Involvement of D1- and D2-like dopamine receptors in the hippocampal CA1 region in mediating the restraint stress-induced analgesia in the rats.

Acute stress exposure can elicit analgesic responses in multiple pain models. Research indicates that dopaminergic pathways in the hippocampus contribute to the analgesic responses elicited by forced swim stress, considered a combination of physical and psychological stress. Since psychological and physical stresses can trigger different brain pathways and areas, this study has examined how dopaminergic receptors in the CA1 region of the hippocampus affect the pain relief induced by restraint stress (RS), generally considered a psychological stress, in an acute pain model. Ninety-six Wistar rats underwent stereotaxic surgery, during which a cannula was unilaterally implanted in the CA1 region of the hippocampus. Five minutes prior to exposure to RS, D1- and D2-like dopamine receptor antagonists (SCH23390 and sulpiride, respectively) or their respective carriers, saline and DMSO, were administered in different doses (0.25, 1, and 4 µg/0.5 µl per rat) into the CA1 area. The analgesic effects of RS were examined with and without dopaminergic receptor antagonists using the tail-flick test. This study's findings indicated that the administration of SCH23390 and sulpiride into the CA1 area of the hippocampus at the maximal doses (4 µg/0.5 µl;