Heebøll Sara, Thomsen Karen Louise, Pedersen Steen B, Vilstrup Hendrik, George Jacob, Grønbæk Henning
Sara Heebøll, Karen Louise Thomsen, Hendrik Vilstrup, Henning Grønbæk, Department of Hepatology and Gastroenterology, Aarhus University Hospital, 8000 Aarhus C, Denmark.
World J Hepatol. 2014 Apr 27;6(4):188-98. doi: 10.4254/wjh.v6.i4.188.
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.
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。