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大黄素预处理对LPS/ATP诱导的人脐静脉内皮细胞焦亡的影响

吴树宁 王凯 施思 夏中元

山西医科大学学报2019,Vol.50Issue(4):410-414,5.
山西医科大学学报2019,Vol.50Issue(4):410-414,5.DOI:10.13753/j.issn.1007-6611.2019.04.006

大黄素预处理对LPS/ATP诱导的人脐静脉内皮细胞焦亡的影响

Effects of emodin pretreatment on pyrotosis of hunan umbilical vein endothelial cells induced by LPS/ATP

吴树宁 1王凯 1施思 1夏中元1

作者信息

  • 1. 武汉大学人民医院麻醉科,武汉 430060
  • 折叠

摘要

Abstract

Objective To investigate the effect of emodin(EMO) pretreatment on pyroptosis induced by LPS /ATP in human umbilical vein endothelial cells(HUVECs). Methods HUVECs with good growth status were randomly divided into three groups: normal control group(C group),LPS /ATP group,LSP/ATP + EMO group(EMO group). The HUVEC cells in LPS /ATP group were stimulated with 1 μg /ml lipopolysaccharide(LPS) for 24 h,and then stimulated with 5. 5 mmol /L adenosine triphosphate(ATP) for 4 h. The HUVEC cells in EMO group were pretreated with emodin 60 μmol /L for 24 h,the cells were stimulated with 1 μg /ml lipopolysaccharide(LPS) for 24 h,and then stimulated with 5. 5 mmol /L adenosine triphosphate(ATP) for 4 h. The levels of LDH and ROS in the supernatant were detected by ELISA and the changes of NLRP3,caspase-1,IL-1β,IL-18 protein were detected by Western blot. Results Compared with normal control group,the levels of LDH and ROS in LPS /ATP group were increased significantly(P < 0. 05), and the expression of NLRP3,caspase-1,IL-1β and IL-18 was increased significantly(P < 0. 05). Compared with LPS /ATP group, the levels of LDH and ROS in the supernatant of the cells was decreased significantly in EMO group(P < 0. 05),and the expression of NLRP3,caspase-1,IL-1β and IL-18 in the cells was decreased significantly(P < 0. 05). Conclusion Emodin can inhibit the cell apoptosis and reduce the cell injury,which may be related to the inhibition of intracellular ROS by emodin.

关键词

大黄素/细胞焦亡/人脐静脉内皮细胞/脂多糖/三磷酸腺苷

Key words

emodin/pyroptosis/human umbilical vein endothelial cells/LPS/ATP

分类

医药卫生

引用本文复制引用

吴树宁,王凯,施思,夏中元..大黄素预处理对LPS/ATP诱导的人脐静脉内皮细胞焦亡的影响[J].山西医科大学学报,2019,50(4):410-414,5.

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