The effect of phencyclidine on the basal and high potassium evoked extracellular GABA levels in the striatum of freely-moving rats: an in vivo microdialysis study |
| |
Authors: | Hisao Hondo Tatsuo Nakahara Kaoru Nakamura Makoto Hirano Hideyuki Uchimura Nobutada Tashiro |
| |
Affiliation: | aLaboratory of Neurochemistry, Center for Emotional and Behavioral Disorders, Hizen National Mental Hospital, Kanzaki Saga 842-01, Japan;bDepartment of Chemistry, Faculty of Science, Kyushu University, Hakozaki, Higashiku, Fukuoka 812, Japan;cDepartment of Neuropsychiatry, Faculty of Medicine, Kyushu University, Maidashi, Higashiku, Fukuoka 812, Japan |
| |
Abstract: | The effect of phencyclidine (PCP) on the γ-aminobutyric acid-ergic (GABAergic) transmission in the striatum of freely-moving rats was investigated using an in vivo microdialysis. The high potassium (100 mM) increased the extracellular GABA level to 4000% of the basal level. Although the basal GABA level in the striatal dialysate did not show either calcium dependency or tetrodotoxin (TTX) sensitivity, the high potassium evoked GABA level was reduced by 82% under calcium-free conditions (with 12.5 mM magnesium) and by 54% in the presence of 10 μM TTX. The systemic administration of PCP (7.5 mg/kg) or the local perfusion of PCP (100 μM and 1 mM) significantly inhibited the high potassium evoked GABA release in the rat striatum. The local perfusion of MK-801 (10 μM and 100 μM), a more potent and selective N-methyl--aspartate (NMDA) receptor antagonist, also inhibited the high potassium evoked striatal GABA release. These drugs did not show any significant effect on the basal extracellular GABA level. NMDA (1 mM) either partly or completely blocked the effect of PCP (1 mM) or MK-801 (100 μM) on the high potassium evoked striatal GABA release. On the other hand, nomifensine (100 μM), a dopamine uptake blocker, did not show any effect on the high potassium evoked GABA release. These results suggest that PCP inhibited the striatal GABAergic neuronal transmission through its antagonism of the NMDA receptor. |
| |
Keywords: | Phencyclidine MK-801 γ -Aminobutyric acid N-Methyl--aspartate Striatum Microdialysis |
本文献已被 ScienceDirect 等数据库收录! |
|