JO1784, a novel σ ligand, potentiates [3H]acetylcholine release from rat hippocampal slices

Author:

Junien Jean L.,Roman François J.,Brunelle Gilles,Pascaud Xavier

Publisher

Elsevier BV

Subject

Pharmacology

Reference11 articles.

1. The dissociative anesthetics, ketamine and phenyclidine, selectively reduce excitation of central mammalian neurones by N-methylaspartate;Ansi;Br. J. Pharmacol.,1983

2. Drugs acting on a and phencyclidine receptors: a review of their nature, function and possible therapeutic importance;Junien;Clin. Neuropharmacol.,1989

3. Pharmacological and autoradiographic discrimination of sigma and phencyclidine receptor binding sites in brain with (+)-[3H]SKF10,047, (+)-[3H]-3-[3-hydroxyphenyl]-N-(1-propyl)piperidil and [3H]-1-[1-(2-thiényl) cyclohexyl]piperidine;Largent;J. Pharmacol. Exp. Ther.,1986

4. Effects of phencyclidine on the release of radioactivity from rat striatal slices labeled with [3H]choline;Leventer;J. Pharmacol. Exp. Ther.,1983

5. N-Methyl-D-aspartate-induced neuronal activation is selectively modulated by σ receptors;Monnet;Eur. J. Pharmacol.,1990

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