Host-Gut Microbiota Crosstalk in Intestinal Adaptation

Cellular and Molecular Gastroenterology and Hepatology - Tập 6 - Trang 149-162 - 2018
Justine Marchix1, Gillian Goddard2, Michael A. Helmrath1,2
1Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
2Department of General Surgery, University of Cincinnati, Cincinnati, Ohio

Tài liệu tham khảo

Dehmer, 2011, Management of pediatric intestinal failure, Adv Pediatr, 58, 181, 10.1016/j.yapd.2011.03.012

Pironi, 2015, ESPEN endorsed recommendations. Definition and classification of intestinal failure in adults, Clin Nutr, 34, 171, 10.1016/j.clnu.2014.08.017

Cole, 2010, The rate of bloodstream infection is high in infants with short bowel syndrome: relationship with small bowel bacterial overgrowth, enteral feeding, and inflammatory and immune responses, J Pediatr, 156, 941, 10.1016/j.jpeds.2009.12.008

Wales, 2010, Short bowel syndrome: epidemiology and etiology, Semin Pediatr Surg, 19, 3, 10.1053/j.sempedsurg.2009.11.001

Sangild, 2014, Animal models of gastrointestinal and liver diseases. Animal models of infant short bowel syndrome: translational relevance and challenges, Am J Physiol Gastrointest Liver Physiol, 307, G1147, 10.1152/ajpgi.00088.2014

Helmrath, 1998, Enterocyte apoptosis is increased following small bowel resection, J Gastrointest Surg, 2, 44, 10.1016/S1091-255X(98)80102-9

Dowling, 1967, Structural and functional changes following small intestinal resection in the rat, Clin Sci, 32, 139

Turner, 2011, Novel neonatal piglet models of surgical short bowel syndrome with intestinal failure, J Pediatr Gastroenterol Nutr, 52, 9, 10.1097/MPG.0b013e3181f18ca0

Schall, 2015, Adult zebrafish intestine resection: a novel model of short bowel syndrome, adaptation, and intestinal stem cell regeneration, Am J Physiol Gastrointest Liver Physiol, 309, G135, 10.1152/ajpgi.00311.2014

Sigalet, 1998, Mechanisms underlying intestinal adaptation after massive intestinal resection in the rat, J Pediatr Surg, 33, 889, 10.1016/S0022-3468(98)90667-4

Dekaney, 2007, Expansion of intestinal stem cells associated with long-term adaptation following ileocecal resection in mice, Am J Physiol Gastrointest Liver Physiol, 293, G1013, 10.1152/ajpgi.00218.2007

Gillingham, 2000, Differential jejunal and colonic adaptation due to resection and IGF-I in parenterally fed rats, Am J Physiol Gastrointest Liver Physiol, 278, G700, 10.1152/ajpgi.2000.278.5.G700

Vegge, 2013, Glucagon-like peptide-2 induces rapid digestive adaptation following intestinal resection in preterm neonates, Am J Physiol Gastrointest Liver Physiol, 305, G277, 10.1152/ajpgi.00064.2013

Aunsholt, 2015, Prematurity reduces functional adaptation to intestinal resection in piglets, JPEN J Parenter Enteral Nutr, 39, 668, 10.1177/0148607114528714

Helmrath, 2007, Rapid expansion of intestinal secretory lineages following a massive small bowel resection in mice, Am J Physiol Gastrointest Liver Physiol, 292, G215, 10.1152/ajpgi.00188.2006

Martin, 2009, Intestinal resection induces angiogenesis within adapting intestinal villi, J Pediatr Surg, 44, 1077, 10.1016/j.jpedsurg.2009.02.036

Rowland, 2012, Immediate alterations in intestinal oxygen saturation and blood flow after massive small bowel resection as measured by photoacoustic microscopy, J Pediatr Surg, 47, 1143, 10.1016/j.jpedsurg.2012.03.020

Tappenden, 2014, Intestinal adaptation following resection, JPEN J Parenter Enteral Nutr, 38, 23S, 10.1177/0148607114525210

Weale, 2005, Intestinal adaptation after massive intestinal resection, Postgrad Med J, 81, 178, 10.1136/pgmj.2004.023846

