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首页|期刊导航|眼科新进展|沉默调节因子相关酶1(SIRT1)对近视豚鼠脉络膜血管密度及内皮素-1表达的影响

沉默调节因子相关酶1(SIRT1)对近视豚鼠脉络膜血管密度及内皮素-1表达的影响

张宁晖 钱继存 辛雅琴 解孝锋 田庆梅 毕宏生

眼科新进展2026,Vol.46Issue(2):108-114,7.
眼科新进展2026,Vol.46Issue(2):108-114,7.DOI:10.13389/j.cnki.rao.2026.0019

沉默调节因子相关酶1(SIRT1)对近视豚鼠脉络膜血管密度及内皮素-1表达的影响

Effect of sirtuin 1 on choroidal vascular density and endothelin-1 expression in myopic guinea pigs

张宁晖 1钱继存 2辛雅琴 1解孝锋 3田庆梅 3毕宏生3

作者信息

  • 1. 250014 山东省济南市,山东中医药大学
  • 2. 250014 山东省济南市,山东中医药大学||250002 山东省济南市,山东中医药大学第二附属医院
  • 3. 250014 山东省济南市,山东中医药大学||250002 山东省济南市,山东中医药大学附属眼科医院,山东省中西医结合眼病防治重点实验室,山东省眼病防治研究院
  • 折叠

摘要

Abstract

Objective To investigate the regulatory effect of sirtuin 1(SIRT1)on choroidal vascular density in the lens-induced myopia(LIM)models of guinea pigs and explore its potential molecular mechanisms.Methods The lens in-duction method was used to establish a myopia model in the left eye(experimental eye)of guinea pigs,with the right eye as the self-control eye.The LIM group and blank control group were set up,respectively.Immunofluorescence staining was performed to evaluate the changes in choroidal vascular density after modeling.Choroidal endothelial cells in primary guinea pigs were isolated and purified using the density gradient centrifugation method.The cells were divided into the control group[treated with dimethyl sulfoxide(DMSO)],the SIRT1 agonist group(treated with SRT1720+DMSO),and the SIRT1 inhibitor group(treated with EX527+DMSO).The cell counting kit-8 cytotoxicity experiment screened the optimal concen-tration of cell drugs(the optimal concentrations of SRT1720 and EX527 were 12.5 μmol·L-1 and 10.0 μmol·L-1,respec-tively).Flow cytometry was used to detect the expression levels of reactive oxygen species(ROS)in choroidal tissue and in vitro cells of guinea pigs.Real-time fluorescence quantitative polymerase chain reaction,enzyme-linked immunosorbent assay,and Western blot were used to measure the mRNA and protein expression levels of SIRT1,endothelin-1(ET-1),and hypoxia-inducible factor-1α(HIF-1α)in choroidal tissue and in vitro cells of guinea pigs.Results Compared with the blank control group,the LIM group showed a significant reduction in choroidal vascular fluorescence signal and vascular density,a significant increase in ROS expression levels in the choroidal tissue and the mRNA and protein expression levels of ET-1 and HIF-1α,and a significant decrease in the expression level of SIRT1 protein,and the differences were statistically significant(all P<0.05).Compared with the control group,the SIRT1 inhibitor group showed increased expression levels of ROS,ET-1 mRNA and protein in cells,while the SIRT1 agonist group showed decreased expression levels of ROS,HIF-1αmRNA and protein,and SIRT1 protein in cells,and the differences were statistically significant(all P<0.05).Compared with the SIRT1 agonist group,the SIRT1 inhibitor group showed a decrease in both SIRT1 mRNA and protein expression lev-els in cells and an increase in the mRNA and protein expression levels of ET-1 and HIF-1α,and the differences were statisti-cally significant(all P<0.05).The Western blot analysis results showed that there were statistically significant differences in the expression of SIRT1,ET-1,and HIF-1α proteins in the choroidal tissue and cells of guinea pigs in each group(all P<0.05).Conclusion The decrease in choroidal vascular density in myopic guinea pigs is related to the downregulation of SIRT1 expression in the choroidal tissue.Its mechanism may be that the downregulation of SIRT1 expression leads to in-creased oxidative stress in choroidal endothelial cells,and accumulated ROS stabilizes and activates HIF-1α protein to drive ET-1 expression,ultimately leading to choroidal vascular dysfunction and reduced blood perfusion.

关键词

病理性近视/弥漫性脉络膜萎缩/沉默调节因子相关酶1/脉络膜血管密度/氧化应激

Key words

pathological myopia/diffuse choroidal atrophy/sirtuin 1/choroidal vascular density/oxidative stress

分类

医药卫生

引用本文复制引用

张宁晖,钱继存,辛雅琴,解孝锋,田庆梅,毕宏生..沉默调节因子相关酶1(SIRT1)对近视豚鼠脉络膜血管密度及内皮素-1表达的影响[J].眼科新进展,2026,46(2):108-114,7.

基金项目

国家自然科学基金项目(编号:82305322) (编号:82305322)

山东省自然科学基金项目(编号:ZR2020QH314) (编号:ZR2020QH314)

山东省中医药科技发展项目(编号:M-2022162) (编号:M-2022162)

眼科新进展

1003-5141

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