• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

表观遗传学在酒精作用中的新作用。

Emerging role of epigenetics in the actions of alcohol.

作者信息

Shukla Shivendra D, Velazquez Jose, French Samuel W, Lu Shelly C, Ticku Maharaj K, Zakhari Samir

机构信息

Department of Medical Pharmacology & Physiology, University of Missouri Columbia, Missouri 65212, USA.

出版信息

Alcohol Clin Exp Res. 2008 Sep;32(9):1525-34. doi: 10.1111/j.1530-0277.2008.00729.x. Epub 2008 Jul 9.

DOI:10.1111/j.1530-0277.2008.00729.x
PMID:18616668
Abstract

This review deals with the recent developments on the epigenetic effects of ethanol. A large body of data have come from studies in liver and in neuronal systems and involve post-translational modifications in histones and methylations in DNA. Ethanol causes site selective acetylation, methylation, and phosphorylation in histone. With respect to methylations the methyl group donating system involving S-adenosyl methionine appears to play a central role. There is contrasting effect of acetylation versus methylation on the same site of histone, as it relates to the transcriptional activation. Epigenetic memory also appears to correlate with liver pathology and Mallory body formation. Experimental evidence supports transcriptional regulation of genes in the CNS by DNA methylations. These studies are contributing towards a better understanding of a novel epigenetic regulation of gene expression in the context of alcohol. The critical steps and the enzymes (e.g., histone acetyltransferase, histone deacetylase, DNA methyltransferase) responsible for the epigenetic modifications are prime targets for intense investigation. The emerging data are also beginning to offer novel insight towards defining the molecular actions of ethanol and may contribute to potential therapeutic targets at the nucleosomal level. These epigenetic studies have opened up a new avenue of investigation in the alcohol field.

摘要

本综述探讨了乙醇表观遗传效应的最新进展。大量数据来自肝脏和神经系统的研究,涉及组蛋白的翻译后修饰和DNA甲基化。乙醇会导致组蛋白发生位点选择性乙酰化、甲基化和磷酸化。就甲基化而言,涉及S-腺苷甲硫氨酸的甲基供体系统似乎起着核心作用。组蛋白同一位点上的乙酰化与甲基化对转录激活具有相反的作用。表观遗传记忆似乎也与肝脏病理学和马洛里小体形成相关。实验证据支持DNA甲基化对中枢神经系统基因的转录调控。这些研究有助于更好地理解酒精环境下基因表达的新型表观遗传调控。负责表观遗传修饰的关键步骤和酶(如组蛋白乙酰转移酶、组蛋白脱乙酰酶、DNA甲基转移酶)是深入研究的主要靶点。新出现的数据也开始为确定乙醇的分子作用提供新的见解,并可能有助于在核小体水平确定潜在的治疗靶点。这些表观遗传学研究为酒精领域开辟了一条新的研究途径。

相似文献

1
Emerging role of epigenetics in the actions of alcohol.表观遗传学在酒精作用中的新作用。
Alcohol Clin Exp Res. 2008 Sep;32(9):1525-34. doi: 10.1111/j.1530-0277.2008.00729.x. Epub 2008 Jul 9.
2
Epigenetic mechanisms in AML - a target for therapy.急性髓系白血病中的表观遗传机制——一个治疗靶点
Cancer Treat Res. 2010;145:19-40. doi: 10.1007/978-0-387-69259-3_2.
3
Small molecule modulators in epigenetics: implications in gene expression and therapeutics.表观遗传学中的小分子调节剂:对基因表达和治疗的影响
Subcell Biochem. 2007;41:397-428.
4
Epigenetic interplay between histone modifications and DNA methylation in gene silencing.基因沉默中组蛋白修饰与DNA甲基化之间的表观遗传相互作用。
Mutat Res. 2008 Jul-Aug;659(1-2):40-8. doi: 10.1016/j.mrrev.2008.02.004. Epub 2008 Feb 29.
5
AtMBD9 modulates Arabidopsis development through the dual epigenetic pathways of DNA methylation and histone acetylation.AtMBD9通过DNA甲基化和组蛋白乙酰化的双重表观遗传途径调控拟南芥的发育。
Plant J. 2009 Jul;59(1):123-35. doi: 10.1111/j.1365-313X.2009.03860.x. Epub 2009 Mar 27.
6
Epigenetic mechanisms are involved in the regulation of ethanol consumption in mice.表观遗传机制参与了小鼠乙醇摄入的调节。
Int J Neuropsychopharmacol. 2014 Oct 31;18(2):pyu072. doi: 10.1093/ijnp/pyu072.
7
Epigenetic gene regulation in cancer.癌症中的表观遗传基因调控
Adv Genet. 2008;61:247-67. doi: 10.1016/S0065-2660(07)00009-0.
8
Epigenetics, disease, and therapeutic interventions.表观遗传学、疾病与治疗干预
Ageing Res Rev. 2006 Nov;5(4):449-67. doi: 10.1016/j.arr.2006.07.001. Epub 2006 Sep 11.
9
A new paradigm in toxicology and teratology: altering gene activity in the absence of DNA sequence variation.毒理学和致畸学的新范式:在无DNA序列变异的情况下改变基因活性。
Reprod Toxicol. 2007 Jul;24(1):20-30. doi: 10.1016/j.reprotox.2007.05.002. Epub 2007 May 22.
10
Acute myeloid leukemia: therapeutic impact of epigenetic drugs.急性髓系白血病:表观遗传药物的治疗作用
Int J Biochem Cell Biol. 2005 Sep;37(9):1752-62. doi: 10.1016/j.biocel.2005.04.019.

