Intra-dorsolateral striatal AMPA receptor antagonism reduces binge-like alcohol drinking in male and female C57BL/6J mice

Behav Brain Res. 2022 Feb 10:418:113631. doi: 10.1016/j.bbr.2021.113631. Epub 2021 Oct 26.

Abstract

The dorsolateral striatum (DLS) is involved in addiction, reward, and alcohol related behaviors. The DLS primarily receives excitatory inputs which are gated by post-synaptic AMPA receptors. We antagonized AMPA receptors in the DLS to investigate how such modulation affects binge-like alcohol drinking in male and female C57BL/6J mice and whether an associated alcohol drinking history alters dorsomedial striatum (DMS) and DLS AMPA receptor expression. We also investigated the effect of intra-DLS NBQX on locomotor activity and saccharin drinking in mice. Mice were allowed free access to 20% alcohol for two hours each day for a total of seven days. Mice received an intra-DLS infusion of one of four concentrations of NBQX (saline, 0.15, 0.5, or 1.5 μg/side), an AMPA receptor antagonist, immediately prior to alcohol access on day 7. Two-hour binge alcohol intakes, locomotor activity, and blood alcohol concentrations were determined. Intra-DLS NBQX reduced binge-like alcohol drinking in a U-shaped manner in male and female mice. Intake predicted blood alcohol concentration, and locomotor activity was not affected. In a follow up experiment, we assessed whether the most effective NBQX concentration for reducing alcohol consumption also reduced saccharin drinking, finding intra-DLS NBQX did not alter saccharin drinking in male and female mice. These data suggest that AMPA receptors in the DLS play a role in the modulation of binge-like alcohol drinking. These findings further validate the importance of the DLS for alcohol related behaviors and alcohol use disorder.

Keywords: AMPA receptor; Alcohol; Binge; Dorsolateral striatum; Dorsomedial striatum.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Binge Drinking / metabolism*
  • Blood Alcohol Content
  • Excitatory Amino Acid Antagonists / pharmacology*
  • Female
  • Locomotion
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Motor Activity / drug effects
  • Neostriatum / metabolism*
  • Quinoxalines / pharmacology*
  • Receptors, AMPA / antagonists & inhibitors*
  • Saccharin / administration & dosage

Substances

  • Blood Alcohol Content
  • Excitatory Amino Acid Antagonists
  • Quinoxalines
  • Receptors, AMPA
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Saccharin