Dopamine decreases NMDA currents in the oval bed nucleus of the stria terminalis of cocaine self-administering rats

Dopamine (DA) and N-methyl-d-aspartate receptors (NMDARs) contribute in the neural processes underlying drug-driven behaviors. DA is a potent modulator of NMDAR, but few studies have investigated the functional interaction between DA and NMDAR in the context of substance abuse. We combined the rat model of cocaine self-administration with brain slice electrophysiology to study DA modulation of NMDA currents in the oval bed nucleus of the stria terminalis (ovBNST), a dense DA terminal field involved in maintenance of cocaine self-administration amongst other drug related behaviors. Long-Evans rats self-administered intravenous cocaine (0.75mg/kg/injection) on a progressive ratio (PR) schedule of reinforcement for 15days and whole-cell patch-clamp recordings were done on the 16th day. DA reduced NMDA currents in brain-slices from cocaine self-administering rats, but not in those of drug-naïve and sucrose self-administering, or when cocaine exposure was passive (yoked), revealing a mechanism unique to voluntary cocaine intake. DA reduced NMDA currents by activating G-protein-coupled D1- and D2-like receptors that converged on phospholipase C and protein phosphatases. Accordingly, our study reveals a mechanism that may contribute to dysfunctional synaptic plasticity associated with drug-driven behaviors during acute withdrawal. •Dopamine reduced NMDA currents in the ovBNST of cocaine self-administering rats.•Dopamine reduced NMDA currents through G-protein/PLC/phosphatase D1R and D2R.•Dopamine preferentially reduced GluN2A-containing NMDA currents.