Forced Abstinence from Volitional Ethanol Intake Drives a Vulnerable Period of Hyperexcitability in BNST-Projecting Insular Cortex Neurons

• Published in: The Journal of neuroscience Vol. 44; no. 4; p. e1121232023
• Main Authors: Taylor, Anne, Adank, Danielle N., Young, Phoebe A., Quan, Yizhen, Nabit, Brett P., Winder, Danny G.
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 24.01.2024
• Subjects: Abstinence; Animals; Cortex (insular); Cortex (somatosensory); Drinking; Drinking behavior; Electrophysiology; Emotional behavior; Ethanol; Ethanol - pharmacology; Excitability; Female; Gene expression; Homeostatic plasticity; Humans; Hybridization; Insular Cortex; Integrated circuits; Large-Conductance Calcium-Activated Potassium Channels - metabolism; Mice; Neurons; Neurons - physiology; Phenotypes; Potassium channels (calcium-gated); Septal Nuclei - physiology; Stria terminalis; Sucrose; BNST; chronic ethanol; BK channels; insular cortex
• ISSN: 0270-6474; 1529-2401; 1529-2401
• DOI: 10.1523/JNEUROSCI.1121-23.2023

The insular cortex (IC) integrates sensory and interoceptive cues to inform downstream circuitry executing adaptive behavioral responses. The IC communicates with areas involved canonically in stress and motivation. IC projections govern stress and ethanol recruitment of bed nucleus of the stria terminalis (BNST) activity necessary for the emergence of negative affective behaviors during alcohol abstinence. Here, we assess the impact of the chronic drinking forced abstinence (CDFA) volitional home cage ethanol intake paradigm on synaptic and excitable properties of IC neurons that project to the BNST (IC →BNST ). Using whole-cell patch-clamp electrophysiology, we investigated IC →BNST circuitry 24 h or 2 weeks following forced abstinence (FA) in female C57BL6/J mice. We find that IC →BNST cells are transiently more excitable following acute ethanol withdrawal. In contrast, in vivo ethanol exposure via intraperitoneal injection, ex vivo via ethanol wash, and acute FA from a natural reward (sucrose) all failed to alter excitability. In situ hybridization studies revealed that at 24 h post FA BK channel mRNA expression is reduced in IC. Further, pharmacological inhibition of BK channels mimicked the 24 h FA phenotype, while BK activation was able to decrease AP firing in control and 24 h FA subjects. All together these data suggest a novel mechanism of homeostatic plasticity that occurs in the IC →BNST circuitry following chronic drinking.