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알레르기성 비염에서 황련-감초 하태독법의 IL-4활성 조절을 통한 항염증효과Anti-inflammatory effects of Hataedock with Coptidis Rhizoma and Glycyrrhiza Uralensis on Allergic Rhinitis through Regulating IL-4 Activation

Other Titles
Anti-inflammatory effects of Hataedock with Coptidis Rhizoma and Glycyrrhiza Uralensis on Allergic Rhinitis through Regulating IL-4 Activation
Authors
정아람
Issue Date
Apr-2019
Publisher
한의병리학회
Keywords
Hataedock; Coptidis Rhizoma; Glycyrrhiza Uralensis; Allergic rhinitis; Inflammation
Citation
동의생리병리학회지, v.33, no.2, pp.116 - 122
Journal Title
동의생리병리학회지
Volume
33
Number
2
Start Page
116
End Page
122
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/54645
DOI
10.15188/kjopp.2019.04.33.2.116
ISSN
1738-7698
Abstract
The aim of this study is to evaluate the anti-inflammatory effect of Hataedock treatment using Coptidis Rhizome and Glycyrrhiza Uralensis (CG) mixed extract in allergic rhinitis induced NC/Nga mice. We divided NC/Nga mice into 3 groups as follows; allergic rhinitis-induced group after CG Hataedock treatment (CGT, n=10), no treatment group (Ctrl), allergic rhinitis elicited group (ARE). To induce allergic rhinitis, NC/Nga mice of 3 weeks age were sensitized on 7, 8 and 9week by Ovalbumin (OVA) antigen in intranasal space. Hataedock using CG extract was administered on week 3 in allergic rhinitis-induced group (CGT) after Hataedock treatment. To identify distribution of Interlukin (IL)-4, Cluster of differentiation 40 (CD40), high-affinity IgE receptor (FcɛRI), substance P, Matrix metallopeptidase 9 (MMP-9), Nuclear factor-κB (NF-κB) p65, Inducible nitric oxide synthase (iNOS) and Cycloxygenase-2 (COX-2), we used histological examination. CGT significantly inhibited IL-4 and CD40 response compared with ARE. The reduction of Th2 cytokine expression decreased inflammatory mediators such as FcɛRI, substance P, MMP-9, NF-κB p65, iNOS and COX-2. Such immunological improvement induced reduction of respiratory epithelial damage and mucin secretion in goblet cell. These results indicate that Hataedock treatment suppresses allergic rhinitis through modulating of Th2 responses and diminishing various inflammatory mediators in nasal mucosal tissue. It might have potential applications for prevention and treatment of allergic rhinitis.
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