Spatholobus suberectus Ameliorates Diabetes-Induced Renal Damage by Suppressing Advanced Glycation End Products in db/db Mice

被引:39
作者
Do, Moon Ho [1 ]
Hur, Jinyoung [1 ,2 ]
Choi, Jiwon [1 ]
Kim, Yoonsook [1 ]
Park, Ho-Young [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
关键词
advanced glycation end products (AGEs); diabetic nephropathy; nuclear factor erythroid 2-related factor 2 (Nrf2); glyoxalase 1 (Glo1); Spatholobus suberectus; INTENSIVE TREATMENT; DISEASE; RAGE; DYSLIPIDEMIA; EXPRESSION; MELLITUS; RECEPTOR; IMPROVES; CELLS; AGE;
D O I
10.3390/ijms19092774
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Spatholobus suberectus (SS) is a medicinal herb commonly used in Asia to treat anemia, menoxenia and rheumatism. However, its effect of diabetes-induced renal damage and mechanisms of action against advanced glycation end-products (AGEs) are unclear. In this study, we evaluated the effects of SS on diabetes-induced renal damage and explored the possible underlying mechanisms using db/db type 2 diabetes mice. db/db mice were administered SS extract (50 mg/kg) orally for 6 weeks. SS-treated group did not change body weight, blood glucose and glycated hemoglobin (HbA1c) levels. However, SS treatment reversed diabetes-induced dyslipidemia and urinary albumin/creatinine ratio in db/db mice. Moreover, SS administration showed significantly increased protein expression of nuclear factor erythroid 2-related factor 2 (Nrf2), which is a transcription factor for antioxidant enzyme. SS significantly upregulated glyoxalase 1 (Glo1) and NADPH quinine oxidoreductase 1 (NQO1) expression but reduced CML accumulation and downregulated receptor for AGEs (RAGE). Furthermore, SS showed significant decrease of periodic acid-Schiff (PAS)-positive staining and AGEs accumulation in histological and immunohistochemical analyses of kidney tissues. Taken together, we concluded that SS ameliorated the renal damage by inhibiting diabetes-induced glucotoxicity, dyslipidemia and oxidative stress, through the Nrf2/antioxidant responsive element (ARE) stress-response system.
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页数:13
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