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还原型谷胱甘肽调控Nrf2/iNOS信号对DR大鼠视网膜的保护机制
引用本文:杨馥宇,苏 杰,王 玲,王林洪,张 蒙. 还原型谷胱甘肽调控Nrf2/iNOS信号对DR大鼠视网膜的保护机制[J]. 转化医学杂志, 2022, 11(1): 36-41
作者姓名:杨馥宇  苏 杰  王 玲  王林洪  张 蒙
作者单位:华北理工大学附属医院
基金项目:河北省卫生健康委2021年度医学科学研究项目(20210909 )
摘    要:目的 探讨还原型谷胱甘肽调控Nrf2/iNOS信号对DR大鼠视网膜的保护机制.方法 选取48只SD大鼠,随机分成健康组、病变组、他汀组、甘肽组,每组均为12只大鼠,除健康组外其余组别均建立糖尿病视网膜病变大鼠模型,建模成功后健康组与病变组不进行用药,他汀组大鼠给予辛伐他汀灌胃,甘肽组大鼠采用还原型谷胱甘肽干预,各组大鼠...

关 键 词:还原型谷胱甘肽  Nrf2  iNOS  糖尿病视网膜病变  应激反应

The protective mechanism of reduced glutathione regulating Nrf2/iNOS signal on the retina of DR rats
YANG Fuyu,SU Jie,WANG Ling,WANG Linhong,ZHANG Meng. The protective mechanism of reduced glutathione regulating Nrf2/iNOS signal on the retina of DR rats[J]. Translational Medicine Journal, 2022, 11(1): 36-41
Authors:YANG Fuyu  SU Jie  WANG Ling  WANG Linhong  ZHANG Meng
Affiliation:Affiliated Hospital of North China University of Science and Technology, Tangshan Hebei 063000,China
Abstract:Objective To explore the protective mechanism of prototype glutathione regulating Nrf2/iNOS signal on the retina of DR rats.Methods 48 SD rats (half male and half female) were randomly divided into four groups: healthy group, pathological group, tatin group and glycine group, with 12 rats in each group.Except for the normal group, all the other groups were established diabetic retinopathy rat models. After successful modeling, the normal group and the model group were not given medication, and the rats in the statin group were given simvastatin intragastric administration.The rats in the peptide group were treated with prototype glutathione for 14 consecutive days.He staining, oxidative stress index, protein expression levels of Nrf2, HO-1, NO and iNOS, mRNA expression levels of Nrf2 and HO-1 were detected in pathological tissues of rats in each group.Results HHE staining results showed that retinal cells in healthy group were closely arranged and the surface was smooth and smooth. The cells in the pathological group were irregular and the surface was not smooth.The cell arrangement of the statin group and the glycine group was more regular, and the pathological changes were significantly improved. Compared with the healthy group, the expression levels of ROS, MDA, NO, iNOS and SOD and GSH-Px in the diseased group were significantly increased, while the levels of SOD and GSH-Px were decreased (P<0.05).Compared with the diseased group, the expression levels of ROS, MDA, NO and iNOS in the statatin group and the glycine group were decreased, while the levels of SOD and GSH-Px were increased (P<0.05).Compared with the statine group, the expression levels of ROS, MDA, NO and iNOS in the glycine group were significantly decreased, while the levels of SOD and GSH-Px were significantly increased (P<0.05).Compared with the healthy group, the mrna levels of Nrf2, HO-1, Nrf2 and HO-1 in the pathological group were decreased (P<0.05).Compared with the lesion group, the mrna levels of Nrf2, HO-1, Nrf2 and HO-1 in the statine group and the glycine group were significantly increased (P<0.05).Compared with the statine group, the mrna levels of Nrf2, HO-1, Nrf2 and HO-1 in glycine group were significantly increased (P<0.05).Conclusions Prototype glutathione can regulate Nrf2/iNOS signaling pathway, improve oxidative stress response, and protect diabetic retinopathy.
Keywords:Prototype glutathione   Nrf2   INOS  Diabetic retinopathy  Stress response
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