Administration of Danhong Injection to diabetic db/db mice inhibits the development of diabetic retinopathy and nephropathy

被引:41
作者
Liu, Mengyang [1 ,2 ]
Pan, Quan [1 ,2 ]
Chen, Yuanli [1 ,3 ]
Yang, Xiaoxiao [1 ,2 ]
Zhao, Buchang [4 ]
Jia, Lifu [4 ]
Zhu, Yan [5 ]
Zhang, Boli [5 ]
Gao, Xiumei [5 ]
Li, Xiaoju [2 ]
Han, Jihong [1 ,3 ]
Duan, Yajun [1 ,3 ]
机构
[1] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
[3] Nankai Univ, Collaborat Innovat Ctr Biotherapy, Tianjin 300071, Peoples R China
[4] Buchang Pharmaceut Co Ltd, Xian 712000, Peoples R China
[5] Tianjin Univ Tradit Chinese Med, Tianjin 300193, Peoples R China
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
美国国家科学基金会;
关键词
GLYCATION END-PRODUCTS; GROWTH-FACTOR; INSULIN-SENSITIVITY; SALVIANOLIC ACID; LITHOSPERMATE-B; HIGH GLUCOSE; ACTIVATION; RECEPTOR; LIVER; CELLS;
D O I
10.1038/srep11219
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Danhong Injection (DHI), a Chinese medicine for treatment of patients with coronary heart disease, inhibits primary abdominal aortic aneurysms in apoE deficient (apoE(-/-)) mice. Formation of microaneurysms plays an important role in the development of diabetic retinopathy and nephropathy. It remains unknown if DHI can reduce these diabetic complications. In this study, diabetic db/db mice in two groups were injected with saline and DHI, respectively, for 14 weeks. Blood and tissue samples were collected to determine serum glucose, lipids and tissue structure. DHI reduced diabetes-induced body weight gain, serum cholesterol and glucose levels. In retinas, DHI blocked the shrink of whole retina and retinal sub-layers by inhibiting expression of caspase 3, matrix metalloproteinase 2 (MMP-2) and MMP-9, accumulation of carbohydrate macromolecules and formation of acellular capillaries. DHI improved renal functions by inhibiting mesangial matrix expansion, expression of vascular endothelial growth factor A, fibronectin and advanced glycation end products in kidneys. Mechanistically, DHI induced expression of glucokinase, AMPK alpha/phosphorylated AMPK alpha, insulin receptor substrate 1, fibroblast growth factor 21 and peroxisome proliferator-activated.. Expression of genes responsible for energy expenditure was also activated by DHI. Therefore, DHI inhibits diabetic retinopathy and nephropathy by ameliorating glucose metabolism and demonstrates a potential application in clinics.
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页数:14
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