• 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

酒精性、非酒精性和毒物相关性脂肪性肝炎:机制上的异同

Alcoholic, Nonalcoholic, and Toxicant-Associated Steatohepatitis: Mechanistic Similarities and Differences.

作者信息

Joshi-Barve Swati, Kirpich Irina, Cave Matthew C, Marsano Luis S, McClain Craig J

机构信息

Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Louisville, Louisville, Kentucky; Department of Medicine, School of Medicine, University of Louisville, Louisville, Kentucky; Department of Pharmacology and Toxicology, School of Medicine, University of Louisville, Louisville, Kentucky.

Division of Gastroenterology, Hepatology and Nutrition, School of Medicine, University of Louisville, Louisville, Kentucky; Department of Medicine, School of Medicine, University of Louisville, Louisville, Kentucky; Department of Pharmacology and Toxicology, School of Medicine, University of Louisville, Louisville, Kentucky; Robley Rex Veterans Affairs Medical Center, Louisville, Kentucky.

出版信息

Cell Mol Gastroenterol Hepatol. 2015 Jun 3;1(4):356-367. doi: 10.1016/j.jcmgh.2015.05.006. eCollection 2015 Jul.

DOI:10.1016/j.jcmgh.2015.05.006
PMID:28210688
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5301292/
Abstract

Hepatic steatosis and steatohepatitis are common histologic findings that can be caused by multiple etiologies. The three most frequent causes for steatosis/steatohepatitis are alcohol (alcoholic steatohepatitis, ASH), obesity/metabolic syndrome (nonalcoholic steatohepatitis, NASH), and environmental toxicants (toxicant-associated steatohepatitis, TASH). Hepatic steatosis is an early occurrence in all three forms of liver disease, and they often share common pathways to disease progression/severity. Disease progression is a result of both direct effects on the liver as well as indirect alterations in other organs/tissues such as intestine, adipose tissue, and the immune system. Although the three liver diseases (ASH, NASH, and TASH) share many common pathogenic mechanisms, they also exhibit distinct differences. Both shared and divergent mechanisms can be potential therapeutic targets. This review provides an overview of selected important mechanistic similarities and differences in ASH, NASH, and TASH.

摘要

肝脂肪变性和脂肪性肝炎是常见的组织学表现,可由多种病因引起。脂肪变性/脂肪性肝炎最常见的三个病因是酒精(酒精性脂肪性肝炎,ASH)、肥胖/代谢综合征(非酒精性脂肪性肝炎,NASH)和环境毒物(毒物相关性脂肪性肝炎,TASH)。肝脂肪变性在所有这三种肝病形式中都是早期出现的情况,并且它们通常具有疾病进展/严重程度的共同途径。疾病进展是对肝脏的直接影响以及其他器官/组织(如肠道、脂肪组织和免疫系统)的间接改变共同作用的结果。虽然这三种肝病(ASH、NASH和TASH)有许多共同的致病机制,但它们也表现出明显的差异。共同机制和不同机制都可能成为潜在的治疗靶点。本综述概述了ASH、NASH和TASH中选定的重要机制异同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8066/5301292/57812b20be17/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8066/5301292/d3d276017105/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8066/5301292/57812b20be17/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8066/5301292/d3d276017105/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8066/5301292/57812b20be17/gr2.jpg

