Postprandial changes in the proteome are modulated by dietary fat in patients with metabolic syndrome

Journal of Nutritional Biochemistry

Volumn 24, Issue 1, 2013, Pages 318-324

  Camargo, Antonio ^a   Rangel Zúñiga, Oriol Alberto ^a   Peña Orihuela, Patricia ^a   Marín, Carmen ^a   Pérez Martínez, Pablo ^a   Delgado Lista, Javier ^a   Gutierrez Mariscal, Francisco Miguel ^a   Malagón, María M ^b   Roche, Helen M ^c   Tinahones, Francisco José ^d,e   Perez Jimenez, Francisco ^a   Lopez Miranda, José ^a  

^a HOSPITAL UNIVERSITARIO REINA SOFÍA   (Spain)

^b UNIVERSITY OF CÓRDOBA   (Spain)

^c UNIVERSITY COLLEGE DUBLIN   (Ireland)

^d HOSPITAL UNIVERSITARIO VIRGEN DE LA VICTORIA   (Spain)

^e Instituto de Salud Carlos III   (Spain)

Author keywords

Atherothrombosis; Diet; Metabolic syndrome; Oxidative stress; Proteomic

Indexed keywords

CHOLESTEROL; DNA; FATTY ACID; HEAT SHOCK 70 KDA PROTEIN 1A; HEAT SHOCK PROTEIN; HIGH MONOUNSATURATED FATTY ACID; HIGH POLYUNSATURATED FATTY ACID; HIGH SATURATED FATTY ACID; INSULIN; MONOUNSATURATED FATTY ACID; OMEGA 3 FATTY ACID; PLACEBO; POLYUNSATURATED FATTY ACID; PROTEASOME; PROTEASOME ACTIVATOR SUBUNIT 1 ISOFORM 1; PROTEIN DISULFIDE ISOMERASE; PROTEOME; RETINOL; SATURATED FATTY ACID; STRUCTURAL MAINTENANCE OF CHROMOSOME 6 PROTEIN; STRUCTURAL PROTEIN; UNCLASSIFIED DRUG;

ANTIINFLAMMATORY ACTIVITY; ARTICLE; CELL FRACTIONATION; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; CYTOPLASM; DIET SUPPLEMENTATION; DIET THERAPY; DNA DAMAGE; FAT INTAKE; FATTY ACID OXIDATION; FEMALE; HUMAN; HUMAN CELL; MALE; MEAL; METABOLIC SYNDROME X; OXIDATIVE STRESS; PERIPHERAL BLOOD MONONUCLEAR CELL; PEROXISOME; POSTPRANDIAL STATE; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN SYNTHESIS; PROTEOMICS; RANDOMIZED CONTROLLED TRIAL; RECEPTOR DOWN REGULATION; RECEPTOR UPREGULATION; SIGNAL TRANSDUCTION; WALNUT; WESTERN BLOTTING;

BLOOD PROTEINS; BLOTTING, WESTERN; DIET; DIETARY FATS; DNA DAMAGE; FATTY ACIDS, MONOUNSATURATED; FATTY ACIDS, OMEGA-3; FATTY ACIDS, UNSATURATED; HUMANS; JUGLANS; LEUKOCYTES, MONONUCLEAR; METABOLIC SYNDROME X; MIDDLE AGED; POSTPRANDIAL PERIOD; REPRODUCIBILITY OF RESULTS;

JUGLANS;

EID: 84870418174     PISSN: 09552863     EISSN: 18734847     Source Type: Journal    
DOI: 10.1016/j.jnutbio.2012.06.014     Document Type: Article

References (53)

