[1]霍彦龙,郝璞珩,田 道 △.丙泊酚抑制缺氧/复氧HUVECs细胞中miR15b表达 及细胞凋亡的实验研究*[J].陕西医学杂志,2019,(2):144-147.
 HUO Yanlong,HAO Puheng,TIAN Dao..Propofol inhibits miR15b expression and apoptosis in hypoxia/reoxygenation HUVECs[J].,2019,(2):144-147.
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丙泊酚抑制缺氧/复氧HUVECs细胞中miR15b表达 及细胞凋亡的实验研究*
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《陕西医学杂志》[ISSN:1000-7377/CN:61-1281/TN]

卷:
期数:
2019年2期
页码:
144-147
栏目:
基础研究
出版日期:
2020-02-05

文章信息/Info

Title:
Propofol inhibits miR15b expression and apoptosis in hypoxia/reoxygenation HUVECs
文章编号:
DOI: 10.3969/j.issn.10007377.2019.02.002
作者:
霍彦龙12郝璞珩3田 道14 △
1.延安大学附属医院(延安716000);2.陕西省吴起县人民医院麻醉科(吴起717600); 3.西安医学院第一附属医院神经外科(西安710077);4. 陕西省荣誉军人康复医院麻醉科(渭南714200)
Author(s):
HUO Yanlong HAO PuhengTIAN Dao.
Affiliated Hospital of Yan’an University(Yan’an 716000)
关键词:
丙泊酚微RNAs抗凋亡蛋白细胞凋亡缺氧/复氧细胞模型血管内皮细胞
Keywords:
Key words PropofolMicroRNAsAntiapoptotic proteinApoptosisHypoxia/reoxygenation cell modelVascular endothelial cells
分类号:
R915
文献标志码:
A
摘要:
摘 要 〖JP2〗目的:研究丙泊酚在缺氧/复氧细胞模型中对微小RNA15b(miR15b)及血管内皮细胞凋亡的影响。方法:建立缺氧/复氧细胞模型[人脐静脉内皮细胞(HUVECs)],设置实验组、对照组、空白组,其中实验组HUVECs缺氧/复氧培养24 h后,加入丙泊酚(150 μmol/L)干预培养6 h;实时定量PCR(RTqPCR)检测各组HUVECs 中miR15b 的表达情况;RTqPCR、Westernblot检测各组HUVECs 中miR15b靶基因B淋巴细胞瘤2 (bcl2)的表达情况;流式细胞术检测各组细胞凋亡能力。结果:RTqPCR结果显示,实验组miR15b的表达水平低于对照组(P<0.05);RTqPCR及Westernblot结果显示,实验组bcl2在mRNA和蛋白水平的表达均高于对照组(P<0.05);实验组HUVECs的细胞凋亡率低于对照组(P<0.05)。结论:丙泊酚能够抑制缺氧/复氧HUVECs细胞中miR15b的表达,并影响其靶基因抗凋亡蛋白bcl2的表达,从而降低细胞凋亡率。
Abstract:
Abstract Objective:To investigate the effect of Propofol on expression of microRNA15b (miR15b) and vascular endothelial cells apoptosis in hypoxia/reoxygenation cell model. Methods: The hypoxia/reoxygenation cell model [human umbilical vein endothelial cells(HUVECs)] was established. The experimental group, the control group and the blank group were set up. HUVECs were incubated with hypoxia/reoxygenation for 24h, then treated with 150 μmol/L Propofol for 6h. The expression of miR15b in each group of HUVECs was detected by realtime quantitative PCR (RTqPCR). The expression of B lymphoblastoma2 (bcl2) expression were detected by RTqPCR and Westernblot. Flow cytometry was used to detect apoptosis in each group. Results: RTqPCR results showed that the expression level of miR15b in the experimental group was lower than that in the control group (P<0.05). The results of RTqPCR and Westernblot showed that the expression of bcl2 mRNA and protein in the experimental group were higher than that in the control (P<0.05). The apoptosis rate of HUVECs in experimental group was lower than that in control group (P<0.05). Conclusion: Propofol can inhibit the expression of miR15b in hypoxia/reoxygenation HUVECs and affect the expression of its target gene bcl2(antiapoptotic protein, thus reducing the apoptosis rate.

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备注/Memo

备注/Memo:
*陕西省教育厅科学研究计划项目(16JK1656)
更新日期/Last Update: 2019-03-13