Department of Neuroscience, Waggoner Center for Alcohol and Addiction Research, Center for Learning and Memory, University of Texas at Austin, Austin, Texas, United States of America.
Department of Biology, Johns Hopkins University, Baltimore, Maryland, United States of America.
PLoS One. 2022 Oct 18;17(10):e0271849. doi: 10.1371/journal.pone.0271849. eCollection 2022.
Alcohol abuse and dependence have a substantial heritable component. Although the genome has been considered the sole vehicle of heritable phenotypes, recent studies suggest that drug or alcohol exposure may induce alterations in gene expression that are transmitted across generations. Still, the transgenerational impact of alcohol use (and abuse) remains largely unexplored in part because multigenerational studies using rodent models present challenges for time, sample size, and genetic heterogeneity. Here, we took advantage of the extremely short generation time, large broods, and clonal form of reproduction of the nematode Caenorhabditis elegans. We developed a model of pre-fertilization parental alcohol exposure to test alterations in behavioral responses to acute alcohol treatment (referred to in short as intoxication) in subsequent F1, F2 and F3 generations. We found that chronic and intermittent alcohol-treatment paradigms resulted in opposite changes to intoxication sensitivity of F3 progeny that were only apparent when controlling for yoked trials. Chronic alcohol-treatment paradigm in the parental generation resulted in alcohol-naïve F3 progeny displaying moderate resistance to intoxication. Intermittent treatment resulted in alcohol-naïve F3 progeny displaying moderate hypersensitivity to intoxication. Further study of these phenomena using this new C. elegans model may yield mechanistic insights into how transgenerational effects may occur in other animals.
酗酒和酒精依赖有很大的遗传因素。虽然基因组被认为是遗传表型的唯一载体,但最近的研究表明,药物或酒精暴露可能会诱导基因表达的改变,这种改变会在代际之间传递。尽管如此,酒精使用(和滥用)的跨代影响在很大程度上仍未得到探索,部分原因是使用啮齿动物模型的多代研究在时间、样本量和遗传异质性方面存在挑战。在这里,我们利用秀丽隐杆线虫(Caenorhabditis elegans)的极短世代时间、大量繁殖和无性繁殖形式。我们开发了一种在受精前暴露于酒精的亲代模型,以测试在随后的 F1、F2 和 F3 代中对急性酒精处理(简称醉酒)的行为反应的改变。我们发现,慢性和间歇性酒精处理模式导致 F3 后代对醉酒敏感性的相反变化,只有在控制配对试验时才会出现这些变化。亲代的慢性酒精处理模式导致酒精敏感的 F3 后代对醉酒表现出中度抵抗。间歇性治疗导致酒精敏感的 F3 后代对醉酒表现出中度超敏反应。使用这种新的秀丽隐杆线虫模型进一步研究这些现象可能会深入了解跨代效应如何在其他动物中发生。