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Changes of Antimicrobial Peptides and Transepidermal Water Loss After Topical Application of Tacrolimus and Ceramide-dominant Emollient in Patients with Atopic Dermatitisopen access

Authors
Park, Kui YoungKim, Dong HaJeong, Mi SookLi, KapsokSeo, Seong Jun
Issue Date
May-2010
Publisher
KOREAN ACAD MEDICAL SCIENCES
Keywords
Antimicrobial peptide; Dermatitis, Atopic; Ceramides; Permeability Barrier; Tacrolimus
Citation
JOURNAL OF KOREAN MEDICAL SCIENCE, v.25, no.5, pp 766 - 771
Pages
6
Journal Title
JOURNAL OF KOREAN MEDICAL SCIENCE
Volume
25
Number
5
Start Page
766
End Page
771
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22476
DOI
10.3346/jkms.2010.25.5.766
ISSN
1011-8934
1598-6357
Abstract
Increased transepidermal water loss (TEWL) and downregulated antimicrobial peptides (AMPs) are observed in patients with atopic dermatitis (AD). Tacrolimus and ceramide-dominant emollients are effective in the treatment of AD by preventing the production of inflammatory cytokines and by correcting skin barrier dysfunctions, respectively. Present study was designed to investigate the relationship between antimicrobial and barrier factors by measuring the changes of AMPs and TEWL after topical application of tacrolimus and ceramide-dominant emollient in the patients with AD. A total of three patients with AD were treated with tacrolimus in one lesion and ceramide-dominant emollient in another lesion for 4 weeks. RT-PCR and western blotting revealed that the mRNA and protein expression levels of hBD-2 and LL-37 were increased on the both study sites. Immunohistochemical analysis showed significant increase of AMPs and IL-1 alpha, while, IL-4 was decreased on the both study sites. The mean changes of TEWL and AMPs showed no statistical difference between both sites. Tacrolimus and ceramide-dominant emollient influence on both TEWL and AMPs expression in patients with AD, namely they have similar effects on both of the two. This study shows that restoration of permeability barrier function is accompanied by the concomitant improvement of antimicrobial defense in patients with AD.
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