Macht Victoria, de Castro Sagan, Vetreno Ryan P
Bowles Center for Alcohol Studies, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Department of Psychiatry, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Adv Exp Med Biol. 2025;1473:179-208. doi: 10.1007/978-3-031-81908-7_9.
Adolescence is a conserved neurodevelopmental period encompassing maturation of glia and the innate immune system that parallels refinement of brain structures, neurotransmitter systems, and neurocircuitry. Given the vast neurodevelopmental processes occurring during adolescence, spanning brain structural and neurocircuitry refinement to maturation of neurotransmitter systems, glia, and the innate immune system, insults incurred during this critical period of neurodevelopment, could have profound effects on brain function and behavior that persist into adulthood. Adolescent binge drinking is common and associated with many adverse outcomes that may underlie the lifelong increased risk of alcohol-related problems and development of an alcohol use disorder (AUD). In this chapter, we examined the impact of adolescent binge drinking models using the adolescent intermittent ethanol (AIE) model on adult neurobiology. These studies implicate proinflammatory neuroimmune signaling across glia and neurons in persistent AIE-induced neuropathology. Some of these changes are reversible, providing unique opportunities for the development of treatments to prevent many of the long-term consequences of adolescent alcohol misuse.
青春期是一个保守的神经发育时期,涵盖神经胶质细胞和先天免疫系统的成熟,这与脑结构、神经递质系统和神经回路的细化过程并行。鉴于青春期会发生大量的神经发育过程,从脑结构和神经回路的细化到神经递质系统、神经胶质细胞和先天免疫系统的成熟,在这个关键的神经发育时期所遭受的损伤,可能会对脑功能和行为产生深远影响,并持续至成年期。青少年暴饮很常见,且与许多不良后果相关,这些后果可能是与酒精相关问题的终生风险增加以及酒精使用障碍(AUD)发生的潜在原因。在本章中,我们使用青少年间歇性乙醇(AIE)模型研究了青少年暴饮模型对成年神经生物学的影响。这些研究表明,在持续的AIE诱导的神经病理学中,神经胶质细胞和神经元之间存在促炎神经免疫信号传导。其中一些变化是可逆的,这为开发预防青少年酒精滥用的许多长期后果的治疗方法提供了独特的机会。