Baicalin protects human retinal pigment epithelial cell lines against high glucose-induced cell injury by up-regulation of microRNA-145

2019 ◽  
Vol 106 ◽  
pp. 123-130 ◽  
Author(s):  
Chunhua Dai ◽  
Shanhao Jiang ◽  
Cuiying Chu ◽  
Meng Xin ◽  
Xiufen Song ◽  
...  
2004 ◽  
Vol 40 (1) ◽  
pp. 55-59 ◽  
Author(s):  
Horst Zitzelsberger ◽  
Ludwig Hieber ◽  
Hedwig Richter ◽  
Kristian Unger ◽  
Cecilia V. Briscoe ◽  
...  

2020 ◽  
Vol 167 (5) ◽  
pp. 495-502 ◽  
Author(s):  
Xuejiao Wang ◽  
Hui Li ◽  
Hao Wang ◽  
Jingyun Shi

Abstract Quercetin is a kind of distinctive bioactive flavonoid that has potent anti-oxidant, anti-inflammatory and anti-diabetic properties. The present article was designed to check the effect of quercetin on diabetic retinopathy. Adult retinal pigment epithelial cell line (ARPE)-19 cells were pre-treated with quercetin and then stimulated by high glucose. Cell damage was evaluated by CCK-8 assay, flow cytometer, quantitative reverse transcriptase polymerase chain reaction (qRT-PCR), enzyme-linked immunosorbent assay, 2,7-dichlorofluorescein diacetate probe and western blot. The association between quercetin and miR-29b expression as well as the downstream pathways was studied by qRT-PCR and western blot. Pre-treating ARPE-19 cells with quercetin clearly attenuated high glucose-induced viability loss, apoptosis, MCP-1 and IL-6 overproduction and reactive oxygen species (ROS) generation. Quercetin down-regulated p53, Bax and cleaved-caspase-3 expression, while up-regulated CyclinD1, CDK4 and Bcl-2. miR-29b was low expressed in high glucose-treated cell, but quercetin elevated its expression. Moreover, the protective action of quercetin towards ARPE-19 cells was attenuated when miR-29b was suppressed. Also, quercetin promoted PTEN/AKT pathway, while inhibited NF-κB pathway via a miR-29b-dependent way. These data illustrated quercetin possibly possess the anti-diabetic retinopathy potential, as quercetin clearly attenuated high glucose-evoked damage in ARPE-19 cells. The protective action of quercetin may due to its regulation on miR-29b expression as well as PTEN/AKT and NF-κB pathways.


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