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Therapeutic Application of Dendrobium fimbriatum Hook for Retinopathy Caused by Ultraviolet Radiation and Chemotherapy Using ARPE-19 Cells and Mouse Retina.
Cheng, Chi-Feng; Wang, Sheue-Er; Lu, Chen-Wen; Nguyen, Thi Kim Ngan; Shen, Szu-Chuan; Lien, Chia-Ying; Chuang, Wu-Chang; Lee, Ming-Chung; Wu, Chung-Hsin.
Afiliação
  • Cheng CF; School of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
  • Wang SE; Department of Oncology, Taipei City United Hospital, Renai Branch, Taipei 106, Taiwan.
  • Lu CW; Department of Pathological Inspection, Saint Paul's Hospital, Taoyuan 330, Taiwan.
  • Nguyen TKN; School of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
  • Shen SC; School of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
  • Lien CY; School of Life Science, National Taiwan Normal University, Taipei 116, Taiwan.
  • Chuang WC; Master Program of Sport Facility Management and Health Promotion, National Taiwan University, Taipei 116, Taiwan.
  • Lee MC; Sun Ten Pharmaceutical Co., Ltd., New Taipei City 231, Taiwan.
  • Wu CH; Brion Research Institute of Taiwan, New Taipei City 231, Taiwan.
Plants (Basel) ; 13(5)2024 Feb 23.
Article em En | MEDLINE | ID: mdl-38475464
ABSTRACT
Retinopathy caused by ultraviolet radiation and cancer chemotherapy has increased dramatically in humans due to rapid environmental and social changes. Therefore, it is very important to develop therapeutic strategies to effectively alleviate retinopathy. In China, people often choose dendrobium to improve their eyesight. In this study, we explored how Dendrobium fimbriatum extract (DFE) protects ARPE-19 cells and mouse retinal tissue from damage of ultraviolet (UV) radiation and chemotherapy. We evaluated the antioxidant capacity of DFE using the 1,1-diphenyl-2-trinitophenylhydrazine (DPPH) assay. The protective effects of DEF from UV- and oxaliplatin (OXA)-induced damage were examined in ARPE-19 cells using 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and immunofluorescence (IF) stains, and in mouse retinal tissue using immunohistochemistry (IHC) stains. Our results show that DFE has excellent antioxidant capacity. The ARPE-19 cell viability was decreased and the F-actin cytoskeleton structure was damaged by UV radiation and OXA chemotherapy, but both were alleviated after the DFE treatment. Furthermore, DFE treatment can alleviate OXA chemotherapy-induced reduced expressions of rhodopsin and SOD2 and increased expressions of TNF-α and caspase 3 in mouse retinal tissue. Thus, we suggest that DFE can act as suitable treatment for retinopathy through reducing oxidative stress, inflammation, and apoptosis.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article