Adolescent intermittent ethanol exposure decreases perineuronal nets in the hippocampus in a sex dependent manner: Modulation through pharmacological inhibition of RPTPβ/ζ

Adolescence is a critical period for brain maturation in which this organ undergoes critical plasticity mechanisms that increase its vulnerability to the effects of alcohol. Significantly, ethanol-induced disruption of hippocampal neurogenesis has been related to cognitive decline in adulthood. Duri...

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Veröffentlicht in:Neuropharmacology 2024-04, Vol.247, p.109850-109850, Article 109850
Hauptverfasser: Galán-Llario, Milagros, Gramage, Esther, García-Guerra, Alba, Torregrosa, Abraham B., Gasparyan, Ani, Navarro, Daniela, Navarrete, Francisco, García-Gutiérrez, María Salud, Manzanares, Jorge, Herradón, Gonzalo
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container_title Neuropharmacology
container_volume 247
creator Galán-Llario, Milagros
Gramage, Esther
García-Guerra, Alba
Torregrosa, Abraham B.
Gasparyan, Ani
Navarro, Daniela
Navarrete, Francisco
García-Gutiérrez, María Salud
Manzanares, Jorge
Herradón, Gonzalo
description Adolescence is a critical period for brain maturation in which this organ undergoes critical plasticity mechanisms that increase its vulnerability to the effects of alcohol. Significantly, ethanol-induced disruption of hippocampal neurogenesis has been related to cognitive decline in adulthood. During adolescence, the maturation of perineuronal nets (PNNs), extracellular matrix structures highly affected by ethanol consumption, plays a fundamental role in neurogenesis and plasticity in the hippocampus. Receptor Protein Tyrosine Phosphatase (RPTP) β/ζ is a critical anchor point for PNNs on the cell surface. Using the adolescent intermittent access to ethanol (IAE) model, we previously showed that MY10, a small-molecule inhibitor of RPTPβ/ζ, reduces chronic ethanol consumption in adolescent male mice but not in females and prevents IAE-induced neurogenic loss in the male hippocampus. We have now tested if these effects of MY10 are related to sex-dependent modulatory actions on ethanol-induced effects in PNNs. Our findings suggest a complex interplay between alcohol exposure, neural structures, and sex-related differences in the modulation of PNNs and parvalbumin (PV)-positive cells in the hippocampus. In general, IAE increased the number of PV + cells in the female hippocampus and reduced PNNs intensity in different hippocampal regions, particularly in male mice. Notably, we found that pharmacological inhibition of RPTPβ/ζ with MY10 regulates ethanol-induced alterations of PNNs intensity, which correlates with the protection of hippocampal neurogenesis from ethanol neurotoxic effects and may be related to the capacity of MY10 to increase the gene expression of key components of PNNs. [Display omitted] •Chronic ethanol consumption shows gender-specific effect on PNNs during adolescence•IAE increased the number of PV + cells in the female hippocampus•IAE reduced PNNs intensity in different hippocampal regions, particularly in males•Inhibition of RPTPβ/ζ regulates ethanol-induced alterations of PNNs intensity
doi_str_mv 10.1016/j.neuropharm.2024.109850
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subjects Adolescence
Alcohol
Perineuronal nets
Pleiotrophin
RPTPβ/ζ
title Adolescent intermittent ethanol exposure decreases perineuronal nets in the hippocampus in a sex dependent manner: Modulation through pharmacological inhibition of RPTPβ/ζ
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