SS-31 protect retinal pigment epithelial cells from H2 O2 -induced cell injury by reducing apoptosis.
Jie BaiYumei YangDingting WuFan YangPublished in: Clinical and experimental pharmacology & physiology (2021)
Evidence has shown that effects from oxidative stress induced damage of retinal or human retinal pigment epithelial (RPE) cells. Antioxidant supplementation is a plausible strategy to avoid oxidative stress and maintain the function of retina. d-Arg-2,6-dimethyltyrosine-Lys-Phe-NH2 (SS-31) has been used in the treatment of many diseases. In this study, we found that SS-31 attenuated hydrogen peroxide (H2 O2 )-induced loss of cell viability, reduced oxidative damage and cell apoptosis in RPE cells. HO-1, Trx-1 and Nrf-2 expression levels significantly increased on pre-treatment with SS-31 compared with the H2 O2 group. SS-31 inhibited apoptosis through the downregulation of Bax and the upregulation of Bcl-2. Our results suggest that SS-31 had a protective effect against H2 O2 treatment in ARPE-19 cells by enhancing the antioxidative enzymes expression and decreasing apoptosis, which could be considered a promising therapeutic intervention for retinal degeneration.
Keyphrases
- oxidative stress
- induced apoptosis
- cell cycle arrest
- endoplasmic reticulum stress
- diabetic rats
- cell death
- hydrogen peroxide
- pi k akt
- poor prognosis
- signaling pathway
- cell proliferation
- diabetic retinopathy
- dna damage
- randomized controlled trial
- optical coherence tomography
- ischemia reperfusion injury
- anti inflammatory
- mesenchymal stem cells
- cell therapy
- drug induced
- binding protein
- bone marrow
- optic nerve