• 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

丹参通过诱导过氧化物酶体增殖物激活受体α(PPARα)活化及随后的4-羟基壬烯醛(4-HNE)降解来预防小鼠早期酒精性肝病。

Danshen protects against early-stage alcoholic liver disease in mice via inducing PPARα activation and subsequent 4-HNE degradation.

作者信息

Ding Lei, Wo Like, Du Zhongyan, Tang Lihua, Song Zhenyuan, Dou Xiaobing

机构信息

College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, P. R. China.

Zhejiang Provincial Hospital of Traditional Chinese Medical, Hangzhou, P. R. China.

出版信息

PLoS One. 2017 Oct 11;12(10):e0186357. doi: 10.1371/journal.pone.0186357. eCollection 2017.

DOI:10.1371/journal.pone.0186357
PMID:29020055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5636149/
Abstract

Alcoholic liver disease (ALD) is a type of chronic liver disease caused by long-term heavy ethanol consumption. Danshen is one of the most commonly used substances in traditional Chinese medicine and has been widely used for the treatment of various diseases, and most frequently, the ALD. The current study aims to determine the potential beneficial effect of Danshen administration on ALD and to clarify the underlying molecular mechanisms. Danshen administration improved liver pathologies of ALD, attenuated alcohol-induced increment of hepatic 4-Hydroxynonenal (4-HNE) formation, and prevented hepatic Peroxisome proliferators activated receptor alpha (PPARα) suppression in response to chronic alcohol consumption. Cell culture studies revealed that both hepatoprotective effect and increased intracellular 4-HNE clearance instigated by Danshen supplementation are PPARα-dependent. In conclusion, Danshen administration can protect against ALD via inducing PPARα activation and subsequent 4-HNE degradation.

摘要

酒精性肝病(ALD)是一种由长期大量饮用乙醇引起的慢性肝病。丹参是中药中最常用的药材之一,已被广泛用于治疗各种疾病,其中最常见的是酒精性肝病。本研究旨在确定丹参给药对酒精性肝病的潜在有益作用,并阐明其潜在的分子机制。丹参给药改善了酒精性肝病的肝脏病理,减轻了酒精诱导的肝脏4-羟基壬烯醛(4-HNE)生成增加,并防止了慢性酒精摄入引起的肝脏过氧化物酶体增殖物激活受体α(PPARα)抑制。细胞培养研究表明,丹参补充剂所激发的肝保护作用和细胞内4-HNE清除增加均依赖于PPARα。总之,丹参给药可通过诱导PPARα激活和随后的4-HNE降解来预防酒精性肝病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/0d3389fc7326/pone.0186357.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/445ccb41a1b2/pone.0186357.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/23fc552699d9/pone.0186357.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/5c8a7ebafdf6/pone.0186357.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/996ee3daf448/pone.0186357.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/15e3ecece8c9/pone.0186357.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/0d3389fc7326/pone.0186357.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/445ccb41a1b2/pone.0186357.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/23fc552699d9/pone.0186357.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/5c8a7ebafdf6/pone.0186357.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/996ee3daf448/pone.0186357.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/15e3ecece8c9/pone.0186357.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df7/5636149/0d3389fc7326/pone.0186357.g006.jpg

