Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/43901
Title: Gallic acid is the major active component of cortex moutan in inhibiting immune maturation of human monocyte-derived dendritic cells
Authors: Chan, BCL
Li, LF
Hu, SQ
Wat, E
Wong, ECW
Zhang, VX
Lau, CBS
Wong, CK
Hon, KLE
Hui, PCL 
Leung, PC
Keywords: Atopic dermatitis
Cortex moutan
Dendritic cells
Gallic acid
High-speed counter-current chromatography
Penta herb formula
Issue Date: 2015
Publisher: Molecular Diversity Preservation International (MDPI)
Source: Molecules, 2015, v. 20, no. 9, p. 16388-16403 How to cite?
Journal: Molecules 
Abstract: Atopic dermatitis (AD) is a widely prevalent and chronically relapsing inflammatory skin disease. Penta Herbs Formula (PHF) is efficacious in improving the quality of life and reducing topical corticosteroid used in children with AD and one of the active herbs it contains is Cortex Moutan. Recent studies showed that altered functions of dendritic cells (DC) were observed in atopic individuals, suggesting that DC might play a major role in the generation and maintenance of inflammation by their production of pro-inflammatory cytokines. Hence, the aims of the present study were to identify the major active component(s) of Cortex Moutan, which might inhibit DC functions and to investigate their possible interactions with conventional corticosteroid on inhibiting the development of DC from monocytes. Monocyte-derived dendritic cells (moDC) culture model coupled with the high-speed counter-current chromatography (HSCCC), high pressure liquid chromatography (HPLC) and Liquid Chromatography-Mass Spectrometry (LCMS) analyses were used. Gallic acid was the major active component from Cortex Moutan which could dose dependently inhibit interleukin (IL)-12 p40 and the functional cluster of differentiation (CD) surface markers CD40, CD80, CD83 and CD86 expression from cytokine cocktail-activated moDC. Gallic acid could also lower the concentration of hydrocortisone required to inhibit the activation of DC.
URI: http://hdl.handle.net/10397/43901
ISSN: 1420-3049
DOI: 10.3390/molecules200916388
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