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Capsaicin induces atopic dermatitis-like manifestations through dysregulation of proteolytic system and alteration of filaggrin processing in rats

Authors
Kim, SewonBack, Seung KeunNa, Heung SikKee, Sun-Ho
Issue Date
4월-2018
Publisher
WILEY
Keywords
atopic dermatitis; Capsaicin; postnatal development; proteases
Citation
EXPERIMENTAL DERMATOLOGY, v.27, no.4, pp.332 - 339
Indexed
SCIE
SCOPUS
Journal Title
EXPERIMENTAL DERMATOLOGY
Volume
27
Number
4
Start Page
332
End Page
339
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/76288
DOI
10.1111/exd.13527
ISSN
0906-6705
Abstract
Atopic dermatitis (AD) is a complex disease featuring pruritic skin inflammation. Many animal models have been developed. In a rat model, subcutaneous capsaicin injection within 48hours after birth induces AD-like skin manifestations of dermatitis and scratching behaviour 3weeks after the injection. When 2- to 4-week-old rats were injected with capsaicin, the lag period was shortened, and the severity of skin manifestations was significantly reduced, suggesting influences of postnatal development. Lgr6 is an epidermal stem cell marker that is normally restricted to the isthmus area of hair follicles at postnatal 2weeks. Lgr6 persisted in the interfollicular epidermis of capsaicin-injected rats beyond 3weeks after birth, indicating that capsaicin-induced skin manifestations were influenced by postnatal epidermal development. Capsaicin injection induced alteration of proteolytic processing of filaggrin and corneodesmosin, suggesting epidermal barrier dysfunction. Inappropriate degradation of matriptase was observed. Degrees of proteolysis of these proteins were corelated with the severity of manifestations, suggesting that inappropriate proteolysis might be a possible cause of the skin manifestations. These results strongly suggest that capsaicin may dysregulate the protease system, resulting in alteration of profilaggrin and corneodesmosin proteolysis and skin manifestations. These events may be influenced by postnatal epidermal development.
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