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K6PC-5, a novel sphingosine kinase activator, improves long-term ultraviolet light-exposed aged murine skin

Authors
 Hwa-young Park  ;  Jong-Kyung Youm  ;  Mi Jung Kwon  ;  Byeong Deog Park  ;  Seung Hun Lee  ;  Eung Ho Choi 
Citation
 EXPERIMENTAL DERMATOLOGY, Vol.17(10) : 829-836, 2008 
Journal Title
 EXPERIMENTAL DERMATOLOGY 
ISSN
 0906-6705 
Issue Date
2008
MeSH
Amides/pharmacology* ; Animals ; Biomarkers/metabolism ; Cell Division/drug effects ; Collagen/metabolism ; Dermis/cytology ; Dermis/enzymology ; Dermis/radiation effects ; Enzyme Activation/drug effects ; Epidermal Cells ; Epidermis/enzymology* ; Epidermis/radiation effects ; Female ; Fibroblasts/cytology ; Fibroblasts/enzymology ; Fibroblasts/radiation effects ; Lysophospholipids/metabolism ; Mice ; Mice, Hairless ; Phosphotransferases (Alcohol Group Acceptor)/metabolism* ; Skin Aging/drug effects* ; Sphingosine/analogs & derivatives ; Sphingosine/metabolism ; Ultraviolet Rays*
Keywords
anti-aging ; skin barrier ; sphingosine-1-phosphate ; sphingosine kinase activator ; UV light
Abstract
Sphingosine-1-phosphate (S1P), which is formed by phosphorylation of sphingosine through a process catalysed by sphingosine kinase (SK), is a multifunctional mediator of a variety of cellular responses including proliferation, differentiation, motility, and survival. K6PC-5, which was recently synthesized as a novel SK activator, is expected to increase S1P levels. Indeed studies have already demonstrated that K6PC-5 exhibits anti-aging effects on intrinsic aged murine skin by increasing fibroblasts, collagen synthesis, dermal thickness, and epidermal differentiation. However, photoaging and intrinsic aging have highly different clinical and histopathological properties. In this study, we developed a photoaged murine model by exposing mice that were 56 weeks old to ultraviolet (UV)B and UVA radiation for 8 weeks. We then investigated whether K6PC-5, as an SK activator, had anti-aging effects on photoaged murine skin in addition to its effects on intrinsic aged murine skin and determined the mechanism. K6PC-5 increased dermal collagen density in photoaged skin through increases in fibroblasts and collagen production. Photoaged murine skin treated with K6PC-5 showed an increase in stratum corneum (SC) integrity with increased corneodesmosome density and an improvement in barrier recovery rate. Matrix metalloproteinase 13 remained unchanged. These results indicate that topical application of K6PC-5 improves photoaged skin by improving skin barrier and increasing fibroblast count and function. In conclusion, K6PC-5, as an S1P activator, improves long-term UV-exposed aged skin as well as intrinsic aged skin.
Full Text
http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0625.2008.00708.x/abstract
DOI
10.1111/j.1600-0625.2008.00708.x
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
Yonsei Authors
Lee, Seung Hun(이승헌)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/108327
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