Houttuynia cordata Thunb. Volatile Oil Exhibited Anti-inflammatory Effects In Vivo and Inhibited Nitric Oxide and Tumor Necrosis Factor-α Production in LPS-stimulated Mouse Peritoneal Macrophages In Vitro

被引:43
作者
Li, Weifeng [1 ]
Fan, Ting [1 ]
Zhang, Yanmin [1 ]
Fan, Te [1 ]
Zhou, Ping [1 ]
Niu, Xiaofeng [1 ]
He, Langchong [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Med, Xian 710061, Shaanxi Provinc, Peoples R China
关键词
Houttuynia cordata Thunb; inflammation; prostaglandins; nitric oxide; tumor necrosis factor-alpha; MEMBRANE CHROMATOGRAPHY; COMPONENTS; SYNTHASE; PATHOPHYSIOLOGY; MODULATION; ACTIVATION; EXTRACT; DISEASE; VIRUS; TNF;
D O I
10.1002/ptr.4905
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Houttuynia cordata Thunb. (HC) is a medicinal herb that generally used in traditional Chinese medicine for treating allergic inflammation. The present study investigated the inhibitory effect of the volatile oil from HC Thunb. on animal models of inflammation and the production of inflammatory mediators in vivo and in vitro. In vivo, xylene-induced mouse ear edema, formaldehyde-induced paw edema and carrageenan-induced mice paw edema were significantly decreased by HC volatile oil. HC volatile oil showed pronounced inhibition of prostaglandin (PG) E-2 and malondialdehyde production in the edematous exudates. In vitro exposure of mouse resident peritoneal macrophages to 1, 10, 100 and 1000 mu g/mL of HC volatile oil significantly suppressed lipopolysaccharide (LPS)-stimulated production of NO and tumor necrosis factor- (TNF-) in a dose-dependent manner. Exposure to HC volatile oil had no effect on cell viability and systemic toxicity. Furthermore, HC volatile oil inhibited the production of NO and TNF- by down-regulating LPS-stimulated iNOS and TNF- mRNA expression. Western blot analysis showed that HC volatile oil attenuated LPS-stimulated synthesis of iNOS and TNF- protein in the macrophages, in parallel. These findings add a novel aspect to the biological profile of HC and clarify its anti-inflammatory mechanism. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:1629 / 1639
页数:11
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