학술논문

Ultraviolet- and infrared-induced 11 beta-hydroxysteroid dehydrogenase type 1 activating skin photoaging is inhibited by red ginseng extract containing high concentration of ginsenoside Rg3(S).
Document Type
Article
Source
Photodermatology, Photoimmunology & Photomedicine. Nov2017, Vol. 33 Issue 6, p311-320. 10p.
Subject
*COLLAGEN
*EXTRACELLULAR matrix
*GINSENOSIDES
*GENE expression
*FIBROBLASTS
*SKIN diseases
*SKIN aging
*KERATINOCYTES
Language
ISSN
0905-4383
Abstract
Background Sun irradiation is one of major extrinsic stressors responsible for premature skin aging through activation and expression of 11 beta-hydroxysteroid dehydrogenase type 1 (11β- HSD1), which converts inactive cortisone to active cortisol. The aim of this study was to evaluate the inhibitory effects of red ginseng extract containing high concentrations of ginsenoside Rg3 (S) ( GERg3) on 11β- HSD1-induced skin photoaging. Methods To evaluate the inhibitory effects of GERg3 on ultraviolet- ( UV) or infrared ( IR)-induced skin photoaging, human dermal fibroblasts or a normal human 3D skin model was exposed to UV or an IR. RT- PCR, ELISA, Western blot, and H&E staining were used for evaluations. GERg3 was isolated from crude red ginseng. Results GERg3 inhibited the increased expressions of 11β- HSD1, interleukin ( IL)-6, and matrix metalloproteinase-1 ( MMP-1) in UVB- or IR-exposed Hs68 cells. Additionally, the increased cortisol, IL-6, and MMP-1 expressions were effectively reduced by GERg3 in UVA-exposed 3D skin models. The photoinduced decrease in type 1 procollagen also recovered as a result of GERg3 treatment in Hs68 cells and the 3D skin model. In addition, the UVA-exposed dermal thickness was decreased in comparison with the UVA-protected 3D skin model, recovered with GERg3 treatment. Conclusion GERg3 had antiphotoaging effects in UV- or IR-exposed human dermal fibroblasts and normal human 3D skin model. [ABSTRACT FROM AUTHOR]