1. Grundy S.M., Cleeman J.I., Daniels S.R., et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute scientific statement. Circulation 2005, 112:2735-2752.
2. Phillips C., Lopez-Miranda J., Perez-Jimenez F., McManus R., Roche H.M. Genetic and nutrient determinants of the metabolic syndrome. Curr Opin Cardiol 2006, 21:185-193.
3. van Oostrom A.J., Rabelink T.J., Verseyden C., et al. Activation of leukocytes by postprandial lipemia in healthy volunteers. Atherosclerosis 2004, 177:175-182.
4. Parks E.J. Recent findings in the study of postprandial lipemia. Curr Atheroscler Rep 2001, 3:462-470.
5. Magne J, Mariotti F, Fischer R, Mathe V, Tome D, Huneau JF. Early postprandial low-grade inflammation after high-fat meal in healthy rats: possible involvement of visceral adipose tissue. J Nutr Biochem 2010;21:550-5.
6. Khoury D.E., Hwalla N., Frochot V., Lacorte J.M., Chabert M., Kalopissis A.D. Postprandial metabolic and hormonal responses of obese dyslipidemic subjects with metabolic syndrome to test meals, rich in carbohydrate, fat or protein. Atherosclerosis 2010, 210:307-313.
7. Ruotolo G., Howard B.V. Dyslipidemia of the metabolic syndrome. Curr Cardiol Rep 2002, 4:494-500.
8. Caimari A, Oliver P, Keijer J, Palou A. Peripheral blood mononuclear cells as a model to study the response of energy homeostasis-related genes to acute changes in feeding conditions. Omics 2010;14:129-41.
9. Burczynski M.E., Dorner A.J. Transcriptional profiling of peripheral blood cells in clinical pharmacogenomic studies. Pharmacogenomics 2006, 7:187-202.
10. Bouwens M., Afman L.A., Muller M. Fasting induces changes in peripheral blood mononuclear cell gene expression profiles related to increases in fatty acid beta-oxidation: functional role of peroxisome proliferator activated receptor alpha in human peripheral blood mononuclear cells. Am J Clin Nutr 2007, 86:1515-1523.
11. Baer D.J., Judd J.T., Clevidence B.A., Tracy R.P. Dietary fatty acids affect plasma markers of inflammation in healthy men fed controlled diets: a randomized crossover study. Am J Clin Nutr 2004, 79:969-973.
12. Paschos G.K., Rallidis L.S., Liakos G.K., et al. Background diet influences the anti-inflammatory effect of alpha-linolenic acid in dyslipidaemic subjects. Br J Nutr 2004, 92:649-655.
13. Konstantinidou V., Khymenets O., Fito M., et al. Characterization of human gene expression changes after olive oil ingestion: an exploratory approach. Folia Biol (Praha) 2009, 55:85-91.
14. Crujeiras A.B., Parra D., Milagro F.I., et al. Differential expression of oxidative stress and inflammation related genes in peripheral blood mononuclear cells in response to a low-calorie diet: a nutrigenomics study. Omics 2008, 12:251-261.
15. Ordovas J.M., Corella D. Nutritional genomics. Annu Rev Genomics Hum Genet 2004, 5:71-118.
16. de Roos B., McArdle H.J. Proteomics as a tool for the modelling of biological processes and biomarker development in nutrition research. Br J Nutr 2008, 99(Suppl. 3):S66-S71.
17. Fuchs D., Vafeiadou K., Hall W.L., et al. Proteomic biomarkers of peripheral blood mononuclear cells obtained from postmenopausal women undergoing an intervention with soy isoflavones. Am J Clin Nutr 2007, 86:1369-1375.
18. Garcia-Bailo B, Brenner DR, Nielsen D, et al. Dietary patterns and ethnicity are associated with distinct plasma proteomic groups. Am J Clin Nutr 2012;95:352-61.
19. Grundy S.M., Brewer H.B., Cleeman J.I., Smith S.C., Lenfant C. Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition. Arterioscler Thromb Vasc Biol 2004, 24:e13-e18.
20. Shaw D.I., Tierney A.C., McCarthy S., et al. LIPGENE food-exchange model for alteration of dietary fat quantity and quality in free-living participants from eight European countries. Br J Nutr 2009, 101:750-759.
21. Hernandez-Presa M.A., Ortego M., Tunon J., et al. Simvastatin reduces NF-kappaB activity in peripheral mononuclear and in plaque cells of rabbit atheroma more markedly than lipid lowering diet. Cardiovasc Res 2003, 57:168-177.
22. Gorg A., Drews O., Luck C., Weiland F., Weiss W. 2-DE with IPGs. Electrophoresis 2009, 30(Suppl. 1):S122-S132.
23. Calvano S.E., Xiao W., Richards D.R., et al. A network-based analysis of systemic inflammation in humans. Nature 2005, 437:1032-1037.
24. Hansson G.K., Libby P., Schonbeck U., Yan Z.Q. Innate and adaptive immunity in the pathogenesis of atherosclerosis. Circ Res 2002, 91:281-291.
25. Bonnefont-Rousselot D. Glucose and reactive oxygen species. Curr Opin Clin Nutr Metab Care 2002, 5:561-568.
26. Jain A., Agrawal B.K., Varma M., Jadhav A.A. Antioxidant status and smoking habits: relationship with diet. Singapore Med J 2009, 50:624-627.
