Patterns of neuronal activation following ethanol-induced social facilitation and social inhibition in adolescent cFos-LacZ male and female rats.

Autor: Towner TT; Developmental Exposure Alcohol Research Center (DEARC), Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, USA., Applegate DT; Developmental Exposure Alcohol Research Center (DEARC), Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, USA., Coleman HJ; Developmental Exposure Alcohol Research Center (DEARC), Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, USA., Papastrat KM; Developmental Exposure Alcohol Research Center (DEARC), Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, USA., Varlinskaya EI; Developmental Exposure Alcohol Research Center (DEARC), Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, USA., Werner DF; Developmental Exposure Alcohol Research Center (DEARC), Department of Psychology, Binghamton University, Binghamton, NY 13902-6000, USA. Electronic address: dwerner@binghamton.edu.
Jazyk: angličtina
Zdroj: Behavioural brain research [Behav Brain Res] 2024 Aug 05; Vol. 471, pp. 115118. Date of Electronic Publication: 2024 Jun 19.
DOI: 10.1016/j.bbr.2024.115118
Abstrakt: Alcohol-associated social facilitation together with attenuated sensitivity to adverse alcohol effects play a substantial role in adolescent alcohol use and misuse, with adolescent females being more susceptible to adverse consequences of binge drinking than adolescent males. Adolescent rodents also demonstrate individual and sex differences in sensitivity to ethanol-induced social facilitation and social inhibition, therefore the current study was designed to identify neuronal activation patterns associated with ethanol-induced social facilitation and ethanol-induced social inhibition in male and female adolescent cFos-LacZ rats. Experimental subjects were given social interaction tests on postnatal day (P) 34, 36, and 38 after an acute challenge with 0, 0.5 and 0.75 g/kg ethanol, respectively, and β-galactosidase (β-gal) expression was assessed in brain tissue of subjects socially facilitated and socially inhibited by 0.75 g/kg ethanol. In females, positive correlations were evident between overall social activity and neuronal activation of seven out of 13 ROIs, including the prefrontal cortex and nucleus accumbens, with negative correlations evident in males. Assessments of neuronal activation patterns revealed drastic sex differences between ethanol responding phenotypes. In socially inhibited males, strong correlations were evident among almost all ROIs (90 %), with markedly fewer correlations among ROIs (38 %) seen in socially facilitated males. In contrast, interconnectivity in females inhibited by ethanol was only 10 % compared to nearly 60 % in facilitated subjects. However, hub analyses revealed convergence of brain regions in males and females, with the nucleus accumbens being a hub region in socially inhibited subjects. Taken together, these findings demonstrate individual and sex-related differences in responsiveness to acute ethanol in adolescent rats, with sex differences more evident in socially inhibited by ethanol adolescents than their socially facilitated counterparts.
(Copyright © 2024 Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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