文章摘要

利拉鲁肽对高糖环境下体外培养的人髓核细胞凋亡的影响

作者: 1姚明言, 1舒民, 2张靖, 1李志红, 3马金辉, 4景园园
1 保定市第一中心医院内分泌科,河北 保定 071000
2 河北大学附属医院心内科,河北 保定 071000
3 河北大学附属医院内分泌科,河北 保定 071000
4 保定市第一中心医院营养科,河北 保定 071000
通讯: 李志红 Email: lizhihongmd@163.com
DOI: 10.3978/j.issn.2095-6959.2020.05.001
基金: 国家自然科学基金(31701238)。

摘要

目的:研究不同浓度的利拉鲁肽(liraglutide,LIR)对高糖环境下体外培养的人髓核细胞(nucleus pulposus cells,NPCs)凋亡的影响。方法:培养人髓核细胞株,第三代髓核细胞随机分为对照组(CON组,NPCM细胞培养液培养)、高糖组(HG组,0.2 mol/L高糖培养液培养)、利拉鲁肽10 nmol/L干预组(LIR10组,0.2 mol/L高糖+10 nmol/L利拉鲁肽)、利拉鲁肽100 nmol/L干预组(LIR100组):0.2 mol/L高糖+100 nmol/L利拉鲁肽、利拉鲁肽1 000 nmol/L干预组(LIR1 000组):0.2 mol/L高糖+1 000 nmol/L利拉鲁肽。各组细胞培养48 h,CCK-8对人髓核细胞的增殖活性进行定量分析,流式细胞术及ELISA检测细胞凋亡率,细胞内活性氧(ROS)检测评估氧化应激水平。采用SPSS 22.0软件进行统计学分析。结果:与正常对照组相比,高糖组细胞增殖活性明显减低,细胞内ROS生成及凋亡率明显增加(P<0.05)。利拉鲁肽(10,100,1000 nmol/L)的干预使细胞增殖活性较高糖组明显升高,ROS的水平及细胞凋亡率明显降低(P<0.05)。在浓度为100 nmol/L时,利拉鲁肽的促进细胞增殖,抑制氧化应激及抗凋亡作用最强,各组间差异有统计学意义(P<0.05)。结论:利拉鲁肽通过抗氧化应激抑制了高糖诱导的人髓核细胞凋亡,从而发挥保护作用。
关键词: 利拉鲁肽;人髓核细胞;高糖;凋亡

Effect of liraglutide on apoptosis of human nucleus pulposus cells induced by high glucose

Authors: 1YAO Mingyan, 1SHU Min, 2ZHANG Jing, 1LI Zhihong, 3MA Jinhui, 4JING Yuanyuan
1 Department of Endocrine, Baoding First Central Hospital, Baoding Hebei 071000, China
2 Department of Cardiology, Affiliated Hospital of Hebei University, Baoding Hebei 071000, China
3 Department of Endocrinology, Affiliated Hospital of Hebei University, Baoding Hebei 071000, China
4 Department of Nutrition, Baoding First Central Hospital, Baoding Hebei 071000, China

CorrespondingAuthor: LI Zhihong Email: lizhihongmd@163.com

DOI: 10.3978/j.issn.2095-6959.2020.05.001

Foundation: This work was supported by the National Natural Science Foundation of China (31701238).

Abstract

Objective: To evaluate the protective effect of liraglutide on apoptosis induced by high glucose in nucleus pulposus cells (NPCs). Methods: The third-generation NPCs were randomly categorized as follows: a control (CON) group (cultured in NPCM), a high glucose (HG) group (cultured in 0.2 mol/L high glucose concentration), a high glucose + liraglutide (HG+LIR) group [cultured in the high glucose (0.2 mol/L) medium containing various concentrations of liraglutide (10, 100, or 1 000 nmol/L)]. The cells were all cultured for 48 h, then cell viability was tested using cell counting kit-8; and the apoptosis rate were measured by flow cytometric analysis and ELISA; the intracellular reactive oxygen species (ROS) of the NPCs was measured using a ROS assay kit. All data were analyzed with SPSS software for Windows version 22.0. Results: Compared with the control group, cell viability decreased significantly and ROS levels, cell apoptosis rate increased significantly in the high glucose group (P<0.05). Our data demonstrated that liraglutide evidently increased cell proliferation activity and inhibited the apoptosis of NPCs induced by high glucose (P<0.05). Further analysis suggested that liraglutide suppressed ROS generation (P<0.05). The maximum effect was at 100 nmol/L of liraglutide, and the differences among different groups were statistically significant (P<0.05). Conclusion: Liraglutide could protect NPCs against high glucose-induced apoptosis by inhibiting oxidative stress.
Keywords: apoptosis; liraglutide; nucleus pulposus cells; high glucose

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