Highly heated food rich in Maillard reaction products limit an experimental colitis in mice

被引:18
作者
Anton, Pauline M. [1 ]
Craus, Alexandre [1 ]
Niquet-Leridon, Celine [1 ]
Tessier, Frederic J.
机构
[1] Inst Polytech LaSalle Beauvais, EGEAL, F-60026 Beauvais, France
关键词
GLYCATION END-PRODUCTS; METABOLIC TRANSIT; RECEPTOR; PROTEIN; FLUORESCENCE; MECHANISMS; ALBUMIN; COFFEE; MODEL; RAGE;
D O I
10.1039/c2fo30045a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Maillard reaction products (MRPs) are a mixture of compounds generated after the heat treatment of food. High circulating levels of MRPs have been associated with degenerative pathologies such as diabetes, but little is known about their effect on the gut, the main organ in contact with food-derived MRPs. This study was aimed at determining whether repeated low-level exposure to MRPs, generated via two different heat treatments, can contribute to the modulation of experimental colitis in mice. In the first series of experiments, we tested whether pellets rich in MRPs would increase plasmatic and faecal concentration of MRPs. In the second series, we assessed whether two levels of pellet-derived MRPs would be able to modulate chemically-induced inflammation and affect tissue healing. The ingestion of MRPs correlates with the increase of its plasmatic and faecal concentration. Highly treated pellets were proved to significantly protect against inflammation whereas standard or moderately heated pellets had no effect on the inflammatory course. The chemical analysis of the different pellets indicated that high heating generates more melanoidins. There is a correlation between the exposure to highly heated foods and the reduction of murine inflammation, of which the mechanisms remain to be elucidated.
引用
收藏
页码:941 / 949
页数:9
相关论文
共 39 条
[1]   The effect of a model melanoidin mixture on faecal bacterial populations in vitro [J].
Ames, JM ;
Wynne, A ;
Hofmann, A ;
Plos, S ;
Gibson, GR .
BRITISH JOURNAL OF NUTRITION, 1999, 82 (06) :489-495
[2]   Posttranslationally modified proteins as mediators of sustained intestinal inflammation [J].
Andrassy, Martin ;
Igwe, John ;
Autschbach, Frank ;
Volz, Christian ;
Remppis, Andrew ;
Neurath, Markus F. ;
Schleicher, Erwin ;
Humpert, Per M. ;
Wendt, Thoralf ;
Liliensiek, Birgit ;
Morcos, Michael ;
Schiekofer, Stephan ;
Thiele, Kirsten ;
Chen, Jiang ;
Kientsch-Engel, Rose ;
Schmidt, Ann-Marie ;
Stremmel, Wolfgang ;
Stern, David M. ;
Katus, Hugo A. ;
Nawroth, Peter P. ;
Bierhaus, Angelika .
AMERICAN JOURNAL OF PATHOLOGY, 2006, 169 (04) :1223-1237
[3]   Bread crust melanoldins as potential prebiotic ingredients [J].
Borrelli, RC ;
Fogliano, V .
MOLECULAR NUTRITION & FOOD RESEARCH, 2005, 49 (07) :673-678
[4]  
BRADLEY PP, 1982, BLOOD, V60, P618
[5]   Are food advanced glycation end products toxic in biological systems? [J].
Chuyen, NV ;
Arai, H ;
Nakanishi, T ;
Utsunomiya, N .
MAILLARD REACTION: CHEMISTRY AT THE INTERFACE OF NUTRITION, AGING, AND DISEASE, 2005, 1043 :467-473
[6]  
Ciccocioppo R., 2010, GUT, V59, pA175
[7]   The functional-374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's disease [J].
Daebritz, Jan ;
Friedrichs, Frauke ;
Weinhage, Toni ;
Hampe, Jochen ;
Kucharzik, Torsten ;
Luegering, Andreas ;
Broeckel, Ulrich ;
Schreiber, Stefan ;
Spieker, Tilmann ;
Stoll, Monika ;
Foell, Dirk .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2011, 300 (05) :G823-G832
[8]   Study of the urinary and faecal excretion of N ε-carboxymethyllysine in young human volunteers [J].
Delgado-Andrade, Cristina ;
Tessier, Frederic J. ;
Niquet-Leridon, Celine ;
Seiquer, Isabel ;
Pilar Navarro, M. .
AMINO ACIDS, 2012, 43 (02) :595-602
[9]   Metabolic transit and in vivo effects of melanoidins and precursor compounds deriving from the Maillard reaction [J].
Faist, V ;
Erbersdobler, HF .
ANNALS OF NUTRITION AND METABOLISM, 2001, 45 (01) :1-12
[10]  
Finot PA, 2005, J AOAC INT, V88, P894