دورية أكاديمية

Epigallocatechin-3-gallate combined with alpha lipoic acid attenuates high glucose-induced receptor for advanced glycation end products (RAGE) expression in human embryonic kidney cells

التفاصيل البيبلوغرافية
العنوان: Epigallocatechin-3-gallate combined with alpha lipoic acid attenuates high glucose-induced receptor for advanced glycation end products (RAGE) expression in human embryonic kidney cells
المؤلفون: Leu, Jyh-Gang, Lin, Chin-Yao, Jian, Jhin-Hao, Shih, Chin-Yu, Liang, Yao-Jen
المصدر: Anais da Academia Brasileira de Ciências. June 2013 85(2)
بيانات النشر: Academia Brasileira de Ciências, 2013.
سنة النشر: 2013
مصطلحات موضوعية: diabetic nephropathy, receptor of advanced glycation end products, epigallocatechin gallate, alpha lipoic acid, anti-oxidant
الوصف: The anti-oxidant effects of epigallocatechin gallate (EGCG) and alpha lipoic acid (ALA) have been demonstrated in previous studies. The kidney protection effects of EGCG and ALA in patients with kidney injury are still under investigation. The purpose of this study is to investigate the anti-inflammatory and anti-oxidant effects of EGCG and ALA on high glucose-induced human kidney cell damage. EGCG inhibited high glucose(HG)-induced TNF-α and IL-6 production in human embryonic kidney (HEK) cells. Both EGCG and ALA decreased HG-induced receptor of advanced glycation end products (RAGE) mRNA and protein expressions in HEK cells. EGCG and ALA also recovered HG-inhibited superoxide dismutase production and decreased ROS expressions in HEK cells. The synergism of EGCG and ALA was also studied. The effect of EGCG combined with ALA is greater than the effect of EGCG alone in all anti-inflammation and anti-oxidant experiments. Our studies provide a potential therapeutic application of EGCG and ALA in preventing progression of diabetic nephropathy.
نوع الوثيقة: article
وصف الملف: text/html
اللغة: English
تدمد: 0001-3765
DOI: 10.1590/S0001-37652013005000023
URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652013000200745
حقوق: info:eu-repo/semantics/openAccess
رقم الأكسشن: edssci.S0001.37652013000200745
قاعدة البيانات: SciELO
الوصف
تدمد:00013765
DOI:10.1590/S0001-37652013005000023