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Inhibitory Effects of Ecklonia cava Extract on High Glucose-Induced Hepatic Stellate Cell Activation

机译:Ecklonia cava提取物对高糖诱导的肝星状细胞活化的抑制作用

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摘要

Nonalcoholic steatohepatitis (NASH) is a disease closely associated with obesity and diabetes. A prevalence of type 2 diabetes and a high body mass index in cryptogenic cirrhosis may imply that obesity leads to cirrhosis. Here, we examined the effects of an extract of Ecklonia cava, a brown algae, on the activation of high glucose-induced hepatic stellate cells (HSCs), key players in hepatic fibrosis. Isolated HSCs were incubated with or without a high glucose concentration. Ecklonia cava extract (ECE) was added to the culture simultaneously with the high glucose. Treatment with high glucose stimulated expression of type I collagen and α-smooth muscle actin, which are markers of activation in HSCs, in a dose-dependent manner. The activation of high glucose-treated HSCs was suppressed by the ECE. An increase in the formation of intracellular reactive oxygen species (ROS) and a decrease in intracellular glutathione levels were observed soon after treatment with high glucose, and these changes were suppressed by the simultaneous addition of ECE. High glucose levels stimulated the secretion of bioactive transforming growth factor-β (TGF-β) from the cells, and the stimulation was also suppressed by treating the HSCs with ECE. These results suggest that the suppression of high glucose-induced HSC activation by ECE is mediated through the inhibition of ROS and/or GSH and the downregulation of TGF-β secretion. ECE is useful for preventing the development of diabetic liver fibrosis.
机译:非酒精性脂肪性肝炎(NASH)是与肥胖和糖尿病密切相关的疾病。隐源性肝硬化的2型糖尿病患病率和高体重指数可能暗示肥胖会导致肝硬化。在这里,我们检查了褐藻海藻Ecklonia cava提取物对高糖诱导的肝星状细胞(HSC)(肝纤维化的关键参与者)的激活的影响。在有或没有高葡萄糖浓度的情况下孵育分离的HSC。 Ecklonia cava提取物(ECE)与高葡萄糖同时加入培养物中。用高葡萄糖治疗以剂量依赖的方式刺激了I型胶原蛋白和α-平滑肌肌动蛋白的表达,这是HSCs激活的标志。 ECE抑制了高葡萄糖处理的HSC的活化。在用高葡萄糖处理后不久,观察到细胞内反应性氧(ROS)形成的增加和细胞内谷胱甘肽水平的降低,并且通过同时添加ECE抑制了这些变化。高葡萄糖水平刺激了细胞分泌生物活性转化生长因子-β(TGF-β),并且通过用ECE处理HSC也抑制了刺激。这些结果表明,通过抑制ROS和/或GSH以及下调TGF-β的分泌来介导ECE对高葡萄糖诱导的HSC活化的抑制。 ECE可用于预防糖尿病性肝纤维化的发展。

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