Stress inoculation during adolescence attenuates social stress-induced increase in ethanol intake in adult male mice

被引:0
|
作者
Reguilon, Marina D. [1 ]
Manzanedo, Carmen [1 ]
Minarro, Jose [1 ]
Rodriguez-Arias, Marta [1 ,2 ]
机构
[1] Univ Valencia, Fac Psicol, Dept Psicobiol, Un Invest Psicobiol Drogodependencias, Valencia, Spain
[2] Univ Valencia, Fac Psicol, Dept Psicobiol, Avda Blasco Ibanez, 21, Valencia 46010, Spain
关键词
Stress inoculation; Social defeat; Resilience; Ethanol; CX3CL1; IL-6; DEFEAT STRESS; INDUCED NEUROINFLAMMATION; ALCOHOL-CONSUMPTION; RESILIENCE; VULNERABILITY; BRAIN; SUSCEPTIBILITY; COCAINE; RATS; NEUROBIOLOGY;
D O I
10.1016/j.neuropharm.2024.109838
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Social stress exposure heightens the risk of substance abuse disorder development, especially when endured during adolescence, influencing long-term mental health. This study investigates early-life stress's potential to confer resilience against later-life stressors. To investigate this hypothesis, we examined the impact of a single social defeat (SD) incident during adolescent mice's lives on subsequent voluntary ethanol consumption following repeated adult social stress exposure. Half of the adolescent mice experienced SD at postnatal day 28. Three weeks later (postnatal day 49), defeated groups encountered four confrontations with aggressive residents every 72 h, while control groups were exposed to non-resident exploration. A day after the last SD, defeated mice were classified as resilient or susceptible based on their response to a social interaction test (SIT), a model for depressive behavior. To assess ethanol consumption during young adulthood, researchers used the 'drinking in the dark' and oral ethanol self-administration paradigms. Stress inoculation (IS) slightly increased resilient animals in the SIT. In mice without IS exposure during adolescence, susceptible defeated mice displayed higher ethanol consumption and motivation than control and resilient mice. IS in adolescence effectively counteracted this effect, as IS-SD groups, whether resilient or susceptible, showed no increase in ethanol intake. These groups also exhibited similar motivation to control, measured by the progressive ratio. Notably, elevated IL-6 levels seen in SD-S mice were absent in IS-exposed mice. Additionally, IS-exposed groups had lower prefrontal cortex IL-6 and CX3CL1 levels. These findings support the hypothesis that IS, induced by moderate-intensity stress during adolescence, can enhance resilience to more severe stressors in adulthood.
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页数:12
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