These results indicate that the steroid promegestone is an AChR noncompetitive antagonist that may alter AChR function by interactions at the lipid-protein interface." @default.
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• W1860217984 date "1999-02-01" @default.
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• W1860217984 title "The Steroid Promegestone Is a Noncompetitive Antagonist of the<i>Torpedo</i>Nicotinic Acetylcholine Receptor that Interacts with the Lipid-Protein Interface" @default.
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• W1860217984 doi "https://doi.org/10.1124/mol.55.2.269" @default.
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