相似文献

1
Danshen protects against early-stage alcoholic liver disease in mice via inducing PPARα activation and subsequent 4-HNE degradation.丹参通过诱导过氧化物酶体增殖物激活受体α(PPARα)活化及随后的4-羟基壬烯醛(4-HNE)降解来预防小鼠早期酒精性肝病。
PLoS One. 2017 Oct 11;12(10):e0186357. doi: 10.1371/journal.pone.0186357. eCollection 2017.
2
Inhibition of NF-κB activation by 4-hydroxynonenal contributes to liver injury in a mouse model of alcoholic liver disease.4-羟基壬烯醛通过抑制 NF-κB 激活,有助于酒精性肝病小鼠模型中的肝损伤。
Am J Pathol. 2012 Nov;181(5):1702-10. doi: 10.1016/j.ajpath.2012.08.004. Epub 2012 Sep 13.
3
A Biomedical Investigation of the Hepatoprotective Effect of Radix salviae miltiorrhizae and Network Pharmacology-Based Prediction of the Active Compounds and Molecular Targets.丹参保肝作用的生物医学研究及基于网络药理学的活性成分与分子靶点预测
Int J Mol Sci. 2017 Mar 13;18(3):620. doi: 10.3390/ijms18030620.
4
[Synergistic action of 4-hydroxynonenal and tumor necrosis factor involving the NF-kB/IkBa signaling pathway in alcohol-induced liver injury].[4-羟基壬烯醛与肿瘤坏死因子在酒精性肝损伤中涉及核因子κB/核因子κB抑制蛋白α信号通路的协同作用]
Zhonghua Gan Zang Bing Za Zhi. 2013 Oct;21(10):747-52. doi: 10.3760/cma.j.issn.1007-3418.2013.10.007.
5
NIK links inflammation to hepatic steatosis by suppressing PPARα in alcoholic liver disease.NIK 通过抑制酒精性肝病中的 PPARα 将炎症与肝脂肪变性联系起来。
Theranostics. 2020 Feb 18;10(8):3579-3593. doi: 10.7150/thno.40149. eCollection 2020.
6
The hepatic BMAL1/AKT/lipogenesis axis protects against alcoholic liver disease in mice via promoting PPARα pathway.肝 BMAL1/AKT/脂肪生成轴通过促进 PPARα 通路保护小鼠免受酒精性肝病的影响。
Hepatology. 2018 Sep;68(3):883-896. doi: 10.1002/hep.29878. Epub 2018 May 20.
7
Modulation of fatty acid and bile acid metabolism by peroxisome proliferator-activated receptor α protects against alcoholic liver disease.过氧化物酶体增殖物激活受体α对脂肪酸和胆汁酸代谢的调节可预防酒精性肝病。
Alcohol Clin Exp Res. 2014 Jun;38(6):1520-31. doi: 10.1111/acer.12424. Epub 2014 Apr 28.
8
Regulation of NOX/p38 MAPK/PPARα pathways and miR-155 expression by boswellic acids reduces hepatic injury in experimentally-induced alcoholic liver disease mouse model: novel mechanistic insight.桦木酸通过调节 NOX/p38 MAPK/PPARα 通路和 miR-155 的表达减轻实验性酒精性肝病小鼠模型的肝损伤:新的机制见解。
Arch Pharm Res. 2023 Apr;46(4):323-338. doi: 10.1007/s12272-023-01441-6. Epub 2023 Mar 23.
9
Chunggan extract, a traditional herbal formula, ameliorated alcohol-induced hepatic injury in rat model.传统草药配方中肝提取物可改善大鼠模型中酒精诱导的肝损伤。
World J Gastroenterol. 2014 Nov 14;20(42):15703-14. doi: 10.3748/wjg.v20.i42.15703.
10
Monascus-fermented red mold dioscorea protects mice against alcohol-induced liver injury, whereas its metabolites ankaflavin and monascin regulate ethanol-induced peroxisome proliferator-activated receptor-γ and sterol regulatory element-binding transcription factor-1 expression in HepG2 cells.红曲发酵的红曲薯蓣可保护小鼠免受酒精诱导的肝损伤,而其代谢产物红曲黄素和红曲红素可调节乙醇诱导的HepG2细胞中过氧化物酶体增殖物激活受体-γ和甾醇调节元件结合转录因子-1的表达。
J Sci Food Agric. 2018 Mar;98(5):1889-1898. doi: 10.1002/jsfa.8670. Epub 2017 Oct 12.

引用本文的文献

1
The Functional Components and Hepatic Protective Mechanism of Wolfberry Vinegar by Mixed-Culture Fermentation.混合发酵枸杞醋的功能成分及肝脏保护机制
Foods. 2025 Apr 7;14(7):1278. doi: 10.3390/foods14071278.
2
Protective effects of Longhu Rendan on chronic liver injury and fibrosis in mice.龙虎人丹对小鼠慢性肝损伤和肝纤维化的保护作用
Liver Res. 2021 May 9;6(2):93-102. doi: 10.1016/j.livres.2021.05.002. eCollection 2022 Jun.
3
Novel intervention for alcohol-associated liver disease.新型酒精性肝病干预措施。

