Acute and Chronic Fluoxetine Treatment Decreases the Sensitivity of Rats to Rewarding Brain Stimulation
Overview
Pharmacology
Psychology
Social Sciences
Authors
Affiliations
The effects of fluoxetine on rewarding brain stimulation were determined in eight Wistar rats using a rate-independent discrete-trial threshold measure. Rats were implanted with bipolar, stainless steel electrodes either into the ventral tegmental area (VTA) or medial forebrain bundle (MFB). Acute administration of fluoxetine significantly raised the reward threshold (decreased sensitivity) at doses of 2.5, 5.0, 10.0, and 20.0 mg/kg, i.p., without altering latency of response. There were no significant differences between VTA and MFB groups. To determine the effects of chronic treatment, daily injections of 5.0 mg/kg fluoxetine were administered to rats for 21 days. Chronic treatment of fluoxetine continued to significantly elevate reward thresholds with no evidence of tolerance. The results of these experiments suggest that fluoxetine does not possess abuse potential and that serotonin produces an inhibitory effect on the mesolimbic dopaminergic reward system. Furthermore, these results suggest that the antidepressant effects of fluoxetine are not the direct result of excitation of brain reward systems, at least in the same manner as abused substances, for example, cocaine.
Cantero-Garcia N, Flores-Burgess A, de Guevara-Miranda D, Serrano A, Garcia-Duran L, Puigcerver A Biomedicines. 2022; 10(2).
PMID: 35203621 PMC: 8962322. DOI: 10.3390/biomedicines10020412.
Kirsch M, Mertens W Front Psychol. 2018; 9:616.
PMID: 29774002 PMC: 5943553. DOI: 10.3389/fpsyg.2018.00616.
Browne C, Fletcher P Neuropsychopharmacology. 2016; 41(10):2566-76.
PMID: 27125304 PMC: 4987855. DOI: 10.1038/npp.2016.63.
Browne C, Fletcher P, Zeeb F Psychopharmacology (Berl). 2015; 233(6):983-93.
PMID: 26690588 DOI: 10.1007/s00213-015-4178-5.
Intracranial self-stimulation to evaluate abuse potential of drugs.
Negus S, Miller L Pharmacol Rev. 2014; 66(3):869-917.
PMID: 24973197 PMC: 4081730. DOI: 10.1124/pr.112.007419.