4.7 Article

Central nucleus of the amygdala projections onto the nucleus accumbens core regulate binge-like alcohol drinking in a CRF-dependent manner

期刊

NEUROPHARMACOLOGY
卷 203, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2021.108874

关键词

Chemogenetics; Binge drinking; Nucleus accumbens; Central amygdala; Corticotropin releasing factor; Mice

资金

  1. US Department of Veterans Affairs [IK2 BX002488, BX004699]
  2. NIH [AA013519, AA010760, AA007468, AA028686, AA027692]

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The study demonstrates that manipulating neuronal activity from the central amygdala to the nucleus accumbens core can reduce binge-like ethanol intake in mice. Additionally, intra-NAc core CRF injection can mimic the effects of this pathway's chemogenetic stimulation, further decreasing binge drinking behavior. However, testing shows that the effects of NPY and SST on binge drinking are minimal, while intra-NAc CRF antagonism can prevent reductions in drinking induced by CeA to NAc core projections.
Rationale: The nucleus accumbens (NAc) is important for regulating a number of behaviors, including alcohol and substance use. We previously found that chemogenetically manipulating neuronal activity in the NAc core regulates binge-like drinking in mice. The central amygdala (CeA) is also an important regulator of alcohol drinking, and projects to the NAc core. We tested whether neuronal projections from the CeA to the NAc core, or neuropeptides released by the CeA in the NAc core, could regulate binge drinking. Methods: For experiment 1, mice were administered AAV2 Cre-GFP into the NAc core and a Cre-inducible DREADD [AAV2 DIO- hM3Dq, -hM4Di, or -mCherry control] into the CeA. We tested the effects of altering CeA to NAc core activity on binge-like ethanol intake (via Drinking in the Dark, DID). For experiment 2, we bilaterally microinfused corticotropin releasing factor (CRF), neuropeptide Y (NPY), or somatostatin (SST) into the NAc core prior to DID. For experiment 3, we tested whether intra-NAc CRF antagonism prevented reductions in drinking induced by CNO/hM3Dq stimulation of CeA->NAc projections. Results: Chemogenetically increasing activity in neurons projecting from the CeA to NAc core decreased bingelike ethanol drinking (p < 0.01). Intra-NAc core CRF mimicked chemogenetic stimulation of this pathway (p < 0.05). Binge-like drinking was unaffected by the doses of NPY and SST tested. Lastly, we found that intra-NAc CRF antagonism prevented reductions in drinking induced by chemogenetic stimulation of CeA->NAc projections. These findings demonstrate that neurons projecting from the CeA to NAc core that release CRF are capable of regulating binge-like drinking in mice.

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