Modification of serotonin responses in rat dorsolateral septal nucleus neurons by acute and chronic cocaine

We used standard intracellular current-clamp electrophysiological recording techniques in a brain slice preparation to determine whether chronic cocaine administration would: 1) alter the sensitivity of septal neurons to exogenous serotonin (5-HT) application and 2) modify the interaction of 5-HT with cocaine in vitro. Recordings were made from neurons in rat brain slices that contained the dorsolateral septal nucleus obtained from drug naive (DN) rats or rats given cocaine (15 mg/kg, i.p., 2 x daily) for periods of 7 (CC7) or 14 (CC14) days. In addition, some of these rats also received intraventricular pertussis toxin (PTX) injections 2 to 3 days before experimentation to abolish the postsynaptic 5-HT1A receptor-mediated membrane hyperpolarization and to unmask a 5-HT-induced depolarization. In comparison with DN and CC7, CC14 slices showed an increased sensitivity to 5-HT as revealed by a 2-fold leftward shift in the 5-HT EC(50) values. In addition, in PTX-CC14 slices, 5-HT could hyperpolarize the cell membrane, whereas the 5-HT1A agonist, 8-OH-DPAT, and the gamma-aminobutyric acid(B) agonist, baclofen, failed to do so. We also observed that cocaine (3 mu M) in CC14 slices did not significantly potentiate and prolong 5-HT hyperpolarizations as found in DN slices. We conclude that in the CC14 septal slice a 5-HT transporter is down-regulated and that an atypical 5-HT response can be elicited. Additionally, 5-HT1A receptor up-regulation and/or 5-HT, receptor down-regulation may contribute to the increased sensitivity of septal neurons to 5-HT.