Hesperidin promotes cyclobutane pyrimidine dimer repair in UVB-exposed mice epidermis

Ir J Med Sci. 2011 Sep;180(3):709-14. doi: 10.1007/s11845-010-0503-5. Epub 2010 Jun 11.

Abstract

Purpose: To investigate whether topical application of hesperin affords protection to Balb/C mice epidermis from UVB-induced cyclobutane pyrimidine dimers (CPDs).

Methods: A DNA damage model of UVB irradiation-induced mice epidermis was established. The immunohistochemical staining and southwestern dot blotting were used for CPDs detection; western blotting was used for P53 detection.

Results: Topical application of hesperidin on Balb/C mice skin significantly decreased the amount of epidermal CPDs 24 and 48 h after 180 mJ/cm(2) of UVB irradiation as compared to untreated mice. UVB-induced p53 expression was more pronounced in hesperidin-treated mice epidermis compared to that of untreated mice.

Conclusion: Taken together, these results suggest that topical hesperidin application promotes DNA photo-damage repair. Hesperidin is therefore a promising protective substance against UVB radiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Topical
  • Animals
  • Blotting, Southwestern
  • Blotting, Western
  • DNA Damage / drug effects*
  • DNA Repair Enzymes / physiology
  • Epidermis / drug effects
  • Epidermis / metabolism
  • Female
  • Hesperidin / administration & dosage
  • Hesperidin / chemistry
  • Hesperidin / therapeutic use*
  • Immunohistochemistry
  • Mice
  • Mice, Inbred BALB C
  • Oxidative Stress / physiology
  • Pyrimidine Dimers / metabolism*
  • Tumor Suppressor Protein p53 / metabolism
  • Ultraviolet Rays / adverse effects*

Substances

  • Pyrimidine Dimers
  • Tumor Suppressor Protein p53
  • Hesperidin
  • DNA Repair Enzymes