Sex-specific maturational trajectory of endocannabinoid plasticity in the rat prefrontal cortex

Published: Oct. 10, 2020, 10:02 a.m.

Link to bioRxiv paper: http://biorxiv.org/cgi/content/short/2020.10.09.332965v1?rss=1 Authors: Bernabeu, A., Bara, A., Manduca, A., Borsoi, M., Lassalle, O., Pelissier-Alicot, A.-L., MANZONI, O. J. Abstract: The prefrontal cortex (PFC) develops until early adulthood in rodents and humans, but how synaptic plasticity evolves throughout postnatal development is not known. Here, we used a cross-sectional approach to establish the postnatal maturational trajectories of intrinsic properties and synaptic plasticity in the PFC of rats of both sexes. We found that while layer 5 PFC pyramidal neurons from rats of both sexes displayed similar current-voltage relationships, rheobases and resting potentials across all age groups, excitability was lower in female adults compared to the other developmental stages. NMDAR-dependent long-term potentiation and mGluR2-3-mediated long-term depression (LTD) were equally expressed at the juvenile, pubescent and adult developmental stages in animals of both sexes. However, the developmental course of endocannabinoid (eCB)-mediated LTD was sexually dimorphic. First, eCB-LTD started at the juvenile period in females, but although CB1R were functional in both sexes at all developmental stages, eCB-LTD first manifestation was delayed to pubescence in male. Second, eCB-LTD engaged distinct receptors in male and female depending on their developmental stages. Female rats employ both CB1R and TRPV1R to produce eCB-LTD at the juvenile stage but solely CB1R at pubescence followed by only TRPV1R at adulthood. In contrast, in pubescent and adult males eCB-LTD always and exclusively depended on CB1R. Pharmacological blockade of 2AG principal degrading enzyme allowed incompetent male juvenile synapses to express eCB-LTD. The data reveal different maturational trajectories in the PFC of male and female rats and provide new cellular substrates to the sex-specific behavioral and synaptic abnormalities caused by adolescent exposure to cannabinoids. Copy rights belong to original authors. Visit the link for more info