RETRACTED: Effect of 2-dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione, isolated from Averrhoa carambola L. (Oxalidaceae) roots, on advanced glycation end-product-mediated renal injury in type 2 diabetic KKAy mice (Retracted Article)

被引:32
|
作者
Zheng, Ni [1 ]
Lin, Xing [1 ]
Wen, Qingwei [1 ]
Kintoko [1 ]
Zhang, Shijun [1 ]
Huang, Jianchun [1 ]
Xu, Xiaohui [1 ]
Huang, Renbin [1 ]
机构
[1] Guangxi Med Univ, Dept Pharmacol, Nanning 530021, Guangxi Zhuang, Peoples R China
基金
中国国家自然科学基金;
关键词
2-Dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione; Diabetic nephropathy; Advanced glycation end products; Transforming growth factor-beta 1; Nuclear factor-kappa B; Renoprotection; OXIDATIVE STRESS; LIPID-PEROXIDATION; IV COLLAGEN; NEPHROPATHY; RECEPTOR; EXTRACT; DISEASE; EXPRESSION; REDUCTION; INDUCTION;
D O I
10.1016/j.toxlet.2013.03.001
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The roots of Averrhoa carambola L. (Oxalidaceae) have a long history of medical use in traditional Chinese medicine for treating diabetes and diabetic nephropathy. 2-Dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione (DMDD) was isolated from the tuberous roots of A. carambola L. The purpose of this study was to investigate the beneficial effect of DMDD on the advanced glycation end-product-mediated renal injury in type 2 diabetic KKAy mice with regard to prove its efficacy by local traditional practitioners in the treatment of kidney frailties in diabetics. KKAy mice were orally administrated DMDD (12.5, 25, 50 mg/kg body weight/d) or aminoguanidine (200 mg/kg body weight/d) for 8 weeks. Hyperglycemia, renal AGE formation, and the expression of related proteins, such as the AGE receptor, nuclear factor-kappa B, transforming growth factor-beta 1, and N-epsilon-(carboxymethyl)lysine, were markedly decreased by DMDD. Diabetes-dependent alterations in proteinuria, serum creatinine, creatinine clearance, and serum urea-N and glomerular mesangial matrix expansion were attenuated after treatment with DMDD for 8 weeks. The activities of superoxide dismutase and glutathione peroxidase, which are reduced in the kidneys of KKAy mice, were enhanced by DMDD. These findings suggest that DMDD may inhibit the progression of diabetic nephropathy and may be a therapeutic agent for regulating several pharmacological targets to treat or prevent of diabetic nephropathy. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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