Polypodium leucotomos extract decreases UV-induced Cox-2 expression and inflammation, enhances DNA repair, and decreases mutagenesis in hairless mice Journal Article


Authors: Zattra, E.; Coleman, C.; Arad, S.; Helms, E.; Levine, D.; Bord, E.; Guillaume, A.; El-Hajahmad, M.; Zwart, E.; Van Steeg, H.; González-Rodríguez, S.; Kishore, R.; Goukassian, D. A.
Article Title: Polypodium leucotomos extract decreases UV-induced Cox-2 expression and inflammation, enhances DNA repair, and decreases mutagenesis in hairless mice
Abstract: UV-irradiated skin and UV-induced tumors overexpress the inducible isoform of cyclooxygenase-2 (Cox-2), and Cox-2 inhibition reduces photocarcinogenesis. To evaluate photoprotective effects of Polypodium leucotomos extract (PL), hairless Xpc<sup>+/-</sup> mice were fed for 10 days with PL (300 mg/kg) or vehicle then UV-irradiated, once. By 24 hours, UV-induced Cox-2 levels were increased in vehicle-fed and PL-fed mice, whereas by 48 and 72 hours, Cox-2 levels were four- to fivefold lower in PL-fed mice (P &lt; 0.05). p53 expression/activity was increased in PL-fed versus vehicle-fed then UV-irradiated mice. UV-induced inflammation was decreased in PL-fed mice, as shown by ∼60% decrease (P &lt; 0.001) in neutrophil infiltration at 24 hours, and macrophages by ∼50% (&lt;0.02) at 24 and 48 hours. By 72 hours, 54 ± 5% cyclobutane pyrimidine dimers remained in vehicle-fed versus 31 ± 5% in PL-fed skin (P &lt; 0.003). The number of 8-hydroxy-2′- deoxyguanosine-positive cells were decreased before UV irradiation by ∼36% (P &lt; 0.01), suggesting that PL reduces constitutive oxidative DNA damage. By 6 and 24 hours, the number of 8-hydroxy-2′-deoxyguanosine-positive cells were ∼59% (P &lt; 0.01) and ∼79% (P &lt; 0.03) lower in PL-fed versus vehicle-fed mice. Finally, UV-induced mutations in PL-fed-mice were decreased by ∼25% when assessed 2 weeks after the single UV exposure. These data demonstrate that PL extract supplementation affords the following photoprotective effects: p53 activation and reduction of acute inflammation via Cox-2 enzyme inhibition, increased cyclobutane pyrimidine dimer removal, and reduction of oxidative DNA damage. Copyright © American Society for Investigative Pathology.
Keywords: controlled study; protein expression; unclassified drug; drug activity; nonhuman; ultraviolet radiation; mouse; animals; mice; animal tissue; dna damage; dna repair; enzyme inhibition; cell infiltration; animal experiment; animal model; inflammation; mutational analysis; protein p53; radiation exposure; skin; cyclooxygenase 2; tumor suppressor protein p53; deoxyguanosine; plant extracts; dietary supplements; dna mutational analysis; macrophage; macrophages; ultraviolet rays; mutagenesis; neutrophil chemotaxis; polypodium leucotomos extract; ultraviolet irradiation; polypodium; 8 hydroxydeoxyguanosine; cyclobutane derivative; cyclobutane pyrimide dimer derivative; hairless mouse; mice, hairless; pyrimidine dimers
Journal Title: American Journal of Pathology
Volume: 175
Issue: 5
ISSN: 0002-9440
Publisher: Elsevier Science, Inc.  
Date Published: 2009-01-01
Start Page: 1952
End Page: 1961
Language: English
DOI: 10.2353/ajpath.2009.090351
PUBMED: 19808641
PROVIDER: scopus
PMCID: PMC2774059
DOI/URL:
Notes: --- - "Cited By (since 1996): 2" - "Export Date: 30 November 2010" - "CODEN: AJPAA" - "Source: Scopus"
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  1. Salvador Gonzalez Rodriguez
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