Biological models for phytochemical research: from cell to human organism

被引:15
作者
Mortensen, Alicja [2 ]
Sorensen, Ilona K. [2 ]
Wilde, Colin [3 ]
Dragoni, Stefania [4 ]
Mullerova, Dana [5 ]
Toussaint, Olivier [6 ]
Zloch, Zdenek [5 ]
Sgaragli, Giampietro [5 ]
Ovesna, Jaroslava [1 ]
机构
[1] Res Inst Crop Prod, CR-16106 Prague 6, Czech Republic
[2] Tech Univ Denmark, Natl Food Inst, DK-2860 Soborg, Denmark
[3] AvantiCell Sci Ltd, Auchincruive KA6 5HW, Ayr, Scotland
[4] Univ Siena, Dept Biomed Sci, I-53110 Siena 55, Italy
[5] Charles Univ Prague, Med Fac Pilsen, Inst Hlth Promot, Plzen 30166, Czech Republic
[6] Univ Namur FUNDP, Unit Cellular Biochem & Biol, Dept Biol, F-5000 Namur, France
关键词
Nutrigenomics; In vitro models; Animal models; Human studies;
D O I
10.1017/S0007114508965806
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Nutrigenomics represents a shift of nutrition research from epidemiology and physiology to molecular biology and genetics. Nutrigenomics seeks to understand nutrition influences on homeostasis, the mechanism of genetic predispositions for diseases, to identify the genes influencing risk of diet related diseases. This review presents some in vitro models applicable in nutrigenomic studies, and discuses the use of animal models, their advantages and limitations and relevance for human situation. In vitro and in vivo models are suitable for performance of DNA microarrays, proteomic and transcriptomic analyses. In vitro models (intracellular organelles and suborganellar compartments, cell cultures, or tissue samples/cultures) give insight in metabolic pathways and responses to test stimuli on cellular and molecular levels. Animal models allow evaluation of the biological significance of the effects recorded in vitro and testing of the hypothesis on how a specific factor affects specific species under specific circumstances. Therefore, the evaluation of the data in relation to human organism should be done carefully, considering the species differences. The use of in vitro and in vivo models is likely to continue as the effects of nutrition on health and disease cannot be fully explained without understanding of nutrients action at nuclear level and their role in the intra-and intercellular signal transduction. Through advances in cell and molecular biology (including genomic and proteomic), the use of these models should become more predictively accurate. However, this predictive value relies on an underpinning knowledge of the advantages and limitations of the model in nutrigenomic research as in other fields of biomedical research.
引用
收藏
页码:ES118 / ES126
页数:9
相关论文
共 102 条
[41]  
Hau J, 1988, SCAND J LAB ANIM SCI, V15, P81
[42]  
Hausner EA, 1995, LAB ANIM SCI, V45, P663
[43]   TRANSPORT OF BILE-ACIDS IN A HUMAN INTESTINAL EPITHELIAL-CELL LINE, CACO-2 [J].
HIDALGO, IJ ;
BORCHARDT, RT .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1035 (01) :97-103
[44]  
HOCHMAN JH, 1994, J PHARMACOL EXP THER, V269, P813
[45]   Enhanced functional maturation of fetal porcine hepatocytes in three-dimensional poly-L-lactic acid scaffolds: A culture condition suitable for engineered liver tissues in large-scale animal studies [J].
Huang, Hongyun ;
Hanada, Sanshiro ;
Kojima, Nobuhiko ;
Sakai, Yasuyuki .
CELL TRANSPLANTATION, 2006, 15 (8-9) :799-809
[46]   Effects of fruit and vegetable consumption on plasma antioxidant concentrations and blood pressure: a randomised controlled trial [J].
John, JH ;
Ziebland, S ;
Yudkin, P ;
Roe, LS ;
Neil, HAW .
LANCET, 2002, 359 (9322) :1969-1974
[47]   CACO-2 CELLS CULTURED IN SERUM-FREE MEDIUM AS A MODEL FOR THE STUDY OF ENTEROCYTIC DIFFERENTIATION INVITRO [J].
JUMARIE, C ;
MALO, C .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 149 (01) :24-33
[48]   BASEMENT-MEMBRANE COMPLEXES WITH BIOLOGICAL-ACTIVITY [J].
KLEINMAN, HK ;
MCGARVEY, ML ;
HASSELL, JR ;
STAR, VL ;
CANNON, FB ;
LAURIE, GW ;
MARTIN, GR .
BIOCHEMISTRY, 1986, 25 (02) :312-318
[49]   The A-204C polymorphism in the cholesterol 7α-hydroxylase (CYP7A1) gene determines the cholesterolemia responsiveness to a high-fat diet [J].
Kovár, J ;
Suchánek, P ;
Hubácek, JA ;
Poledne, R .
PHYSIOLOGICAL RESEARCH, 2004, 53 (05) :565-568
[50]   Inhibition of xenobiotic-induced genotoxicity in cultured precision-cut human and rat liver slices [J].
Lake, BG ;
Beamand, JA ;
Tredger, JM ;
Barton, PT ;
Renwick, AB ;
Price, RJ .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1999, 440 (01) :91-100