Abstract:ObjectiveTo investigate the effects and mechanism of glucagonlike peptide1 (GLP1) on high glucoseinduced human umbilical vein endothelial cells (HUVECs) oxidative stress.MethodsHUVECs was isolated and cultured in vitro, randomly divided into control group ,high glucose(30 mmol/L) group and GLP1 group (100 nmol/L GLP1+high glucose).Endothelial toxicity was evaluated by lactate dehydrogenase (LDH) method.Intracellular reactive oxygen species (ROS) production and activity of superoxide dismutase (SOD) reflects the oxidative stress state in the cell.Fluorescence enzymelabeled instrument was used to detect the production of ROS.The activity of SOD was detected by xanthine oxidase method.Results(1)GLP1 could reduce toxicity of high glucose.After high glucose trestment, the ratio of LDH leakage was markly increased to 1.8 times of the control group.However, the ratio of LDH leakage in cells pretreated with 100 nmol/L GLP1 significantly decreased to 1.3 times of the control group(P<0.05).(2)Comparing with control group, ROS production was increased more than 1 times(P<0.05) and the activity of SOD had no significant changes in high glucose group.After GLP1 pretreatment, ROS was lowered to the level of control group and activity of SOD was increased by 64.64%(P<0.05).ConclusionsGLP1 has a direct protective effect on HUVECs function under high glucose condition,which is probably related to the mitigation of oxidative stress.