Suppr超能文献

青少年期接触可卡因对具有不同情感表型的成年雄性大鼠的精神运动致敏和表观遗传谱有不同影响。

Adolescent cocaine differentially impacts psychomotor sensitization and epigenetic profiles in adult male rats with divergent affective phenotypes.

作者信息

Parsegian Aram, García-Fuster M Julia, Hebda-Bauer Elaine, Watson Stanley J, Flagel Shelly B, Akil Huda

机构信息

Michigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, United States.

IUNICS, University of the Balearic Islands, Palma, Spain.

出版信息

Front Psychiatry. 2022 Oct 12;13:1024617. doi: 10.3389/fpsyt.2022.1024617. eCollection 2022.

Abstract

Adolescent drug use reliably predicts increased addiction liability in adulthood, but not all individuals are equally impacted. To explore the biological bases of this differential reactivity to early life drug experience, we used a genetic rat model of temperament and evaluated the impact of adolescent cocaine exposure on adult psychomotor sensitization. Relative to adult bred low-responder (bLR) rats, bred high-responders (bHR) are more sensitive to the psychomotor-activating effects of cocaine and reinstate drug-seeking behavior more readily following prolonged cocaine exposure and/or abstinence. We found that a 7-day sensitizing cocaine regimen (15 mg/kg/day) during either adolescence or adulthood produced psychomotor sensitization in bHRs only, while a dual cocaine exposure prevented further sensitization, suggesting limits on neuroplasticity. By contrast, adolescent cocaine in bLRs shifted their resilient phenotype, rendering them more responsive to cocaine in adulthood following adolescent cocaine. To begin to explore the neural correlates of these behavioral phenotypes, we assessed two functionally opposite epigenetic chromatin modifications implicated in addiction liability, permissive acetylation (ac) and repressive tri-methylation (me3) on Histone 3 Lysine 9 (H3K9), in four striatal sub-regions. In bHRs, decreased H3K9me3 and increased acH3K9 in the nucleus accumbens (NAc) core associated with cocaine sensitization. In bLRs, the combination of cocaine exposure in adolescence and adulthood, which lead to an increased response to a cocaine challenge, also increased acH3K9 in the core. Thus, adolescent cocaine experience interacts with genetic background to elicit different behavioral profiles relevant to addiction in adulthood, with concurrent modifications in the epigenetic histone profiles in the NAc that associate with cocaine sensitization and with metaplasticity.

摘要

青少年药物使用能可靠地预测成年后成瘾倾向的增加,但并非所有个体受到的影响都相同。为了探究这种对早期生活药物经历的差异反应性的生物学基础,我们使用了一种气质遗传大鼠模型,并评估了青少年接触可卡因对成年后精神运动性敏感化的影响。相对于成年培育的低反应者(bLR)大鼠,培育的高反应者(bHR)对可卡因的精神运动激活作用更敏感,并且在长时间接触可卡因和/或戒断后更容易恢复觅药行为。我们发现,在青少年期或成年期进行为期7天的可卡因致敏方案(15毫克/千克/天)仅在bHR大鼠中产生了精神运动性敏感化,而双重可卡因暴露则阻止了进一步的敏感化,这表明神经可塑性存在限制。相比之下,bLR大鼠在青少年期接触可卡因改变了它们的适应表型,使它们在成年后对青少年期接触可卡因后的可卡因反应更强。为了开始探究这些行为表型的神经相关性,我们在四个纹状体亚区域评估了与成瘾倾向相关的两种功能相反的表观遗传染色质修饰,即组蛋白3赖氨酸9(H3K9)上的允许性乙酰化(ac)和抑制性三甲基化(me3)。在bHR大鼠中,伏隔核(NAc)核心区域的H3K9me3减少和acH3K9增加与可卡因敏感化相关。在bLR大鼠中,青少年期和成年期接触可卡因的联合作用导致对可卡因激发的反应增加,同时也增加了核心区域的acH3K9。因此,青少年期可卡因经历与遗传背景相互作用,引发了与成年后成瘾相关的不同行为特征,同时NAc中与可卡因敏感化和可塑性相关的表观遗传组蛋白谱也发生了改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ecc/9599748/9c308abedbf3/fpsyt-13-1024617-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验