Thompson, 1995, Surgical approach to short-bowel syndrome. Experience in a population of 160 patients, Ann Surg, 222, 600, 10.1097/00000658-199522240-00016

McDuffie, 2011, Intestinal adaptation after small bowel resection in human infants, J Pediatr Surg, 46, 1045, 10.1016/j.jpedsurg.2011.03.027

Doldi, 1991, Intestinal adaptation following jejuno-ileal bypass, Clin Nutr, 10, 138, 10.1016/0261-5614(91)90049-I

Joly, 2010, Drastic changes in fecal and mucosa-associated microbiota in adult patients with short bowel syndrome, Biochimie, 92, 753, 10.1016/j.biochi.2010.02.015

O'Keefe, 1994, Long-acting somatostatin analogue therapy and protein metabolism in patients with jejunostomies, Gastroenterology, 107, 379, 10.1016/0016-5085(94)90162-7

Ziegler, 2002, Distribution of the H+/peptide transporter PepT1 in human intestine: up-regulated expression in the colonic mucosa of patients with short-bowel syndrome, Am J Clin Nutr, 75, 922, 10.1093/ajcn/75.5.922

Scott, 1998, GLP-2 augments the adaptive response to massive intestinal resection in rat, Am J Physiol, 275, G911

Jeppesen, 2012, Teduglutide, a novel glucagon-like peptide 2 analog, in the treatment of patients with short bowel syndrome, Therap Adv Gastroenterol, 5, 159, 10.1177/1756283X11436318

Jeppesen, 2011, Randomised placebo-controlled trial of teduglutide in reducing parenteral nutrition and/or intravenous fluid requirements in patients with short bowel syndrome, Gut, 60, 902, 10.1136/gut.2010.218271

Seidner, 2013, Increased intestinal absorption in the era of teduglutide and its impact on management strategies in patients with short bowel syndrome-associated intestinal failure, JPEN J Parenter Enteral Nutr, 37, 201, 10.1177/0148607112472906

Jeppesen, 2001, Glucagon-like peptide 2 improves nutrient absorption and nutritional status in short-bowel patients with no colon, Gastroenterology, 120, 806, 10.1053/gast.2001.22555

Jeppesen, 2005, Teduglutide (ALX-0600), a dipeptidyl peptidase IV resistant glucagon-like peptide 2 analogue, improves intestinal function in short bowel syndrome patients, Gut, 54, 1224, 10.1136/gut.2004.061440

Jeppesen, 2012, Teduglutide reduces need for parenteral support among patients with short bowel syndrome with intestinal failure, Gastroenterology, 143, 1473, 10.1053/j.gastro.2012.09.007

Madsen, 2013, Acute effects of continuous infusions of glucagon-like peptide (GLP)-1, GLP-2 and the combination (GLP-1+GLP-2) on intestinal absorption in short bowel syndrome (SBS) patients. A placebo-controlled study, Regul Pept, 184, 30, 10.1016/j.regpep.2013.03.025

Sigalet, 2004, GLP-2 levels in infants with intestinal dysfunction, Pediatr Res, 56, 371, 10.1203/01.PDR.0000134250.80492.EC

Tappenden, 2013, Teduglutide enhances structural adaptation of the small intestinal mucosa in patients with short bowel syndrome, J Clin Gastroenterol, 47, 602, 10.1097/MCG.0b013e3182828f57

Schwartz, 2016, Long-term teduglutide for the treatment of patients with intestinal failure associated with short bowel syndrome, Clin Transl Gastroenterol, 7, e142, 10.1038/ctg.2015.69

Watson, 2014, An in vivo model of human small intestine using pluripotent stem cells, Nat Med, 20, 1310, 10.1038/nm.3737

Juno, 2002, A serum factor after intestinal resection stimulates epidermal growth factor receptor signaling and proliferation in intestinal epithelial cells, Surgery, 132, 377, 10.1067/msy.2002.125724

Tappenden, 2014, Pathophysiology of short bowel syndrome: considerations of resected and residual anatomy, JPEN J Parenter Enteral Nutr, 38, 14S, 10.1177/0148607113520005

Goulet, 2005, Outcome and long-term growth after extensive small bowel resection in the neonatal period: a survey of 87 children, Eur J Pediatr Surg, 15, 95, 10.1055/s-2004-821214

