- Author:
So Hee NAM
1
;
Seung Eun JUNG
;
Yoen Kyung LEE
;
Ji Eun KIM
;
Eon Pil LEE
;
Hae Wook CHOI
;
Hong Sung KIM
;
Jae Ho LEE
;
Young Jin JUNG
;
Chung Yeol LEE
;
Hong Ju SON
;
Hyun Woong LEE
;
Jung Sik CHO
;
Byeong Cheol KANG
;
Dae Youn HWANG
Author Information
- Publication Type:Original Article
- Keywords: Selenium; photoaging; UV-irradiation; MMP
- MeSH: Animals; Blotting, Western; Mice; Mice, Hairless; Phosphorylation; Selenium; Skin; Skin Aging
- From:Laboratory Animal Research 2010;26(1):37-45
- CountryRepublic of Korea
- Language:Korean
- Abstract: Ultraviolet (UV) irradiation is an environmental factor that causes skin aging, and is also a major factor leading to cumulative alterations of skin structure, function and appearance. To investigate the effects of Selenium (Sel) on UV-induced skin aging, hairless mice were treated for 4 weeks with UV irradiation and topical application of Sel. Then, the effects of Sel were measured in the skin of these mice via histological analysis and Western blotting. According to the results of wrinkle formation analysis, the topical application of Sel induced a reduction in wrinkling formation in the damaged skin of the UV-irradiated mice. Additionally, our histological analysis demonstrated that the skin thickness in the Sel-treated group was less than in the UV-irradiated group. Furthermore, in an effort to investigate the mechanisms underlying the effects of Sel, the expression levels of matrix-metalloproteinase (MMP) and MAPK protein were assessed in both groups. The application of Sel induced a reduction in MMP-1 expression levels to the levels observed in the non-irradiated group. However, the expression level of MMP-9 was increased slightly in the Sel application group as compared with the vehicle application group. Additionally, the levels of ERK phosphorylation were increased by the application of Sel, but the levels of JNK and p38 were not altered by Sel treatment. These results suggest the possibility that Sel should be considered as a skin aging-protective and therapeutic drug candidate, which functions via the regulation of MMP expression levels.