Hypocretin Neurotransmission Within the Central Amygdala Mediates Escalated Cocaine Self-administration and Stress-Induced Reinstatement in Rats

Biol Psychiatry. 2017 Apr 1;81(7):606-615. doi: 10.1016/j.biopsych.2016.06.010. Epub 2016 Jun 16.

Abstract

Background: Cocaine addiction is characterized by patterns of compulsive drug-taking, including preoccupation with obtaining cocaine and loss of control over drug intake. The lateral hypothalamic hypocretin/orexin (HCRT) system has been implicated in drug-taking and the reinstatement of drug-seeking. Evidence suggests that HCRT may drive drug-seeking through activation of specific brain regions implicated in stress system dysfunction, including the central amygdala (CeA). The role of HCRT in the persistence of compulsive-like cocaine-taking has yet to be fully elucidated.

Methods: Systemic and intra-CeA microinfusions of the HCRT-receptor 1 antagonist, SB-334867, were administered to rats allowed either short (1 hour; ShA) or long (6 hours; LgA) access to cocaine self-administration. Animals were tested for fixed and progressive ratio responding for cocaine and stress-induced reinstatement of drug-seeking. In addition, using electrophysiological techniques on in vitro slices, we investigated gamma-aminobutyric acidergic (GABAergic) neurotransmission in the medial CeA and the sensitivity of GABAergic synapses to modulation of the HCRT system in ShA or LgA rats.

Results: We found systemic administration of SB-334867 (0, 7.5, 15, 30 mg/kg) dose dependently decreased cocaine intake specifically in LgA rats but not in ShA rats. Microinjections of SB-334867 (20 nmol) bilaterally into the CeA significantly reduced cocaine intake in LgA rats. We also observed a significant attenuation of yohimbine-induced reinstatement of cocaine-seeking after intra-CeA SB-334867 (10 nmol) administration. Finally, electrophysiological data indicated enhanced GABAergic neurotransmission within the medial CeA in LgA rats, which was blocked with SB-334867 (10 μmol/L).

Conclusions: These findings suggest that HCRT neurotransmission within the CeA is implicated in compulsive-like cocaine-seeking.

Keywords: Central amygdala; Cocaine; Drug dependence; Hypocretin/orexin; Intravenous self-administration; Reinstatement.

MeSH terms

  • Animals
  • Benzoxazoles / administration & dosage
  • Central Amygdaloid Nucleus / drug effects*
  • Central Amygdaloid Nucleus / physiology*
  • Cocaine / administration & dosage*
  • Drug-Seeking Behavior*
  • Inhibitory Postsynaptic Potentials
  • Male
  • Naphthyridines
  • Orexin Receptor Antagonists / administration & dosage
  • Orexin Receptors / physiology*
  • Rats
  • Rats, Wistar
  • Reinforcement Schedule
  • Self Administration
  • Stress, Psychological / physiopathology*
  • Urea / administration & dosage
  • Urea / analogs & derivatives
  • gamma-Aminobutyric Acid / physiology

Substances

  • 1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl urea
  • Benzoxazoles
  • Hcrtr1 protein, rat
  • Naphthyridines
  • Orexin Receptor Antagonists
  • Orexin Receptors
  • gamma-Aminobutyric Acid
  • Urea
  • Cocaine