Purpose: To investigate the effects of circ_0001953/miR-186 on human retinal vascular endothelial cell (HRVEC) injury evoked by high glucose. Methods: A cell model (HG group) was established using high glucose-treated HRVECs, while untreated HRVECs were used as the control group (Con group). The levels of endothelin-1 (ET-1), ICAM-1 and IL-6 were evaluated by ELISA and the content of malondialdehyde (MDA) and superoxide dismutase (SOD) in HRVECs were determined. Apoptosis rate was tested adopting flow cytometry. The interrelationship between circ_0001953 and miR-186 was assessed using dual luciferase reporter assay. Measurement of Bax and Bcl-2 was implemented via western blot. Results: In HG group, circ_0001953 increased while miR-186 was downregulated, ET-1, IL-6, ICAM-1, and apoptosis rate increased and accompanied with up-regulated Bax content and declined Bcl-2 protein level. Furthermore, the content of MDA increased and SOD decreased. MiR-186 was a target of circ_0001953. Conclusion: Inhibition of circ_0001953 can repress inflammation, oxidative stress and apoptosis in HRVECs by up-regulating the expression of miR-186.
第一作者机构:[1]Fourth Hosp Hebei Med Univ, Dept Ophthalmol, Shijiazhuang 050000, Hebei, Peoples R China
通讯作者:
通讯机构:[1]Fourth Hosp Hebei Med Univ, Dept Ophthalmol, Shijiazhuang 050000, Hebei, Peoples R China
推荐引用方式(GB/T 7714):
Yuan Yazhen,Guan Yongqing,Shao Chenjun,et al.Circ_0001953 contribute to retinal vascular endothelial cell injury induced by high glucose through regulating miR-186[J].TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH.2023,22(3):563-569.doi:10.4314/tjpr.v22i3.13.
APA:
Yuan, Yazhen,Guan, Yongqing,Shao, Chenjun,Wang, Hui&Zhang, Shuangmei.(2023).Circ_0001953 contribute to retinal vascular endothelial cell injury induced by high glucose through regulating miR-186.TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH,22,(3)
MLA:
Yuan, Yazhen,et al."Circ_0001953 contribute to retinal vascular endothelial cell injury induced by high glucose through regulating miR-186".TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH 22..3(2023):563-569