PPP1R1B differentially modulates alcohol intake and emotional comorbidity through distinct prefrontal circuits.

Authors

Fei Li, Minghui Chen, Xiang Li, Zunyue Zhang, Huayou Luo, Mei Zhu, Huawei Wang, Yu Xu, Fengrong Chen, Kunhua Wang

Published in

Proceedings of the National Academy of Sciences of the United States of America. Volume 123. Issue 46. Pages e2611266123. Nov 17, 2026. Epub Nov 11, 2026.

Abstract

Excessive alcohol consumption frequently co-occurs with anxiety and depression in alcohol use disorder (AUD), yet the specific neural circuits and molecular mechanisms coordinating these comorbid conditions remain poorly defined. The medial prefrontal cortex (mPFC), particularly its prelimbic (PL) and infralimbic (IL) subregions, projects to key reward and emotion centers like the nucleus accumbens (Nac) and basolateral amygdala (BLA), but the functional heterogeneity of these projections is unclear. Using chemogenetics, retrograde tracing, electrophysiology, spatial proteomics, and cell-type-specific gene editing in mice subjected to a 4-wk intermittent access to alcohol (IAA) paradigm, we selectively manipulated glutamatergic projections from the PL and IL to the Nac core, Nac shell, and BLA and assessed alcohol intake, anxiety-like, and depression-like behaviors. Chemogenetic activation of PL-Nac core projections reduced short-term alcohol intake, anxiety-, and depression-like behaviors, while IL-BLA activation decreased alcohol consumption and anxiety-like behaviors only. Retrograde tracing revealed mirror-image anatomical segregation of projection-defined neuronal subpopulations within PL/IL linking spatial organization to functional divergence. IAA induced pathway-specific synaptic adaptations. Spatial proteomics nominated protein phosphatase 1 regulatory subunit 1B (PPP1R1B) as a candidate molecule in PL-Nac core neurons. Independent immunostaining confirmed PPP1R1B downregulation, and circuit-specific knockout recapitulated alcohol-related and affective phenotypes, whereas overexpression reversed them. In IL-BLA neurons, PPP1R1B manipulation modulated alcohol intake and anxiety, but not depression. These findings define a subregion- and projection-specific organizational logic in the mPFC for differentially regulating alcohol consumption and emotional comorbidity, with PPP1R1B as a key molecular determinant. This provides a neural pathway-molecule framework for targeted intervention in AUD.

PMID:
43013539
Bibliographic data and abstract were imported from PubMed on 12 Nov 2026.

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