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Intestinal Sucrase as a Novel Target Contributing to the Regulation of Glycemia by Prebiotics

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  1. Sim Lyann, Willemsma Carly, Mohan Sankar, Naim Hassan Y., Pinto B. Mario, Rose David R., Structural Basis for Substrate Selectivity in Human Maltase-Glucoamylase and Sucrase-Isomaltase N-terminal Domains, 10.1074/jbc.m109.078980
  2. Williamson Gary, Possible effects of dietary polyphenols on sugar absorption and digestion, 10.1002/mnfr.201200511
  3. Bindels Laure B., Delzenne Nathalie M., Cani Patrice D., Walter Jens, Towards a more comprehensive concept for prebiotics, 10.1038/nrgastro.2015.47
  4. Hutkins Robert W, Krumbeck Janina A, Bindels Laure B, Cani Patrice D, Fahey George, Goh Yong Jun, Hamaker Bruce, Martens Eric C, Mills David A, Rastal Robert A, Vaughan Elaine, Sanders Mary Ellen, Prebiotics: why definitions matter, 10.1016/j.copbio.2015.09.001
  5. 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
  6. Delzenne Nathalie M., Cani Patrice D., Everard Amandine, Neyrinck Audrey M., Bindels Laure B., Gut microorganisms as promising targets for the management of type 2 diabetes, 10.1007/s00125-015-3712-7
  7. Delzenne Nathalie M., Neyrinck Audrey M., Bäckhed Fredrik, Cani Patrice D., Targeting gut microbiota in obesity: effects of prebiotics and probiotics, 10.1038/nrendo.2011.126
  8. Everard Amandine, Lazarevic Vladimir, Derrien Muriel, Girard Myriam, Muccioli Giulio G., Neyrinck Audrey M., Possemiers Sam, Van Holle Ann, François Patrice, de Vos Willem M., Delzenne Nathalie M., Schrenzel Jacques, Cani Patrice D., Responses of Gut Microbiota and Glucose and Lipid Metabolism to Prebiotics in Genetic Obese and Diet-Induced Leptin-Resistant Mice, 10.2337/db11-0227
  9. Cani P. D., Possemiers S., Van de Wiele T., Guiot Y., Everard A., Rottier O., Geurts L., Naslain D., Neyrinck A., Lambert D. M., Muccioli G. G., Delzenne N. M., Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability, 10.1136/gut.2008.165886
  10. Cani P. D., Knauf C., Iglesias M. A., Drucker D. J., Delzenne N. M., Burcelin R., Improvement of Glucose Tolerance and Hepatic Insulin Sensitivity by Oligofructose Requires a Functional Glucagon-Like Peptide 1 Receptor, 10.2337/db05-1360
  11. PD Cani, Br J Nutr, 1 (2007)
  12. Maurer Alannah D., Chen Qixuan, McPherson Christine, Reimer Raylene A., Changes in satiety hormones and expression of genes involved in glucose and lipid metabolism in rats weaned onto diets high in fibre or protein reflect susceptibility to increased fat mass in adulthood : Early high fibre or protein diets, 10.1113/jphysiol.2008.161844
  13. JE Urias-Silvas, Br J Nutr, 99, 254 (2008)
  14. Oki Tomoyuki, Matsui Toshiro, Osajima Yutaka, Inhibitory Effect of α-Glucosidase Inhibitors Varies According to Its Origin, 10.1021/jf980788t
  15. Oku Tsuneyuki, Murata-Takenoshita Yoko, Yamazaki Yuko, Shimura Fumio, Nakamura Sadako, d-Sorbose inhibits disaccharidase activity and demonstrates suppressive action on postprandial blood levels of glucose and insulin in the rat, 10.1016/j.nutres.2014.09.009
  16. Dahlqvist Arne, Assay of intestinal disaccharidases, 10.1016/0003-2697(68)90263-7
  17. Bindels Laure B., Neyrinck Audrey M., Salazar Nuria, Taminiau Bernard, Druart Céline, Muccioli Giulio G., François Emmanuelle, Blecker Christophe, Richel Aurore, Daube Georges, Mahillon Jacques, de los Reyes-Gavilán Clara G., Cani Patrice D., Delzenne Nathalie M., Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice, 10.1371/journal.pone.0131009
  18. , Scientific Opinion on the substantiation of a health claim related to non digestible carbohydrates and a reduction of post prandial glycaemic responses pursuant to Article 13(5) of Regulation (EC) No 1924/2006, 10.2903/j.efsa.2014.3513
  19. Fukunaga Tetsuya, Sasaki Masaya, Araki Yoshio, Okamoto Toshihiko, Yasuoka Takashi, Tsujikawa Tomoyuki, Fujiyama Yoshihide, Bamba Tadao, Effects of the Soluble Fibre Pectin on Intestinal Cell Proliferation, Fecal Short Chain Fatty Acid Production and Microbial Population, 10.1159/000069705
  20. Brownlee Iain A., Havler Mike E., Dettmar Peter W., Allen Adrian, Pearson Jeffrey P., Colonic mucus: secretion and turnover in relation to dietary fibre intake, 10.1079/pns2003206
  21. Hedemann M. S., Eskildsen M., Lærke H. N., Pedersen C., Lindberg J. E., Laurinen P., Knudsen K. E. Bach, Intestinal morphology and enzymatic activity in newly weaned pigs fed contrasting fiber concentrations and fiber properties, 10.2527/2006.8461375x
  22. LR Jacobs, Am J Physiol, 246, G378 (1984)
  23. JR Lupton, J Nutr, 118, 840 (1988)
