Phloroglucinol Attenuates DNA Damage and Apoptosis Induced by Oxidative Stress in Human Retinal Pigment Epithelium ARPE-19 Cells by Blocking the Production of Mitochondrial ROS

• Published in: Antioxidants 2022-11, Vol.11 (12), p.2353
• Main Authors: Park, Cheol, Cha, Hee-Jae, Kim, Min Yeong, Bang, EunJin, Moon, Sung-Kwon, Yun, Seok Joong, Kim, Wun-Jae, Noh, Jeong Sook, Kim, Gi-Young, Cho, Suengmok, Lee, Hyesook, Choi, Yung Hyun
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Antibodies; Antioxidants; Apoptosis; Autophagy; Bcl-2 protein; Caspase-3; Cell viability; Cytochrome c; Cytotoxicity; DNA damage; Enzymes; Epithelium; Hydrogen peroxide; Macular degeneration; Mitochondrial DNA; mitochondrial ROS; Observations; Oxidative stress; Phenolic compounds; phloroglucinol; Physiological aspects; Reactive oxygen species; Retina; Retinal pigment epithelium; Ribose
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox11122353

Phloroglucinol, a phenolic compound, is known to possess a potent antioxidant ability. However, its role in retinal cells susceptible to oxidative stress has not been well elucidated yet. Thus, the objective of this study was to evaluate whether phloroglucinol could protect against oxidative damage in cultured human retinal pigment epithelium ARPE-19 cells. For this purpose, ARPE-19 cells were stimula ted with hydrogen peroxide (H O ) to mimic oxidative stress. Cell viability, cytotoxicity, apoptosis, reactive oxygen species (ROS) generation, mitochondrial function, DNA damage, and autophagy were then assessed. Our results revealed that phloroglucinol ameliorated cell viability, cytotoxicity, and DNA damage in H O -exposued ARPE-19 cells and blocked production of ROS. Phloroglucinol also counteracted H O -induced apoptosis by reducing Bax/Bcl-2 ratio, blocking activation of caspase-3, and inhibiting degradation of poly (ADP-ribose) polymerase. H O caused mitochondrial impairment and increased expression levels of mitophagy markers such as PINK1and PARKIN known to be associated with mitochondrial ROS (mtROS) generation and cytosolic release of cytochrome . However, these changes were significantly attenuated by phloroglucinol. Mito-TEMPO, a selective mitochondrial antioxidant, further enhanced the protective effect of phloroglucinol against dysfunctional mitochondria. Furthermore, H O induced autophagy, but not when ARPE-19 cells were pretreated with phloroglucinol, meaning that autophagy by H O contributed to the pro-survival mechanism and that phloroglucinol protected ARPE-19 cells from apoptosis by blocking autophagy. Taken together, these results suggest that phloroglucinol can inhibit oxidative stress-induced ARPE-19 cell damage and dysfunction by protecting DNA damage, autophagy, and subsequent apoptosis through mitigation of mtROS generation. Thus, phloroglucinol might have therapeutic potential to prevent oxidative stress-mediated damage in RPE cells.