Conditioned stress prevents cue-primed cocaine reinstatement only in stress-responsive rats

Stress. 2016 Jul;19(4):406-18. doi: 10.1080/10253890.2016.1189898. Epub 2016 Jun 3.

Abstract

Neurobiological mechanisms underlying comorbid posttraumatic stress disorder (PTSD) and cocaine use disorder (CUD) are unknown. We aimed to develop an animal model of PTSD + CUD to examine the neurobiology underlying cocaine-seeking in the presence of PTSD comorbidity. Rats were exposed to cat urine once for 10-minutes and tested for anxiety-like behaviors one week later. Subsequently, rats underwent long-access (LgA) cocaine self-administration and extinction training. Rats were re-exposed to the trauma context and then immediately tested for cue-primed reinstatement of cocaine-seeking. Plasma and brains were collected afterwards for corticosterone assays and real-time qPCR analysis. Urine-exposed (UE; n = 23) and controls not exposed to urine (Ctrl; n = 11) did not differ in elevated plus maze behavior, but UE rats displayed significantly reduced habituation of the acoustic startle response (ASR) relative to Ctrl rats. A median split of ASR habituation scores was used to classify stress-responsive rats. UE rats (n = 10) self-administered more cocaine on Day 1 of LgA than control rats (Ctrl + Coc; n = 8). Re-exposure to the trauma context prevented cocaine reinstatement only in stress-responsive rats. Ctrl + Coc rats had lower plasma corticosterone concentrations than Ctrls, and decreased gene expression of corticotropin releasing hormone (CRH) and Glcci1 in the hippocampus. Rats that self-administered cocaine displayed greater CRH expression in the amygdala that was independent of urine exposure. While we did not find that cat urine exposure induced a PTSD-like phenotype in our rats, the present study underscores the need to separate stressed rats into cohorts based on anxiety-like behavior in order to study individual vulnerability to PTSD + CUD.

Keywords: Addiction; CRH; FKBP5; Glcci1; PTSD; corticosterone.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amygdala / drug effects
  • Animals
  • Cocaine / pharmacology*
  • Cocaine-Related Disorders / genetics
  • Cocaine-Related Disorders / metabolism
  • Cocaine-Related Disorders / physiopathology
  • Corticosterone / blood
  • Corticotropin-Releasing Hormone / genetics
  • Corticotropin-Releasing Hormone / metabolism
  • Cues
  • Disease Models, Animal
  • Dopamine Uptake Inhibitors / pharmacology*
  • Extinction, Psychological / drug effects*
  • Hippocampus / drug effects
  • Hippocampus / physiopathology
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Reflex, Startle / drug effects
  • Self Administration
  • Stress, Psychological / genetics
  • Stress, Psychological / metabolism
  • Stress, Psychological / physiopathology*

Substances

  • Dopamine Uptake Inhibitors
  • Corticotropin-Releasing Hormone
  • Cocaine
  • Corticosterone