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Systemic Administration of the AMPA Receptor Antagonist, NBQX, Reduces Alcohol Drinking in Male C57BL/6J, But Not Female C57BL/6J or High‐Alcohol‐Preferring, Mice
Author(s) -
Bauer Meredith R.,
Garcy Daniel P.,
Boehm Stephen L.
Publication year - 2020
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/acer.14461
Subject(s) - nbqx , ampa receptor , alcohol , antagonist , chemistry , binge drinking , ionotropic effect , medicine , endocrinology , glutamate receptor , pharmacology , receptor , alcohol consumption , biochemistry
Background α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptors are ionotropic glutamate receptors that have been investigated for their role in modulating alcohol consumption. However, little is known about the role of AMPA receptors in the control of binge‐like or free‐access alcohol drinking in C57BL/6J or in selectively bred high‐alcohol‐preferring (HAP) mice. The purpose of this experiment was to assess the role of systemic administration of the AMPA receptor antagonist, 2,3‐dioxo‐6‐nitro‐7‐sulfamoyl‐benzo[f]quinoxaline (NBQX), on alcohol consumption using a model of binge‐like drinking, drinking in the dark (DID) and free‐access 2‐bottle choice (2BC) in male and female C57BL/6J and HAP mice. Methods C57BL/6J mice were allowed free access to 20% (v/v) alcohol for 2 hours each day beginning 3 hours into the dark cycle for 4 days. On day 5, mice were intraperitoneally injected with one of 4 doses of NBQX (0, 3, 10, or 30 mg/kg; n = 10) 15 minutes before alcohol presentation and were given 4‐hour alcohol access (extended DID). HAP mice were given 24‐hour free access to 10% (v/v) alcohol and water for 19 days. On day 20, mice were intraperitoneally injected with one of 4 doses of NBQX (0, 3, 10, or 30 mg/kg; n = 9) 15 minutes before alcohol and water presentation. Results In the first 2 hours of DID, at 30 mg/kg, male, but not female C57BL/6J or HAP, mice drank significantly less alcohol compared with controls and 30 mg/kg NBQX did not alter saccharin intake in the males. Although male HAP mice drank significantly less alcohol than female mice following 10 mg/kg NBQX, neither sex exhibited drinking that differed significantly from controls. NBQX did not reduce locomotor behavior at any dose, sex, or genotype. Conclusions These data suggest that AMPA receptors play a key role in modulating binge‐like alcohol consumption without altering saccharin consumption or general locomotion and that this effect is specific to sex and genotype.