Biomol Ther.  2024 May;32(3):329-340. 10.4062/biomolther.2023.175.

Activation of Heme Oxygenase-1 by Mangiferin in Human Retinal Pigment Epithelial Cells Contributes to Blocking Oxidative Damage

Affiliations
  • 1Division of Basic Sciences, College of Liberal Studies, Dong-eui University, Busan 47340, Republic of Korea
  • 2Department of Parasitology and Genetics, Kosin University College of Medicine, Busan 49104, Republic of Korea
  • 3Anti-Aging Research Center, Dong-eui University, Busan 47340, Republic of Korea
  • 4Department of Biochemistry, College of Korean Medicine, Dong-eui University, Busan 47227, Republic of Korea
  • 5Department of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 46241, Republic of Korea
  • 6Department of Urology, Chungbuk National University College of Medicine, Cheongju 28644, Republic of Korea
  • 7Department of Food and Nutrition, Chung-Ang University, Ansung 17546, Republic of Korea
  • 8Institute of Urotech, Cheongju 28120, Republic of Korea
  • 9Department of Marine Life Sciences, Jeju National University, Jeju 63243, Republic of Korea
  • 10Department of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan 58554, Republic of Korea
  • 11The China-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan 450008, China

Abstract

Mangiferin is a kind of natural xanthone glycosides and is known to have various pharmacological activities. However, since the beneficial efficacy of this compound has not been reported in retinal pigment epithelial (RPE) cells, this study aimed to evaluate whether mangiferin could protect human RPE ARPE-19 cells from oxidative injury mimicked by hydrogen peroxide (H 2O 2). The results showed that mangiferin attenuated H 2O 2-induced cell viability reduction and DNA damage, while inhibiting reactive oxygen species (ROS) production and preserving diminished glutathione (GSH). Mangiferin also antagonized H 2O 2-induced inhibition of the expression and activity of antioxidant enzymes such as manganese superoxide dismutase and GSH peroxidase, which was associated with inhibition of mitochondrial ROS production. In addition, mangiferin protected ARPE-19 cells from H 2O 2-induced apoptosis by increasing the Bcl-2/Bax ratio, decreasing caspase-3 activation, and blocking poly(ADP-ribose) polymerase cleavage. Moreover, mangiferin suppressed the release of cytochrome c into the cytosol, which was achieved by interfering with mitochondrial membrane disruption. Furthermore, mangiferin increased the expression and activity of heme oxygenase-1 (HO-1) and nuclear factor-erythroid-2 related factor 2 (Nrf2). However, the inhibition of ROS production, cytoprotective and anti-apoptotic effects of mangiferin were significantly attenuated by the HO-1 inhibitor, indicating that mangiferin promoted Nrf2-mediated HO-1 activity to prevent ARPE-19 cells from oxidative injury. The results of this study suggest that mangiferin, as an Nrf2 activator, has potent ROS scavenging activity and may have the potential to protect oxidative stress-mediated ocular diseases.

Keyword

Mangiferin; Reactive oxygen species; DNA damage; Apoptosis; Nrf2/HO-1
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