Antioxidant enzymes immobilized on gold and silver nanoparticles enhance DNA repairing systems of rat skin after exposure to ultraviolet radiation

Nanomedicine. 2022 Jul:43:102558. doi: 10.1016/j.nano.2022.102558. Epub 2022 Apr 4.

Abstract

The aim of the study was to investigate in vivo whether the application of immobilized superoxide dismutase (SOD) and catalase (CAT) could enhance DNA repairing systems and reduce level of CPD (cyclobutane pyrimidine dimers) and 6-4PP ((6-4) pyrimidine-pyrimidone photoproducts), and whether the immobilization on gold (AuNPs) and silver (AgNPs) nanoparticles affects the outcome. The study presents secondary analysis of our previous research. Three-day application of SOD and CAT in all forms of solution decreased the levels of CPD and 6-4PP boosted by UV irradiation. The mRNA expression level of the nucleotide excision repair (NER) system genes (XPA, XPC, ERCC1, ERCC2, ERCC3, LIG1) increased after application of immobilized and free enzymes. Increased by UV irradiation, p53 mRNA expression level normalized with the enzyme application. In conclusion, application of free and immobilized antioxidant enzymes accelerates removal of harmful effects of UV radiation in the rat skin by increasing expression level of NER genes.

Keywords: Catalase; DNA repair; Gold nanoparticles; In vivo skin damage; Silver nanoparticles; Superoxide dismutase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants
  • DNA / genetics
  • DNA Damage
  • DNA Repair
  • Gold
  • Metal Nanoparticles*
  • RNA, Messenger
  • Rats
  • Silver / pharmacology
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Ultraviolet Rays*

Substances

  • Antioxidants
  • RNA, Messenger
  • Silver
  • Gold
  • DNA
  • Superoxide Dismutase