Alcohol Effects on Colon Epithelium are Time-Dependent.

IF 3.2 3区 医学 Q1 Medicine
Alcoholism, clinical and experimental research Pub Date : 2019-09-01 Epub Date: 2019-07-22 DOI:10.1111/acer.14141
Faraz Bishehsari, Lijuan Zhang, Robin M Voigt, Natalie Maltby, Bita Semsarieh, Eyas Zorub, Maliha Shaikh, Sherry Wilber, Andrew R Armstrong, Seyed Sina Mirbagheri, Nailliw Z Preite, Peter Song, Alessia Stornetta, Silvia Balbo, Christopher B Forsyth, Ali Keshavarzian
{"title":"Alcohol Effects on Colon Epithelium are Time-Dependent.","authors":"Faraz Bishehsari, Lijuan Zhang, Robin M Voigt, Natalie Maltby, Bita Semsarieh, Eyas Zorub, Maliha Shaikh, Sherry Wilber, Andrew R Armstrong, Seyed Sina Mirbagheri, Nailliw Z Preite, Peter Song, Alessia Stornetta, Silvia Balbo, Christopher B Forsyth, Ali Keshavarzian","doi":"10.1111/acer.14141","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Alcohol intake increases the risk of developing colon cancer. Circadian disruption promotes alcohol's effect on colon carcinogenesis through unknown mechanisms. Alcohol's metabolites induce DNA damage, an early step in carcinogenesis. We assessed the effect of time of alcohol consumption on markers of tissue damage in the colonic epithelium.</p><p><strong>Methods: </strong>Mice were treated by alcohol or phosphate-buffered saline (PBS), at 4-hour intervals for 3 days, and their colons were analyzed for (i) proliferation (Ki67) and antiapoptosis (Bcl-2) markers, (ii) DNA damage (γ-H2AX), and (iii) the major acetaldehyde (AcH)-DNA adduct, N<sup>2</sup> -ethylidene-dG. To model circadian disruption, mice were shifted once weekly for 12 h and then were sacrificed at 4-hour intervals. Samples of mice with a dysfunctional molecular clock were analyzed. The dynamics of DNA damage repair from AcH treatment as well as role of xeroderma pigmentosum, complementation group A (XPA) in their repair were studied in vitro.</p><p><strong>Results: </strong>Proliferation and survival of colonic epithelium have daily rhythmicity. Alcohol induced colonic epithelium proliferation in a time-dependent manner, with a stronger effect during the light/rest period. Alcohol-associated DNA damage also occurred more when alcohol was given at light. Levels of DNA adduct did not vary by time, suggesting rather lower repair efficiency during the light versus dark. XPA gene expression, a key excision repair gene, was time-dependent, peaking at the beginning of the dark. XPA knockout colon epithelial cells were inefficient in repair of the DNA damage induced by alcohol's metabolite.</p><p><strong>Conclusions: </strong>Time of day of alcohol intake may be an important determinant of colon tissue damage and carcinogenicity.</p>","PeriodicalId":7410,"journal":{"name":"Alcoholism, clinical and experimental research","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2019-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722020/pdf/nihms-1038080.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alcoholism, clinical and experimental research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/acer.14141","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/7/22 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Alcohol intake increases the risk of developing colon cancer. Circadian disruption promotes alcohol's effect on colon carcinogenesis through unknown mechanisms. Alcohol's metabolites induce DNA damage, an early step in carcinogenesis. We assessed the effect of time of alcohol consumption on markers of tissue damage in the colonic epithelium.

Methods: Mice were treated by alcohol or phosphate-buffered saline (PBS), at 4-hour intervals for 3 days, and their colons were analyzed for (i) proliferation (Ki67) and antiapoptosis (Bcl-2) markers, (ii) DNA damage (γ-H2AX), and (iii) the major acetaldehyde (AcH)-DNA adduct, N2 -ethylidene-dG. To model circadian disruption, mice were shifted once weekly for 12 h and then were sacrificed at 4-hour intervals. Samples of mice with a dysfunctional molecular clock were analyzed. The dynamics of DNA damage repair from AcH treatment as well as role of xeroderma pigmentosum, complementation group A (XPA) in their repair were studied in vitro.

Results: Proliferation and survival of colonic epithelium have daily rhythmicity. Alcohol induced colonic epithelium proliferation in a time-dependent manner, with a stronger effect during the light/rest period. Alcohol-associated DNA damage also occurred more when alcohol was given at light. Levels of DNA adduct did not vary by time, suggesting rather lower repair efficiency during the light versus dark. XPA gene expression, a key excision repair gene, was time-dependent, peaking at the beginning of the dark. XPA knockout colon epithelial cells were inefficient in repair of the DNA damage induced by alcohol's metabolite.

Conclusions: Time of day of alcohol intake may be an important determinant of colon tissue damage and carcinogenicity.

Abstract Image

Abstract Image

Abstract Image

酒精对结肠上皮细胞的影响具有时间依赖性。
背景:酒精摄入会增加患结肠癌的风险。昼夜节律紊乱通过未知机制促进酒精对结肠癌发生的影响。酒精的代谢物会诱发 DNA 损伤,这是致癌的早期步骤。我们评估了饮酒时间对结肠上皮组织损伤标志物的影响:方法:用酒精或磷酸盐缓冲盐水(PBS)对小鼠进行为期 3 天、每隔 4 小时一次的处理,然后分析小鼠结肠中(i)增殖(Ki67)和抗凋亡(Bcl-2)标记物、(ii)DNA 损伤(γ-H2AX)和(iii)主要乙醛(AcH)-DNA 加合物 N2-亚乙基-dG。为了模拟昼夜节律紊乱,小鼠每周换班一次,每次 12 小时,然后每隔 4 小时处死一次。对分子钟失调的小鼠样本进行了分析。在体外研究了AcH处理引起的DNA损伤修复的动态以及A互补组色素性红斑(XPA)在其修复中的作用:结果:结肠上皮细胞的增殖和存活具有日节律性。酒精诱导结肠上皮细胞增殖与时间有关,在光照/休息期间影响更大。在光照下饮酒时,与酒精相关的 DNA 损伤也更严重。DNA 加合物的水平并不随时间而变化,这表明在光照和黑暗条件下的修复效率更低。XPA基因是一种关键的切除修复基因,其表达与时间有关,在黑暗开始时达到高峰。XPA基因敲除的结肠上皮细胞对酒精代谢物诱导的DNA损伤的修复效率较低:结论:每天摄入酒精的时间可能是决定结肠组织损伤和致癌性的重要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.90
自引率
9.40%
发文量
219
审稿时长
1 months
期刊介绍: Alcoholism: Clinical and Experimental Research''s scope spans animal and human clinical research, epidemiological, experimental, policy, and historical research relating to any aspect of alcohol abuse, dependence, or alcoholism. This journal uses a multi-disciplinary approach in its scope of alcoholism, its causes, clinical and animal effect, consequences, patterns, treatments and recovery, predictors and prevention.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信