暴饮暴食后青春期雄性小鼠NAc mRNA谱的比较分析

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-06-25 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0322576
Mario E Lloret Torres, Arelys Rivas Jiménez, Eduardo L Tosado Rodríguez, Kiara Cardona Jordan, Xiany X Lay Rivera, Yaren L Peña Señeriz, Joseph L Capella Muñiz, Marieliz Dieppa Rodríguez, Daniel F Ruiz Bolívar, Jovangelis González Del Toro, John A Florian Alsina, Paola A Colón Rivera, Jose O Garcia Colon, Abiel Roche-Lima, Cristina Velázquez-Marrero
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引用次数: 0

摘要

压力相关障碍经常与酒精使用障碍(AUD)共同发生。这就需要了解造成这种关系的生理和遗传因素。酗酒是青少年男性中最常见的饮酒方式,并显著增加了并发压力相关疾病和澳元的风险。在模拟青春期雄性小鼠单次酗酒的影响的实验中,我们观察到上下文消失学习的明显缺陷。通过每隔一天(EOD)两瓶选择饮用试验测量,这种暴露导致了第一天随后自愿饮酒的显着初始增加,此后正常化。方法:在本研究中,我们对小鼠伏隔核(NAc)进行了mRNASeq分析,该区域在EOD后复杂地参与调节厌恶情境恐惧反应和奖励,以描述该区域mrna的差异表达。我们还使用冠状脑切片的免疫组织化学来表征纹状体、伏隔核(NAc)、海马和基底外侧杏仁核(BLA)中与应激相关疾病和分子酒精耐受性相关的蛋白质的表达,如FKBP5、GSK3ß和ß-catenin。结果:比较mRNA谱分析显示,即使在初次暴露后30天,狂饮样酒精暴露诱导的基因表达也会发生显著的长期变化。免疫组织化学显示,在EOD之前,先前观察到的目标蛋白水平改变完全恢复。结论:这些发现表明,特定基因亚群的时间激活在AUD和应激相关疾病的合并症中起着至关重要的作用。了解这些机制有助于开发更有效的综合治疗方法,以改善受影响个体的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative mRNA profile analysis from NAc of adolescent male mice after binge-like alcohol exposure eliciting deficits in context fear extinction learning.

Introduction: Stressor-related disorders frequently co-occur with alcohol use disorder (AUD). This necessitates an understanding of the physiological and genetic factors contributing to this relationship. Binge drinking is the most common method of alcohol consumption among adolescent males and significantly increases the risk of developing comorbid stressor-related disorders and AUD. In experiments modeling the effects of a single binge-like alcohol exposure in male adolescent mice, we observed a clear deficit in context extinction learning. This exposure led to a significant initial increase in subsequent voluntary drinking on day one, as measured by the every-other-day (EOD) two-bottle choice drinking assay, which normalized thereafter.

Methods: For this study we performed an mRNASeq analysis of mice nucleus accumbens (NAc), a region intricately involved in regulating both aversive contextual fear responses and reward, after EOD to profile the differential expression of mRNAs within this region. We also used immunohistochemistry of coronal brain slices to characterize expression of proteins associated with stress-related disorders and molecular alcohol tolerance, such as FKBP5, GSK3ß, and ß-catenin, within the striatum, nucleus accumbens (NAc), hippocampus, and basolateral amygdala (BLA).

Results: Comparative mRNA profile analysis reveals significant long-term changes in gene expression induced by binge-like alcohol exposure, even 30 days after the initial exposure. Immunohistochemistry showed a full recovery of previously observed altered levels of target proteins prior to EOD.

Conclusions: These findings suggest that the temporal activation of specific gene subsets plays a crucial role in the comorbidity of AUD and stressor-related diseases. Understanding these mechanisms can help develop more effective, integrated treatment approaches to improve outcomes for affected individuals.

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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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