Eucommia ulmoides Ameliorates Glucotoxicity by Suppressing Advanced Glycation End-Products in Diabetic Mice Kidney

被引:54
作者
Do, Moon Ho [1 ]
Hur, Jinyoung [1 ,2 ]
Choi, Jiwon [1 ]
Kim, Mina [1 ]
Kim, Min Jung [1 ]
Kim, Yoonsook [1 ]
Ha, Sang Keun [1 ,2 ]
机构
[1] Korea Food Res Inst, 245 Nongsaengmyeong Ro, Wanju Gun 55365, Jeollabuk Do, South Korea
[2] Univ Sci & Technol, Div Food Biotechnol, Daejeon 305350, South Korea
来源
NUTRIENTS | 2018年 / 10卷 / 03期
关键词
glucotoxicity; advanced glycation end-product; nuclear factor erythroid 2-related factor 2; glyoxalase; OLIVER LEAF EXTRACT; PROTEIN GLYCATION; GENIPOSIDIC ACID; CULINARY HERBS; GLYOXALASE-I; METHYLGLYOXAL; NEPHROPATHY; INHIBITION; GLUCOSE; CELLS;
D O I
10.3390/nu10030265
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Eucommia ulmoides Oliv. (EU), also known as Du-Zhong, is a medicinal herb commonly used in Asia to treat hypertension and diabetes. Despite evidence of the protective effects of EU against diabetes, its precise effects and mechanisms of action against advanced glycation end-products (AGEs) are unclear. In this study, we evaluated the effects of EU on AGEs-induced renal disease and explored the possible underlying mechanisms using streptozotocin (STZ)-induced diabetic mice. STZ-induced diabetic mice received EU extract (200 mg/kg) orally for 6 weeks. EU treatment did not change blood glucose and glycated hemoglobin (HbA1c) levels in diabetic mice. However, the EU-treated group showed a significant increase in the protein expression and activity of glyoxalase 1 (Glo1), which detoxifies the AGE precursor, methylglyoxal (MGO). EU significantly upregulated nuclear factor erythroid 2-related factor 2 (Nrf2) expression but downregulated that of receptor for AGE (RAGE). Furthermore, histological and immunohistochemical analyses of kidney tissue showed that EU reduced periodic acid -Schiff (PAS)-positive staining, AGEs, and MGO accumulation in diabetic mice. Based on these findings, we concluded that EU ameliorated the renal damage in diabetic mice by inhibiting AGEs formation and RAGE expression and reducing oxidative stress, through the Glo1 and Nrf2 pathways.
引用
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页数:13
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