Abstract
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.
Highlights
A prevalence of type 2 diabetes mellitus and a high body mass index in cryptogenic cirrhosis may imply that obesity leads to cirrhosis [1,2]
hepatic stellate cells (HSCs) are a major source of extracellular matrix (ECM), and during fibrogenesis, they undergo an activation process that is characterized by increased proliferation and collagen synthesis
We examined the influence of Ecklonia cava extract (ECE) on high glucose-induced HSC activation and found that ECE suppressed the activation by decreasing the production of reactive oxygen species (ROS) and transforming growth factor-β (TGF-β)
Summary
A prevalence of type 2 diabetes mellitus and a high body mass index in cryptogenic cirrhosis may imply that obesity leads to cirrhosis [1,2]. It has been shown that an induction of collagen gene expression in renal fibroblasts by high glucose levels is one of the mechanisms of diabetic nephropathy. Hyperglycemia has been shown to be functionally related to fibrogenesis in a model of diabetic nephropathy in which the progressive accumulation of extracellular matrix (ECM) components was observed in the glomerular mesangium and tubulointerstitium [5]. It is important to establish an in vitro model of diabetic fibrosis with HSCs to clarify the mechanism of high glucose-induced fibrogenesis in nonalcoholic steatohepatitis (NASH).
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