The interactions of alcohol and cocaine regulate the expression of genes involved in the GABAergic, glutamatergic and endocannabinoid systems of male and female rats

Neuropharmacology. 2022 Mar 15:206:108937. doi: 10.1016/j.neuropharm.2021.108937. Epub 2021 Dec 26.

Abstract

Although the pharmacological and behavioural interactions between cocaine and alcohol are well established, less is known about how polyconsumption of these drugs affects the neurotransmitter systems involved in their psychoactive effects and in particular, in the process of addiction. Here, rats of both sexes at two stages of development were studied under a chronic regime of intravenous cocaine and/or alcohol administration. Brain samples from the medial prefrontal cortex, nucleus accumbens, hippocampus and amygdala were extracted to analyse the mRNA expression of genes encoding subunits of the GABA, NMDA and AMPA receptors, as well as the expression of the CB1 receptor, and that of enzymes related to the biosynthesis and degradation of endocannabinoids. Moreover, two synaptic scaffold proteins related to GABA and NMDA receptors, gephyrin and PSD-95, were quantified in Western blots. Significant interactions between cocaine and alcohol were common, affecting the GABAergic and endocannabinoid systems in the medial prefrontal cortex and amygdala of young adults, whereas such interactions were evident in the glutamatergic and endocannabinoid systems in adults, as well as a more pronounced sex effect. Significant interactions between these drugs affecting the scaffold proteins were evident in the medial prefrontal cortex and nucleus accumbens of young adults, and in the nucleus accumbens and amygdala of adults, but not in the hippocampus. These results highlight the importance of considering the interactions between cocaine and alcohol on neurotransmitter systems in the context of polyconsumption, specifically when treating problems of abuse of these two substances.

Keywords: Co-abuse; Cocaine; Ethanol; GABAergic; Glutamatergic and endocannabinoid systems; Mesocorticolimbic system; Rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Central Nervous System Depressants / administration & dosage
  • Central Nervous System Depressants / pharmacology*
  • Cerebrum / drug effects*
  • Cocaine / administration & dosage
  • Cocaine / pharmacology*
  • Dopamine Uptake Inhibitors / administration & dosage
  • Dopamine Uptake Inhibitors / pharmacology*
  • Drug Interactions
  • Ethanol / administration & dosage
  • Ethanol / pharmacology*
  • Female
  • Gene Expression Regulation / drug effects*
  • Male
  • Rats
  • Receptors, AMPA / drug effects*
  • Receptors, Cannabinoid / drug effects*
  • Receptors, GABA / drug effects*
  • Receptors, N-Methyl-D-Aspartate / drug effects*
  • Sex Characteristics

Substances

  • Central Nervous System Depressants
  • Dopamine Uptake Inhibitors
  • Receptors, AMPA
  • Receptors, Cannabinoid
  • Receptors, GABA
  • Receptors, N-Methyl-D-Aspartate
  • Ethanol
  • Cocaine