Psidium guajava']java extract inhibits thymus and activation-regulated chemokine (TARC/CCL17) production in human keratinocytes by inducing heme oxygenase-1 and blocking NF-κB and STAT1 activation

被引:27
|
作者
Han, Eun Hee [1 ]
Hwang, Yong Pil [1 ]
Choi, Jae Ho [1 ]
Yang, Ji Hye [1 ]
Seo, Jong Kwon [2 ]
Chung, Young Chul [2 ]
Jeong, Hye Gwang [1 ]
机构
[1] Chungnam Natl Univ, Dept Toxicol, Coll Pharm, Taejon 305764, South Korea
[2] Korea Int Univ, Div Food Sci, Jinju, South Korea
关键词
Psidium gua[!text type='java']java[!/text; Atopic dermatitis; TARC; Heme oxygenase-1; EPSTEIN-BARR-VIRUS; ATOPIC-DERMATITIS; CC-CHEMOKINE; HACAT CELLS; MDC/CCL22; PRODUCTION; MOLECULAR-CLONING; DENDRITIC CELLS; IFN-GAMMA; TNF-ALPHA; EXPRESSION;
D O I
10.1016/j.etap.2011.04.004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Psidium guajava (P. guajava) is a food and medicinal plant with antioxidant, anti-inflammatory, and anti-allergic activities that support its traditional uses. The aim of this study was to determine the effects of P. guajava ethyl acetate extract (PGEA) on atopic dermatitis and to investigate the possible mechanisms by which PGEA inhibits cytokine-induced Th2 chemokine expression in HaCaT human keratinocyte cells. We found that PGEA suppressed the IFN-gamma/TNF-alpha-co-induced production of thymus and activation-regulated chemokine (TARC) protein and mRNA in HaCaT cells. Additionally, PGEA inhibited the TNF-alpha/IFN-gamma-co-induced activation of NF-kappa B and STAT1 and increased the expression of heme oxygenase-1 (HO-1) protein and mRNA. HO-1 inhibitor enhanced the suppressive effects of PGEA on TNF-alpha/IFN-gamma-co-induced TARC production and gene expression. Collectively, these data demonstrate that PGEA inhibits chemokine expression in keratinocytes by inducing HO-1 expression and it suggests a possible therapeutic application in atopic dermatitis and other inflammatory skin diseases. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 145
页数:10
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