Nordgaard, 1994, Colon as a digestive organ in patients with short bowel, Lancet, 343, 373, 10.1016/S0140-6736(94)91220-3

McMellen, 2010, Growth factors: possible roles for clinical management of the short bowel syndrome, Semin Pediatr Surg, 19, 35, 10.1053/j.sempedsurg.2009.11.010

Warner, 2016, The pathogenesis of resection-associated intestinal adaptation, Cell Mol Gastroenterol Hepatol, 2, 429, 10.1016/j.jcmgh.2016.05.001

Scolapio, 1997, Effect of growth hormone, glutamine, and diet on adaptation in short-bowel syndrome: a randomized, controlled study, Gastroenterology, 113, 1074, 10.1053/gast.1997.v113.pm9322500

Nucci, 2004, Results of growth trophic therapy in children with short bowel syndrome, J Pediatr Surg, 39, 335, 10.1016/j.jpedsurg.2003.11.022

Goulet, 2010, Effect of recombinant human growth hormone on intestinal absorption and body composition in children with short bowel syndrome, JPEN J Parenter Enteral Nutr, 34, 513, 10.1177/0148607110362585

Guo, 2016, Early intestinal rehabilitation therapy ameliorates intestinal adaptation in children with short bowel syndrome: the long-term outcome, Am Surg, 82, 1215, 10.1177/000313481608201229

Byrne, 2005, Growth hormone, glutamine, and an optimal diet reduces parenteral nutrition in patients with short bowel syndrome, Ann Surg, 242, 655, 10.1097/01.sla.0000186479.53295.14

Gu, 2001, Effects of growth hormone (rhGH) and glutamine supplemented parenteral nutrition on intestinal adaptation in short bowel rats, Clin Nutr, 20, 159, 10.1054/clnu.2000.0379

Sigalet, 2005, A pilot study of the use of epidermal growth factor in pediatric short bowel syndrome, J Pediatr Surg, 40, 763, 10.1016/j.jpedsurg.2005.01.038

Erwin, 1999, Intestinal overexpression of EGF in transgenic mice enhances adaptation after small bowel resection, Am J Physiol, 277, G533

Shin, 1998, Epidermal growth factor augments adaptation following small bowel resection: optimal dosage, route, and timing of administration, J Surg Res, 77, 11, 10.1006/jsre.1998.5336

Chaet, 1994, Epidermal growth factor enhances intestinal adaptation after massive small bowel resection, J Pediatr Surg, 29, 1035, 10.1016/0022-3468(94)90274-7

Rowland, 2012, Enterocyte expression of epidermal growth factor receptor is not required for intestinal adaptation in response to massive small bowel resection, J Pediatr Surg, 47, 1748, 10.1016/j.jpedsurg.2012.03.089

Sun, 2014, Insulin-like growth factor 2 and its enterocyte receptor are not required for adaptation in response to massive small bowel resection, J Pediatr Surg, 49, 966, 10.1016/j.jpedsurg.2014.01.035

Lim, 2017, Synergy of glucagon-like peptide-2 and epidermal growth factor coadministration on intestinal adaptation in neonatal piglets with short bowel syndrome, Am J Physiol Gastrointest Liver Physiol, 312, G390, 10.1152/ajpgi.00281.2016

Martin, 2004, Glucagon-like peptide-2 induces intestinal adaption in parenterally fed rats with short bowel syndrome, Am J Physiol, 286, G964

Lim, 2016, Differential effects on intestinal adaptation following exogenous glucagon-like peptide 2 therapy with and without enteral nutrition in neonatal short bowel syndrome, JPEN J Parenter Enteral Nutr, 41, 156, 10.1177/0148607116665812

Drucker, 1996, Induction of intestinal epithelial proliferation by glucagon-like peptide 2, Proc Natl Acad Sci U S A, 93, 7911, 10.1073/pnas.93.15.7911

Tsai, 1997, Intestinal growth-promoting properties of glucagon-like 2 in mice, Am J Physiol, 273, E77

Sigalet, 2006, Glucagon-like peptide-2 induces a specific pattern of adaptation in remnant jejunum, Dig Dis Sci, 51, 1557, 10.1007/s10620-006-9077-5

