Divergent opioid-mediated suppression of inhibition between hippocampus and neocortex across species and development
Adam CaccavanoiD, Anna VlachosiD, Nadiya McLean, Sarah Kimmel, June Hoan KimiD, Geoffrey A. VargishiD, Vivek MahadevaniD, Lauren T. HewittiD, Anthony M. Rossi, Ilona Spineux, Sherry Jingjing WuiD, Elisabetta FurlanisiD, Min DaiiDauthor, Brenda Leyva GarciaiD, Yating WangiD, Ramesh ChittajalluiD, Edra LondoniD, Xiaoqing Q YuaniD, Steven HuntiD, Daniel T. Abebe, Mark A. G. EldridgeiD, Alex C. Cummins, Brendan E. HinesiD, Anya S. PlotnikovaiD, Arya Mohanty, , Chris J. McBainiD
Abstract
Within the adult rodent hippocampus, opioids suppress inhibitory parvalbumin-expressing interneurons (PV-INs), thus disinhibiting local micro-circuits. However, it is unknown if this disinhibitory motif is conserved in other cortical regions, species, or across development. We observed that PV-IN mediated inhibition is robustly suppressed by opioids in hippocampus proper but not primary neocortex in mice and nonhuman primates, with spontaneous inhibitory tone in resected human tissue also following a consistent dichotomy. This hippocampal disinhibitory motif was established in early development when PV-INs and opioids were found to regulate early population activity. Acute opioid-mediated modulation was partially occluded with morphine pretreatment, with implications for the effects of opioids on hippocampal network activity important for learning and memory. Together, these findings demonstrate that PV-INs exhibit a divergence in opioid sensitivity across brain regions that is remarkably conserved across evolution and highlights the underappreciated role of opioids acting through immature PV-INs in shaping hippocampal development.
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