The Inhibition of RasGRF2, But Not RasGRF1, Alters Cocaine Reward in Mice

J Neurosci. 2019 Aug 7;39(32):6325-6338. doi: 10.1523/JNEUROSCI.1120-18.2019. Epub 2019 Jun 10.

Abstract

Ras/Raf/MEK/ERK (Ras-ERK) signaling has been implicated in the effects of drugs of abuse. Inhibitors of MEK1/2, the kinases upstream of ERK1/2, have been critical in defining the role of the Ras-ERK cascade in drug-dependent alterations in behavioral plasticity, but the Ras family of small GTPases has not been extensively examined in drug-related behaviors. We examined the role of Ras Guanine Nucleotide Releasing Factor 1 (RasGRF1) and 2 (RasGRF2), upstream regulators of the Ras-ERK signaling cascade, on cocaine self-administration (SA) in male mice. We first established a role for Ras-ERK signaling in cocaine SA, demonstrating that pERK1/2 is upregulated following SA in C57BL/6N mice in striatum. We then compared RasGRF1 and RasGRF2 KO mouse lines, demonstrating that cocaine SA in RasGRF2 KO mice was increased relative to WT controls, whereas RasGRF1 KO and WT mice did not differ. This effect in RasGRF2 mice is likely mediated by the Ras-ERK signaling pathway, as pERK1/2 upregulation following cocaine SA was absent in RasGRF2 KO mice. Interestingly, the lentiviral knockdown of RasGRF2 in the NAc had the opposite effect to that in RasGRF2 KO mice, reducing cocaine SA. We subsequently demonstrated that the MEK inhibitor PD325901 administered peripherally prior to cocaine SA increased cocaine intake, replicating the increase seen in RasGRF2 KO mice, whereas PD325901 administered into the NAc decreased cocaine intake, similar to the effect seen following lentiviral knockdown of RasGRF2. These data indicate a role for RasGRF2 in cocaine SA in mice that is ERK-dependent, and suggest a differential effect of global versus site-specific RasGRF2 inhibition.SIGNIFICANCE STATEMENT Exposure to drugs of abuse activates a variety of intracellular pathways, and following repeated exposure, persistent changes in these pathways contribute to drug dependence. Downstream components of the Ras-ERK signaling cascade are involved in the acute and chronic effects of drugs of abuse, but their upstream mediators have not been extensively characterized. Here we show, using a combination of molecular, pharmacological, and lentiviral techniques, that the guanine nucleotide exchange factor RasGRF2 mediates cocaine self-administration via an ERK-dependent mechanism, whereas RasGRF1 has no effect on responding for cocaine. These data indicate dissociative effects of mediators of Ras activity on cocaine reward and expand the understanding of the contribution of Ras-ERK signaling to drug-taking behavior.

Keywords: RasGRF1; RasGRF2; cocaine; extracellular signal-regulated kinase; histone h3; self-administration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Benzamides / pharmacology
  • Cocaine / administration & dosage
  • Cocaine / pharmacology*
  • Cocaine-Related Disorders / physiopathology*
  • Conditioning, Operant
  • Corpus Striatum / drug effects
  • Corpus Striatum / physiopathology*
  • Diphenylamine / analogs & derivatives
  • Diphenylamine / pharmacology
  • Gene Knockdown Techniques
  • Genetic Vectors / genetics
  • Histones / metabolism
  • Lentivirus / genetics
  • MAP Kinase Signaling System / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nucleus Accumbens / drug effects
  • Nucleus Accumbens / physiopathology
  • Organ Specificity
  • Phosphorylation
  • Protein Processing, Post-Translational
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / pharmacology
  • Reward*
  • Self Administration
  • ras Guanine Nucleotide Exchange Factors / deficiency
  • ras Guanine Nucleotide Exchange Factors / genetics
  • ras Guanine Nucleotide Exchange Factors / physiology*
  • ras-GRF1 / deficiency
  • ras-GRF1 / genetics
  • ras-GRF1 / physiology

Substances

  • Benzamides
  • Histones
  • RNA, Small Interfering
  • Rasgrf1 protein, mouse
  • Rasgrf2 protein, mouse
  • ras Guanine Nucleotide Exchange Factors
  • ras-GRF1
  • mirdametinib
  • Diphenylamine
  • Cocaine