2013
DOI: 10.3390/ijms141019846
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Development of Nonalcoholic Hepatopathy: Contributions of Oxidative Stress and Advanced Glycation End Products

Abstract: Advanced glycation end products (AGEs) are generated spontaneously in cells; however, under conditions of hyperglycemia and lipid peroxidation, their levels are higher than usual, which contribute to the development of diseases such as the nonalcoholic fatty liver disease (NAFLD). NAFLD is associated with oxidative stress (OS), which is linked to the transition of steatosis to steatohepatitis due to lipid peroxidation. The AGE-receptor interaction in hepatic stellate cells leads to an increase in reactive oxyg… Show more

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Cited by 65 publications
(53 citation statements)
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“…Presence of AGEs has been shown in the liver of patients with non-alcoholic steatohepatitis using immunohistochemical methods, and serum AGE levels were found related with the severity of hepatic disorder (18)(19)(20).…”
Section: Hepatic Diseasesmentioning
confidence: 98%
“…Presence of AGEs has been shown in the liver of patients with non-alcoholic steatohepatitis using immunohistochemical methods, and serum AGE levels were found related with the severity of hepatic disorder (18)(19)(20).…”
Section: Hepatic Diseasesmentioning
confidence: 98%
“…Повреждение (сшивки) матричных белков в почечной ткани; снижение скорости клубочковой фильтрации; нефротоксичность (на примере лабора-торных животных) [24][25][26] Заболевания печени Биохимические изменения в крови; жировое перерождение и цирроз печени (на примере лабораторных животных) [27][28][29] …”
Section: заболевания почекunclassified
“…It is well known that oxidative species favours the glycoxidation reaction of proteins in presence of reducing sugars, thus resulting in AGEs accumulation. In turn, AGEs exert a prooxidant effect compromising antioxidant enzymes activity and mitochondrial functions, thus creating a vicious cycle [81]. In this regard, a very recent study evidenced that fructose feeding activates in rats the so-called AROS axis, featured by the consecutive enhancement in plasma AGEs level -tissue RAGE activation -mitochondrial ROS production, with subsequent intracellular AGEs formation [82].…”
Section: Interference On Mitochondrial Function and Oxidative Stressmentioning
confidence: 99%