27. Schmitt E., Gehrmann M., Brunet M., Multhoff G., Garrido C. Intracellular and extracellular functions of heat shock proteins: repercussions in cancer therapy. J Leukoc Biol 2007, 81:15-27.
28. Daoud S.S., Munson P.J., Reinhold W., et al. Impact of p53 knockout and topotecan treatment on gene expression profiles in human colon carcinoma cells: a pharmacogenomic study. Cancer Res 2003, 63:2782-2793.
29. Perez-Martinez P., Garcia-Quintana J.M., Yubero-Serrano E.M., et al. Postprandial oxidative stress is modified by dietary fat: evidence from a human intervention study. Clin Sci (Lond) 2010, 119:251-261.
30. Appella E., Anderson C.W. Post-translational modifications and activation of p53 by genotoxic stresses. Eur J Biochem 2001, 268:2764-2772.
31. Sablina A.A., Budanov A.V., Ilyinskaya G.V., Agapova L.S., Kravchenko J.E., Chumakov P.M. The antioxidant function of the p53 tumor suppressor. Nat Med 2005, 11:1306-1313.
32. Gutierrez-Mariscal FM, Perez-Martinez P, Delgado-Lista J, et al. Mediterranean diet supplemented with coenzyme Q10 induces postprandial changes in p53 in response to oxidative DNA damage in elderly subjects. Age (Dordr) 2012;34:389-403.
33. McKeown N.M., Meigs J.B., Liu S., Saltzman E., Wilson P.W., Jacques P.F. Carbohydrate nutrition, insulin resistance, and the prevalence of the metabolic syndrome in the Framingham Offspring Cohort. Diabetes Care 2004, 27:538-546.
34. Roberts W, Magwenzi S, Aburima A, Naseem KM. Thrombospondin-1 induces platelet activation through CD36-dependent inhibition of the cAMP/protein kinase A signaling cascade. Blood 2010;116:4297-306.
35. Jennings L.K. Role of platelets in atherothrombosis. Am J Cardiol 2009, 103:4A-10A.
36. Iacoviello L., Vischetti M., Zito F., Benedetta Donati M. Genes encoding fibrinogen and cardiovascular risk. Hypertension 2001, 38:1199-1203.
37. Redman C.M., Xia H. Fibrinogen biosynthesis. Assembly, intracellular degradation, and association with lipid synthesis and secretion. Ann N Y Acad Sci 2001, 936:480-495.
38. Smith A., Patterson C., Yarnell J., Rumley A., Ben-Shlomo Y., Lowe G. Which hemostatic markers add to the predictive value of conventional risk factors for coronary heart disease and ischemic stroke? The Caerphilly Study. Circulation 2005, 112:3080-3087.
39. Pebernard S., Perry J.J., Tainer J.A., Boddy M.N. Nse1 RING-like domain supports functions of the Smc5-Smc6 holocomplex in genome stability. Mol Biol Cell 2008, 19:4099-4109.
40. Ahn K., Erlander M., Leturcq D., Peterson P.A., Fruh K., Yang Y. In vivo characterization of the proteasome regulator PA28. J Biol Chem 1996, 271:18237-18242.
41. Li J., Powell S.R., Wang X. Enhancement of proteasome function by PA28α overexpression protects against oxidative stress. Faseb J 2011, 25:883-893.
42. Murakumo Y., Ogura Y., Ishii H., et al. Interactions in the error-prone postreplication repair proteins hREV1, hREV3, and hREV7. J Biol Chem 2001, 276:35644-35651.
43. Jessop C.E., Bulleid N.J. Glutathione directly reduces an oxidoreductase in the endoplasmic reticulum of mammalian cells. J Biol Chem 2004, 279:55341-55347.
44. Fernandez-Sanchez A, Madrigal-Santillan E, Bautista M, et al. Inflammation, oxidative stress, and obesity. Int J Mol Sci 2011;12:3117-32.
45. Codoner-Franch P, Valls-Belles V, Arilla-Codoner A, Alonso-Iglesias E. Oxidant mechanisms in childhood obesity: the link between inflammation and oxidative stress. Transl Res 2010;158:369-84.
46. Gregor M.F., Hotamisligil G.S. Thematic review series: adipocyte biology. Adipocyte stress: the endoplasmic reticulum and metabolic disease. J Lipid Res 2007, 48:1905-1914.
47. Minamino T., Komuro I., Kitakaze M. Endoplasmic reticulum stress as a therapeutic target in cardiovascular disease. Circ Res 2010, 107:1071-1082.
48. Reddy J.K., Hashimoto T. Peroxisomal beta-oxidation and peroxisome proliferator-activated receptor alpha: an adaptive metabolic system. Annu Rev Nutr 2001, 21:193-230.
49. Carpentier Y.A., Portois L., Malaisse W.J. n-3 fatty acids and the metabolic syndrome. Am J Clin Nutr 2006, 83:1499S-1504S.
50. Hamel F.G., Bennett R.G., Upward J.L., Duckworth W.C. Insulin inhibits peroxisomal fatty acid oxidation in isolated rat hepatocytes. Endocrinology 2001, 142:2702-2706.
51. FitzPatrick D.R., Germain-Lee E., Valle D. Isolation and characterization of rat and human cDNAs encoding a novel putative peroxisomal enoyl-CoA hydratase. Genomics 1995, 27:457-466.
52. Wang P., Heitman J. The cyclophilins. Genome Biol 2005, 6:226.
53. Wall R, Ross RP, Fitzgerald GF, Stanton C. Fatty acids from fish: the anti-inflammatory potential of long-chain omega-3 fatty acids. Nutr Rev 2010;68:280-9.