Increased oxidative DNA damage, lipid peroxidation, and reactive oxygen species in cultured orbital fibroblasts from patients with Graves ophthalmopathy: Evidence that oxidative stress has a role in this disorder

C. C. Tsai, S. B. Wu, C. Y. Cheng, S. C. Kao, H. C. Kau, S. H. Chiou, Wen-Ming Hsu, Y. H. Wei

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Purpose: We investigated the oxidative stress in orbital fibroadipose tissues and cultured orbital fibroblasts from patients with Graves ophthalmopathy (GO). Methods: The content of 8-hydroxy 2′-deoxyguanosine (8-OHdG), an important biomarker of oxidative DNA damage, was measured in orbital fibroadipose tissues and cultured orbital fibroblasts from patients with GO and compared with age-matched normal controls. A product of lipid peroxidation, malondialdehyde (MDA), and intracellular reactive oxygen species (ROS) in cultured orbital fibroblasts was also determined. Results: There was no significant difference in the 8-OHdG content of orbital fibroadipose tissues between patients with GO and age-matched normal controls (P=0.074). However, the levels of 8-OHdG and MDA in GO orbital fibroblasts were significantly higher than those of normal controls (P=0.0026 and P=0.001, respectively). In addition, GO orbital fibroblasts had higher contents of superoxide anions and hydrogen peroxide compared with those of normal controls (P=0.0133 and 0.0025, respectively). Conclusion: sOrbital fibroblasts represent the most abundant cell type among orbital connective tissues and exhibit great differences in their phenotypes. Increased oxidative DNA damage and lipid peroxidation, as well as higher intracellular ROS levels in GO orbital fibroblasts may have a role in the pathogenesis of GO.

Original languageEnglish
Pages (from-to)1520-1525
Number of pages6
JournalEye
Volume24
Issue number9
DOIs
Publication statusPublished - Jan 1 2010

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Graves Ophthalmopathy
Lipid Peroxidation
DNA Damage
Reactive Oxygen Species
Oxidative Stress
Fibroblasts
Malondialdehyde
Superoxides
Connective Tissue
Hydrogen Peroxide
Biomarkers
Phenotype

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems

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Increased oxidative DNA damage, lipid peroxidation, and reactive oxygen species in cultured orbital fibroblasts from patients with Graves ophthalmopathy : Evidence that oxidative stress has a role in this disorder. / Tsai, C. C.; Wu, S. B.; Cheng, C. Y.; Kao, S. C.; Kau, H. C.; Chiou, S. H.; Hsu, Wen-Ming; Wei, Y. H.

In: Eye, Vol. 24, No. 9, 01.01.2010, p. 1520-1525.

Research output: Contribution to journalArticle

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abstract = "Purpose: We investigated the oxidative stress in orbital fibroadipose tissues and cultured orbital fibroblasts from patients with Graves ophthalmopathy (GO). Methods: The content of 8-hydroxy 2′-deoxyguanosine (8-OHdG), an important biomarker of oxidative DNA damage, was measured in orbital fibroadipose tissues and cultured orbital fibroblasts from patients with GO and compared with age-matched normal controls. A product of lipid peroxidation, malondialdehyde (MDA), and intracellular reactive oxygen species (ROS) in cultured orbital fibroblasts was also determined. Results: There was no significant difference in the 8-OHdG content of orbital fibroadipose tissues between patients with GO and age-matched normal controls (P=0.074). However, the levels of 8-OHdG and MDA in GO orbital fibroblasts were significantly higher than those of normal controls (P=0.0026 and P=0.001, respectively). In addition, GO orbital fibroblasts had higher contents of superoxide anions and hydrogen peroxide compared with those of normal controls (P=0.0133 and 0.0025, respectively). Conclusion: sOrbital fibroblasts represent the most abundant cell type among orbital connective tissues and exhibit great differences in their phenotypes. Increased oxidative DNA damage and lipid peroxidation, as well as higher intracellular ROS levels in GO orbital fibroblasts may have a role in the pathogenesis of GO.",
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AU - Cheng, C. Y.

AU - Kao, S. C.

AU - Kau, H. C.

AU - Chiou, S. H.

AU - Hsu, Wen-Ming

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