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Protein Oxidation Levels After Different Corneal Collagen Cross-Linking Methods

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Date

2016

Author

Türkcü, ÜmmÜhani Özel
Yüksel, Nilay
Novruzlu, Şahin
Yalınbaş, Duygu
Bilgihan, Ayse
Bilgihan, Kamil
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Referenced in 1 patents
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Abstract

Purpose: To evaluate advanced oxidation protein products (AOPP) levels, superoxide dismutase (SOD) enzyme activity, and total sulfhydryl (TSH) levels in rabbit corneas after different corneal collagen cross-linking (CXL) methods. Methods: Eighteen eyes of 9 adult New Zealand rabbits were divided into 3 groups of 6 eyes. The standard CXL group was continuously exposed to UV-A at a power setting of 3 mW/cm(2) for 30 minutes. The accelerated CXL (A-CXL) group was continuously exposed to UV-A at a power setting of 30 mW/cm(2) for 3 minutes. The pulse light-accelerated CXL (PLA-CXL) group received UV-A at a power setting of 30 mW/cm(2) for 6 minutes of pulsed exposure (1 second on, 1 second off). Corneas were obtained after 1 hour of UV-A exposure, and 360-degree keratotomy was performed. SOD enzyme activity, AOPP, and TSH levels were measured in the corneal tissues. Results: Compared with the standard CXL and A-CXL groups (133.2 +/- 8.5 and 140.2 +/- 6.2 mu mol/mg, respectively), AOPP levels were found to be significantly increased in the PLA-CXL group (230.7 +/- 30.2 mu mol/mg) (P = 0.005 and 0.009, respectively). SOD enzyme activities and TSH levels did not differ between the groups (P = 0.167 and 0.187, respectively). Conclusions: CXL creates covalent bonds between collagen fibers because of reactive oxygen species. This means that more oxygen concentration during the CXL method will produce more reactive oxygen species and, thereby, AOPP. This means that in which CXL method occurs in more oxygen concentration that will produce more reactive oxygen species and thereby AOPP. This study demonstrated that PLA-CXL results in more AOPP formation than did standard CXL and A-CXL.

Source

Cornea

Volume

35

Issue

3

URI

https://doi.org/10.1097/ICO.0000000000000731
https://hdl.handle.net/20.500.12809/2576

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  • PubMed İndeksli Yayınlar Koleksiyonu [2082]
  • Scopus İndeksli Yayınlar Koleksiyonu [6219]
  • Temel Tıp Bilimleri Bölümü Koleksiyonu [193]
  • WoS İndeksli Yayınlar Koleksiyonu [6466]



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