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Anti-inflammatory activity of ethanol extracts from ready to eat stir-fried chicken with red curry in lipopolysaccharide-induced RAW264.7 murine macrophages

Published online by Cambridge University Press:  04 June 2010

S. Tuntipopipat
Affiliation:
Institute of Nutrition, Mahidol University, Putthamonthon4, Salaya, Nakhon-Pathom 73170, Thailand
C. Muangnoi
Affiliation:
Institute of Nutrition, Mahidol University, Putthamonthon4, Salaya, Nakhon-Pathom 73170, Thailand
P. Chingsuwanrote
Affiliation:
Institute of Nutrition, Mahidol University, Putthamonthon4, Salaya, Nakhon-Pathom 73170, Thailand
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2009

Phytochemicals in individual spice/herb have been extensively investigated to diminish pro-inflammatory mediator productions(Reference Chainani-Wu1Reference Aggarwal and Shishodia4). Pro-inflammatory mediators play biological roles on pathogenesis of several non-communicable diseases(Reference Aggarwal5). Although individual spices/herbs have been demonstrated to suppress pro-inflammatory mediator productions, investigation of such activity in complex diets has been limited. This study evaluated the anti-inflammatory activity of extract from a popular Thai diet ‘ready to eat stir-fried chicken with red curry’. The anti-inflammatory activities of the food extract were evaluated by measuring NO2, iNOS and COX-2 expression in LPS-activated RAW264.7 cells. The mechanism of action was examined by determining the activation of mitogen-activated protein kinases (MAPKs) signalling proteins.

The ready to eat food was prepared by stir-fried less sodium red chilli paste and skinless chicken meat with vegetable oil until cooked. Pea and round eggplants with green peppercorn were added with palm sugar, sorbitol and seasoned with kaffir lime and sweet basil leaves. The food was freeze dried and extracted at ratio 1:3 with 90% ethanol. RAW264.7 cells were cultured in DMEM with 10% FBS at 37°C at 5% CO2. Cells were pretreated with the ethanol extract of food at 60–240 μg/ml for 1 h prior to stimulate with LPS for 24 h. Culture medium and cell lysate were collected for measuring NO2 and iNOS, COX-2 and MAPKs protein, respectively. The effects on iNOS and COX-2 mRNA levels were examined by RT–PCR. The food extract significantly suppressed NO2 production (data not shown) and diminished iNOS, COX-2 protein and mRNA levels (Figs 1 and 2, respectively) by dose-dependent without cytotoxicity. It inactivated MAPKs proteins by blocking phosphorylation of p38, ERK1/2 and JNK (Fig. 3) by dose dependent without alteration of total p38, ERK1/2 and JNK level.

These results suggested that the ethanol extract from this complex diet containing several spices/herbs possesses high potential to attenuate LPS-induced pro-inflammatory mediators in part by inactivation of MAPKs signalling protein. The health benefit of stir-fried chicken with red curry warrants further investigations in vivo. (Supported by Mahidol University Fund.).

References

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