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Gut microbial metabolites of polyunsaturated fatty acids correlate with specific fecal bacteria and serum markers of metabolic syndrome in obese women

Bibliographic reference Druart, Céline ; Dewulf, Evelyne M. ; Cani, Patrice D. ; Neyrinck, Audrey M. ; Thissen, Jean-Paul ; et. al. Gut microbial metabolites of polyunsaturated fatty acids correlate with specific fecal bacteria and serum markers of metabolic syndrome in obese women. In: Lipids, Vol. 49, no. 4, p. 397-402 (2014)
Permanent URL http://hdl.handle.net/2078.1/145840
  1. Delzenne Nathalie M., Neyrinck Audrey M., Cani Patrice D., Gut microbiota and metabolic disorders: how prebiotic can work?, 10.1017/s0007114512004047
  2. Nicholson J. K., Holmes E., Kinross J., Burcelin R., Gibson G., Jia W., Pettersson S., Host-Gut Microbiota Metabolic Interactions, 10.1126/science.1223813
  3. Bhattacharya Arunabh, Banu Jameela, Rahman Mizanur, Causey Jennifer, Fernandes Gabriel, Biological effects of conjugated linoleic acids in health and disease, 10.1016/j.jnutbio.2006.02.009
  4. Meyer D, Stasse-Wolthuis M, The bifidogenic effect of inulin and oligofructose and its consequences for gut health, 10.1038/ejcn.2009.64
  5. Ramirez-Farias Carlett, Slezak Kathleen, Fuller Zoë, Duncan Alan, Holtrop Grietje, Louis Petra, Effect of inulin on the human gut microbiota: stimulation of Bifidobacterium adolescentis and Faecalibacterium prausnitzii, 10.1017/s0007114508019880
  6. Roberfroid Marcel, Gibson Glenn R., Hoyles Lesley, McCartney Anne L., Rastall Robert, Rowland Ian, Wolvers Danielle, Watzl Bernhard, Szajewska Hania, Stahl Bernd, Guarner Francisco, Respondek Frederique, Whelan Kevin, Coxam Veronique, Davicco Marie-Jeanne, Léotoing Laurent, Wittrant Yohann, Delzenne Nathalie M., Cani Patrice D., Neyrinck Audrey M., Meheust Agnes, Prebiotic effects: metabolic and health benefits, 10.1017/s0007114510003363
  7. Dewulf Evelyne M, Cani Patrice D, Claus Sandrine P, Fuentes Susana, Puylaert Philippe GB, Neyrinck Audrey M, Bindels Laure B, de Vos Willem M, Gibson Glenn R, Thissen Jean-Paul, Delzenne Nathalie M, Insight into the prebiotic concept: lessons from an exploratory, double blind intervention study with inulin-type fructans in obese women, 10.1136/gutjnl-2012-303304
  8. O'Shea Eileen F., Cotter Paul D., Stanton Catherine, Ross R. Paul, Hill Colin, Production of bioactive substances by intestinal bacteria as a basis for explaining probiotic mechanisms: Bacteriocins and conjugated linoleic acid, 10.1016/j.ijfoodmicro.2011.05.025
  9. Gorissen Lara, Raes Katleen, Weckx Stefan, Dannenberger Dirk, Leroy Frédéric, De Vuyst Luc, De Smet Stefaan, Production of conjugated linoleic acid and conjugated linolenic acid isomers by Bifidobacterium species, 10.1007/s00253-010-2713-1
  10. Coakley M., Ross R.P., Nordgren M., Fitzgerald G., Devery R., Stanton C., Conjugated linoleic acid biosynthesis by human-derived Bifidobacterium species, 10.1046/j.1365-2672.2003.01814.x
  11. Moya-Camarena SY, Vanden Heuvel JP, Blanchard SG, Leesnitzer LA, Belury MA (1999) Conjugated linoleic acid is a potent naturally occurring ligand and activator of PPARalpha. J Lipid Res 40:1426–1433
  12. Belury Martha A, Moya-Camarena Silvia Y, Lu Ming, Shi Lingling, Leesnitzer Lisa M, Blanchard Steven G, Conjugated linoleic acid is an activator and ligand for peroxisome proliferator-activated receptor-gamma (PPARγ), 10.1016/s0271-5317(02)00393-7
