2004
DOI: 10.1016/j.jaad.2004.06.027
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Oral Polypodium leucotomos extract decreases ultraviolet-induced damage of human skin

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Cited by 133 publications
(121 citation statements)
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“…The incidence of phototoxicity was demonstrated to decrease after oral PL administration in subjects receiving psoralen-UVA (PUVA) treatment [99], as well as in normal healthy subjects [100]. In another study, PL-treated keratinocytes and fibroblasts exposed to UV displayed significantly ameliorated membrane integrity, mitigated lipid peroxidation, increased elastin expression and inhibited MMP-1 expression [101].…”
Section: Some Notable Anti-oxidantsmentioning
confidence: 98%
“…The incidence of phototoxicity was demonstrated to decrease after oral PL administration in subjects receiving psoralen-UVA (PUVA) treatment [99], as well as in normal healthy subjects [100]. In another study, PL-treated keratinocytes and fibroblasts exposed to UV displayed significantly ameliorated membrane integrity, mitigated lipid peroxidation, increased elastin expression and inhibited MMP-1 expression [101].…”
Section: Some Notable Anti-oxidantsmentioning
confidence: 98%
“…Moreover, oral administration of extracts of natural compounds such Polypodium leucotomos (PL) had been reported to induce photoprotective mechanisms through reduction of UV-induced reactive oxygen species and formation of free radicals, which in turn reduces post-UV inflammation, photodamage, and phototoxicity. 5,15 The mouse homologue of the human gene xeroderma pigmentosum group C (Xpc) has been cloned, and subsequently, knockout and heterozygote mice have been generated. 16 The Xpc heterozygote mice display a skin cancer proneness that is highly comparable with that observed in mild human XP syndromes, which may also model age-associated increase in skin cancer predisposition due to decline in DNA repair capacity, 17 as well as exaggerated inflammation secondary to UV exposure.…”
mentioning
confidence: 99%
“…* Polypodium leucotomos extract (PL) can also be administered orally with very low toxicity, in addition to its topical use as already described.Oral PL scavenges free radicals and reactive oxygen species such as superoxide anion, singlet oxygen, hydroxyl radical and hydrogen peroxide, and prevents lipid peroxidation [47,48]. Besides the effects already mentioned, PL also prevents oxidative DNA damage (8-hydroxyguanine) and accelerates repair of thymine dimers [24,49]. In addition, it also inhibitstrans-urocanic acid photo-induced isomerization and inactivation, as well as UVA-induced cyclobutane pyrimidine dimer deletions and mitochondrial DNA damage [50,51].…”
Section: Systemic Sunscreensmentioning
confidence: 96%
“…It is a potent antioxidant and has shown immunemodulating capability and inhibition of pro-inflammatory cytokines, such as TNF-α or IL-6 [22]. PL also inhibits the depletion of langerhan cells induced by irradiation with UV light and PUVA therapy [22][23][24] and reduces chronic elastosis and matrix metalloprotease expression [25,26]. * Dihydroxy-acetone: Photo-protective agent that provides SPF 3-4 and protects against UVA photons [27].…”
Section: Antioxidantsmentioning
confidence: 99%