Abstract

Skin aging can be attributed to photoaging (extrinsic) and chronological (intrinsic) aging. Photoaging and intrinsic aging are induced by damage to human skin attributable to repeated exposure to ultraviolet (UV) irradiation and to the passage of time, respectively. In our previous report, eicosapentaenoic acid (EPA) was found to inhibit UV-induced matrix metalloproteinase-1 (MMP-1) expression in human dermal fibroblasts. Therefore, we investigated the effects of EPA on UV-induced skin damage and intrinsic aging by applying EPA topically to young and aged human skin, respectively. By immunohistochemical analysis and Western blotting, we found that topical application of EPA reduced UV-induced epidermal thickening and inhibited collagen decrease induced by UV light. It was also found that EPA attenuated UV-induced MMP-1 and MMP-9 expression by inhibiting UV-induced c-Jun phosphorylation, which is closely related to UV-induced activator protein-1 activation, and by inhibiting JNK and p38 activation. EPA also inhibited UV-induced cyclooxygenase-2 (COX-2) expression without altering COX-1 expression. Moreover, it was found that EPA increased collagen and elastic fibers (tropoelastin and fibrillin-1) expression by increasing transformin growth factor-beta expression in aged human skin. Together, these results demonstrate that topical EPA has potential as an anti-skin-aging agent.

Highlights

  • Skin aging can be attributed to photoaging and chronological aging

  • We demonstrated that eicosapentaenoic acid (EPA) inhibits UV-induced matrix metalloproteinase (MMP)-1 expression in human dermal fibroblasts and that it is mediated by the inhibition of the MEK1/ ERK/c-Fos and SEK1/JNK/c-Jun pathways [15]

  • We demonstrated that EPA inhibits UV-induced matrix metalloproteinase-1 (MMP-1) expression in human dermal fibroblasts [15] and that treating human dermal fibroblasts with EPA inhibited UV-induced activator protein-1 (AP-1) activation, which has an important role in MMP-1 expression

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Summary

Introduction

Skin aging can be attributed to photoaging (extrinsic) and chronological (intrinsic) aging. Photoaging and intrinsic aging are induced by damage to human skin attributable to repeated exposure to ultraviolet (UV) irradiation and to the passage of time, respectively. Eicosapentaenoic acid (EPA) was found to inhibit UV-induced matrix metalloproteinase-1 (MMP-1) expression in human dermal fibroblasts. It was found that EPA increased collagen and elastic fibers (tropoelastin and fibrillin-1) expression by increasing transformin growth factor-b expression in aged human skin. Together, these results demonstrate that topical EPA has potential as an anti-skin-aging agent.—Kim, H. UV-induced AP-1 transcriptional activity that is closely related to MMP expression is limited by c-Jun expression, because c-Fos is constitutively expressed [7]. This article is available online at http://www.jlr.org

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