5-HT1D-LIKE RECEPTORS INHIBIT THE RELEASE OF ENDOGENOUSLY FORMED [H-3] GABA IN HUMAN, BUT NOT IN RABBIT, NEOCORTEX

Citation
Tj. Feuerstein et al., 5-HT1D-LIKE RECEPTORS INHIBIT THE RELEASE OF ENDOGENOUSLY FORMED [H-3] GABA IN HUMAN, BUT NOT IN RABBIT, NEOCORTEX, Neuroscience letters, 209(3), 1996, pp. 210-214
Citations number
26
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
03043940
Volume
209
Issue
3
Year of publication
1996
Pages
210 - 214
Database
ISI
SICI code
0304-3940(1996)209:3<210:5RITRO>2.0.ZU;2-5
Abstract
Both human and rabbit brain contain the 5-hydroxytryptamine (5-HT)(1D) subtype of 5-HT1 receptors, We studied the effects of 5-HT1D receptor stimulation on neocortical [H-3]gamma-aminobutyric acid (GABA) releas e from GABAergic neurons in these species. The 5-HT1D receptor agonist sumatriptan depressed [H-3]GABA release in human neocortex and the 5- HT1 receptor antagonist metitepin prevented this depression with poten cies suggesting mediation by 5-HT1D-like receptors. In rabbit neocorte x, however, 5-HT1D agonists did not affect the release of [H-3]GABA. S ince 5-HT and GABA seem to function antagonistically in anxiety disord ers their neocortical interaction may be (patho)physiologically releva nt.