Protective effect of folic acid on oxidative stress injury and apoptosis of SH-SY5Y cells induced by arsenic
10.3760/cma.j.issn.2095-4255.2019.06.005
- VernacularTitle:叶酸对砷诱导SH-SY5Y细胞氧化应激损伤及凋亡的保护作用研究
- Author:
Qi ZHOU
1
;
Qiaoyu WANG
;
Teng WANG
;
Yanmei YANG
;
Yanhui GAO
;
Hongna SUN
;
Dianjun SUN
Author Information
1. 哈尔滨医科大学中国疾病预防控制中心地方病控制中心地氟病防治研究所 150081
- Keywords:
Arsenicals;
Folic acid;
Oxidative stress;
Apoptosis
- From:
Chinese Journal of Endemiology
2019;38(6):453-457
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effects of arsenic trioxide (As2O3) on oxidative stress and apoptosis of neuroblastoma cells (SH-SY5Y) and the protective effect of folic acid (FA).Methods SH-SY5Y cells were cultured in vitro,and were divided into six groups:control group,low arsenic group (2.5 μmol/L As2O3),medium arsenic group (5.0 μmol/L As2O3),high arsenic group (10.0 μmol/L As2O3),FA intervention group (10.0 μmol/L As2O3,0.3 mmol/L FA),and FA control group (0.3 mmol/L FA).Each group of cells was cultured for 24 h or 5 h.Cell chromatin agglutination was observed by fluorescence staining.The ultrastructure of cells was observed by transmission electron microscope.The changes of oxidative stress related indicators of glutathione (GSH),malondialdehyde (MDA),superoxide dismutase (SOD),and reactive oxygen species (ROS) were detected;caspase 3 activity was also detected.Results Under fluorescence microscope,as the dose of arsenic increased,the nucleus became increasingly highlighted and a small number of cells in the medium and high arsenic groups showed chromatin agglutination,and FA intervention reduced chromatin agglutination.Under transmission electron microscope,the mitochondria of low and medium arsenic groups were slightly swollen and the endoplasmic reticulum was expanded;while the mitochondria of high arsenic group were significantly swollen and the nuclear membrane was ruptured,and the apoptotic bodies were observed.Mitochondria were slightly swollen after FA intervention.There were statistically significant differences in GSH content,SOD activity,ROS level and caspase 3 activity between groups (F =14.905,6.120,12.714,36.657,P ＜ 0.05).GSH content and SOD activity in high arsenic group [0.104 ± 0.074,(12.673 ± 5.106) U/mg prot] were lower than those in control group [1.000 ± 0.000,(34.699 ±3.998) U/mg prot,P ＜ 0.05].GSH content in FA intervention group (0.411 ± 0.344) was higher than that in high arsenic group (P ＜ 0.05).The ROS level and caspase 3 activity in high arsenic group were higher than those in control group (P ＜ 0.05),and the ROS level and caspase 3 activity in FA intervention group were lower than those in high arsenic group (P ＜ 0.05).There was no significant difference in MDA content between groups (F =8.207,P ＜ 0.05).Conclusions Arsenic exposure can inhibit the activity of antioxidants,cause oxidative stress injury,and increase the activity of caspase 3,leading to cell apoptosis.FA plays an antagonistic role in arsenicinduced oxidative damage and apoptosis of nerve cells.
