Premium
Kinetics of Drug‐Induced Changes in Dopamine and Serotonin Metabolite Concentrations in the CSF of the Rat
Author(s) -
Mignot E.,
Laude D.,
Elghozi J. L.
Publication year - 1984
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1984.tb02754.x
Subject(s) - homovanillic acid , chemistry , endocrinology , medicine , metabolite , dopamine , tranylcypromine , haloperidol , dopaminergic , cerebrospinal fluid , monoamine oxidase , decarboxylase inhibitor , serotonin , receptor , biochemistry , levodopa , enzyme , disease , parkinson's disease
Cerebrospinal fluid (CSF) was removed at a constant flow rate of 1 μl/min from the third ventricle of anesthetized rats. Every 15 min, CSF dihydroxyphenyl‐acetic acid (DOPAC), homovanillic acid (HVA), and 5‐hydroxyindoleacetic acid (5‐HIAA) concentrations were determined by direct injection of CSF into a liquid chromatographic system coupled with electrochemical detection. Mean CSF concentrations of DOPAC, HVA, and 5‐HIAA were 1.29 μ M , 0.88 μ M , and 2.00 μ M , respectively. In order to determine the turnover rates of dopamine (DA) and serotonin, experiments using monoamine oxidase (MAO) inhibition were performed. Tranylcypromine (20 mg/kg i.p.) induced a sharp exponential decrease of CSF DOPAC, HVA, and 5‐HIAA, with respective half‐lives of 15.60 min, 16.91 min, and 77.23 min. Their respective turnover rates were 3.74, 2.22, and 1.18 nmol ml −1 . h −1 . m ‐Hydroxybenzylhydrazine (NSD‐1015, 100 mg/kg i.p.) and monofluoromethyl‐DOPA (100 mg/kg i.p.), two decarboxylase inhibitors, induced a slow exponential decrease of all three CSF metabolites, α‐Methyl‐ p ‐tyrosine (250 mg/kg i.p.) also induced a slow exponential decrease of DOPAC and HVA. These decreases of CSF DOPAC and HVA induced by DA synthesis inhibitors may reflect the turnover of DA in vivo . Haloperidol (0.5 mg/kg i.p.) considerably enhanced CSF DOPAC and HVA without affecting 5‐HIAA, confirming that dopaminergic receptors modulate DA neurotrans‐mission in vivo . Haloperidol administered 1.5 h after NSD‐1015 did not increase DOPAC and HVA, in contrast to reserpine (5 mg/kg i.p.) injected under the same conditions. These findings indicate that the effect of haloperidol on DA metabolites may involve newly synthesized DA, but not the DA storage pool.