Innate cocaine-seeking vulnerability arising from loss of serotonin-mediated aversive effects of cocaine in rats

Cell Rep. 2023 May 30;42(5):112404. doi: 10.1016/j.celrep.2023.112404. Epub 2023 Apr 20.

Abstract

Cocaine blocks dopamine reuptake, thereby producing rewarding effects that are widely studied. However, cocaine also blocks serotonin uptake, which we show drives, in rats, individually variable aversive effects that depend on serotonin 2C receptors (5-HT2CRs) in the rostromedial tegmental nucleus (RMTg), a major GABAergic afferent to midbrain dopamine neurons. 5-HT2CRs produce depolarizing effects in RMTg neurons that are particularly strong in some rats, leading to aversive effects that reduce acquisition of and relapse to cocaine seeking. In contrast, 5-HT2CR signaling is largely lost after cocaine exposure in other rats, leading to reduced aversive effects and increased cocaine seeking. These results suggest a serotonergic biological marker of cocaine-seeking vulnerability that can be targeted to modulate drug seeking.

Keywords: 5-HT; CP: Neuroscience; RMTg; VTA; addiction; aversion; cocaine; dopamine; serotonin; serotonin receptor 2c.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cocaine* / pharmacology
  • Dopaminergic Neurons / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Serotonin / pharmacology
  • Serotonin Agents / pharmacology
  • Tegmentum Mesencephali
  • Ventral Tegmental Area / physiology

Substances

  • Cocaine
  • Serotonin
  • Serotonin Agents