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  4. Inhibitory effects of ethyl acetate extract of andrographis paniculata on NF-κB trans-activation activity and LPS-induced acute inflammation in mice
 
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Inhibitory effects of ethyl acetate extract of andrographis paniculata on NF-κB trans-activation activity and LPS-induced acute inflammation in mice

Journal
Evidence-based Complementary and Alternative Medicine
Journal Volume
2011
Date Issued
2011
Author(s)
Chao, Wen-Wan
Kuo, Yueh-Hsiung
Hsieh, Shie-Liang
BI-FONG LIN  
DOI
10.1093/ecam/nep120
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-79953273783&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/367000
Abstract
This study was to investigate anti-inflammatory effect of Andrographis paniculata (Burm. f.) Nees (Acanthaceae) (AP). The effects of ethyl acetate (EtOAc) extract from AP on the level of inflammatory mediators were examined first using nuclear factor kappa B (NF-B) driven luciferase assay. The results showed that AP significantly inhibited NF-B luciferase activity and tumor necrosis factor (TNF-), interleukin 6 (IL-6), macrophage inflammatory protein-2 (MIP-2) and nitric oxide (NO) secretions from lipopolysaccharide (LPS)/interferon- stimulated Raw264.7 cells. To further evaluate the anti-inflammatory effects of AP in vivo, BALB/c mice were tube-fed with 0.78 (AP1), 1.56 (AP2), 3.12 (AP3) and 6.25 (AP4)mgkg-1 body weight (BW)/day in soybean oil, while the control and PDTC (pyrrolidine dithiocarbamate, an anti-inflammatory agent) groups were tube-fed with soybean oil only. After 1 week of tube-feeding, the PDTC group was injected with 50mgkg-1 BW PDTC and 1 h later, all of the mice were injected with 15mgkg-1 BW LPS. The results showed that the AP1, AP2, AP3 and PDTC groups, but not AP4, had significantly higher survival rate than the control group. Thus, the control, AP1, AP2, AP3 and PDTC groups were repeated for in vivo parameters. The results showed that the AP and PDTC groups had significantly lower TNF-, IL-12p40, MIP-2 or NO in serum or peritoneal macrophages and infiltration of inflammatory cells into the lung of mice. The AP1 group also had significantly lower MIP-2 mRNA expression in brain. This study suggests that AP can inhibit the production of inflammatory mediators and alleviate acute hazards at its optimal dosages. Copyright © 2011 Wen-Wan Chao et al.
Type
journal article

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