Souccar_1994_Gen.Pharmacol_25_1397

Reference

Title : Prejunctional effect of quaternary derivatives of l-hyoscyamine at the rat neuromuscular junction. A structure-activity relationship study - Souccar_1994_Gen.Pharmacol_25_1397
Author(s) : Souccar C , Soldera Jdo C , Cysneiros RM , Goncalo Mdo C , Lapa AJ
Ref : General Pharmacology , 25 :1397 , 1994
Abstract :

1. The effects of phenthonium and related compounds on the spontaneous release of acetylcholine (ACh) were investigated with electrophysiological and radiolabelled techniques to correlate the prejunctional effect with their cholinolytic activities and to determine the structure-activity relationship. 2. Phenthonium and endophen are N-(4-phenyl)-phenacyl derivatives of l-hyoscyamine in "exo" and "endo" conformation, respectively. Tropol is N-(4-phenyl) phenacyl tropan-3-ol whereas ipratropium is 8-isopropyl-noratropine. 3. Only phenthonium increased the frequency of miniature endplate potentials and the resting efflux of spontaneous [3H]-ACh in rat diaphragm muscles. 4. The rank order of the antimuscarinic potency was: ipratropium > atropine > phenthonium = endophen > tropol. The rank order of the antinicotinic activity was: phenthonium = endophen > tropol > atropine > ipratropium. 5. It is concluded that the prejunctional facilitatory effect of phenthonium is associated with the N-phenyl-phenacyl group at "exo" conformation but the effect is unrelated to its cholinolytic properties.

PubMedSearch : Souccar_1994_Gen.Pharmacol_25_1397
PubMedID: 7896051

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Citations formats

Souccar C, Soldera Jdo C, Cysneiros RM, Goncalo Mdo C, Lapa AJ (1994)
Prejunctional effect of quaternary derivatives of l-hyoscyamine at the rat neuromuscular junction. A structure-activity relationship study
General Pharmacology 25 :1397

Souccar C, Soldera Jdo C, Cysneiros RM, Goncalo Mdo C, Lapa AJ (1994)
General Pharmacology 25 :1397