Gimenez-Gomez Pablo, Le Timmy, Zinter Max, M'Angale Peter, Duran-Laforet Violeta, Freels Timothy G, Pavchinskiy Rebecca, Molas Susanna, Schafer Dorothy P, Tapper Andrew R, Thomson Travis, Martin Gilles E
Brudnick Neuropsychiatric Research Institute, Department of Neurobiology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Department of Neurobiology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Nat Neurosci. 2025 Jun 10. doi: 10.1038/s41593-025-01970-x.
Alcohol consumption remains a significant global health challenge, directly and indirectly causing millions of deaths annually. Alcohol abuse causes dysregulated activity of the prefrontal cortex, yet effects on specific prefrontal circuits remain to be elucidated. Here, we identify a discrete GABAergic neuronal ensemble in the mouse medial orbitofrontal cortex (mOFC) that is selectively recruited in response to binge alcohol drinking and limits further drinking behavior. Optogenetic silencing of this population, or its ablation, results in uncontrolled binge alcohol consumption. This neuronal ensemble is specific to alcohol and is not recruited by other rewarding substances. Neurons in this ensemble project widely throughout the brain, but projections specifically to the mediodorsal thalamus regulate binge alcohol drinking. Together, these results identify a brain circuit in the mOFC that serves to protect against binge drinking by reducing alcohol intake, which may offer avenues for the development of mOFC neuronal ensemble-targeted interventions.
饮酒仍然是一项重大的全球健康挑战,每年直接或间接导致数百万人死亡。酒精滥用会导致前额叶皮质活动失调,但对特定前额叶回路的影响仍有待阐明。在此,我们在小鼠内侧眶额皮质(mOFC)中鉴定出一个离散的γ-氨基丁酸能神经元群体,该群体在暴饮酒精时被选择性激活,并限制进一步的饮酒行为。对该群体进行光遗传学沉默或切除会导致不受控制的暴饮酒精行为。这个神经元群体对酒精具有特异性,不会被其他奖励性物质激活。该群体中的神经元广泛投射到整个大脑,但特别投射到丘脑背内侧核的投射调节暴饮酒精行为。总之,这些结果确定了mOFC中的一个脑回路,该回路通过减少酒精摄入量来防止暴饮,这可能为开发针对mOFC神经元群体的干预措施提供途径。