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Cited 3 time in webofscience Cited 3 time in scopus
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Papain Suppresses Atopic Skin Inflammation through Anti-Inflammatory Activities Using In Vitro and In Vivo Modelsopen access

Authors
Kim, Hye-MinKang, Yun-MiLee, MinhoAn, Hyo-Jin
Issue Date
Aug-2024
Publisher
MDPI AG
Keywords
atopic dermatitis; Dermatophagoides farinae body; keratinocytes; NC/Nga; papain
Citation
Antioxidants, v.13, no.8, pp 1 - 17
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
Antioxidants
Volume
13
Number
8
Start Page
1
End Page
17
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/23035
DOI
10.3390/antiox13080928
ISSN
2076-3921
2076-3921
Abstract
Papain (PN) is a proteolytic enzyme derived from Carica Papaya L. While the pharmacological effects of PN have not been extensively studied compared to its enzymatic activity, PN also holds potential benefits beyond protein digestion. This study aimed to investigate the potential effects of PN against skin inflammation in house dust mite Dermatophagoides farinae body (Dfb)-exposed NC/Nga atopic dermatitis (AD) mice and human HaCaT keratinocytes and their underlying mechanisms. The effects of PN on the skin were assessed via histological examination, measurements of transepidermal water loss (TEWL), quantitative reverse transcription-polymerase chain reaction, Western blotting, and enzyme-linked immunosorbent assay. Our findings indicated that the oral intake of PN decreased the severity scores of lesions resembling AD, TEWL, and the levels of inflammatory cytokines and serum immunoglobulin E in Dfb-induced AD mice, along with a reduction in epidermal thickness and mast cell infiltration. Additionally, PN inhibited the activation of the mitogen-activated protein kinases (MAPKs) and the signal transducer and activator of transcription (STAT) pathways in Dfb-induced AD mice and HaCaT keratinocytes. Moreover, PN improved survival and reduced ROS production in H2O2-damaged HaCaT keratinocytes and enhanced the expression of antioxidant enzymes in Dfb-induced AD mice. Concludingly, the oral administration of PN suppressed inflammatory mediators and downregulated the MAPKs/STAT pathway, suggesting its potential role in AD pathogenesis. © 2024 by the authors.
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