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Traditional Chinese medicine for atopic eczema: PentaHerbs formula suppresses inflammatory mediators release from mast cells

PentaHerbs formula (PHF) containing Cortex Moutan, root bark of Paeonia suffruticosa Andr. (Ranunculaceae), Cortex Phellodendri, bark of Phellodendron chinensis Schneid. (Rutaceae), Flos Lonicerae, flower of Lonicera japonica Thunb. (Capri-foliaceae), Herba Menthae, aerial part of Mentha haplocalyx...

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Bibliographic Details
Published in:Journal of ethnopharmacology 2008-10, Vol.120 (1), p.85-91
Main Authors: Chan, Ben Chung Lap, Hon, Kam Lun Ellis, Leung, Ping Chung, Sam, Sze Wing, Fung, Kwok Pui, Lee, Mavis Yuk Ha, Lau, Hang Yung Alaster
Format: Article
Language:English
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Summary:PentaHerbs formula (PHF) containing Cortex Moutan, root bark of Paeonia suffruticosa Andr. (Ranunculaceae), Cortex Phellodendri, bark of Phellodendron chinensis Schneid. (Rutaceae), Flos Lonicerae, flower of Lonicera japonica Thunb. (Capri-foliaceae), Herba Menthae, aerial part of Mentha haplocalyx Briq. (Labiatae) and Rhizoma Atractylodis, rhizome of Atractylodes lancea (Thunb.) DC. (Compositae) at the ratio of 2:2:2:1:2 was useful in the management of eczema. Since the mechanism of action of PHF is not known, we aimed to investigate the actions of PHF on mast cell activation. Effects of aqueous extracts of PHF and individual component herb on mediator release from rat peritoneal mast cells (RPMCs) and cytokine production from HMC-1 were investigated. PHF, Cortex Moutan and Herba Menthae significantly attenuated histamine release and prostaglandin D 2 synthesis from RPMC activated by anti-IgE and compound 48/80 ( p < 0.05). While Flos Lonicerae and Rhizoma Atractylodis suppressed only mediator release from compound 48/80 activated RPMC, Cortex Phellodendri potentiated only anti-IgE induced mediator release ( p < 0.05). However, with the exception of Cortex Moutan, PHF and the other four component herbs failed to affect cytokine production in HMC-1. Although individual herbs demonstrated different modulating effects on mast cells, inhibition of inflammatory mediator release from mast cells would contribute to the therapeutic efficacy of PHF.
ISSN:0378-8741
1872-7573
DOI:10.1016/j.jep.2008.07.034