相似文献

1
Alcoholic, Nonalcoholic, and Toxicant-Associated Steatohepatitis: Mechanistic Similarities and Differences.酒精性、非酒精性和毒物相关性脂肪性肝炎:机制上的异同
Cell Mol Gastroenterol Hepatol. 2015 Jun 3;1(4):356-367. doi: 10.1016/j.jcmgh.2015.05.006. eCollection 2015 Jul.
2
The Riddle of Nonalcoholic Fatty Liver Disease: Progression From Nonalcoholic Fatty Liver to Nonalcoholic Steatohepatitis.非酒精性脂肪性肝病之谜:从非酒精性脂肪肝到非酒精性脂肪性肝炎的进展
J Clin Exp Hepatol. 2015 Jun;5(2):147-58. doi: 10.1016/j.jceh.2015.02.002. Epub 2015 Feb 16.
3
Decoding cell death signals in liver inflammation.解析肝炎症中的细胞死亡信号。
J Hepatol. 2013 Sep;59(3):583-94. doi: 10.1016/j.jhep.2013.03.033. Epub 2013 Apr 6.
4
The ratio of aspartate aminotransferase to alanine aminotransferase: potential value in differentiating nonalcoholic steatohepatitis from alcoholic liver disease.天冬氨酸氨基转移酶与丙氨酸氨基转移酶的比值:在区分非酒精性脂肪性肝炎与酒精性肝病中的潜在价值。
Am J Gastroenterol. 1999 Apr;94(4):1018-22. doi: 10.1111/j.1572-0241.1999.01006.x.
5
Macrophage-derived thrombospondin 1 promotes obesity-associated non-alcoholic fatty liver disease.巨噬细胞衍生的血小板反应蛋白1促进肥胖相关的非酒精性脂肪性肝病。
JHEP Rep. 2020 Oct 9;3(1):100193. doi: 10.1016/j.jhepr.2020.100193. eCollection 2021 Feb.
6
Peroxisome proliferator-activated receptors alpha and gamma2 polymorphisms in nonalcoholic fatty liver disease: a study in Brazilian patients.过氧化物酶体增殖物激活受体α和γ2 多态性与非酒精性脂肪性肝病:巴西患者的研究。
Gene. 2013 Oct 25;529(2):326-31. doi: 10.1016/j.gene.2013.06.091. Epub 2013 Jul 24.
7
Will Studies in Nonalcoholic Steatohepatitis Help Manage Alcoholic Steatohepatitis?非酒精性脂肪性肝炎研究能否有助于酒精性脂肪性肝炎的治疗管理?
Clin Liver Dis. 2019 Feb;23(1):157-165. doi: 10.1016/j.cld.2018.09.008.
8
Alcohol, microbiome, life style influence alcohol and non-alcoholic organ damage.酒精、微生物群、生活方式会影响酒精性和非酒精性器官损伤。
Exp Mol Pathol. 2017 Feb;102(1):162-180. doi: 10.1016/j.yexmp.2017.01.003. Epub 2017 Jan 7.
9
Therapeutic opportunities for alcoholic steatohepatitis and nonalcoholic steatohepatitis: exploiting similarities and differences in pathogenesis.酒精性脂肪性肝炎和非酒精性脂肪性肝炎的治疗机会:从发病机制的异同中寻找突破。
JCI Insight. 2017 Sep 7;2(17). doi: 10.1172/jci.insight.95354.
10
Serum intercellular adhesion molecule-1 in patients with nonalcoholic steatohepatitis: comparison with alcoholic hepatitis.非酒精性脂肪性肝炎患者血清细胞间黏附分子-1:与酒精性肝炎的比较
Alcohol Clin Exp Res. 2007 Jan;31(1 Suppl):S83-7. doi: 10.1111/j.1530-0277.2006.00292.x.

引用本文的文献

1
Inflammatory and metabolic markers mediate the association between urinary metals and non-alcoholic fatty liver disease in U.S. adults: a cross-sectional study.炎症和代谢标志物介导美国成年人尿金属与非酒精性脂肪性肝病之间的关联:一项横断面研究。
Front Public Health. 2025 Jul 4;13:1564302. doi: 10.3389/fpubh.2025.1564302. eCollection 2025.
2
The correlation between heavy metal ions in blood and metabolic dysfunction-associated steatotic liver disease from 1999 to 2018 based on NHANES data.基于美国国家健康与营养检查调查(NHANES)数据,1999年至2018年血液中重金属离子与代谢功能障碍相关脂肪性肝病之间的相关性。
Front Public Health. 2025 Jan 7;12:1512901. doi: 10.3389/fpubh.2024.1512901. eCollection 2024.
3