  13. Plourde Mélanie, Jew Stephanie, Cunnane Stephen C, Jones Peter JH, Conjugated linoleic acids: why the discrepancy between animal and human studies? : Nutrition Reviews©, Vol. 66, No. 7, 10.1111/j.1753-4887.2008.00051.x
  14. Houseknecht Karen L., Heuvel John P.Vanden, Moya-Camarena Silvia Y., Portocarrero Carla P., Peck Louise W., Nickel Kwangok P., Belury Martha A., Dietary Conjugated Linoleic Acid Normalizes Impaired Glucose Tolerance in the Zucker Diabetic Fattyfa/faRat, 10.1006/bbrc.1998.8303
  15. Kelley NS, Hubbard NE, Erickson KL (2007) Conjugated linoleic acid isomers and cancer. J Nutr 137:2599–2607
  16. Reynolds C.M., Roche H.M., Conjugated linoleic acid and inflammatory cell signalling, 10.1016/j.plefa.2010.02.021
  17. Wang Y W, Jones P J H, Conjugated linoleic acid and obesity control: efficacy and mechanisms, 10.1038/sj.ijo.0802641
  18. Clément Lionel, Poirier Hélène, Niot Isabelle, Bocher Virginie, Guerre-Millo Michèle, Krief Stéphane, Staels Bart, Besnard Philippe, Dietarytrans-10,cis-12conjugated linoleic acid induces hyperinsulinemia and fatty liver in the mouse, 10.1194/jlr.m20008-jlr200
  19. Onakpoya Igho J., Posadzki Paul P., Watson Leala K., Davies Lucy A., Ernst Edzard, The efficacy of long-term conjugated linoleic acid (CLA) supplementation on body composition in overweight and obese individuals: a systematic review and meta-analysis of randomized clinical trials, 10.1007/s00394-011-0253-9
  20. Martin Jean-Charles, Valeille Karine, Conjugated linoleic acids: all the same or to everyone its own function?, 10.1051/rnd:2002042
  21. Loscher C. E., Draper E., Leavy O., Kelleher D., Mills K. H. G., Roche H. M., Conjugated Linoleic Acid Suppresses NF- B Activation and IL-12 Production in Dendritic Cells through ERK-Mediated IL-10 Induction, 10.4049/jimmunol.175.8.4990
  22. Moloney F., Toomey S., Noone E., Nugent A., Allan B., Loscher C. E., Roche H. M., Antidiabetic Effects of cis-9, trans-11-Conjugated Linoleic Acid May Be Mediated via Anti-Inflammatory Effects in White Adipose Tissue, 10.2337/db06-0384
  23. Poirier H., Shapiro J. S., Kim R. J., Lazar M. A., Nutritional Supplementation With trans-10, cis-12-Conjugated Linoleic Acid Induces Inflammation of White Adipose Tissue, 10.2337/db06-0036
  24. Park Yeonhwa, Storkson Jayne M., Albright Karen J., Liu Wei, Pariza Michael W., Evidence that the trans-10,cis-12 isomer of conjugated linoleic acid induces body composition changes in mice, 10.1007/s11745-999-0358-8
  25. Tricon S, Burdge GC, Kew S, Banerjee T, Russell JJ, Jones EL, Grimble RF, Williams CM, Yaqoob P, Calder PC (2004) Opposing effects of cis-9,trans-11 and trans-10,cis-12 conjugated linoleic acid on blood lipids in healthy humans. Am J Clin Nutr 80:614–620
  26. Riserus U., Arner P., Brismar K., Vessby B., Treatment With Dietary trans10cis12 Conjugated Linoleic Acid Causes Isomer-Specific Insulin Resistance in Obese Men With the Metabolic Syndrome, 10.2337/diacare.25.9.1516
  27. Tricon Sabine, Yaqoob Parveen, Conjugated linoleic acid and human health: a critical evaluation of the evidence : , 10.1097/01.mco.0000214567.44568.fb
  28. Folch J, Lees M, Sloane Stanley GH (1957) A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 226:497–509
