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      Homeostasis alteration within small intestinal mucosa after acute enteral refeeding in total parenteral nutrition mouse model

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          Abstract

          Feeding strategies to care for patients who transition from enteral nutrient deprivation while on total parenteral nutrition (TPN) to enteral feedings generally proceed to full enteral nutrition once the gastrointestinal tract recovers; however, an increasing body of literature suggests that a subgroup of patients may actually develop an increased incidence of adverse events, including death. To examine this further, we studied the effects of acute refeeding in a mouse model of TPN. Interestingly, refeeding led to some beneficial effects, including prevention in the decline in intestinal epithelial cell (IEC) proliferation. However, refeeding led to a significant increase in mucosal expression of proinflammatory cytokines, including tumor necrosis factor-α (TNF-α), as well as an upregulation in Toll-like receptor 4 (TLR-4). Refeeding also failed to prevent TPN-associated increases in IEC apoptosis, loss of epithelial barrier function, and failure of the leucine-rich repeat-containing G protein-coupled receptor 5-positive stem cell expression. Transitioning from TPN to enteral feedings led to a partial restoration of the small bowel microbial population. In conclusion, while acute refeeding led to some restoration of normal gastrointestinal physiology, enteral refeeding led to a significant increase in mucosal inflammatory markers and may suggest alternative strategies to enteral refeeding should be considered.

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          Author and article information

          Journal
          Am J Physiol Gastrointest Liver Physiol
          Am. J. Physiol. Gastrointest. Liver Physiol
          ajpgi
          ajpgi
          AJPGI
          American Journal of Physiology - Gastrointestinal and Liver Physiology
          American Physiological Society (Bethesda, MD )
          0193-1857
          1522-1547
          3 December 2015
          15 February 2016
          15 February 2017
          : 310
          : 4
          : G273-G284
          Affiliations
          [1] 1Section of Pediatric Surgery, Department of Surgery, the University of Michigan Medical School and the C. S. Mott Children's Hospital, Ann Arbor, Michigan;
          [2] 2General Surgery, Department of Surgery, the University of Michigan Medical School, Ann Arbor, Michigan;
          [3] 3University of Michigan, Ann Arbor, Michigan; and
          [4] 4Department of Pediatric Surgery, Juntendo Hospital, Juntendo University, Tokyo, Japan
          Author notes
          [*]

          Y. Feng and D. H. Teitelbaum contributed equally to this work.

          Address for reprint requests and other correspondence: D. H. Teitelbaum, Section of Pediatric Surgery, Univ. of Michigan, Mott Children's Hospital F3970, Ann Arbor, MI, USA 48109-5245 (e-mail: dttlbm@ 123456umich.edu ).
          Article
          PMC4754738 PMC4754738 4754738 GI-00335-2015
          10.1152/ajpgi.00335.2015
          4754738
          26635320
          a4d1de0f-9527-4787-9526-f3c09643bd34
          Copyright © 2016 the American Physiological Society
          History
          : 21 September 2015
          : 24 November 2015
          Funding
          Funded by: 100000060 HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
          Award ID: RO1-AI44076
          Categories
          Nutrient Sensing, Nutrition, and Metabolism

          tumor necrosis factor-α,intestinal epithelial cell proliferation,enteral nutrition

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