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Anti-allergic and Profilaggrin (ProFLG)-mRNA expression modulatory effects of sacran.

Authors :
Ngatu, Nlandu R.
Motoyama, Keiichi
Nishimura, Yasumitsu
Okajima, Maiko Kaneko
Hirota, Ryoji
Higashi, Taishi
Lee, Suni
Arima, Hidetoshi
Ikeda, Mitsunori
Nojima, Sayumi
Kaneko, Tatsuo
Source :
International Journal of Biological Macromolecules. Dec2017 Part 2, Vol. 105, p1532-1538. 7p.
Publication Year :
2017

Abstract

Atopic dermatitis (AD) is a skin disorder characterized by filaggrin (FLG) defect. We evaluated sacran’s effects on dust-mite extracts (DME)-induced AD-like disease and also its effect on profilaggrin (proFLG) in a murine model of 2,4- dinitroflurobenze (DNFB)-induced contact hypersensitivity. In the murine AD-like disease model, allergic NC/Nga mice (N = 60) were randomly divided into five treatment groups of 12 animals each: 0.2% and 1%sacran; 0.1% Tacrolimus ; Vaseline and buffer-treated controls. Blood samples were drawn and serum levels of representative Th-1, Th-2 and also Th-17 (IL-17A) cytokines were assayed by Cytometric Bead Array (CBA). In the contact hypersensitivity model, diseased NC/Nga mice (N = 20) were divided into four groups of five mice each [0.05%sacran, 0.05% chondroitin sulfate (CS), 0.5% prednisolone (PD), non-treated control group] and were treated for 14 days. Skin biopsies were performed for the measurement of proFLG-mRNA by real-time PCR. Sacran solutions and 0.1% Tacrolimus reduced disease severity, suppressed histological changes and decreased the serum Th-1 (IFN-γ, TNF-α, IL-2) and Th-2 (IL-4, IL-6, IL-10) cytokines in allergic mice (vs. controls). Additionally, a marked increase of proFLG-mRNA expression was observed in 0.05%sacran group (vs. control 0.05% CS and 0.5% PD groups). Thus, Sacran might be useful as a natural skin barrier enhancer and anti-allergic agent. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01418130
Volume :
105
Database :
Academic Search Index
Journal :
International Journal of Biological Macromolecules
Publication Type :
Academic Journal
Accession number :
125806049
Full Text :
https://doi.org/10.1016/j.ijbiomac.2017.05.049