Mechanism for differential recruitment of orbitostriatal transmission during actions and outcomes following chronic alcohol exposure
Year: 2021
Type: article
Abstract: Psychiatric disease often produces symptoms that have divergent effects on neural activity. For example, in drug dependence, dysfunctional value-based decision-making and compulsive-like actions have been linked to hypo- and hyperactivity of orbital frontal cortex (OFC)-basal ganglia circuits, respectively; however, the underlying mechanisms are unknown. Here we show that alcohol-exposed mice have enhanced activity in OFC terminals in dorsal striatum (OFC-DS) associated with actions, but reduced activity of the same terminals during periods of outcome retrieval, corresponding with a loss of outcome control over decision-making. Disrupted OFC-DS terminal activity was due to a dysfunction of dopamine-type 1 receptors on spiny projection neurons (D1R SPNs) that resulted in increased retrograde endocannabinoid signaling at OFC-D1R SPN synapses reducing OFC-DS transmission. Blocking CB1 receptors restored OFC-DS activity in vivo and rescued outcome-based control over decision-making. These findings demonstrate a circuit-, synapse-, and computation-specific mechanism gating OFC activity in alcohol-exposed mice.
Source: eLife
DOI: 10.7554/elife.67065
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,500
Awards: Graduate Research Fellowship Program (GRFP), Graduate Research Fellowship Program (GRFP), G4094912120, Chronic ethanol induced disruption of goal-directed circuits, G5277970811, G5893467534, G6288925769, G684805955, G7424419118, G8954942264, G9000035882, G9000058780, G9000264153, Dependence induced dysfunction of decision-making circuits
OpenAlex ID: W3137913033