本文引用的文献

1
[Drug-induced Nonalcoholic Steatohepatitis].
Yakugaku Zasshi. 2016;136(4):579-82. doi: 10.1248/yakushi.15-00264-3.
2
Antioxidant role of glutathione S-transferases: 4-Hydroxynonenal, a key molecule in stress-mediated signaling.谷胱甘肽S-转移酶的抗氧化作用:4-羟基壬烯醛,应激介导信号传导中的关键分子。
Toxicol Appl Pharmacol. 2015 Dec 15;289(3):361-70. doi: 10.1016/j.taap.2015.10.006. Epub 2015 Oct 23.
3
Obesity in a model of gpx4 haploinsufficiency uncovers a causal role for lipid-derived aldehydes in human metabolic disease and cardiomyopathy.在gpx4单倍体不足模型中的肥胖揭示了脂质衍生醛在人类代谢疾病和心肌病中的因果作用。
World J Gastroenterol. 2024 Oct 21;30(39):4308-4312. doi: 10.3748/wjg.v30.i39.4308.
4
Ethyl Acetate Fractions of Bunge (Danshen) Crude Extract Modulate Fibrotic Signals to Ameliorate Diabetic Kidney Injury.Bunge(丹参)粗提物的乙酸乙酯馏分通过调节纤维化信号改善糖尿病肾病损伤。
Int J Mol Sci. 2024 Aug 18;25(16):8986. doi: 10.3390/ijms25168986.
5
Protective Effects of Murray against Acute Alcoholic Liver Disease in Mice via the Nrf2/HO-1/NF-κB Signaling Pathway.通过Nrf2/HO-1/NF-κB信号通路探讨光叶菝葜对小鼠急性酒精性肝病的保护作用
Pharmaceuticals (Basel). 2024 Apr 13;17(4):497. doi: 10.3390/ph17040497.
6
Proteomics reveals the potential mechanism of Tanshinone IIA in promoting the expansion of human bone marrow mesenchymal stem cells.蛋白质组学揭示丹参酮IIA促进人骨髓间充质干细胞增殖的潜在机制。
Regen Ther. 2022 Nov 24;21:560-573. doi: 10.1016/j.reth.2022.11.004. eCollection 2022 Dec.
7
Bge. (Danshen) in the Treating Non-alcoholic Fatty Liver Disease Based on the Regulator of Metabolic Targets.基于代谢靶点调节剂的丹参治疗非酒精性脂肪性肝病
Front Cardiovasc Med. 2022 Apr 22;9:842980. doi: 10.3389/fcvm.2022.842980. eCollection 2022.
8
Comprehensive Analysis of the Expression Profiles of Hepatic lncRNAs in the Mouse Model of Alcoholic Liver Disease.酒精性肝病小鼠模型中肝脏长链非编码RNA表达谱的综合分析
Front Pharmacol. 2021 Jul 29;12:709287. doi: 10.3389/fphar.2021.709287. eCollection 2021.
9
PPARs as Metabolic Sensors and Therapeutic Targets in Liver Diseases.过氧化物酶体增殖物激活受体作为肝脏疾病的代谢传感器和治疗靶点。
Int J Mol Sci. 2021 Aug 2;22(15):8298. doi: 10.3390/ijms22158298.
10
Activation of the AMPK-SIRT1 pathway contributes to protective effects of Salvianolic acid A against lipotoxicity in hepatocytes and NAFLD in mice.AMPK-SIRT1通路的激活有助于丹酚酸A对肝细胞脂毒性及小鼠非酒精性脂肪性肝病的保护作用。
Front Pharmacol. 2020 Nov 30;11:560905. doi: 10.3389/fphar.2020.560905. eCollection 2020.
Mol Metab. 2015 Apr 21;4(6):493-506. doi: 10.1016/j.molmet.2015.04.001. eCollection 2015 Jun.
4
Increased 4-hydroxynonenal protein adducts in male GSTA4-4/PPAR-α double knockout mice enhance injury during early stages of alcoholic liver disease.在酒精性肝病早期阶段,雄性 GSTA4-4/PPAR-α 双重基因敲除小鼠中增加的 4-羟基壬烯醛蛋白加合物增强了损伤。
Am J Physiol Gastrointest Liver Physiol. 2015 Mar 1;308(5):G403-15. doi: 10.1152/ajpgi.00154.2014. Epub 2014 Dec 11.
5
Modulation of fatty acid and bile acid metabolism by peroxisome proliferator-activated receptor α protects against alcoholic liver disease.过氧化物酶体增殖物激活受体α对脂肪酸和胆汁酸代谢的调节可预防酒精性肝病。
Alcohol Clin Exp Res. 2014 Jun;38(6):1520-31. doi: 10.1111/acer.12424. Epub 2014 Apr 28.
6
Activation of peroxisome proliferator activated receptor alpha ameliorates ethanol mediated liver fibrosis in mice.过氧化物酶体增殖物激活受体α的激活可改善乙醇诱导的小鼠肝纤维化。
Lipids Health Dis. 2013 Feb 6;12:11. doi: 10.1186/1476-511X-12-11.
7
Inhibition of NF-κB activation by 4-hydroxynonenal contributes to liver injury in a mouse model of alcoholic liver disease.4-羟基壬烯醛通过抑制 NF-κB 激活,有助于酒精性肝病小鼠模型中的肝损伤。
Am J Pathol. 2012 Nov;181(5):1702-10. doi: 10.1016/j.ajpath.2012.08.004. Epub 2012 Sep 13.
8
Inhibition of hydrogen peroxide signaling by 4-hydroxynonenal due to differential regulation of Akt1 and Akt2 contributes to decreases in cell survival and proliferation in hepatocellular carcinoma cells.由于 Akt1 和 Akt2 的差异调节,4-羟基壬烯醛抑制过氧化氢信号,导致肝癌细胞中细胞存活和增殖减少。
Free Radic Biol Med. 2012 Jul 1;53(1):1-11. doi: 10.1016/j.freeradbiomed.2012.04.021. Epub 2012 May 1.
9
Tanshinones from Chinese medicinal herb Danshen (Salvia miltiorrhiza Bunge) suppress prostate cancer growth and androgen receptor signaling.丹参(丹参)中的丹参酮抑制前列腺癌生长和雄激素受体信号传导。
Pharm Res. 2012 Jun;29(6):1595-608. doi: 10.1007/s11095-012-0670-3. Epub 2012 Jan 27.
10
Interactions of glutathione transferases with 4-hydroxynonenal.谷胱甘肽转移酶与 4-羟基壬烯醛的相互作用。
Drug Metab Rev. 2011 May;43(2):165-78. doi: 10.3109/03602532.2011.558092. Epub 2011 Mar 14.