Garrison, 2009, Early but not late administration of glucagon-like peptide-2 following ileo-cecal resection augments putative intestinal stem cell expansion, Am J Physiol Gastrointest Liver Physiol, 296, G643, 10.1152/ajpgi.90588.2008

Naberhuis, 2017, Teduglutide-stimulated intestinal adaptation is complemented and synergistically enhanced by partial enteral nutrition in a neonatal piglet model of short bowel syndrome, JPEN J Parenter Enteral Nutr, 41, 853, 10.1177/0148607115602891

Krsek, 2002, Plasma ghrelin levels in patients with short bowel syndrome, Endocr Res, 28, 10.1081/ERC-120004535

Lund, 1998, Molecular basis of intestinal adaptation: the role of the insulin-like growth factor system, Ann N Y Acad Sci, 859, 18, 10.1111/j.1749-6632.1998.tb11108.x

Knott, 2004, Smooth muscle overexpression of IGF-I induces a novel adaptive response to small bowel resection, Am J Physiol Gastrointest Liver Physiol, 287, G562, 10.1152/ajpgi.00438.2003

Dahly, 2003, IGF-I augments resection-induced mucosal hyperplasia by altering enterocyte kinetics, Am J Physiol Regul Integr Comp Physiol, 285, R800, 10.1152/ajpregu.00014.2003

Vanderhoof, 1992, Truncated and native insulin like growth factor I enhance mucosal adaptation after jejunoileal resection, Gastroenterology, 102, 1949, 10.1016/0016-5085(92)90318-S

Choi, 2013, IGF-2 mediates intestinal mucosal hyperplasia in retinoblastoma protein (Rb)-deficient mice, J Pediatr Surg, 48, 1340, 10.1016/j.jpedsurg.2013.03.042

Falcone, 1999, Intestinal adaptation occurs independent of transforming growth factor-alpha, J Pediatr Surg, 35, 365, 10.1016/S0022-3468(00)90042-3

Sukhotnik, 2002, Effect of transforming growth factor-α on intestinal adaptation in a rat model of short bowel syndrome, J Surg Res, 108, 235, 10.1006/jsre.2002.6556

Sukhotnik, 2008, Responsiveness of intestinal epithelial cell turnover to TGF-alpha after bowel resection in a rat is correlated with EGF receptor expression along the villus-crypt axis, Pediatr Surg Int, 24, 21, 10.1007/s00383-007-2038-z

Sukhotnik, 2006, Effect of leptin on intestinal re-growth following massive small bowel resection in rat, Pediatr Surg Int, 22, 9, 10.1007/s00383-005-1572-9

Sukhotnik, 2009, Leptin affects intestinal epithelial cell turnover in correlation with leptin receptor expression along the villus-crypt axis after massive small bowel resection in a rat, Pediatr Res, 66, 648, 10.1203/PDR.0b013e3181be9f84

Pearson, 2001, Novel effect of leptin on small intestine adaptation, J Surg Res, 97, 192, 10.1006/jsre.2001.6153

Kiely, 2006, Altered small intestinal absorptive enzyme activities in leptin-deficient obese mice: influence of bowel resection, J Pediatr Surg, 41, 1243, 10.1016/j.jpedsurg.2006.03.047

Guyton, 2017, The gut microbiota and gastrointestinal surgery, Nat Rev Gastroenterol Hepatol, 14, 43, 10.1038/nrgastro.2016.139

Begley, 2005, The interaction between bacteria and bile, FEMS Microbiol Rev, 29, 625, 10.1016/j.femsre.2004.09.003

Devine, 2013, Impact of ileocecal resection and concomitant antibiotics on the microbiome of the murine jejunum and colon, PLoS One, 8, e73140, 10.1371/journal.pone.0073140

Lapthorne, 2013, Gut microbial diversity is reduced and is associated with colonic inflammation in a piglet model of short bowel syndrome, Gut Microbes, 4, 212, 10.4161/gmic.24372

Sommovilla, 2015, Small bowel resection induces long-term changes in the enteric microbiota of mice, J Gastrointest Surg, 19, 56, 10.1007/s11605-014-2631-0

