Abstinence from cocaine-self-administration activates the nELAV/GAP -43 pathway in the hippocampus: A stress-related effect?

Hippocampus. 2016 Jun;26(6):700-4. doi: 10.1002/hipo.22572. Epub 2016 Feb 25.

Abstract

We previously demonstrated that nELAV/GAP-43 pathway is pivotal for learning and its hippocampal expression is up-regulated by acute stress following repeated cocaine administration. We therefore hypothesized that abstinence-induced stress may sustain nELAV/GAP-43 pathway during early abstinence following 2 weeks of cocaine self-administration. We found that contingent, but not non-contingent, cocaine exposure selectively increases hippocampal nELAV, but not GAP-43, expression immediately after the last self-administration session, an effect that wanes after 24 h and that comes back 7 days later when nELAV activation becomes associated with increased expression of GAP-43, an effect again observed only in animals self-administering the psychostimulant. Such effect is specific for nELAV since the ubiquitous ELAV/HuR is unchanged. This nELAV profile suggests that its initial transient alteration is perhaps related to the daily administration of cocaine, while the increase in the nELAV/GAP-43 pathway following a week of abstinence may reflect the activation of this cascade as a target of stressful conditions associated with drug-related memories. © 2016 Wiley Periodicals, Inc.

Keywords: GAP-43; cocaine; hippocampus; nELAV; self-administration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Central Nervous System Stimulants / administration & dosage*
  • Cocaine / administration & dosage*
  • Cocaine-Related Disorders / metabolism
  • Cocaine-Related Disorders / psychology
  • Disease Models, Animal
  • ELAV-Like Protein 1 / metabolism
  • GAP-43 Protein* / metabolism
  • Hippocampus / metabolism*
  • Rats
  • Self Administration
  • Signal Transduction
  • Stress, Psychological / etiology
  • Stress, Psychological / metabolism
  • Substance Withdrawal Syndrome / metabolism*

Substances

  • Central Nervous System Stimulants
  • ELAV-Like Protein 1
  • Elavl1 protein, rat
  • GAP-43 Protein
  • Cocaine