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Res Pharm Sci. 2025 Jun 17;20(3):434-444. doi: 10.4103/RPS.RPS_220_24. eCollection 2025 Jun.
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Food Sci Nutr. 2025 Mar 4;13(3):e70073. doi: 10.1002/fsn3.70073. eCollection 2025 Mar.
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A healthier approach to clinical trials evaluating resveratrol for primary prevention of age‐related diseases in healthy populations.一种更健康的临床试验方法,用于评估白藜芦醇对健康人群原发性预防与年龄相关疾病的作用。
Aging (Albany NY). 2013 Jul;5(7):495-506. doi: 10.18632/aging.100579.
2
Current role of fenofibrate in the prevention and management of non-alcoholic fatty liver disease.非诺贝特在非酒精性脂肪性肝病预防和管理中的当前作用。
World J Hepatol. 2013 Sep 27;5(9):470-8. doi: 10.4254/wjh.v5.i9.470.
3
Effects of resveratrol on obesity-related inflammation markers in adipose tissue of genetically obese rats.白藜芦醇对遗传性肥胖大鼠脂肪组织中肥胖相关炎症标志物的影响。
Nutrition. 2013 Nov-Dec;29(11-12):1374-80. doi: 10.1016/j.nut.2013.04.014. Epub 2013 Sep 5.
4
Resveratrol modulates autophagy and NF-κB activity in a murine model for treating non-alcoholic fatty liver disease.白藜芦醇在治疗非酒精性脂肪肝病的小鼠模型中调节自噬和 NF-κB 活性。
Food Chem Toxicol. 2014 Jan;63:166-73. doi: 10.1016/j.fct.2013.08.036. Epub 2013 Aug 24.
5
Probiotics as a novel treatment for non-alcoholic Fatty liver disease; a systematic review on the current evidences.益生菌作为非酒精性脂肪性肝病的一种新型治疗方法:对当前证据的系统评价
Hepat Mon. 2013 Apr 9;13(4):e7233. doi: 10.5812/hepatmon.7233. Print 2013 Apr.
6
Emerging drugs for non-alcoholic steatohepatitis.非酒精性脂肪性肝炎的新兴药物。
Expert Opin Emerg Drugs. 2013 Sep;18(3):279-90. doi: 10.1517/14728214.2013.811232. Epub 2013 Jul 13.
7
Resveratrol suppresses PAI-1 gene expression in a human in vitro model of inflamed adipose tissue.白藜芦醇可抑制人炎症性脂肪组织体外模型中 PAI-1 基因的表达。
Oxid Med Cell Longev. 2013;2013:793525. doi: 10.1155/2013/793525. Epub 2013 Jun 2.
8
The effects of chronic AMPK activation on hepatic triglyceride accumulation and glycerol 3-phosphate acyltransferase activity with high fat feeding.高脂喂养时慢性 AMPK 激活对肝甘油三酯积累和甘油-3-磷酸酰基转移酶活性的影响。
Diabetol Metab Syndr. 2013 May 31;5:29. doi: 10.1186/1758-5996-5-29. eCollection 2013.
9
Melatonin attenuates high fat diet-induced fatty liver disease in rats.褪黑素可减轻高脂饮食诱导的大鼠脂肪肝疾病。
World J Hepatol. 2013 Apr 27;5(4):160-9. doi: 10.4254/wjh.v5.i4.160.
10
Resveratrol suppresses T0901317-induced hepatic fat accumulation in mice.白藜芦醇抑制 T0901317 诱导的小鼠肝脂肪堆积。
AAPS J. 2013 Jul;15(3):744-52. doi: 10.1208/s12248-013-9473-7. Epub 2013 Apr 17.

白藜芦醇在实验性和临床非酒精性脂肪性肝病中的作用

Effects of resveratrol in experimental and clinical non-alcoholic fatty liver disease.

作者信息

Heebøll Sara, Thomsen Karen Louise, Pedersen Steen B, Vilstrup Hendrik, George Jacob, Grønbæk Henning

机构信息

Sara Heebøll, Karen Louise Thomsen, Hendrik Vilstrup, Henning Grønbæk, Department of Hepatology and Gastroenterology, Aarhus University Hospital, 8000 Aarhus C, Denmark.

出版信息

World J Hepatol. 2014 Apr 27;6(4):188-98. doi: 10.4254/wjh.v6.i4.188.

DOI:10.4254/wjh.v6.i4.188
PMID:24799987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4009474/
Abstract

The prevalence of obesity and related conditions like non-alcoholic fatty liver disease (NAFLD) is increasing worldwide and therapeutic options are limited. Alternative treatment options are therefore intensively sought after. An interesting candidate is the natural polyphenol resveratrol (RSV) that activates adenosinmonophosphate-activated protein kinase (AMPK) and silent information regulation-2 homolog 1 (SIRT1). In addition, RSV has known anti-oxidant and anti-inflammatory effects. Here, we review the current evidence for RSV-mediated effects on NAFLD and address the different aspects of NAFLD and non-alcoholic steatohepatitis (NASH) pathogenesis with respect to free fatty acid (FFA) flux from adipose tissue, hepatic de novo lipogenesis, inadequate FFA β-oxidation and additional intra- and extrahepatic inflammatory and oxidant hits. We review the in vivo evidence from animal studies and clinical trials. The abundance of animal studies reports a decrease in hepatic triglyceride accumulation, liver weight and a general improvement in histological fatty liver changes, along with a reduction in circulating insulin, glucose and lipid levels. Some studies document AMPK or SIRT1 activation, and modulation of relevant markers of hepatic lipogenesis, inflammation and oxidation status. However, AMPK/SIRT1-independent actions are also likely. Clinical trials are scarce and have primarily been performed with a focus on overweight/obese participants without a focus on NAFLD/NASH and histological liver changes. Future clinical studies with appropriate design are needed to clarify the true impact of RSV treatment in NAFLD/NASH patients.

摘要

肥胖及非酒精性脂肪性肝病(NAFLD)等相关疾病在全球范围内的患病率正在上升,而治疗选择却很有限。因此,人们正在积极寻找替代治疗方案。一种有趣的候选物质是天然多酚白藜芦醇(RSV),它可激活腺苷单磷酸激活的蛋白激酶(AMPK)和沉默信息调节因子2同源物1(SIRT1)。此外,RSV还具有已知的抗氧化和抗炎作用。在此,我们综述了目前关于RSV对NAFLD影响的证据,并从脂肪组织中游离脂肪酸(FFA)通量、肝脏从头脂肪生成、FFAβ氧化不足以及肝内外额外的炎症和氧化应激等方面探讨了NAFLD和非酒精性脂肪性肝炎(NASH)发病机制的不同方面。我们回顾了动物研究和临床试验的体内证据。大量动物研究报告显示,肝脏甘油三酯积累减少、肝脏重量减轻、组织学脂肪肝变化总体改善,同时循环胰岛素、葡萄糖和脂质水平降低。一些研究记录了AMPK或SIRT1的激活以及肝脏脂肪生成、炎症和氧化状态相关标志物的调节。然而,也可能存在不依赖AMPK/SIRT1的作用。临床试验很少,主要针对超重/肥胖参与者进行,而没有关注NAFLD/NASH和肝脏组织学变化。需要进行设计合理的未来临床研究,以阐明RSV治疗对NAFLD/NASH患者的真正影响。