Dehydroepiandrosterone increases tonic and phasic dopamine release in the striatum

• Published in: Neuroscience letters Vol. 734; p. 135095
• Main Authors: Pérez-Neri, Iván, Parra, Doris, Aquino-Miranda, Guillermo, Coffeen, Ulises, Ríos, Camilo
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 24.08.2020
• Subjects: Animals; Antipsychotic; Corpus Striatum - drug effects; Corpus Striatum - metabolism; Dehydroepiandrosterone; Dehydroepiandrosterone - pharmacology; Dopamine - metabolism; Dopamine transporter; Male; Microdialysis; Motor Activity - drug effects; Neuroprotection; Rats; Rats, Wistar; Schizophrenia; DHEA; Neuroprotection; DOPAC; Schizophrenia; COMT; HVA; Dehydroepiandrosterone; Microdialysis; DAT; Antipsychotic; Dopamine transporter; MAO; DA; HPLC
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2020.135095

[Display omitted] •Dehydroepiandrosterone increases tonic dopamine release in the striatum.•DHEA increases depolarization-induced dopamine release in the striatum.•DHEA increases striatal dopamine release while reducing its turnover.•DHEA reduces motor activity despite increasing striatal dopamine release. Dehydroepiandrosterone (DHEA) modulates dopaminergic neurotransmission. It takes part in neurologic and psychiatric diseases involving monoamine neurotransmitters. Earlier results show that DHEA (120-min treatment) reduced striatal dopamine (DA) turnover in rats, suggesting a reduced DA release. Some investigations report that DHEA increases DA release but inhibits motor activity, which seems contradictory. This research examines the effect of DHEA on striatal DA release, its metabolism and motor activity. Male Wistar rats were implanted in the striatum with a cannula for in vivo microdialysis. DHEA was administered (120 mg/kg) and dialysates were collected for 280 min. A depolarizing stimulus was applied at 120 min. Samples were analyzed by HPLC-ED to determine the concentration of DA and its metabolites. The effect of DHEA on motor activity was also evaluated during 120 min. Extracellular DA concentration was greater in treated animals both before and after depolarization. In contrast, DHEA reduced the areas below the curves for DA metabolites and DA/metabolite ratios. DHEA also reduced motor activity, remarkably in the first 20 min after treatment. In summary, DHEA yielded a stimulatory effect on striatal DA release that was not reflected in neither DA metabolism nor motor activity. Thus, DHEA resembles the effect of typical antipsychotics, increasing DA release but reducing behavioral activation.