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Titolo:
DEPOLARIZATION INACTIVATION OF DOPAMINE NEURONS - TERMINAL RELEASE CHARACTERISTICS
Autore:
MOGHADDAM B; BUNNEY BS;
Indirizzi:
YALE UNIV,VA MED CTR 116A2,DEPT PSYCHIAT NEW HAVEN CT 06510 YALE UNIV,VA MED CTR 116A2,DEPT PHARMACOL NEW HAVEN CT 06510
Titolo Testata:
Synapse
fascicolo: 3, volume: 14, anno: 1993,
pagine: 195 - 200
SICI:
0887-4476(1993)14:3<195:DIODN->2.0.ZU;2-Q
Fonte:
ISI
Lingua:
ENG
Soggetto:
CHRONIC HALOPERIDOL TREATMENT; NUCLEUS-ACCUMBENS; STRIATAL DOPAMINE; INVIVO MICRODIALYSIS; ANTIPSYCHOTIC-DRUGS; PREFRONTAL CORTEX; BASAL DOPAMINE; RAT; METABOLISM; TOLERANCE;
Keywords:
HALOPERIDOL; STRIATUM; GLUTAMATE; DOPAMINE; MICRODIALYSIS; SCHIZOPHRENIA;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
26
Recensione:
Indirizzi per estratti:
Citazione:
B. Moghaddam e B.S. Bunney, "DEPOLARIZATION INACTIVATION OF DOPAMINE NEURONS - TERMINAL RELEASE CHARACTERISTICS", Synapse, 14(3), 1993, pp. 195-200

Abstract

The functional consequences of chronic treatment with haloperidol (0.5 mg(kg s.c. for 21-23 days) on striatal extracellular levels of dopamine and excitatory amino acids, aspartate and glutamate, were examinedusing microdialysis techniques. Our studies indicate that, in both awake and anesthetized animals, chronic haloperidol treatment does not appear to change basal outflow of dopamine and its response to an exogenous antagonist (i.e., a challenge dose of haloperidol). Furthermore, in chronic haloperidol and vehicle-treated animals, extracellular dopamine levels were decreased below our limit of detection following perfusion of tetrodotoxin through the probe, or into the medial forebrain bundle, suggesting that in both groups of animals extracellular dopamine levels are neuronally derived and seemed to depend equally on impulse flow. However, some differences were observed between the vehicle and haloperidol-treated animals: the excitatory action of 30 mM K+ on extracellular dopamine levels was decreased, and extracellular levels of glutamate were significantly increased, in animals treated chronically with haloperidol. The alterations in extracellular glutamate levelssuggests that events at the terminal may be involved in maintaining the ''normal'' extracellular dopamine levels. Furthermore, the decreasein response to stimulation by K+ suggests that chronic haloperidol treatment may decrease the responsivity of the striatal dopamine system to stimuli. (C) 1993 Wiley-Liss, Inc.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/04/20 alle ore 13:12:51