N-methyl- d-aspartate receptors modulate extracellular dopamine concentration and metabolism in rat hippocampus and striatum in vivo

The effects of infusingN-methyl- d-aspartate (NMDA), and the specific NMDA receptor antagonist d-2-amino-5-phosphonoproprionic acid ( d-AP5) into rat hippocampus and stiatum on extracellular dopamine (DA) and its metabolites dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were studied...

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Veröffentlicht in:Brain research 1994-01, Vol.635 (1), p.312-316
Hauptverfasser: Whitton, P.S., Maione, S., Biggs, C.S., Fowler, L.J.
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container_title Brain research
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Maione, S.
Biggs, C.S.
Fowler, L.J.
description The effects of infusingN-methyl- d-aspartate (NMDA), and the specific NMDA receptor antagonist d-2-amino-5-phosphonoproprionic acid ( d-AP5) into rat hippocampus and stiatum on extracellular dopamine (DA) and its metabolites dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were studied using intracerebral microdialysis. In striatum NMDA increased DA extracellularly in a concentration-dependent manner. Against a 10 μM concentration of NMDA the increase in striatal DA was opposed by D-AP5 (10 μM in all experiments), which when infused alone significanlty reduced DA concentration. Infusion of NMDA and DOPAC level in a complex manner, with 10 μM concentration causing a significant increase 2 h after infusion, while 100 μM NMDA caused a transcient decrease in the metabolite. None of the treatments altered striatal dialysate HVA. In hippocampus NMDA infusion decreased dialysate DA concentration-dependent manner, and the decrease caused by 10 μM NMDA was reversed by D-AP5. When given alone the antagonist was without effect. NMDA infusion elevated hippocampal dialysate DOPAC and HVA, while HVA was decreased following D-AP5 infusion. These data indicate that DA release is reginally controlled by excitatory amino acids, but in differential manner.
doi_str_mv 10.1016/0006-8993(94)91453-2
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In striatum NMDA increased DA extracellularly in a concentration-dependent manner. Against a 10 μM concentration of NMDA the increase in striatal DA was opposed by D-AP5 (10 μM in all experiments), which when infused alone significanlty reduced DA concentration. Infusion of NMDA and DOPAC level in a complex manner, with 10 μM concentration causing a significant increase 2 h after infusion, while 100 μM NMDA caused a transcient decrease in the metabolite. None of the treatments altered striatal dialysate HVA. In hippocampus NMDA infusion decreased dialysate DA concentration-dependent manner, and the decrease caused by 10 μM NMDA was reversed by D-AP5. When given alone the antagonist was without effect. NMDA infusion elevated hippocampal dialysate DOPAC and HVA, while HVA was decreased following D-AP5 infusion. 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ispartof Brain research, 1994-01, Vol.635 (1), p.312-316
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subjects 3,4-Dihydroxyphenylacetic Acid - metabolism
Alanine - administration & dosage
Alanine - analogs & derivatives
Animals
Biological and medical sciences
Central nervous system
Central neurotransmission. Neuromudulation. Pathways and receptors
Corpus Striatum - metabolism
DOPAC
Dopamine
Dopamine - metabolism
Fundamental and applied biological sciences. Psychology
Hippocampus - metabolism
Homovanillic Acid - metabolism
HVA
Intracerebral dialysis
Male
Microdialysis
N-Methylaspartate - administration & dosage
NDMA
Organophosphonates - administration & dosage
Rats
Rats, Wistar
Receptors, N-Methyl-D-Aspartate - analysis
Receptors, N-Methyl-D-Aspartate - physiology
Vertebrates: nervous system and sense organs
title N-methyl- d-aspartate receptors modulate extracellular dopamine concentration and metabolism in rat hippocampus and striatum in vivo
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