mRNA and microRNA analysis reveals modulation of biochemical pathways related to addiction in the ventral tegmental area of methamphetamine self-administering rats

BMC Neurosci. 2015 Jul 19:16:43. doi: 10.1186/s12868-015-0186-y.

Abstract

Background: Methamphetamine is a highly addictive central nervous system stimulant with increasing levels of abuse worldwide. Alterations to mRNA and miRNA expression within the mesolimbic system can affect addiction-like behaviors and thus play a role in the development of drug addiction. While many studies have investigated the effects of high-dose methamphetamine, and identified neurotoxic effects, few have looked at the role that persistent changes in gene regulation play following methamphetamine self-administration. Therefore, the aim of this study was to identify RNA changes in the ventral tegmental area following methamphetamine self-administration. We performed microarray analyses on RNA extracted from the ventral tegmental area of Sprague-Dawley rats following methamphetamine self-administration training (2 h/day) and 14 days of abstinence.

Results: We identified 78 miRNA and 150 mRNA transcripts that were differentially expressed (fdr adjusted p < 0.05, absolute log2 fold change >0.5); these included genes not previously associated with addiction (miR-125a-5p, miR-145 and Foxa1), loci encoding receptors related to drug addiction behaviors and genes with previously recognized roles in addiction such as miR-124, miR-181a, DAT and Ret.

Conclusion: This study provides insight into the effects of methamphetamine on RNA expression in a key brain region associated with addiction, highlighting the possibility that persistent changes in the expression of genes with both known and previously unknown roles in addiction occur.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamine-Related Disorders / metabolism
  • Animals
  • Catheters, Indwelling
  • Central Nervous System Stimulants / administration & dosage*
  • Drug-Seeking Behavior / physiology
  • Male
  • Methamphetamine / administration & dosage*
  • MicroRNAs / metabolism*
  • Microarray Analysis
  • RNA, Messenger / metabolism*
  • Random Allocation
  • Rats, Sprague-Dawley
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Self Administration
  • Ventral Tegmental Area / drug effects*
  • Ventral Tegmental Area / metabolism*

Substances

  • Central Nervous System Stimulants
  • MicroRNAs
  • RNA, Messenger
  • Methamphetamine