1380400

gamma-Aminobutyric acid, through GABAA receptors, inhibits the potassium-stimulated release of calcitonin gene-related peptide- but not that of substance P-like material from rat spinal cord slices.

Article date: 1992/6/26

PubMed ID: 1380400

Journal name: Brain research (ISSN: 0006-8993)

ABSTRACT

Superfusion of slices of the dorsal zone of the lumbar enlargement with an artificial cerebrospinal fluid was used to investigate the possible modulation by GABA receptor ligands of the in vitro release of calcitonin gene-related peptide- and substance P-like materials (CGRPLM and SPLM) from the rat spinal cord. Whereas the spontaneous outflow of both peptides remained unaffected, the K+ (30 mM)-evoked overflow of CGRPLM could be partially inhibited (approx. -30%) by GABA (1 microM-0.1 mM) and muscimol (10 microM-0.1 mM) but not by baclofen (1-10 microM). Bicuculline methiodide (1 microM) completely prevented the inhibition by GABA (1 microM) and muscimol (10 microM) as expected from an action through GABAA receptors. By contrast, the K(+)-evoked SPLM overflow was altered neither by GABA nor muscimol and baclofen. These data further support that GABA exerts a presynaptic inhibitory control of (CGRP-containing) primary afferent fibres within the rat dorsal horn.

This document is available from: http://directlinks.cc/files/muscimol/1380400.pdf

Author List: Bourgoin S, Pohl M, Benoliel J J, Mauborgne A, Collin E, Hamon M, Cesselin F

Publication Types: Journal Article; Research Support, Non-U.S. Gov't

Substances mentioned in the article: Receptors, GABA-A; Muscimol; Substance P; gamma-Aminobutyric Acid; Calcitonin Gene-Related Peptide; Baclofen; Potassium; Bicuculline;

Mesh terms: Animals; Baclofen/pharmacology; Bicuculline/pharmacology; Calcitonin Gene-Related Peptide/secretion; Dose-Response Relationship, Drug; In Vitro Techniques; Male; Muscimol/pharmacology; Potassium/pharmacology; Rats; Rats, Inbred Strains; Receptors, GABA-A/drug effects; Spinal Cord/drug effects; Substance P/secretion; gamma-Aminobutyric Acid/pharmacology;

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