Alstonia scholaris R. Br. Significantly Inhibits Retinoid-Induced Skin Irritation In Vitro and In Vivo

被引:107
作者
Lee, Soo-Jin [1 ]
Cho, Sun-A [1 ]
An, Su-Sun [1 ]
Na, Yong-Joo [1 ]
Park, Nok-Hyun [1 ]
Kim, Han-Sung [1 ]
Lee, Chan-Woo [1 ]
Kim, Han-Kon [1 ]
Kim, Eun-Kyung [2 ]
Jang, Young-Pyo [2 ]
Kim, Jin-Woong [3 ]
机构
[1] Amorepacific Co R&D Ctr, Yongin 449729, Gyeonggi Do, South Korea
[2] Kyung Hee Univ, Coll Pharm, Seoul 130701, South Korea
[3] Hanyang Univ, Dept Appl Chem, Ansan 426791, Gyeonggi Do, South Korea
关键词
GENE-RELATED PEPTIDE; TOPICAL TRETINOIN; INDOLE ALKALOIDS; CONSTITUENTS; MECHANISMS; CAPSAICIN; BARK; MADECASSOSIDE; RECEPTORS; EXTRACTS;
D O I
10.1155/2012/190370
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Topical retinoids inhibit matrix metalloproteinases and accelerate collagen synthesis, thereby triggering antiaging effects in the skin. However, topical retinoids can cause severe skin reactions, including scaling, erythema, papules, and inflammation. The present study demonstrates that the ethanolic bark extract of Alstonia scholaris R. Br. can significantly inhibit all-trans retinoic acid-induced inflammation in human HaCat keratinocyte cells. Furthermore, two representative retinoid-induced proinflammatory cytokines, monocyte chemoattractant protein-1 and interleukin-8, were significantly suppressed by A. scholaris extract (by 82.1% and 26.3% at 100 ppm, and dose-dependently across the tested concentrations) in vitro. In a cumulative irritation patch test, A. scholaris extract decreased retinol-induced skin irritation, while strengthening the ability of retinoids to inhibit matrix metalloproteinase-1 expression, which is strongly associated with aging effects. These results suggest that A. scholaris is a promising compound that may increase the antiaging function of retinoids while reducing their ability to cause skin irritation.
引用
收藏
页数:11
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