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Sirtuin1 在肝损伤中的作用:分子机制和新的治疗靶点。

The role of sirtuin1 in liver injury: molecular mechanisms and novel therapeutic target.

机构信息

Department of Medical Instrumental Analysis, Zunyi Medical University, Zunyi, Guizhou, China.

Department of Infectious Diseases, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.

出版信息

PeerJ. 2024 Mar 29;12:e17094. doi: 10.7717/peerj.17094. eCollection 2024.


DOI:10.7717/peerj.17094
PMID:38563003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10984179/
Abstract

Liver disease is a common and serious threat to human health. The progression of liver diseases is influenced by many physiologic processes, including oxidative stress, inflammation, bile acid metabolism, and autophagy. Various factors lead to the dysfunction of these processes and basing on the different pathogeny, pathology, clinical manifestation, and pathogenesis, liver diseases are grouped into different categories. Specifically, Sirtuin1 (SIRT1), a member of the sirtuin protein family, has been extensively studied in the context of liver injury in recent years and are confirmed the significant role in liver disease. SIRT1 has been found to play a critical role in regulating key processes in liver injury. Further, SIRT1 seems to cause divers outcomes in different types of liver diseases. Recent studies have showed some therapeutic strategies involving modulating SIRT1, which may bring a novel therapeutic target. To elucidate the mechanisms underlying the role of sirtuin1 in liver injury and its potentiality as a therapeutic target, this review outlines the key signaling pathways associated with sirtuin1 and liver injury, and discusses recent advances in therapeutic strategies targeting sirtuin1 in liver diseases.

摘要

肝脏疾病是人类健康的常见且严重的威胁。肝脏疾病的进展受到许多生理过程的影响,包括氧化应激、炎症、胆汁酸代谢和自噬。各种因素导致这些过程的功能障碍,基于不同的病因、病理、临床表现和发病机制,肝脏疾病被分为不同的类别。具体来说,Sirtuin1(SIRT1)是 sirtuin 蛋白家族的一员,近年来在肝脏损伤方面的研究中得到了广泛的研究,并被证实对肝脏疾病具有重要作用。SIRT1 被发现对肝脏损伤的关键过程具有调节作用。此外,SIRT1 在不同类型的肝脏疾病中似乎导致了不同的结果。最近的研究表明,一些涉及调节 SIRT1 的治疗策略可能为肝脏疾病提供新的治疗靶点。为了阐明 SIRT1 在肝脏损伤中的作用机制及其作为治疗靶点的潜力,本综述概述了与 SIRT1 和肝脏损伤相关的关键信号通路,并讨论了针对肝脏疾病中 SIRT1 的治疗策略的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/23121de2072c/peerj-12-17094-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/a069e85197cb/peerj-12-17094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/8d9d78b09592/peerj-12-17094-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/7cd9befe87cf/peerj-12-17094-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/5176b74e389e/peerj-12-17094-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/23121de2072c/peerj-12-17094-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/a069e85197cb/peerj-12-17094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/8d9d78b09592/peerj-12-17094-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/7cd9befe87cf/peerj-12-17094-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/5176b74e389e/peerj-12-17094-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7cd/10984179/23121de2072c/peerj-12-17094-g005.jpg

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本文引用的文献

[1]
Anti-miR-873-5p improves alcohol-related liver disease by enhancing hepatic deacetylation via SIRT1.

JHEP Rep. 2023-9-30

[2]
Aging aggravates liver fibrosis through downregulated hepatocyte SIRT1-induced liver sinusoidal endothelial cell dysfunction.

Hepatol Commun. 2024-1-1

[3]
Sirtuin 1 alleviates alcoholic liver disease by inhibiting HMGB1 acetylation and translocation.

PeerJ. 2023

[4]
SIRT1 regulates hepatocyte programmed cell death via GSDME - IL18 axis in human and mouse liver transplantation.

Cell Death Dis. 2023-11-23

[5]
Ethanol Extract of Ameliorates Acetaminophen-Induced Liver Injury via Upregulating Sirt1 and Subsequent Potentiation of LKB1/AMPK/Nrf2 Cascade in Hepatocytes.

Molecules. 2023-10-28

[6]
Pioglitazone attenuates tamoxifen-induced liver damage in rats via modulating Keap1/Nrf2/HO-1 and SIRT1/Notch1 signaling pathways: In-vivo investigations, and molecular docking analysis.

Mol Biol Rep. 2023-12

[7]
Tributyrin Mitigates Ethanol-Induced Lysine Acetylation of Histone-H3 and p65-NFκB Downregulating CCL2 Expression and Consequent Liver Inflammation and Injury.

Nutrients. 2023-10-17

[8]
Sinensetin Attenuated Macrophagic NLRP3 Inflammasomes Formation SIRT1-NRF2 Signaling.

ACS Omega. 2023-9-7

[9]
Pachymic acid protects hepatic cells against oxygen-glucose deprivation/reperfusion injury by activating sirtuin 1 to inhibit HMGB1 acetylation and inflammatory signaling.

Chin J Physiol. 2023

[10]
The Potential Effects of Quercetin-Loaded Nanoliposomes on Amoxicillin/Clavulanate-Induced Hepatic Damage: Targeting the SIRT1/Nrf2/NF-κB Signaling Pathway and Microbiota Modulation.

Antioxidants (Basel). 2023-7-25

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