The protective effect of smilax glabra extract on advanced glycation end products-induced endothelial dysfunction in HUVECs via RAGE-ERK1/2-NF-κB pathway

被引:25
作者
Sang, Hai-qiang [1 ]
Gu, Jun-fei [2 ,3 ]
Yuan, Jia-rui [2 ,3 ]
Zhang, Ming-hua [2 ]
Jia, Xiao-bin [2 ]
Feng, Liang [2 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Cardiol, Zhengzhou 450052, Henan, Peoples R China
[2] Jiangsu Prov Acad Chinese Med, Key Lab Delivery Syst Chinese Meteria Med, Nanjing 210028, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Coll Pharm, Nanjing 210023, Jiangsu, Peoples R China
关键词
Smilax glabra Roxb; Endothelial dysfunction; Advanced glycation end products; RAGE-ERK1/2-NF-kappa B pathway; Diabetic vascular complications; INDUCED OXIDATIVE STRESS; DIABETIC-NEPHROPATHY; VASCULAR DYSFUNCTION; ALDOSE REDUCTASE; CELL DYSFUNCTION; IN-VITRO; RAGE; AGES; RATS; APOPTOSIS;
D O I
10.1016/j.jep.2014.06.028
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Smilax glabra Roxb. (SGR) is a traditional Chinese herb that has been used in folk for the treatment of diabetic vascular complications. Advanced glycation end products (AGEs)-induced endothelial dysfunction has been thought to be a major cause of diabetic vascular complications. The present study was conducted to investigate the protective effect of SGR extract on AGEs-induced endothelial dysfunction and its underlying mechanisms. Materials and methods: Human umbilical vein endothelial cells (HUVECs) were exposed to 200 mu g/ml AGEs to induce endothelial dysfunction. Acridine orange/ethidium bromide (AO/EB) fluorescence assay and Annexin-V/PI double-staining were performed to determine endothelium apoptosis. Dihydroethidium (DHE) fluorescence probe, SOD and MDA kits were used to evaluate oxidative stress. The effect of SGR extract on AGEs-induced TGF-beta1 expression was determined by immunocytochemistry and western blotting. Attenuations of SGR extract on receptor for AGEs (RAGE) expression, extracellular regulated protein kinases (ERK1/2) activation and NF-kappa B phosphorylation were determined by immunofluorescence assay and western blotting. The blockade assays for RAGE and ERK1/2 were carried out using a specific RAGE-antibody (RAGE-Ab) or a selective ERK1/2 inhibitor PD98059 in immunofluorescence assay. Results: The pretreatment of SGR extract (0.125, 0.25 and 0.5 mg crude drug/ml) significantly attenuated AGEs-induced endothelium apoptosis, and down-regulated TGF-beta1 protein expression in HUVECs. It was also well shown that SGR extract could down-regulate dose-dependently ROS over-generation, MDA content, TGF-beta1 expression, ERK1/2 and NF-kappa B activation whereas increase significantly SOD activity. Furthermore, the AGEs-induced ERK1/2 activation could be attenuated by the blockade of RAGE-Ab (5 mu g/ml) while the NF-kappa B activation was ameliorated by ERK1/2 inhibitor PD98059 (10 mu M). Conclusion: These results indicated that SGR extract could attenuate AGEs-induced endothelial dysfunction via RAGE-ERK1/2-NF-kappa B pathways. Our findings suggest that SGR extract may be beneficial for attenuating endothelial dysfunction in diabetic vascular complications. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:785 / 795
页数:11
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