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本文引用的文献

1
Alcoholic liver disease and the gut-liver axis.酒精性肝病与肠-肝轴。
World J Gastroenterol. 2010 Mar 21;16(11):1321-9. doi: 10.3748/wjg.v16.i11.1321.
2
The role of zinc deficiency in alcohol-induced intestinal barrier dysfunction.锌缺乏在酒精诱导的肠道屏障功能障碍中的作用。
Am J Physiol Gastrointest Liver Physiol. 2010 May;298(5):G625-33. doi: 10.1152/ajpgi.00350.2009. Epub 2010 Feb 18.
3
AMPK and SIRT1: a long-standing partnership?AMPK 与 SIRT1:长期的合作关系?
Am J Physiol Endocrinol Metab. 2010 Apr;298(4):E751-60. doi: 10.1152/ajpendo.00745.2009. Epub 2010 Jan 26.
4
Global burden of disease and injury and economic cost attributable to alcohol use and alcohol-use disorders.饮酒及酒精使用障碍所致的全球疾病负担、伤害及经济成本。
Lancet. 2009 Jun 27;373(9682):2223-33. doi: 10.1016/S0140-6736(09)60746-7.
5
Signalling pathways in alcohol-induced liver inflammation.酒精性肝炎症中的信号通路。
J Hepatol. 2009 Jun;50(6):1258-66. doi: 10.1016/j.jhep.2009.03.007. Epub 2009 Mar 28.
6
Alphavbeta3-targeted nanotherapy suppresses inflammatory arthritis in mice.靶向αvβ3的纳米疗法可抑制小鼠的炎性关节炎。
FASEB J. 2009 Sep;23(9):2978-85. doi: 10.1096/fj.09-129874. Epub 2009 Apr 17.
7
Redox regulation of tumor necrosis factor signaling.肿瘤坏死因子信号的氧化还原调节。
Antioxid Redox Signal. 2009 Sep;11(9):2245-63. doi: 10.1089/ars.2009.2611.
8
Pentoxifylline versus prednisolone for severe alcoholic hepatitis: a randomized controlled trial.己酮可可碱与泼尼松龙治疗重症酒精性肝炎的随机对照试验
World J Gastroenterol. 2009 Apr 7;15(13):1613-9. doi: 10.3748/wjg.15.1613.
9
Fibrin accumulation plays a critical role in the sensitization to lipopolysaccharide-induced liver injury caused by ethanol in mice.纤维蛋白积累在小鼠中乙醇所致对脂多糖诱导肝损伤的致敏作用中起关键作用。
Hepatology. 2009 May;49(5):1545-53. doi: 10.1002/hep.22847.
10
PGC-1alpha, SIRT1 and AMPK, an energy sensing network that controls energy expenditure.PGC-1α、SIRT1和AMPK,一个控制能量消耗的能量感应网络。
Curr Opin Lipidol. 2009 Apr;20(2):98-105. doi: 10.1097/MOL.0b013e328328d0a4.

酒精性肝病的发病机制和细胞信号转导。

Mechanisms and cell signaling in alcoholic liver disease.

机构信息

Department of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, KY 40292, USA.

出版信息

Biol Chem. 2010 Nov;391(11):1249-64. doi: 10.1515/BC.2010.137.

DOI:10.1515/BC.2010.137
PMID:20868231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3755482/
Abstract

Alcoholic liver disease (ALD) remains a major cause of morbidity and mortality worldwide. For example, the Veterans Administration Cooperative Studies reported that patients with cirrhosis and superimposed alcoholic hepatitis had a 4-year mortality of >60%. The poor prognosis of ALD implies that preventing disease progression would be more effective than treating end-stage liver disease. An obvious avenue of prevention would be to remove the damaging agent; however, the infamously high rate of recidivism in alcoholics makes maintaining abstinence a difficult treatment goal to prevent ALD. Indeed, although the progression of ALD is well-characterized, there is no universally accepted therapy available to halt or reverse this process in humans. With better understanding of the mechanism(s) and risk factors that mediate the initiation and progression of ALD, rational targeted therapy can be developed to treat or prevent ALD. The purpose of this review is to summarize the established and proposed mechanisms by which chronic alcohol abuse damages the liver and to highlight key signaling events known or hypothesized to mediate these effects.

摘要

酒精性肝病(ALD)仍然是全球发病率和死亡率的主要原因。例如,退伍军人管理局合作研究报告称,患有肝硬化和叠加性酒精性肝炎的患者 4 年死亡率>60%。ALD 的预后不良意味着预防疾病进展将比治疗终末期肝病更有效。一个明显的预防途径是去除致病因子;然而,酗酒者复发率极高,这使得保持戒酒成为预防 ALD 的一个困难治疗目标。事实上,尽管 ALD 的进展已经得到很好的描述,但目前还没有被广泛接受的疗法可以阻止或逆转人类的这一过程。通过更好地了解介导 ALD 发生和进展的机制和风险因素,可以开发合理的靶向治疗来治疗或预防 ALD。本文综述的目的是总结慢性酒精滥用损害肝脏的既定和提出的机制,并强调已知或假设介导这些效应的关键信号事件。