Engstrand Lilja, 2015, Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome, Microbiome, 3, 18, 10.1186/s40168-015-0084-7

Korpela, 2017, Intestinal microbiota signatures associated with histological liver steatosis in pediatric-onset intestinal failure, JPEN J Parenter Enteral Nutr, 41, 238, 10.1177/0148607115584388

Tolga Muftuoglu, 2011, Effects of probiotics on experimental short-bowel syndrome, Am J Surg, 202, 461, 10.1016/j.amjsurg.2011.03.005

Mao, 1996, The effects of Lactobacillus strains and oat fiber on methotrexate-induced enterocolitis in rats, Gastroenterology, 111, 334, 10.1053/gast.1996.v111.pm8690198

Pereira-Fantini, 2017, Unravelling the metabolic impact of SBS-associated microbial dysbiosis: insights from the piglet short bowel syndrome model, Sci Rep, 7, 43326, 10.1038/srep43326

Kamath, 1988, Short-chain fatty acids stimulate ileal motility in humans, Gastroenterology, 95, 1496, 10.1016/S0016-5085(88)80068-4

Royall, 1992, Evidence for colonic conservation of malabsorbed carbohydrate in short bowel syndrome, Am J Gastroenterol, 87, 751

Sobhani, 2011, Microbial dysbiosis in colorectal cancer (CRC) patients, PLoS One, 6, e16393, 10.1371/journal.pone.0016393

Ley, 2006, Microbial ecology: human gut microbes associated with obesity, Nature, 444, 1022, 10.1038/4441022a

Mondot, 2016, Structural robustness of the gut mucosal microbiota is associated with Crohn's disease remission after surgery, Gut, 65, 954, 10.1136/gutjnl-2015-309184

Shogan, 2014, Intestinal anastomotic injury alters spatially defined microbiome composition and function, Microbiome, 2, 35, 10.1186/2049-2618-2-35

Speck, 2011, Inflammation enhances resection-induced intestinal adaptive growth in IL-10 null mice, J Surg Res, 168, 62, 10.1016/j.jss.2009.09.051

Willing, 2007, Enterocyte proliferation and apoptosis in the caudal small intestine is influenced by the composition of colonizing commensal bacteria in the neonatal gnotobiotic pig, J Anim Sci, 85, 3256, 10.2527/jas.2007-0320

Juno, 2003, Characterization of small bowel resection and intestinal adaptation in germ-free rats, Surgery, 134, 582, 10.1016/S0039-6060(03)00281-2

Dekaney, 2008, Bacterial-dependent up-regulation of intestinal bile acid binding protein and transport is FXR-mediated following ileo-cecal resection, Surgery, 144, 174, 10.1016/j.surg.2008.03.035

Banasaz, 2002, Increased enterocyte production in gnotobiotic rats mono-associated with Lactobacillus rhamnosus GG, Appl Environ Microbiol, 68, 3031, 10.1128/AEM.68.6.3031-3034.2002

Ichikawa, 1999, Probiotic bacteria stimulate gut epithelial cell proliferation in rat, Dig Dis Sci, 44, 2119, 10.1023/A:1026647024077

Reddy, 2013, Role of probiotics in short bowel syndrome in infants and children–a systematic review, Nutrients, 5, 679, 10.3390/nu5030679

Kanamori, 2004, Experience of long-term synbiotic therapy in seven short bowel patients with refractory enterocolitis, J Pediatr Surg, 39, 1686, 10.1016/j.jpedsurg.2004.07.013

Sentongo, 2008, Intestinal permeability and effects of Lactobacillus rhamnosus therapy in children with short bowel syndrome, J Pediatr Gastroenterol Nutr, 46, 41, 10.1097/01.mpg.0000304452.92175.f5

Gillard, 2017, Microbiota is involved in post-resection adaptation in humans with short bowel syndrome, Front Physiol, 8, 224, 10.3389/fphys.2017.00224

Mowat, 2014, Regional specialization within the intestinal immune system, Nat Rev Immunol, 14, 667, 10.1038/nri3738

Round, 2009, The gut microbiome shapes intestinal immune responses during health and disease, Nat Rev Immunol, 9, 313, 10.1038/nri2515

