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母体甲基苯丙胺暴露会影响后代的行为敏化和伏隔核DNA甲基化。

Maternal Methamphetamine Exposure Influences Behavioral Sensitization and Nucleus Accumbens DNA Methylation in Subsequent Generation.

作者信息

Dong Nan, Zhu Jie, Wang Rui, Wang Shuai, Chen Yanjiong, Wang Changhe, Goh Eyleen L K, Chen Teng

机构信息

College of Forensic Medicine, Xi'an Jiaotong University Health Science Center, Xi'an, China.

The Key Laboratory of Health Ministry for Forensic Science, Xi'an Jiaotong University, Xi'an, China.

出版信息

Front Pharmacol. 2022 Jul 19;13:940798. doi: 10.3389/fphar.2022.940798. eCollection 2022.

Abstract

The deleterious effects of methamphetamine (METH) exposure extend beyond abusers, and may potentially impact the vulnerability of their offspring in developing addictive behaviors. Epigenetic signatures have been implicated in addiction, yet the characteristics to identify prenatal METH abuse to offspring addiction risk remains elusive. Here, we used escalating doses of METH-exposed mouse model in F0 female mice before and during pregnancy to simulate the human pattern of drug abuse and generated METH-induced behavioral sensitization to investigate the addictive behavior in offspring mice. We then utilized whole genome-bisulfite sequencing (WGBS) to investigate the methylation signature of nucleus accumbens (NAc) in male METH-sensitized mice. Interestingly, male but not female offspring exhibited an enhanced response to METH-induced behavioral sensitization. Additionally, the METH-exposed group of male mice underwent a more comprehensive wave of epigenome remodeling over all genomic elements compared with unexposed groups due to drug exposure history. 104,219 DMCs (METH-SAL vs SAL-SAL) induced by prenatal METH-exposure were positively correlated with that of postnatal METH-exposure (38,570, SAL-METH vs SAL-SAL). Moreover, 4,983 DMCs induced by pre- and postnatal METH exposure (METH-METH vs SAL-METH) were negatively correlated with that of postnatal METH exposure, and 371 commonly changed DMCs between the two comparison groups also showed a significantly negative correlation and 86 annotated genes functionally enriched in the pathways of neurodevelopment and addiction. Key annotated genes included , , and , implicated in neurodevelopmental processes, were down-regulated in METH-METH group mice compared with the SAL-METH group. Taken together, we render novel insights into the epigenetic correlation of drug exposure and provide evidence for epigenetic characteristics that link maternal METH exposure to the intensity of the same drug-induced behavioral sensitization in adult offspring.

摘要

甲基苯丙胺(METH)暴露的有害影响不仅限于滥用者,还可能影响其后代形成成瘾行为的易感性。表观遗传特征与成瘾有关,但识别产前METH滥用与后代成瘾风险的特征仍不清楚。在这里,我们在F0雌性小鼠怀孕前和怀孕期间使用递增剂量的METH暴露小鼠模型来模拟人类药物滥用模式,并产生METH诱导的行为敏化,以研究后代小鼠的成瘾行为。然后,我们利用全基因组亚硫酸氢盐测序(WGBS)来研究雄性METH致敏小鼠伏隔核(NAc)的甲基化特征。有趣的是,雄性而非雌性后代对METH诱导的行为敏化表现出增强的反应。此外,由于药物暴露史,与未暴露组相比,METH暴露组的雄性小鼠在所有基因组元件上经历了更全面的表观基因组重塑浪潮。产前METH暴露诱导的104,219个差异甲基化胞嘧啶(METH-SAL与SAL-SAL)与产后METH暴露诱导的差异甲基化胞嘧啶(38,570个,SAL-METH与SAL-SAL)呈正相关。此外,产前和产后METH暴露诱导的4,983个差异甲基化胞嘧啶(METH-METH与SAL-METH)与产后METH暴露诱导的差异甲基化胞嘧啶呈负相关,两个比较组之间371个共同变化的差异甲基化胞嘧啶也显示出显著的负相关,并且86个注释基因在神经发育和成瘾途径中功能富集。关键注释基因包括参与神经发育过程的基因,与SAL-METH组相比,METH-METH组小鼠中的这些基因下调。综上所述,我们对药物暴露的表观遗传相关性有了新的认识,并为将母体METH暴露与成年后代中相同药物诱导的行为敏化强度联系起来的表观遗传特征提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1df6/9343784/4320584a471f/fphar-13-940798-g001.jpg

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