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Michelia alba extract attenuates UVB-induced expression of matrix metalloproteinases via MAP kinase pathway in human dermal fibroblasts
[Display omitted] ► MAE exhibited antioxidant activity. ► MAE inhibited collagenase activity. ► MAE inhibited UVB-induced MMP-1 and MMP-3 expression and MMP-9 activity. ► MAE inhibited UVB-induced ERK and JNK kinase but not p38 kinase expression. ► MAE is an effective agent against UVB-induced photo...
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Published in: | Food and chemical toxicology 2012-12, Vol.50 (12), p.4260-4269 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
► MAE exhibited antioxidant activity. ► MAE inhibited collagenase activity. ► MAE inhibited UVB-induced MMP-1 and MMP-3 expression and MMP-9 activity. ► MAE inhibited UVB-induced ERK and JNK kinase but not p38 kinase expression. ► MAE is an effective agent against UVB-induced photodamage.
Solar ultraviolet (UV) radiation can cause skin photoaging by inducing secretion of matrix metalloproteinases (MMPs). It has been reported that MMPs, especially MMP-1, -3 and -9, reduce elasticity of the dermis by degrading collagen. Polyphenols are a group of compounds that exist mainly in glycosides in the plants and they may transform to aglycone after hydrolysis. Polyphenols can inhibit MMP expression and elastase activity. In this study, we investigated the effects of Michelia alba extract (MAE) on expression and activity of MMPs in human skin fibroblast cultures after UVB exposure. The results showed that MAE and its hydrolysates (MAH) inhibited collagenase and elastase activities. In addition, MAE exhibited antioxidant activity, elevated hyaluronic acid content and inhibited UVB-induced MMP-1, MMP-3 and MMP-9 expression. In addition, the zymography assay revealed that MAE also inhibited MMP-9 activity. We also found that MAE inhibited UVB-induced ERK and JNK kinase but not p38 kinase expression, suggesting that MAE may regulate the UVB-induced expression of MMP-1, MMP-3 and MMP-9 via the ERK and JNK kinase pathway. MAE could restore total collagen synthesis reduced by UVB. The results also suggest that MAE treatment may prevent UVB-induced extracellular matrix damage by inhibiting the expression of MMP-1, MMP-3 and MMP-9 through the MAP kinase pathway. Our findings imply that MAE is an effective agent against UVB-induced photodamage. |
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ISSN: | 0278-6915 1873-6351 |
DOI: | 10.1016/j.fct.2012.08.018 |