本文引用的文献

1
Oligofructose protects against arsenic-induced liver injury in a model of environment/obesity interaction.在环境/肥胖相互作用模型中,低聚果糖可预防砷诱导的肝损伤。
Toxicol Appl Pharmacol. 2015 May 1;284(3):304-14. doi: 10.1016/j.taap.2015.02.022. Epub 2015 Mar 8.
2
Hepatocellular carcinoma.肝细胞癌
Cold Spring Harb Perspect Med. 2015 Feb 2;5(2):a021444. doi: 10.1101/cshperspect.a021444.
3
Hepatic and fecal metabolomic analysis of the effects of Lactobacillus rhamnosus GG on alcoholic fatty liver disease in mice.
Quantitative proteomic analysis unveils a critical role of VARS1 in hepatocellular carcinoma aggressiveness through the modulation of MAGI1 expression.
定量蛋白质组学分析揭示了VARS1通过调节MAGI1表达在肝细胞癌侵袭性中的关键作用。
Mol Cancer. 2025 Jan 14;24(1):15. doi: 10.1186/s12943-024-02206-5.
4
Impact of Endocrine Disrupting Pesticide Use on Obesity: A Systematic Review.内分泌干扰性农药的使用对肥胖的影响:一项系统综述
Biomedicines. 2024 Nov 24;12(12):2677. doi: 10.3390/biomedicines12122677.
5
Dietary therapy of murine primary biliary cholangitis induces hepatocellular steatosis: A cautionary tale.饮食疗法治疗原发性胆汁性胆管炎可诱导肝细胞脂肪变性:一个警示故事。
Liver Int. 2024 Oct;44(10):2834-2846. doi: 10.1111/liv.16060. Epub 2024 Aug 5.
6
Immunological mechanisms in steatotic liver diseases: An overview and clinical perspectives.免疫机制在脂肪性肝病中的作用:综述与临床展望。
Clin Mol Hepatol. 2024 Oct;30(4):620-648. doi: 10.3350/cmh.2024.0315. Epub 2024 Jul 11.
7
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.
8
Alcohol-associated liver disease and behavioral and medical cofactors: unmet needs and opportunities.酒精相关肝病及行为和医疗共病因素:未满足的需求和机会。
Front Public Health. 2024 Apr 4;12:1322460. doi: 10.3389/fpubh.2024.1322460. eCollection 2024.
9
Obesogenic polystyrene microplastic exposures disrupt the gut-liver-adipose axis.肥胖相关的聚苯乙烯微塑料暴露会破坏肠道-肝脏-脂肪轴。
Toxicol Sci. 2024 Mar 26;198(2):210-220. doi: 10.1093/toxsci/kfae013.
10
Contributing roles of mitochondrial dysfunction and hepatocyte apoptosis in liver diseases through oxidative stress, post-translational modifications, inflammation, and intestinal barrier dysfunction.线粒体功能障碍和肝细胞凋亡通过氧化应激、翻译后修饰、炎症和肠道屏障功能障碍在肝脏疾病中的作用。
Cell Mol Life Sci. 2024 Jan 12;81(1):34. doi: 10.1007/s00018-023-05061-7.
鼠李糖乳杆菌GG对小鼠酒精性脂肪肝疾病影响的肝脏和粪便代谢组学分析
J Proteome Res. 2015 Feb 6;14(2):1174-82. doi: 10.1021/pr501121c. Epub 2015 Jan 27.
4
The role of intestinal bacteria overgrowth in obesity-related nonalcoholic fatty liver disease.肠道细菌过度生长在肥胖相关非酒精性脂肪性肝病中的作用。
Nutrients. 2014 Dec 3;6(12):5583-99. doi: 10.3390/nu6125583.
5
Long non-coding RNAs and hepatocellular carcinoma.长链非编码RNA与肝细胞癌
Mol Clin Oncol. 2015 Jan;3(1):13-17. doi: 10.3892/mco.2014.429. Epub 2014 Sep 25.
6
Identification of Environmental Chemicals Associated with the Development of Toxicant-associated Fatty Liver Disease in Rodents.与啮齿动物中毒物相关性脂肪性肝病发生相关的环境化学物质的鉴定。
Toxicol Pathol. 2015 Jun;43(4):482-97. doi: 10.1177/0192623314549960. Epub 2014 Oct 16.
7
Payment or reimbursement for certain medical expenses for Camp Lejeune family members. Interim final rule.为勒琼营家庭成员的某些医疗费用提供支付或报销。暂行最终规则。
Fed Regist. 2014 Sep 24;79(185):57415-21.
8
Exposure to a northern contaminant mixture (NCM) alters hepatic energy and lipid metabolism exacerbating hepatic steatosis in obese JCR rats.暴露于北方污染物混合物(NCM)会改变肥胖JCR大鼠的肝脏能量和脂质代谢,加剧肝脏脂肪变性。
PLoS One. 2014 Sep 15;9(9):e106832. doi: 10.1371/journal.pone.0106832. eCollection 2014.
9
Association of inflammatory response and oxidative injury in the pathogenesis of liver steatosis and insulin resistance following subchronic exposure to malathion in rats.大鼠亚慢性暴露于马拉硫磷后,肝脏脂肪变性和胰岛素抵抗发病机制中炎症反应与氧化损伤的关联
Environ Toxicol Pharmacol. 2014 Sep;38(2):542-53. doi: 10.1016/j.etap.2014.08.007. Epub 2014 Aug 18.
10
Cell death and cell death responses in liver disease: mechanisms and clinical relevance.肝病中的细胞死亡及细胞死亡反应:机制与临床意义
Gastroenterology. 2014 Oct;147(4):765-783.e4. doi: 10.1053/j.gastro.2014.07.018. Epub 2014 Jul 18.