Wang Yan, Nie Minghao, Lu Yanhong, Wang Rui, Li Jin, Yang Bin, Xia Mingyang, Zhang Haiyang, Li Xiurong
Department of Pathology, Heilongjiang Provincial Hospital, Harbin, Heilongjiang 150036, P.R. China.
Int J Mol Med. 2015 Apr;35(4):1067-73. doi: 10.3892/ijmm.2015.2095. Epub 2015 Feb 9.
Fucoidan, an extract of the seaweed, Fucus vesiculosus, has been widely investigated for its antioxidant effects. However, to date and to the best of our knowledge, pathological studies on the effects of fucoidan against diabetic nephropathy (DN) related to spontaneous diabetes have not been carried out. DN is one of the most serious microvascular complications of diabetes. Therefore, in the present study, the effects of fucoidan against DN related to spontaneous diabetes were investigated in vitro and in vivo. Goto-Kakizaki (GK) rats were allowed free access to standard rat food with or without fucoidan for 13 weeks, and Wistar rats were used as controls. Fucoidan did not show any cytotoxicity on glomerular mesangial cells (GMCs) which were separated from rat kidneys. Fasting blood glucose levels were measured using a blood glucose meter, blood urea nitrogen (BUN) and serum creatinine (Cr) levels were measured using an automatic biochemistry analyzer and urine protein levels were measured using an ELISA kit. Collagen Ⅳ levels in the renal cortex were measured using an ELISA kit, and the expression levels of transforming growth factor-β1 (TGF-β1) and fibronectin (FN) in the renal cortex and GMCs, and nuclear factor-κB (NF-κB) in GMCs were determined by western blot analysis. Fasting blood glucose, BUN, serum Cr, urine protein and collagen Ⅳ levels, and the expression of TGF-β1 and FN, as well as NF-κB p65 nuclear translocation all significantly increased in the GK rats compared with the control Wistar rats. The increase in the fasting blood glucose, BUN, serum Cr, urine protein and collagen Ⅳ levels in the renal cortex was reversed in the GK rats which were orally administered fucoidan. The oral administration of fucoidan also decreased the expression of TGF-β1 and FN in the renal cortex and GMCs, as well as the nuclear translocation of NF-κB p65 in the GMCs. Taken together, the data from our in vitro and in vivo experiments indicate that fucoidan attenuates hyperglycemia and prevents or impedes the development of DN related to spontaneous diabetes by attenuating the activation of the NF-κB signaling pathway.
岩藻聚糖是一种从墨角藻中提取的物质,人们已对其抗氧化作用展开了广泛研究。然而,据我们所知,迄今为止尚未开展关于岩藻聚糖对自发性糖尿病相关糖尿病肾病(DN)影响的病理学研究。DN是糖尿病最严重的微血管并发症之一。因此,在本研究中,我们在体外和体内研究了岩藻聚糖对自发性糖尿病相关DN的影响。将Goto-Kakizaki(GK)大鼠自由喂食含或不含岩藻聚糖的标准大鼠饲料13周,以Wistar大鼠作为对照。岩藻聚糖对从大鼠肾脏分离出的肾小球系膜细胞(GMC)未表现出任何细胞毒性。使用血糖仪测量空腹血糖水平,使用自动生化分析仪测量血尿素氮(BUN)和血清肌酐(Cr)水平,使用ELISA试剂盒测量尿蛋白水平。使用ELISA试剂盒测量肾皮质中的Ⅳ型胶原水平,并通过蛋白质印迹分析确定肾皮质和GMC中转化生长因子-β1(TGF-β1)和纤连蛋白(FN)的表达水平以及GMC中核因子-κB(NF-κB)的表达水平。与对照Wistar大鼠相比,GK大鼠的空腹血糖、BUN、血清Cr、尿蛋白和Ⅳ型胶原水平以及TGF-β1和FN的表达以及NF-κB p65核转位均显著增加。口服岩藻聚糖的GK大鼠肾皮质中空腹血糖、BUN、血清Cr、尿蛋白和Ⅳ型胶原水平的升高得到逆转。口服岩藻聚糖还降低了肾皮质和GMC中TGF-β1和FN的表达以及GMC中NF-κB p65的核转位。综上所述,我们体外和体内实验的数据表明,岩藻聚糖通过减弱NF-κB信号通路的激活来减轻高血糖,并预防或阻碍自发性糖尿病相关DN的发展。