Ethanol extract of the tuber of Alisma orientale reduces the pathologic features in a chronic obstructive pulmonary disease mouse model

被引:23
作者
Kim, Kyun Ha [1 ]
Song, Hyuk-Hwan [2 ]
Ahn, Kyung-Seop [3 ]
Oh, Sei-Ryang [3 ]
Sadikot, Ruxana T. [4 ]
Joo, Myungsoo [1 ]
机构
[1] Pusan Natl Univ, Sch Korean Med, Yangsan 626870, South Korea
[2] Agcy Korea Natl Food Cluster, R&D Team, 460 Iksan Daero, Iksan 507749, Jeonbuk, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Nat Med Res Ctr, Ochang 363883, Chung Buk, South Korea
[4] Emory Univ, Sch Med, Pulm Crit Care & Sleep Med, 1670 Clairmont Rd, Decatur, GA 30033 USA
基金
新加坡国家研究基金会;
关键词
Alismataceae Alisma Orientale Juzepzuk; Chronic obstructive pulmonary disease; Animal model; Inflammation; Emphysema; Autophagy; GENOME-WIDE ASSOCIATION; RHIZOMA DRIED RHIZOME; TERPENE COMPONENTS; CIGARETTE-SMOKING; METHANOL EXTRACT; KAPPA-B; AUTOPHAGY; LUNG; EXPRESSION; SUSCEPTIBILITY;
D O I
10.1016/j.jep.2016.05.004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The tuber of Alismataceae Alisma orientate Juzepzuk has been prescribed as a remedy for treating the diseases associated with body fluid dysfunction such as edema and inflammatory lung diseases. Chronic obstructive pulmonary disease (COPD) is a debilitating, inflammatory lung disease without effective treatment. Along with persistent inflammation, autophagy has been recently reported to contribute to COPD. Here, by employing a murine model, we examined whether the tuber of the plant is effective against COPD Materials and methods: The ethanol extract of the tuber of A. orientate Juzepzuk (EEAO) was fingerprinted by HPLC. For the establishment of COPD lung, mice received single intratracheal (i.t.) spraying of elastase and LPS per week for 2 weeks. After approximated to the dose prescribed typically to patients, EEAO was administered to the lung 2 h after each LPS treatment. Morphometric analyses, semi-quantitative RT-PCR, and western blot were performed to evaluate the effects of EEAO on emphysema, inflammation, and autophagy in mouse lungs. The effect of EEAO on autophagy was also assessed by western blot at the cellular level with murine macrophages and human lung epithelial cells. Results: When receiving i.t. elastase and LPS for 2 weeks, mice developed emphysema and inflammation in the lung. EEAO treatment, however, significantly reduced emphysema and inflammatory cell infiltration to the lung with concomitant decrease of the production of pro-inflammatory cytokines including TNF-alpha, IL-6, and TGF-beta, signature cytokines of COPD. Unlike control mice, the lungs of the COPD mice expressed LC3-II, a biomarker for autophagy formation, which was decreased by EEAO treatment. EEAO also lowered the expression of LC3-II in murine macrophage, RAW 264.7, and human lung epithelial cell, BEAS-2B, which was associated with EEAO activating mTOR. Conclusion: EEAO relieved COPD pathologic features in a mouse model, which was associated with suppression of lung inflammation, emphysema, and autophagy. Our results suggest an effectiveness of the tuber of A. orientate in chronic inflammatory lung diseases such as COPD. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 30
页数:10
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