文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

天然产物治疗对乙酰氨基酚诱导的急性肝损伤:综述。

Natural Products for Acetaminophen-Induced Acute Liver Injury: A Review.

机构信息

School of Medicine, Taizhou University, Taizhou 318000, China.

College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian 116000, China.

出版信息

Molecules. 2023 Dec 1;28(23):7901. doi: 10.3390/molecules28237901.


DOI:10.3390/molecules28237901
PMID:38067630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10708418/
Abstract

The liver plays a vital role in metabolism, synthesis, and detoxification, but it is susceptible to damage from various factors such as viral infections, drug reactions, excessive alcohol consumption, and autoimmune diseases. This susceptibility is particularly problematic for patients requiring medication, as drug-induced liver injury often leads to underestimation, misdiagnosis, and difficulties in treatment. Acetaminophen (APAP) is a widely used and safe drug in therapeutic doses but can cause liver toxicity when taken in excessive amounts. This study aimed to investigate the hepatotoxicity of APAP and explore potential treatment strategies using a mouse model of APAP-induced liver injury. The study involved the evaluation of various natural products for their therapeutic potential. The findings revealed that natural products demonstrated promising hepatoprotective effects, potentially alleviating liver damage and improving liver function through various mechanisms such as oxidative stress and inflammation, which cause changes in signaling pathways. These results underscore the importance of exploring novel treatment options for drug-induced liver injury, suggesting that further research in this area could lead to the development of effective preventive and therapeutic interventions, ultimately benefiting patients with liver injury caused by medicine.

摘要

肝脏在新陈代谢、合成和解毒中起着至关重要的作用,但它容易受到各种因素的损害,如病毒感染、药物反应、过量饮酒和自身免疫性疾病。这种易感性对需要药物治疗的患者来说尤其成问题,因为药物性肝损伤常常导致低估、误诊和治疗困难。对乙酰氨基酚(APAP)在治疗剂量下是一种广泛使用且安全的药物,但过量服用会导致肝毒性。本研究旨在使用 APAP 诱导的肝损伤小鼠模型研究 APAP 的肝毒性,并探讨潜在的治疗策略。该研究涉及评估各种天然产物的治疗潜力。研究结果表明,天然产物具有有希望的肝保护作用,可能通过氧化应激和炎症等导致信号通路改变的各种机制减轻肝损伤和改善肝功能。这些结果强调了探索药物性肝损伤新的治疗选择的重要性,表明该领域的进一步研究可能会导致开发有效的预防和治疗干预措施,最终使因药物导致肝损伤的患者受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/4453c48332af/molecules-28-07901-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/aea4b0b3f107/molecules-28-07901-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/27ad344f39c5/molecules-28-07901-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/d25cf3ade595/molecules-28-07901-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/2b16be7c4a82/molecules-28-07901-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/4453c48332af/molecules-28-07901-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/aea4b0b3f107/molecules-28-07901-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/27ad344f39c5/molecules-28-07901-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/d25cf3ade595/molecules-28-07901-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/2b16be7c4a82/molecules-28-07901-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/10708418/4453c48332af/molecules-28-07901-g005.jpg

相似文献

[1]
Natural Products for Acetaminophen-Induced Acute Liver Injury: A Review.

Molecules. 2023-12-1

[2]
Activation of Farnesoid X Receptor by Schaftoside Ameliorates Acetaminophen-Induced Hepatotoxicity by Modulating Oxidative Stress and Inflammation.

Antioxid Redox Signal. 2020-7-10

[3]
Shikonin attenuates acetaminophen-induced acute liver injury via inhibition of oxidative stress and inflammation.

Biomed Pharmacother. 2019-2-25

[4]
Pectolinarigenin ameliorates acetaminophen-induced acute liver injury via attenuating oxidative stress and inflammatory response in Nrf2 and PPARa dependent manners.

Phytomedicine. 2023-5

[5]
Paeoniflorin Protects against Acetaminophen-Induced Liver Injury in Mice via JNK Signaling Pathway.

Molecules. 2022-12-4

[6]
Auriculatone Sulfate Effectively Protects Mice Against Acetaminophen-Induced Liver Injury.

Molecules. 2019-10-9

[7]
Veronica persica ameliorates acetaminophen-induced murine hepatotoxicity via attenuating oxidative stress and inflammation.

Biomed Pharmacother. 2023-12-31

[8]
Hepatoprotective effects of berberine on acetaminophen-induced hepatotoxicity in mice.

Biomed Pharmacother. 2018-5-7

[9]
Autophagy and acetaminophen-induced hepatotoxicity.

Arch Toxicol. 2018-6-6

[10]
Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury.

Int J Mol Sci. 2018-11-28

引用本文的文献

[1]
Salvianolic Acid B Attenuates Liver Fibrosis via Suppression of Glycolysis-Dependent m1 Macrophage Polarization.

Curr Issues Mol Biol. 2025-7-29

[2]
Lactate Metabolism and Lactylation Modification: New Opportunities and Challenges in Cardiovascular Disease.

MedComm (2020). 2025-7-1

[3]
Salvianolic Acid B Alleviates Liver Injury by Regulating Lactate-Mediated Histone Lactylation in Macrophages.

Molecules. 2024-1-1

本文引用的文献

[1]
Leonurine alleviates acetaminophen-induced acute liver injury by regulating the PI3K/AKT signaling pathway in mice.

Int Immunopharmacol. 2023-7

[2]
The E3 ubiquitin ligase NEDD4-1 protects against acetaminophen-induced liver injury by targeting VDAC1 for degradation.

Acta Pharm Sin B. 2023-4

[3]
Evaluation of Hepatoprotective and Gastroprotective Activities of Paspalidium flavidum Leaves Extract in Experimental Animal Models.

Cell Mol Biol (Noisy-le-grand). 2022-9-30

[4]
Salvianolic Acid A Protects against Acetaminophen-Induced Hepatotoxicity via Regulation of the miR-485-3p/SIRT1 Pathway.

Antioxidants (Basel). 2023-4-3

[5]
Liberation of daidzein by gut microbial β-galactosidase suppresses acetaminophen-induced hepatotoxicity in mice.

Cell Host Microbe. 2023-5-10

[6]
IL-33/ST2 antagonizes STING signal transduction via autophagy in response to acetaminophen-mediated toxicological immunity.

Cell Commun Signal. 2023-4-20

[7]
Acetaminophen-induced liver injury: Molecular mechanism and treatments from natural products.

Front Pharmacol. 2023-3-27

[8]
P2rx1 deficiency alleviates acetaminophen-induced acute liver failure by regulating the STING signaling pathway.

Cell Biol Toxicol. 2023-12

[9]
Circulating Cell-Free DNAs as a Biomarker and Therapeutic Target for Acetaminophen-Induced Liver Injury.

Adv Sci (Weinh). 2023-6

[10]
Hepatoprotective effect of methanol extract of Agave americana leaves on paracetamol induced hepatotoxicity in Wistar albino rats.

BMC Complement Med Ther. 2023-4-1

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索