Ethanol extract of Alismatis Rhizoma reduces acute lung inflammation by suppressing NF-κB and activating Nrf2

被引:149
作者
Han, Chang Woo [1 ,2 ]
Kwun, Min Jung [1 ]
Kim, Kyun Ha [1 ]
Choi, Jun-Yong [1 ,2 ]
Oh, Sei-Ryang [3 ]
Ahn, Kyung-Seop [3 ]
Lee, Jang Hoon [4 ]
Joo, Myungsoo [1 ,5 ]
机构
[1] Pusan Natl Univ, Sch Korean Med, Yangsan 626870, South Korea
[2] Pusan Natl Univ, Korean Med Hosp, Yangsan 626789, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Immune Modulator Res Ctr, Ochang 363883, South Korea
[4] Kyung Hee Univ, Coll Oriental Med, Dept Internal Med, Seoul 130701, South Korea
[5] Vanderbilt Univ, Med Ctr, Div Allergy Pulm & Crit Care Med, Nashville, TN 37232 USA
基金
新加坡国家研究基金会;
关键词
Alisma orientale; Acute lung injury; Anti-inflammation; NF-kappa B; Nrf2; RESPIRATORY-DISTRESS-SYNDROME; TERPENE COMPONENTS; METHANOL EXTRACT; DRIED RHIZOME; RECEPTOR; INJURY; ORIENTALE; ENDOTOXIN; ARDS; SESQUITERPENES;
D O I
10.1016/j.jep.2013.01.010
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: The tuber of Alisma orientate Juzepzuk, a medicinal herb that has been used for the treatment of various disorders in Korea, has an anti-inflammatory effect. Here, we investigated a possible underlying mechanism and a protective effect on acute lung injury (ALI). Materials and methods: Alisma orientate tuber was extracted in 80% ethanol and dried. The powder of the ethanol extract of Alisma orientate tuber (EEAO) was dissolved in PBS. The effect of EEAO on NF-kappa B and Nrf2 activities was analyzed with RAW 264.7 cells. The effect of EEAO on lung inflammation was determined by histologic and molecular biological analyses of the lung tissue of C57BL/6 mice that were gavaged once a day with 0.3 or 1.2 g/kg of EEAO for 14 days, prior to an intranasal administration of LPS (0.01 g/kg) for inducing ALI. Results: EEAO pre-treatment of RAW 264.7 cells suppressed NF-kappa B activity and the expression of its dependent genes including.COX-2, IL-1 beta and iNOS. Similar treatment enhanced Nrf2 activity and the expression of Nrf2-regulated genes including NQO-1, HO-1 and GCLC. LPS instillation induced acute neutrophilic lung inflammation, which was significantly suppressed by pre-treatment with EEAO. Analysis of the lungs revealed that EEAO pre-treatment induced the expression of Nrf2-regulated genes, with concomitant down-regulation of inflammatory gene expression. Conclusions: EEAO attenuated lung inflammation in LPS-induced ALI mice, which was associated with differential regulation of NF-kappa B and Nrf2 activities. We suggest that EEAO can be developed as a potential therapeutics for the treatment of ALI. (C) 2013 Elsevier Ireland Ltd, All rights reserved.
引用
收藏
页码:402 / 410
页数:9
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