A ventral pallidal glutamatergic aversive network encodes abstinence from and reexposure to cocaine.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 40700490.
- Also identified by DOI 10.1126/sciadv.adu6074 and PMC identifier 12285697.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Relapse to drugs of abuse can occur after long periods of abstinence. The ventral pallidum (VP) is central to drug addiction, and its glutamatergic neurons (VP<sub>Glu</sub>), whose activation drives aversion, inhibit drug seeking. However, it remains unknown whether these neurons encode the abstinence from and relapse to drugs. We show here that VP<sub>Glu</sub> projections specifically to the aversion-related lateral habenula (LHb) and ventral tegmental area gabaergic (VTA<sub>GABA</sub>) neurons show plasticity induced by abstinence from and reexposure to cocaine or cocaine cues. Both these pathways potentiate during abstinence and restore baseline values upon drug reexposure but with different plasticity mechanisms. Last, inhibiting the VP<sub>Glu</sub> → LHb pathway enhances cocaine preference after abstinence, while inhibiting the VP<sub>Glu</sub> → VTA pathway shows variable effects. These findings establish an aversive circuit orchestrated by VP<sub>Glu</sub> neurons encoding long-term abstinence-driven changes that may contribute to drug relapse.
Medical subject headings
- Cocaine
- Cocaine-Related Disorders
- Basal Forebrain
- Glutamic Acid