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Abstract: Intracerebral microdialysis was used to monitor dopamine release in rat striatal extracellular fluid following the intraperitoneal administration of dopamine's precursor amino acid, l‐tyrosine. Dopamine concentrations in dialysates increased transiently after tyrosine (50–100 mg/kg) administration. Pretreatment with haloperidol or the partial lesioning of nigrostriatal neurons enhanced the effect of tyrosine on dopamine release, and haloperidol also prolonged this effect. These data suggest that nigrostriatal dopaminergic neurons are responsive to changes in precursor availability under basal conditions, but that receptor‐mediated feedback mechanisms limit the magnitude and duration of this effect.
Journal of Neurochemistry – Wiley
Published: May 1, 1989
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