Gensollen, 2016, How colonization by microbiota in early life shapes the immune system, Science, 352, 539, 10.1126/science.aad9378

Moreau, 1978, Increase in the population of duodenal immunoglobulin A plasmocytes in axenic mice associated with different living or dead bacterial strains of intestinal origin, Infect Immun, 21, 532, 10.1128/iai.21.2.532-539.1978

Suzuki, 2002, Regional variations in the distributions of small intestinal intraepithelial lymphocytes in germ-free and specific pathogen-free mice, Exp Mol Pathol, 72, 230, 10.1006/exmp.2002.2433

Tlaskalova-Hogenova, 1983, Development of immunological capacity under germfree and conventional conditions, Ann N Y Acad Sci, 409, 96, 10.1111/j.1749-6632.1983.tb26862.x

Schall, 2017, Short bowel syndrome results in increased gene expression associated with proliferation, inflammation, bile acid synthesis and immune system activation: RNA sequencing a zebrafish SBS model, BMC Genomics, 18, 23, 10.1186/s12864-016-3433-4

Murakami, 2007, Changes in lymphocyte phenotypes and cytokine production by surgical stress in a rat small intestinal resection model, J Clin Biochem Nutr, 40, 216, 10.3164/jcbn.40.216

Barrena, 1995, Lymphocyte subpopulations after extensive small bowel resection in the rat, J Pediatr Surg, 30, 1447, 10.1016/0022-3468(95)90403-4

Hise, 2006, Inflammatory mediators and immune function are altered in home parenteral nutrition patients, Nutrition, 22, 97, 10.1016/j.nut.2005.05.011

Turato, 2016, The impact of intestinal resection on the immune function of short bowel syndrome patients, Hum Immunol, 77, 1202, 10.1016/j.humimm.2016.07.237

Schmidt, 1996, Effect of intestinal resection on human small bowel motility, Gut, 38, 859, 10.1136/gut.38.6.859

Gianino, 2003, GDNF availability determines enteric neuron number by controlling precursor proliferation, Development, 130, 2187, 10.1242/dev.00433

Hitch, 2012, Ret heterozygous mice have enhanced intestinal adaptation after massive small bowel resection, Am J Physiol Gastrointest Liver Physiol, 302, G1143, 10.1152/ajpgi.00296.2011

Lai, 2017, Effects of exogenous glucagon-like peptide-2 and distal bowel resection on intestinal and systemic adaptive responses in rats, PLoS One, 12, e0181453, 10.1371/journal.pone.0181453

Anitha, 2012, Gut microbial products regulate murine gastrointestinal motility via Toll-like receptor 4 signaling, Gastroenterology, 143, 1006, 10.1053/j.gastro.2012.06.034

Muller, 2014, Crosstalk between muscularis macrophages and enteric neurons regulates gastrointestinal motility, Cell, 158, 300, 10.1016/j.cell.2014.04.050

Gabanyi, 2016, Neuro-immune interactions drive tissue programming in intestinal macrophages, Cell, 164, 378, 10.1016/j.cell.2015.12.023

Gaboriau-Routhiau, 2009, The key role of segmented filamentous bacteria in the coordinated maturation of gut helper T cell responses, Immunity, 31, 677, 10.1016/j.immuni.2009.08.020

Ivanov, 2009, Induction of intestinal Th17 cells by segmented filamentous bacteria, Cell, 139, 485, 10.1016/j.cell.2009.09.033

Alam, 2016, The microenvironment of injured murine gut elicits a local pro-restitutive microbiota, Nat Microbiol, 1, 15021, 10.1038/nmicrobiol.2015.21

Sukhotnik, 2016, Effect of bowel resection on TLR signaling during intestinal adaptation in a rat model, Surg Endosc, 30, 4416, 10.1007/s00464-016-4760-x

Bry, 1996, A model of host-microbial interactions in an open mammalian ecosystem, Science, 273, 1380, 10.1126/science.273.5280.1380

Comstock, 2006, Bacterial glycans: key mediators of diverse host immune responses, Cell, 126, 847, 10.1016/j.cell.2006.08.021

Zheng, 2011, The footprints of gut microbial-mammalian co-metabolism, J Proteome Res, 10, 5512, 10.1021/pr2007945