  24. Fletcher Madeleine M., Halls Michelle L., Christopoulos Arthur, Sexton Patrick M., Wootten Denise, The complexity of signalling mediated by the glucagon-like peptide-1 receptor, 10.1042/bst20150244
  25. Liu C., Finegold S. M., Song Y., Lawson P. A., Reclassification of Clostridium coccoides, Ruminococcus hansenii, Ruminococcus hydrogenotrophicus, Ruminococcus luti, Ruminococcus productus and Ruminococcus schinkii as Blautia coccoides gen. nov., comb. nov., Blautia hansenii comb. nov., Blautia hydrogenotrophica comb. nov., Blautia luti comb. nov., Blautia producta comb. nov., Blautia schinkii comb. nov. and description of Blautia wexlerae sp. nov., isolated from human faeces, 10.1099/ijs.0.65208-0
  26. Nakamura Noriko, Lin Henry C., McSweeney Christopher S., Mackie Roderick I., Gaskins H. Rex, Mechanisms of Microbial Hydrogen Disposal in the Human Colon and Implications for Health and Disease, 10.1146/annurev.food.102308.124101
  27. Junicke Helena, Feldman Hannah, Van Loosdrecht Mark C. M., Kleerebezem Robbert, Limitation of syntrophic coculture growth by the acetogen : Role of the Acetogen in a Syntrophic Coculture, 10.1002/bit.25816
  28. S Devkota, Nature, 487, 104 (2012)
  29. Barlow Gillian M., Yu Allen, Mathur Ruchi, Role of the Gut Microbiome in Obesity and Diabetes Mellitus, 10.1177/0884533615609896
  30. David Lawrence A., Maurice Corinne F., Carmody Rachel N., Gootenberg David B., Button Julie E., Wolfe Benjamin E., Ling Alisha V., Devlin A. Sloan, Varma Yug, Fischbach Michael A., Biddinger Sudha B., Dutton Rachel J., Turnbaugh Peter J., Diet rapidly and reproducibly alters the human gut microbiome, 10.1038/nature12820
  31. Schneeberger Marc, Everard Amandine, Gómez-Valadés Alicia G., Matamoros Sébastien, Ramírez Sara, Delzenne Nathalie M., Gomis Ramon, Claret Marc, Cani Patrice D., Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice, 10.1038/srep16643
  32. Tannock G. W., Lawley B., Munro K., Sims I. M., Lee J., Butts C. A., Roy N., RNA-Stable-Isotope Probing Shows Utilization of Carbon from Inulin by Specific Bacterial Populations in the Rat Large Bowel, 10.1128/aem.03799-13
  33. Martínez Inés, Lattimer James M, Hubach Kelcie L, Case Jennifer A, Yang Junyi, Weber Casey G, Louk Julie A, Rose Devin J, Kyureghian Gayaneh, Peterson Daniel A, Haub Mark D, Walter Jens, Gut microbiome composition is linked to whole grain-induced immunological improvements, 10.1038/ismej.2012.104
  34. Everard A., Belzer C., Geurts L., Ouwerkerk J. P., Druart C., Bindels L. B., Guiot Y., Derrien M., Muccioli G. G., Delzenne N. M., de Vos W. M., Cani P. D., Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity, 10.1073/pnas.1219451110
  35. Everard Amandine, Lazarevic Vladimir, Gaïa Nadia, Johansson Maria, Ståhlman Marcus, Backhed Fredrik, Delzenne Nathalie M, Schrenzel Jacques, François Patrice, Cani Patrice D, Microbiome of prebiotic-treated mice reveals novel targets involved in host response during obesity, 10.1038/ismej.2014.45
  36. Salonen Anne, Lahti Leo, Salojärvi Jarkko, Holtrop Grietje, Korpela Katri, Duncan Sylvia H, Date Priya, Farquharson Freda, Johnstone Alexandra M, Lobley Gerald E, Louis Petra, Flint Harry J, de Vos Willem M, Impact of diet and individual variation on intestinal microbiota composition and fermentation products in obese men, 10.1038/ismej.2014.63
  37. Yang Junyi, Bindels Laure B., Segura Munoz Rafael R., Martínez Inés, Walter Jens, Ramer-Tait Amanda E., Rose Devin J., Disparate Metabolic Responses in Mice Fed a High-Fat Diet Supplemented with Maize-Derived Non-Digestible Feruloylated Oligo- and Polysaccharides Are Linked to Changes in the Gut Microbiota, 10.1371/journal.pone.0146144
  38. Y Kawai, Infect Immun, 19, 771 (1978)
  39. DD Whitt, Appl Environ Microbiol, 42, 513 (1981)
  40. Quintero Maria, Maldonado Maria, Perez-Munoz MariaElisa, Jimenez Roberto, Fangman Terry, Rupnow John, Wittke Anja, Russell Michael, Hutkins Robert, Adherence Inhibition of Cronobacter sakazakii to Intestinal Epithelial Cells by Prebiotic Oligosaccharides, 10.1007/s00284-011-9882-8
  41. Zenhom M., Hyder A., de Vrese M., Heller K. J., Roeder T., Schrezenmeir J., Prebiotic Oligosaccharides Reduce Proinflammatory Cytokines in Intestinal Caco-2 Cells via Activation of PPAR  and Peptidoglycan Recognition Protein 3, 10.3945/jn.110.136176
Bibliographic reference Neyrinck, Audrey M. ; Pachikian, Barbara D. ; Taminiau , Bernard ; Daube , Georges ; Frédérick, Raphaël ; et. al. Intestinal Sucrase as a Novel Target Contributing to the Regulation of Glycemia by Prebiotics. In: PLoS One, Vol. 11, no.8, p. e0160488 [1-13] (2016)
Permanent URL http://hdl.handle.net/2078.1/179136