دورية أكاديمية

Impact of 3-Amino-1,2,4-Triazole (3-AT)- Derived Increase in Hydrogen Peroxide Levels on Inflammation and Metabolism in Human Differentiated Adipocytes.

التفاصيل البيبلوغرافية
العنوان: Impact of 3-Amino-1,2,4-Triazole (3-AT)- Derived Increase in Hydrogen Peroxide Levels on Inflammation and Metabolism in Human Differentiated Adipocytes.
المؤلفون: Ruiz-Ojeda, Francisco Javier1, Gomez-Llorente, Carolina1,2,3, Aguilera, Concepción María1,2,3, Gil, Angel1,2,3, Rupérez, Azahara Iris1 azahararuperez@ugr.es
المصدر: PLoS ONE. 3/29/2016, Vol. 11 Issue 3, p1-20. 20p.
مصطلحات موضوعية: *OBESITY, *ADIPOSE tissues, *OXIDATIVE stress, *INFLAMMATION, *GENE expression
مستخلص: Obesity is characterized by an excessive accumulation of fat in adipose tissue, which is associated with oxidative stress and chronic inflammation. Excessive H2O2 levels are degraded by catalase (CAT), the activity of which is decreased in obesity. We investigated the effects of inhibition of catalase activity on metabolism and inflammation by incubating human differentiated adipocytes with 10 mM 3-amino-1,2,4-triazole (3-AT) for 24 h. As expected, the treatment decreased CAT activity and increased intracellular H2O2 levels significantly. Glutathione peroxidase (GPX) activity was also reduced, and the gene expression levels of the antioxidant enzymes GPX4 and peroxiredoxins (1, 3 and 5) were inhibited. Interestingly, this occurred along with lower mRNA levels of the transcription factors nuclear factor (erythroid 2-like 2) and forkhead box O, which are involved in redox homeostasis. However, superoxide dismutase activity and expression were increased. Moreover, 3-AT led to nuclear factor kappa-light-chain-enhancer of activated B cells (NF-®B) activation and increased tumor necrosis alpha and interleukin 6 protein and gene expression levels, while lowering peroxisome proliferator-activated receptor gamma (PPAR?) mRNA and protein levels. These alterations were accompanied by an altered glucose and lipid metabolism. Indeed, adipocytes treated with 3-AT showed reduced basal glucose uptake, reduced glucose transporter type 4 gene and protein expression, reduced lipolysis, reduced AMP-activated protein kinase activation and reduced gene expression of lipases. Our results indicate that increased H2O2 levels caused by 3-AT treatment impair the antioxidant defense system, lower PPAR? expression and initiate inflammation, thus affecting glucose and lipid metabolism in human differentiated adipocytes. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0152550