Koruda, 1986, Harry M. Vars award. The effect of a pectin-supplemented elemental diet on intestinal adaptation to massive small bowel resection, JPEN J Parenter Enteral Nutr, 10, 343, 10.1177/0148607186010004343

Tappenden, 1997, Short-chain fatty acid-supplemented total parenteral nutrition enhances functional adaptation to intestinal resection in rats, Gastroenterology, 112, 792, 10.1053/gast.1997.v112.pm9041241

Koruda, 1988, Effect of parenteral nutrition supplemented with short-chain fatty acids on adaptation to massive small bowel resection, Gastroenterology, 95, 715, 10.1016/S0016-5085(88)80019-2

Tappenden, 1998, Short-chain fatty acid-supplemented total parenteral nutrition alters intestinal structure, glucose transporter 2 (GLUT2) mRNA and protein, and proglucagon mRNA abundance in normal rats, Am J Clin Nutr, 68, 118, 10.1093/ajcn/68.1.118

Tappenden, 2010, Emerging therapies for intestinal failure, Arch Surg, 145, 528, 10.1001/archsurg.2010.102

Bartholome, 2004, Supplementation of total parenteral nutrition with butyrate acutely increases structural aspects of intestinal adaptation after an 80% jejunoileal resection in neonatal piglets, JPEN J Parenter Enteral Nutr, 28, 210, 10.1177/0148607104028004210

Gosselin, 2014, Enteral nutrition in the management of pediatric intestinal failure, J Pediatr, 165, 1085, 10.1016/j.jpeds.2014.08.012

Atia, 2011, JPEN J Parenter Enteral Nutr, 35, 229, 10.1177/0148607110378410

Vieira, 2012, Oral administration of sodium butyrate attenuates inflammation and mucosal lesion in experimental acute ulcerative colitis, J Nutr Biochem, 23, 430, 10.1016/j.jnutbio.2011.01.007

Butzner, 1996, Butyrate enema therapy stimulates mucosal repair in experimental colitis in the rat, Gut, 38, 568, 10.1136/gut.38.4.568

Singh, 2014, Activation of Gpr109a, receptor for niacin and the commensal metabolite butyrate, suppresses colonic inflammation and carcinogenesis, Immunity, 40, 128, 10.1016/j.immuni.2013.12.007

Chang, 2014, The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition, Proc Natl Acad Sci U S A, 111, 2247, 10.1073/pnas.1322269111

Cao, 2017, Dysbiosis contributes to chronic constipation development via regulation of serotonin transporter in the intestine, Sci Rep, 7, 10322, 10.1038/s41598-017-10835-8

Reigstad, 2015, Gut microbes promote colonic serotonin production through an effect of short-chain fatty acids on enterochromaffin cells, FASEB J, 29, 1395, 10.1096/fj.14-259598

Yano, 2015, Indigenous bacteria from the gut microbiota regulate host serotonin biosynthesis, Cell, 161, 264, 10.1016/j.cell.2015.02.047

Soret, 2010, Short-chain fatty acids regulate the enteric neurons and control gastrointestinal motility in rats, Gastroenterology, 138, 1772, 10.1053/j.gastro.2010.01.053

Atarashi, 2008, ATP drives lamina propria T(H)17 cell differentiation, Nature, 455, 808, 10.1038/nature07240

Beulens, 2013, The role of menaquinones (vitamin K2) in human health, Br J Nutr, 110, 1357, 10.1017/S0007114513001013

Cella, 2015, Aryl hydrocarbon receptor: Linking environment to immunity, Semin Immunol, 27, 310, 10.1016/j.smim.2015.10.002

Pols, 2011, The bile acid membrane receptor TGR5 as an emerging target in metabolism and inflammation, J Hepatol, 54, 1263, 10.1016/j.jhep.2010.12.004

Alemi, 2013, The receptor TGR5 mediates the prokinetic actions of intestinal bile acids and is required for normal defecation in mice, Gastroenterology, 144, 145, 10.1053/j.gastro.2012.09.055

Thông tin
Thông tin xuất bản

Cellular and Molecular Gastroenterology and Hepatology

Tập 6

149-162

Thông tin tác giả