• 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

内质网应激在酒精性肝病发病机制中的作用。

Endoplasmic reticulum stress in the pathogenesis of alcoholic liver disease.

机构信息

Department of Pharmacy, The 926th Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, Kaiyuan, Yunan, China.

出版信息

PeerJ. 2023 Nov 14;11:e16398. doi: 10.7717/peerj.16398. eCollection 2023.

DOI:10.7717/peerj.16398
PMID:38025713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10655704/
Abstract

The endoplasmic reticulum (ER) plays a pivotal role in protein synthesis, folding, and modification. Under stress conditions such as oxidative stress and inflammation, the ER can become overwhelmed, leading to an accumulation of misfolded proteins and ensuing ER stress. This triggers the unfolded protein response (UPR) designed to restore ER homeostasis. Alcoholic liver disease (ALD), a spectrum disorder resulting from chronic alcohol consumption, encompasses conditions from fatty liver and alcoholic hepatitis to cirrhosis. Metabolites of alcohol can incite oxidative stress and inflammation in hepatic cells, instigating ER stress. Prolonged alcohol exposure further disrupts protein homeostasis, exacerbating ER stress which can lead to irreversible hepatocellular damage and ALD progression. Elucidating the contribution of ER stress to ALD pathogenesis may pave the way for innovative therapeutic interventions. This review delves into ER stress, its basic signaling pathways, and its role in the alcoholic liver injury.

摘要

内质网 (ER) 在蛋白质合成、折叠和修饰中起着关键作用。在氧化应激和炎症等应激条件下,内质网可能不堪重负,导致错误折叠的蛋白质积累和随之而来的内质网应激。这会触发未折叠蛋白反应 (UPR),旨在恢复内质网的平衡。酒精性肝病 (ALD) 是一种由慢性饮酒引起的谱障碍,包括从脂肪肝和酒精性肝炎到肝硬化的各种疾病。酒精的代谢物会在肝细胞中引发氧化应激和炎症,引发内质网应激。长期饮酒进一步破坏蛋白质的动态平衡,加剧内质网应激,导致不可逆转的肝细胞损伤和 ALD 进展。阐明内质网应激对 ALD 发病机制的贡献可能为创新的治疗干预铺平道路。本综述深入探讨了内质网应激、其基本信号通路以及在酒精性肝损伤中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/a34664c03c79/peerj-11-16398-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/07a87e0b2a83/peerj-11-16398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/dbcf689ea877/peerj-11-16398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/a34664c03c79/peerj-11-16398-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/07a87e0b2a83/peerj-11-16398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/dbcf689ea877/peerj-11-16398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10655704/a34664c03c79/peerj-11-16398-g003.jpg

相似文献

1
Endoplasmic reticulum stress in the pathogenesis of alcoholic liver disease.内质网应激在酒精性肝病发病机制中的作用。
PeerJ. 2023 Nov 14;11:e16398. doi: 10.7717/peerj.16398. eCollection 2023.
2
Endoplasmic reticulum stress in liver disease.内质网应激与肝脏疾病。
J Hepatol. 2011 Apr;54(4):795-809. doi: 10.1016/j.jhep.2010.11.005. Epub 2010 Nov 13.
3
Regulation mechanism of endoplasmic reticulum stress on metabolic enzymes in liver diseases.内质网应激对肝脏疾病代谢酶的调控机制。
Pharmacol Res. 2024 Sep;207:107332. doi: 10.1016/j.phrs.2024.107332. Epub 2024 Jul 30.
4
ASMase is required for chronic alcohol induced hepatic endoplasmic reticulum stress and mitochondrial cholesterol loading.ASMase 对于慢性酒精诱导的肝内质网应激和线粒体胆固醇蓄积是必需的。
J Hepatol. 2013 Oct;59(4):805-13. doi: 10.1016/j.jhep.2013.05.023. Epub 2013 May 23.
5
Sirtuin 6 ameliorates alcohol-induced liver injury by reducing endoplasmic reticulum stress in mice.Sirtuin 6 通过减少小鼠内质网应激改善酒精性肝损伤。
Biochem Biophys Res Commun. 2021 Mar 12;544:44-51. doi: 10.1016/j.bbrc.2021.01.061. Epub 2021 Jan 28.
6
Linking Pathogenic Mechanisms of Alcoholic Liver Disease With Clinical Phenotypes.将酒精性肝病的致病机制与临床表型相联系。
Gastroenterology. 2016 Jun;150(8):1756-68. doi: 10.1053/j.gastro.2016.02.035. Epub 2016 Feb 23.
7
Endoplasmic reticulum stress in liver diseases.肝脏疾病中的内质网应激。
Hepatology. 2023 Feb 1;77(2):619-639. doi: 10.1002/hep.32562. Epub 2022 May 24.
8
The contribution of endoplasmic reticulum stress to liver diseases.内质网应激与肝脏疾病的关系。
Hepatology. 2011 May;53(5):1752-63. doi: 10.1002/hep.24279.
9
The unfolded protein response and hepatic lipid metabolism in non alcoholic fatty liver disease.未折叠蛋白反应与非酒精性脂肪性肝病的肝内脂质代谢。
Pharmacol Ther. 2019 Nov;203:107401. doi: 10.1016/j.pharmthera.2019.107401. Epub 2019 Aug 13.
10
Fatty Acids Inhibit LAMP2-Mediated Autophagy Flux via Activating ER Stress Pathway in Alcohol-Related Liver Disease.脂肪酸通过激活酒精性肝病中的内质网应激通路抑制 LAMP2 介导线粒体自噬流。
Cell Mol Gastroenterol Hepatol. 2021;12(5):1599-1615. doi: 10.1016/j.jcmgh.2021.07.002. Epub 2021 Jul 17.

