Polyphenolic compounds, antioxidant and anti-inflammatory effects of Abeliophyllum distichum Nakai extract

被引:15
作者
Choi, Jae Hyeok [1 ]
Seo, Ean-Jeong [2 ]
Sung, Jeehye [3 ]
Choi, Ki Man [4 ]
Kim, Heekyu [5 ]
Kim, Ju-Sung [6 ]
Lee, Junsoo [3 ]
Efferth, Thomas [2 ]
Hyun, Tae Kyung [1 ]
机构
[1] Chungbuk Natl Univ, Coll Agr Life & Environm Sci, Dept Ind Plant Sci & Technol, Cheongju 28644, South Korea
[2] Johannes Gutenberg Univ Mainz, Dept Pharmaceut Biol, Inst Pharm & Biochem, Mainz, Germany
[3] Chungbuk Natl Univ, Coll Agr Life & Environm Sci, Div Food & Anim Sci, Cheongju, South Korea
[4] Nat Environm Res Pk Gangwon Prov, Hongcheon, South Korea
[5] Gangwon Forest Sci Inst, Chunchon, South Korea
[6] Jeju Natl Univ, Coll Agr & Life Sci, SARI, Jeju, South Korea
基金
新加坡国家研究基金会;
关键词
NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; EXPRESSION; MECHANISMS; MAPK; INFLAMMATION; CELLS; TRANSFORMATION; INHIBITION; INDUCTION;
D O I
10.5073/JABFQ.2017.090.033
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The present study was conducted to evaluate the antioxidant and anti-inflammatory activities of crude methanolic extract of Abeliophyllum distichum Nakai, and those of its partitioned fractions, including hexane, ethyl acetate, n-butanol, and aqueous. The antioxidant activities were analyzed by DPPH free radical scavenging and oxygen radical antioxidant capacity assay. Results showed that the BuOH fraction possessed a strong antioxidant activity through a hydrogen atom transfer reaction-based mechanism and a single electron transfer reaction-based mechanism. In lipopolysaccharide (LPS)-stimulated RAW 264.7 cells, the BuOH fraction of A. distichum methanol extract exhibited a strong inhibitory effect on the nitric oxide production and inhibited the expression of pro-inflammatory mediators, including COX-2, TNF-alpha, and IL-6, through the inhibition of the MEK/ERK signaling pathway. In addition, the BuOH fraction inhibited the LPS-induced ROS level through the NADPH oxidase-independent mechanism. Furthermore, HPLC analysis identified chlorogenic acid, caffeic acid, gentisic acid, rutin, ferulic acid, and quercetin, and suggested that the antioxidant and anti-inflammatory activities of the BuOH fraction should be mediated by the presence of higher amounts of caffeic acid, rutin, and ferulic acid than other fractions. Taken together, these results suggest that A. distichum extract is a source of antioxidant and anti-inflammatory compounds, and could be developed as a potential source for functional food and dietary health supplement.
引用
收藏
页码:266 / +
页数:9
相关论文
共 45 条
[1]  
Al-Dhabi NA, 2015, EXCLI J, V14, P59, DOI 10.17179/excli2014-663
[2]   Reactive Oxygen Species in Health and Disease [J].
Alfadda, Assim A. ;
Sallam, Reem M. .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2012,
[3]   Inflammation: Mechanisms, Costs, and Natural Variation [J].
Ashley, Noah T. ;
Weil, Zachary M. ;
Nelson, Randy J. .
ANNUAL REVIEW OF ECOLOGY, EVOLUTION, AND SYSTEMATICS, VOL 43, 2012, 43 :385-406
[4]  
Atawodi SE, 2005, AFR J BIOTECHNOL, V4, P128
[5]   β-Carotene inhibits inflammatory gene expression in lipopolysaccharide-stimulated macrophages by suppressing redox-based NF-κB activation [J].
Bai, SK ;
Lee, SJ ;
Na, HJ ;
Ha, KS ;
Han, JA ;
Lee, H ;
Kwon, YG ;
Chung, CK ;
Kim, YM .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2005, 37 (04) :323-334
[6]   The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313
[7]   Mechanisms of suppression of inducible nitric oxide synthase (iNOS) expression in RAW 264.7 cells by andrographolide [J].
Chiou, WF ;
Chen, CF ;
Lin, JJ .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (08) :1553-1560
[8]   Alantolactone suppresses inducible nitric oxide synthase and cyclooxygenase-2 expression by down-regulating NF-κB, MAPK and AP-1 via the MyD88 signaling pathway in LPS-activated RAW 264.7 cells [J].
Chun, Jaemoo ;
Choi, Ran Joo ;
Khan, Salman ;
Lee, Dong-Sung ;
Kim, Youn-Chul ;
Nam, Young-Joo ;
Lee, Dong-Ung ;
Kim, Yeong Shik .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2012, 14 (04) :375-383
[9]   Mitochondria contribute to LPS-induced MAPK activation via uncoupling protein UCP2 in macrophages [J].
Emre, Yalin ;
Hurtaud, Corinne ;
Nubel, Tobias ;
Criscuolo, Francois ;
Ricquier, Daniel ;
Cassard-Doulcier, Anne-Marie .
BIOCHEMICAL JOURNAL, 2007, 402 (02) :271-278
[10]   Lipopolysaccharide regulates proinflammatory cytokine expression in mouse myoblasts and skeletal muscle [J].
Frost, RA ;
Nystrom, GJ ;
Lang, CH .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 283 (03) :R698-R709