Objective To investigate the effects of UA in oxidative stress to rats glomerular endothelial cells.Methods Observing the effects of UA((0,4,8,16mg/dl),500μmol/1H2O2and8mg/dlUA+500μmol/lH2O2on the proliferation of RGEC after48hours by MTT.NO and ET-1were detected in supernatant medium by ELISA.Results8mg/d1UA group,16mg/dIUA group,500μamol/lH2O2group and8mg/dIUA+500μmol/lH2O2group could inhibit the proliferation of RGEC compared with control group(p<0.05).8mg/dIUA+500μmol/1H2O2group had a significant difference compared with8mg/dIUA group (p<0.05).8mg/dIUA grcup16mg/dIUA group,500)μmol/1H2O2group and8mg/dIUA+500μmol/lH2O2group inhibited production of NO and stimulated the secretion of ET-1. A significant difference could be found compared with control group (p<0.05).8mg/dlUA+500umol/lH2O2group had significantly difference compared with8mg/dIUA group (p<0.05).Conclusion UA could inhibit the proliferation of RGEC,decrease the production of NO, increase the synthesis and release of ET-1in oxidative stress,leading to dysfunction of the glomerular endothelial cells. |