  29. Christie William W., Dobson Gary, Adlof Richard O., A Practical Guide to the Isolation, Analysis and Identification of Conjugated Linoleic Acid, 10.1007/s11745-007-3107-8
  30. Precht Dietz, Molkentin Joachim, McGuire Mark A., McGuire Michelle K., Jensen Robert G., Overestimates of oleic and linoleic acid contents in materials containing trans fatty acids and analyzed with short packed gas chromatographic columns, 10.1007/s11745-001-0710-z
  31. Kramer John K. G., Hernandez Marta, Cruz-Hernandez Cristina, Kraft Jana, Dugan Michael E. R., Combining Results of Two GC Separations Partly Achieves Determination of All cis and trans 16:1, 18:1, 18:2 and 18:3 Except CLA Isomers of Milk Fat as Demonstrated Using Ag-Ion SPE Fractionation, 10.1007/s11745-007-3143-4
  32. Ritzenthaler KL, McGuire MK, Falen R, Shultz TD, Dasgupta N, McGuire MA (2001) Estimation of conjugated linoleic acid intake by written dietary assessment methodologies underestimates actual intake evaluated by food duplicate methodology. J Nutr 131:1548–1554
  33. Neyrinck Audrey M., Possemiers Sam, Druart Céline, Van de Wiele Tom, De Backer Fabienne, Cani Patrice D., Larondelle Yvan, Delzenne Nathalie M., Prebiotic Effects of Wheat Arabinoxylan Related to the Increase in Bifidobacteria, Roseburia and Bacteroides/Prevotella in Diet-Induced Obese Mice, 10.1371/journal.pone.0020944
  34. Lahti Leo, Salonen Anne, Kekkonen Riina A., Salojärvi Jarkko, Jalanka-Tuovinen Jonna, Palva Airi, Orešič Matej, de Vos Willem M., Associations between the human intestinal microbiota,Lactobacillus rhamnosusGG and serum lipids indicated by integrated analysis of high-throughput profiling data, 10.7717/peerj.32
  35. Devillard E., McIntosh F. M., Duncan S. H., Wallace R. J., Metabolism of Linoleic Acid by Human Gut Bacteria: Different Routes for Biosynthesis of Conjugated Linoleic Acid, 10.1128/jb.01359-06
  36. Or-Rashid Mamun M., AlZahal Ousama, McBride Brian W., Comparative studies on the metabolism of linoleic acid by rumen bacteria, protozoa, and their mixture in vitro, 10.1007/s00253-010-2865-z
  37. Chilliard Yves, Glasser Frédéric, Ferlay Anne, Bernard Laurence, Rouel Jacques, Doreau Michel, Diet, rumen biohydrogenation and nutritional quality of cow and goat milk fat, 10.1002/ejlt.200700080
  38. McIntosh F. M., Shingfield K. J., Devillard E., Russell W. R., Wallace R. J., Mechanism of conjugated linoleic acid and vaccenic acid formation in human faecal suspensions and pure cultures of intestinal bacteria, 10.1099/mic.0.022921-0
  39. Park Hui Gyu, Cho Hyung Taek, Song Myoung-Chong, Kim Sang Bum, Kwon Eung Gi, Choi Nag Jin, Kim Young Jun, Production of a Conjugated Fatty Acid byBifidobacterium breveLMC520 from α-Linolenic Acid: Conjugated Linolenic Acid (CLnA), 10.1021/jf2041559
  40. Alonso L., Cuesta E.P., Gilliland S.E., Production of Free Conjugated Linoleic Acid by Lactobacillus acidophilus and Lactobacillus casei of Human Intestinal Origin, 10.3168/jds.s0022-0302(03)73781-3
  41. Bassett C. M. C., Edel A. L., Patenaude A. F., McCullough R. S., Blackwood D. P., Chouinard P. Y., Paquin P., Lamarche B., Pierce G. N., Dietary Vaccenic Acid Has Antiatherogenic Effects in LDLr-/- Mice, 10.3945/jn.109.105163
  42. Oh K., Dietary Fat Intake and Risk of Coronary Heart Disease in Women: 20 Years of Follow-up of the Nurses' Health Study, 10.1093/aje/kwi085