引用本文的文献

1
Naringin and Naringenin in Liver Health: A Review of Molecular and Epigenetic Mechanisms and Emerging Therapeutic Strategies.柚皮苷和柚皮素对肝脏健康的影响:分子和表观遗传机制及新兴治疗策略综述
Antioxidants (Basel). 2025 Aug 10;14(8):979. doi: 10.3390/antiox14080979.
2
Alpinetin Exhibits Antioxidant and Anti-Inflammatory Effects in C57BL/6 Mice with Alcoholic Liver Disease Induced by the Lieber-DeCarli Ethanol Liquid Diet.山姜素对采用Lieber-DeCarli乙醇液体饲料诱导的酒精性肝病C57BL/6小鼠具有抗氧化和抗炎作用。
Int J Mol Sci. 2024 Dec 26;26(1):86. doi: 10.3390/ijms26010086.
3
Oral supplementation of choline attenuates the development of alcohol-related liver disease (ALD).

本文引用的文献

1
A beneficial adaptive role for CHOP in driving cell fate selection during ER stress.CHOP 在 ER 应激过程中驱动细胞命运选择的有益适应性作用。
EMBO Rep. 2024 Jan;25(1):228-253. doi: 10.1038/s44319-023-00026-0. Epub 2024 Jan 2.
2
Role of the ER-induced UPR pathway, apoptosis, and autophagy in colorectal cancer.内质网应激诱导的未折叠蛋白反应途径、细胞凋亡和自噬在结直肠癌中的作用。
Pathol Res Pract. 2023 Aug;248:154706. doi: 10.1016/j.prp.2023.154706. Epub 2023 Jul 21.
3
Treatment of liver fibrosis: Past, current, and future.肝纤维化的治疗:过去、现在与未来
口服补充胆碱可减轻与酒精相关的肝病 (ALD) 的发展。
Mol Med. 2024 Oct 18;30(1):181. doi: 10.1186/s10020-024-00950-4.
4
AGR2: The Covert Driver and New Dawn of Hepatobiliary and Pancreatic Cancer Treatment.AGR2:肝胆胰癌症治疗的隐蔽驱动因素和新曙光。
Biomolecules. 2024 Jun 23;14(7):743. doi: 10.3390/biom14070743.
World J Hepatol. 2023 Jun 27;15(6):755-774. doi: 10.4254/wjh.v15.i6.755.
4
Experimental models of fatty liver diseases: Status and appraisal.脂肪性肝病的实验模型:现状与评估。
Hepatol Commun. 2023 Jun 28;7(7). doi: 10.1097/HC9.0000000000000200. eCollection 2023 Jul 1.
5
Targeting the ATF6-Mediated ER Stress Response and Autophagy Blocks Integrin-Driven Prostate Cancer Progression.靶向 ATF6 介导的内质网应激反应和自噬可阻断整合素驱动的前列腺癌进展。
Mol Cancer Res. 2023 Sep 1;21(9):958-974. doi: 10.1158/1541-7786.MCR-23-0108.
6
Current and future treatment for alcoholic-related liver diseases.当前和未来治疗酒精性相关肝病的方法。
J Gastroenterol Hepatol. 2023 Aug;38(8):1218-1226. doi: 10.1111/jgh.16257. Epub 2023 Jun 10.
7
The SLIT/ROBO Pathway in Liver Fibrosis and Cancer.SLIT/ROBO 通路在肝纤维化和癌症中的作用。
Biomolecules. 2023 May 1;13(5):785. doi: 10.3390/biom13050785.
8
Redox states in the endoplasmic reticulum directly regulate the activity of calcium channel, inositol 1,4,5-trisphosphate receptors.内质网中的氧化还原状态直接调节钙通道、肌醇 1,4,5-三磷酸受体的活性。
Proc Natl Acad Sci U S A. 2023 May 30;120(22):e2216857120. doi: 10.1073/pnas.2216857120. Epub 2023 May 22.
9
Integrating stress signals-XBP1 as a novel mediator of intercellular crosstalk in non-alcoholic steatohepatitis.整合应激信号——XBP1作为非酒精性脂肪性肝炎细胞间串扰的新型介质
Transl Gastroenterol Hepatol. 2022 Sep 7;8:13. doi: 10.21037/tgh-22-73. eCollection 2023.
10
Iron overload induces islet β cell ferroptosis by activating ASK1/P-P38/CHOP signaling pathway.铁过载通过激活 ASK1/P-P38/CHOP 信号通路诱导胰岛 β 细胞铁死亡。
PeerJ. 2023 Apr 18;11:e15206. doi: 10.7717/peerj.15206. eCollection 2023.