Topical application of Pleurotus eryngii extracts inhibits 2,4-dinitrochlorobenzene-induced atopic dermatitis in NC/Nga mice by the regulation of Th1/Th2 balance
► Effect of Pleurotus eryngii extracts (PEE) on AD-like skin lesions was assayed. ► PEE suppressed dermatitis severity and serum levels of IgE and TARC. ► PEE suppressed mRNA expression of IL-4, IL-5, IL-13, TNF-α, and INF-γ. ► PEE reduced thickness of dermis in ear lesions. ► PEE inhibited infiltra...
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Veröffentlicht in: | Food and chemical toxicology 2013-03, Vol.53, p.38-45 |
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Sprache: | eng |
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Zusammenfassung: | ► Effect of Pleurotus eryngii extracts (PEE) on AD-like skin lesions was assayed. ► PEE suppressed dermatitis severity and serum levels of IgE and TARC. ► PEE suppressed mRNA expression of IL-4, IL-5, IL-13, TNF-α, and INF-γ. ► PEE reduced thickness of dermis in ear lesions. ► PEE inhibited infiltration of inflammatory cells and mast cells in ear lesions.
Pleurotus eryngii is a nutritional and medicinal food rich in polysaccharides that enhance the host immune system as a response to various diseases. The present study investigated the effects of P. eryngii extracts (PEE) on the progress of atopic dermatitis (AD)-like skin lesions in NC/Nga mice induced by 2,4-dinitrochlorobenzene (DNCB). We evaluated skin dermatitis severity, ear thickness, histopathological examination, and cytokines level in DNCB-applied mice treated with PEE. Continuous treatment of PEE inhibited the development of the AD-like skin lesions. PEE suppressed DNCB-induced dermatitis severity, serum level of IgE and thymus and activation-regulated chemokine (TARC), and mRNA expression of TNF-α, INF-γ, IL-4, IL-5, and IL-13 in mice. In addition, PEE reduced thickness of the dermis and dermal infiltration of inflammatory cells and mast cells in histopathological examination. These results indicate that PEE inhibits allergic contact dermatitis through the modulating of T helper (Th)1 and Th2 responses and diminishing the inflammatory cells and mast cells infiltration in the skin lesions in NC/Nga mice. |
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ISSN: | 0278-6915 1873-6351 |
DOI: | 10.1016/j.fct.2012.11.025 |