引用本文的文献

1
Chronic Alcohol Consumption Reprograms Hepatic Metabolism Through Organelle-Specific Acetylation in Mice.长期饮酒通过小鼠细胞器特异性乙酰化重编程肝脏代谢。
Mol Cell Proteomics. 2025 Jun;24(6):100990. doi: 10.1016/j.mcpro.2025.100990. Epub 2025 May 12.
2
Continuous Activation of C/EBPβ Transcription Factor Prevents Fibrosis Resolution After Alcohol Cessation.C/EBPβ转录因子的持续激活会阻碍戒酒后的纤维化消退。
Cell Mol Gastroenterol Hepatol. 2025 Apr 26;19(9):101525. doi: 10.1016/j.jcmgh.2025.101525.
3
Evaluation of Salivary Carcinogenic microR-21 and miR-125a Expression Associated with Alcohol Consumption and Smoking.
与饮酒和吸烟相关的唾液致癌性微小RNA-21和miR-125a表达的评估
Asian Pac J Cancer Prev. 2025 Feb 1;26(2):551-556. doi: 10.31557/APJCP.2025.26.2.551.
4
Synaptic Mechanisms of Ethanol Tolerance and Neuroplasticity: Insights from Invertebrate Models.乙醇耐受和神经可塑性的突触机制:无脊椎动物模型的见解。
Int J Mol Sci. 2024 Jun 21;25(13):6838. doi: 10.3390/ijms25136838.
5
Alcohol-Associated Liver Disease Outcomes: Critical Mechanisms of Liver Injury Progression.酒精性肝病的结局:肝损伤进展的关键机制
Biomolecules. 2024 Mar 27;14(4):404. doi: 10.3390/biom14040404.
6
E-Cigarettes and Associated Health Risks: An Update on Cancer Potential.电子烟及相关健康风险:癌症潜在风险的最新研究。
Adv Respir Med. 2023 Nov 14;91(6):516-531. doi: 10.3390/arm91060038.
7
Introducing Molecular Chaperones into the Causality and Prospective Management of Autoimmune Hepatitis.将分子伴侣引入自身免疫性肝炎的病因及前瞻性管理中。
Dig Dis Sci. 2023 Nov;68(11):4098-4116. doi: 10.1007/s10620-023-08118-6. Epub 2023 Sep 27.
8
Missing Causality and Heritability of Autoimmune Hepatitis.自身免疫性肝炎的因果关系及遗传力缺失
Dig Dis Sci. 2023 Apr;68(4):1585-1604. doi: 10.1007/s10620-022-07728-w. Epub 2022 Oct 19.
9
The increased risk of multiple sclerosis associated with HLA-DRB1*15:01 and smoking is modified by alcohol consumption.与 HLA-DRB1*15:01 和吸烟相关的多发性硬化症风险增加,受饮酒量影响。
Sci Rep. 2021 Oct 27;11(1):21237. doi: 10.1038/s41598-021-00578-y.
10
Ethanol-Induced Cell Damage Can Result in the Development of Oral Tumors.乙醇诱导的细胞损伤可导致口腔肿瘤的发生。
Cancers (Basel). 2021 Jul 30;13(15):3846. doi: 10.3390/cancers13153846.