Chitooligosaccharides Derivatives Protect ARPE-19 Cells against Acrolein-Induced Oxidative Injury.
Cheng YangRongrong YangMing GuJiejie HaoShixin WangChun-Xia LiPublished in: Marine drugs (2023)
Age-related macular degeneration (AMD) is the leading cause of vision loss among the elderly. The progression of AMD is closely related to oxidative stress in the retinal pigment epithelium (RPE). Here, a series of chitosan oligosaccharides (COSs) and N -acetylated derivatives (NACOSs) were prepared, and their protective effects on an acrolein-induced oxidative stress model of ARPE-19 were explored using the MTT assay. The results showed that COSs and NACOs alleviated APRE-19 cell damage induced by acrolein in a concentration-dependent manner. Among these, chitopentaose (COS-5) and its N -acetylated derivative (N-5) showed the best protective activity. Pretreatment with COS-5 or N-5 could reduce intracellular and mitochondrial reactive oxygen species (ROS) production induced by acrolein, increase mitochondrial membrane potential, GSH level, and the enzymatic activity of SOD and GSH-Px. Further study indicated that N-5 increased the level of nuclear Nrf2 and the expression of downstream antioxidant enzymes. This study revealed that COSs and NACOSs reduced the degeneration and apoptosis of retinal pigment epithelial cells by enhancing antioxidant capacity, suggesting that they have the potential to be developed into novel protective agents for AMD treatment and prevention.
Keyphrases
- oxidative stress
- age related macular degeneration
- induced apoptosis
- diabetic rats
- reactive oxygen species
- dna damage
- cell cycle arrest
- cell death
- ischemia reperfusion injury
- poor prognosis
- single cell
- drug delivery
- endoplasmic reticulum stress
- nitric oxide
- hydrogen peroxide
- signaling pathway
- drug induced
- stem cells
- binding protein
- mesenchymal stem cells
- risk assessment
- cell proliferation
- amyotrophic lateral sclerosis
- long non coding rna
- bone marrow
- heat shock protein
- stress induced
- endothelial cells