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Catalpol Protects ARPE-19 Cells against Oxidative Stress via Activation of the Keap1/Nrf2/ARE Pathway.

Abstract
Oxidative damage to retinal pigment epithelial (RPE) has been identified as one of the major regulatory factors in the pathogenesis of age-related macular degeneration (AMD). Catalpol is an iridoid glucoside compound that has been found to possess potential antioxidant activity. In the present study, we aimed to investigate the protective effect of catalpol on RPE cells under oxidative stress and to elucidate the potential molecular mechanism involved. We found that catalpol significantly attenuated hydrogen peroxide (H2O2)-induced cytotoxicity, G0/G1 phase cell cycle arrest, and apoptosis in RPE cells. The overproduction of reactive oxygen species (ROS) and malondialdehyde (MDA) stimulated by oxidative stress and the corresponding reductions in antioxidant glutathione (GSH) and superoxide dismutase (SOD) levels were largely reversed by catalpol pretreatment. Moreover, catalpol pretreatment markedly activated the expression of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) and its downstream antioxidant enzymes, catalase (CAT), heme oxygenase-1 (HO-1), and NADPH dehydrogenase (NQO1). It also increased the expression levels of cyclin E, Bcl-2, cyclin A, and cyclin-dependent kinase 2 (CDK2) and decreased the expression levels of Bax, Fas, cleaved PARP, p-p53, and p21 cleaved caspase-3, 8, and 9. The oxidative stress-induced formation of the Keap1/Nrf2 complex in the cytoplasm was significantly blocked by catalpol pretreatment. These results indicate that catalpol protected RPE cells from oxidative stress through a mechanism involving the activation of the Keap1/Nrf2/ARE pathways and the inactivation of oxidative stress-mediated pathways of apoptosis.
AuthorsLongtai You, Hulinyue Peng, Jing Liu, Mengru Cai, Huimin Wu, Zhiqin Zhang, Jie Bai, Yu Yao, Xiaoxv Dong, Xingbin Yin, Jian Ni
JournalCells (Cells) Vol. 10 Issue 10 (10 02 2021) ISSN: 2073-4409 [Electronic] Switzerland
PMID34685615 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Iridoid Glucosides
  • Kelch-Like ECH-Associated Protein 1
  • NF-E2-Related Factor 2
  • catalpol
  • Hydrogen Peroxide
Topics
  • Antioxidant Response Elements (genetics)
  • Apoptosis (drug effects)
  • Cell Cycle Checkpoints (drug effects)
  • Cell Line
  • Humans
  • Hydrogen Peroxide (toxicity)
  • Iridoid Glucosides (pharmacology)
  • Kelch-Like ECH-Associated Protein 1 (metabolism)
  • Mitochondria (drug effects, metabolism)
  • NF-E2-Related Factor 2 (metabolism)
  • Neuroprotection (drug effects)
  • Oxidative Stress (drug effects, genetics)

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