Novel Facial Cream Containing Carnosine Inhibits Formation of Advanced Glycation End-Products in Human Skin

被引:23
|
作者
Narda, Mridvika [1 ]
Peno-Mazzarino, Laurent [2 ]
Krutmann, Jean [3 ,4 ,5 ]
Trullas, Caries [1 ]
Granger, Corinne [1 ]
机构
[1] ISDIN, Innovat & Dev, Barcelona, Spain
[2] Lab BIO EC, Longjumeau, France
[3] Univ Dusseldorf, Leibniz Res Inst Environm Med, Dusseldorf, Germany
[4] Univ Dusseldorf, Med Fac, Med, Dusseldorf, Germany
[5] Heinrich Heine Univ Dusseldorf, Med Fac, Dusseldorf, Germany
关键词
Advanced glycation end-products; Glycation; Skin aging; Anti-aging; Carnosine; Facial cream;
D O I
10.1159/000492276
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Accumulation of advanced glycation end-products (AGEs) in skin has been associated with skin aging. Inhibition of glycation of proteins of extracellular matrix may help skin texture and appearance. The objective of the study was to demonstrate the antiglycation activity of topically applied carnosine and novel facial cream (FC) containing carnosine in human skin explants ex vivo. Methods: Glycation was induced in human skin explants by methylglyoxal (MG) in culture media. FC containing carnosine (FC-CARN) or carnosine in aqueous solution (AQ-CARN) was applied topically on skin explants. Levels of AGEs carboxymethyl-lysine (CML) and pentosidine were determined in the epidermis and dermis of skin sections and were used to calculate antiglycation activity. Results: Exposure to MG led to increases in CML and pentosidine in skin explants. Antiglycation effect for AQ-CARN was CML: -64 and -41%, pentosidine: -48 and 42% in epidermis and reticular dermis respectively. Antiglycation effect for FC-CARN was CML: -150 and -122%, pentosidine:-108 and -136%, in epidermis and reticular dermis respectively. Conclusion: Topically applied carnosine protects against the glycation induced by MG. Novel FC-CARN significantly reduced levels of AGEs in both epidermis and reticular dermis in human skin explants. (C) 2018 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:324 / 331
页数:8
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