Interneuron-selective HCN channel knockdown in prelimbic cortex of female rats mimics effects of chronic ethanol exposure

• Published in: Alcohol (Fayetteville, N.Y.) Vol. 121; pp. 59 - 67
• Main Authors: Hughes, Benjamin A., O'Buckley, Todd K., Boero, Giorgia, Morrow, A. Leslie
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2024; Elsevier Limited
• Subjects: Alcohol; alcohol dependence; Animal euthanasia; Animals; Channel gating; Down-regulation; Drug abuse; electrophysiology; Ethanol; Ethanol - pharmacology; Female; Females; Food; Gender differences; Gene Knockdown Techniques; HCN channels; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - genetics; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - metabolism; Interneurons; Interneurons - drug effects; Interneurons - metabolism; Ion channels (cyclic nucleotide-gated); Laboratories; Laboratory animals; Male; Males; Matching-to-sample; Maze Learning - drug effects; Memory; Memory, Short-Term - drug effects; Neuroplasticity; Potassium Channels - drug effects; Potassium Channels - genetics; Potassium Channels - metabolism; Prefrontal cortex; Prefrontal Cortex - drug effects; Prefrontal Cortex - metabolism; Rats; Rats, Sprague-Dawley; Rodents; Sex differences; Sexes; working memory; Prefrontal cortex; electrophysiology; working memory; alcohol dependence; HCN channels
• ISSN: 0741-8329; 1873-6823; 1873-6823
• DOI: 10.1016/j.alcohol.2024.07.005

Our laboratory has previously shown that chronic ethanol exposure elicits enhanced working memory performance in female, but not male, adult Sprague–Dawley rats, indicative of a fundamental sex difference in cortical plasticity. Recent studies have furthermore revealed that females display markedly reduced HCN-mediated channel activity in inhibitory Martinotti interneurons after chronic ethanol exposure that is similarly not observed in males. From these observations we hypothesized that alcohol induces facilitated working memory performance via down-regulation of these channels’ activity specifically within interneurons. To test this hypothesis, we employed a Pol-II compatible shRNA expression system to elicit targeted knockdown of HCN channel activity in these cells, and measured performance on a delayed Non-Match-to-Sample (NMS) T-maze test to gauge effects on working memory performance. A significant baseline enhancement of working memory performance with HCN channel knockdown was observed, indicative of a critical role for interneuron-expressed HCNs in maintaining optimal cortical network activity during cognitively-demanding tasks. Consistent with previous observations, ethanol exposure resulted in enhanced NMS T-maze performance, however elevated working memory performance was observed in both scram- and hcn-shRNA infected groups after alcohol administration. We therefore conclude that interneuron-expressed HCN channels, despite representing a minor population of total cortical HCN expression, contribute substantially to maintaining working memory processes. Downregulated HCN channel activity, though, does not alone appear sufficient to manifest alcohol-induced enhancement of working memory performance observed in female rats during acute withdrawal. •Interneuron HCN channel knockdown in prelimbic cortex enhanced working memory in female rats.•HCN knockdown mimicked alcohol exposure-induced HCN channel downregulation and concomitant working memory enhancement.•Somatostatin interneuron-selective HCN knockdown was achieved using a multi-plexed viral strategy and verified electrophysiologically.•Cortical internueron HCN expression regulates working memory and may underlie chronic ethanol effects on T maze performance.