Unsaponifiable fraction from extra virgin olive oil inhibits the inflammatory response in LPS-activated murine macrophages

被引:26
作者
Cardeno, Ana [1 ]
Sanchez-Hidalgo, Marina [1 ]
Aparicio-Soto, Marina [1 ]
Alarcon-de-la-Lastra, Catalina [1 ]
机构
[1] Univ Seville, Fac Pharm, Dept Pharmacol, E-41012 Seville, Spain
关键词
Extra virgin olive oil; Unsaponifiable fraction; LPS-stimulated macrophages; ROS; NF kappa B; MAPK; NF-KAPPA-B; BIOLOGICAL IMPORTANCE; MOLECULAR-MECHANISMS; LIPOPOLYSACCHARIDE; PATHWAYS; MELATONIN; SQUALENE; STRESS;
D O I
10.1016/j.foodchem.2013.09.117
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Extra virgin olive oil (EVOO) has demonstrated great anti-inflammatory properties. Nowadays, it is clear that its minor components have a key role in these beneficial effects. However, the contribution of the unsaponifiable fraction (UF) to these healthy effects remains unknown. The present study was designed to evaluate UF in LPS stimulated peritoneal macrophages isolated from mice. NO production was analysed by the Griess method and intracellular ROS by fluorescence analysis. In addition, MAPK family activation, IKB alpha, degradation, NF kappa B-p65, iNOS and COX-2 expression were determined by Western blot. UF exerted anti-inflammatory and anti-oxidant effects inhibiting LPS-induced intracellular ROS and nitrite production. Additionally, UF decreased COX-2 and iNOS protein expression. These effects were related with a down-regulation in NF kappa B signal signalling pathways and in MAPK phosphorylation. UF of EVOO compounds could play an important role in the anti-inflammatory effect of virgin olive oils and probably provide an attractive complement in management of inflammatory diseases. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 30 条
[1]   Microarray analysis of hepatic genes differentially expressed in the presence of the unsaponitiable fraction of olive oil in apolipoprotein E-deficient mice [J].
Acin, Sergio ;
Navarro, Maria A. ;
Perona, Javier S. ;
Surra, Joaquin C. ;
Guillen, Natalia ;
Arnal, Carmen ;
Sarria, Alfonso J. ;
Arbones-Mainar, Jose M. ;
Carnicer, Ricardo ;
Ruiz-Gutierrez, Valentina ;
Osada, Jesus .
BRITISH JOURNAL OF NUTRITION, 2007, 97 (04) :628-638
[2]   Toll-like receptor signaling pathways [J].
Barton, GM ;
Medzhitov, R .
SCIENCE, 2003, 300 (5625) :1524-1525
[3]   Oleic Acid in Olive Oil: From a Metabolic Framework Toward a Clinical Perspective [J].
Bermudez, Beatriz ;
Lopez, Sergio ;
Ortega, Almudena ;
Varela, Lourdes M. ;
Pacheco, Yolanda M. ;
Abia, Rocio ;
Muriana, Francisco J. G. .
CURRENT PHARMACEUTICAL DESIGN, 2011, 17 (08) :831-843
[4]   Sterols and sterolins: new drugs for the immune system? [J].
Bouic, PJD .
DRUG DISCOVERY TODAY, 2002, 7 (14) :775-778
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]  
Brune B., 2013, ANTIOXIDANT REDOX SI
[7]   Salicylideneamino-2-thiophenol inhibits inflammatory mediator genes (RANTES, MCP-1, IL-8 and HIF-1α) expression induced by tert-butyl hydroperoxide via MAPK pathways in rat peritoneal macrophages [J].
Chung, Jin ;
Lee, Hwa Sun ;
Chung, Hae Young ;
Yoon, Taek Rim ;
Kim, Hyung Keun .
BIOTECHNOLOGY LETTERS, 2008, 30 (09) :1553-1558
[8]  
de la Lastra CA, 2001, CURR PHARM DESIGN, V7, P933
[9]   Effect of squalene on tissue defense system in isoproterenol-induced myocardial infarction in rats [J].
Farvin, KHS ;
Anandan, R ;
Kumar, SHS ;
Shiny, KS ;
Sankar, TV ;
Thankappan, TK .
PHARMACOLOGICAL RESEARCH, 2004, 50 (03) :231-236
[10]   MAPK signalling pathways as molecular targets for anti-inflammatory therapy - from molecular mechanisms to therapeutic benefits [J].
Kaminska, B .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2005, 1754 (1-2) :253-262