Literature DB >> 11844648

Provision of phosphorylatable substrate during hypoxia decreases jejunal barrier function.

Kelly A Tappenden1.   

Abstract

OBJECTIVES: There is an emerging consensus that early enteral nutrition benefits the high-risk surgical patient. However, in patients with inadequate gastrointestinal perfusion, food in the intestine may increase the oxygen demand beyond that which can be satisfied by the available delivery, potentially leading to intestinal malfunction. The effect of metabolic substrate on gastrointestinal function during various oxygenation states was investigated.
METHODS: Jejunal samples obtained from 32 male Sprague-Dawley rats (263 +/- Q15 g) were stripped of the muscularis, mounted in modified Ussing chambers, and randomized to be incubated in media equilibrated with one of four gas mixtures (95%, 75%, 50%, and 25% oxygen). After equilibration, fluorescent probes (4400 and 17 200 molecular weight [MW]) were added to the incubation media on the mucosal side. The rate of probe accumulation on the serosal side was determined before and after the addition of one of four substrates to the mucosal medium: mannitol (an osmotic control), glucose (which is transported, phosphorylated, and metabolized), 2-deoxyglucose (a glucose analog that is transported and phosphorylated but not metabolized), or 3-O-methylglucose (a glucose analog that is transported but not phosphorylated or metabolized).
RESULTS: Lumenal glucose, 2-deoxyglucose, and 3-O-methylglucose increased permeation of the 4400-MW probe at all oxygen levels, whereas mannitol did not alter permeation in the 95% and 75% oxygen groups. Lumenal glucose increased (P < 0.05) the permeation rate of the 17 200-MW probe at all oxygen levels, whereas 2-deoxyglucose and 3-O-methylglucose did not increase the permeation rate of the 17 200-MW probe until oxygen was lowered to 75% and 50%, respectively. Regardless of substrate treatment, jejunal permeation of the 4400-MW (P < 0.001) and 17 200-MW (P < 0.05) probes increased in the 25% and 50% oxygen groups compared with the 75% and 95% oxygen groups.
CONCLUSIONS: These initial results suggest that the provision of lumenal nutrients exacerbates the loss of gastrointestinal barrier function during hypoxia. Although the early provision of nutrients is an important intervention in acutely injured patients, care must be taken to ensure that gastrointestinal perfusion is adequate to allow substrate metabolism and prevent further compromise in gastrointestinal function.

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Year:  2002        PMID: 11844648     DOI: 10.1016/s0899-9007(01)00720-1

Source DB:  PubMed          Journal:  Nutrition        ISSN: 0899-9007            Impact factor:   4.008


  4 in total

Review 1.  Current Knowledge of Necrotizing Enterocolitis in Preterm Infants and the Impact of Different Types of Enteral Nutrition Products.

Authors:  Jocelyn Shulhan; Bryan Dicken; Lisa Hartling; Bodil Mk Larsen
Journal:  Adv Nutr       Date:  2017-01-17       Impact factor: 8.701

2.  The effect of hypoxia on permeability and bacterial translocation in Caco-2 adult and I-407 fetal enterocyte cell culture models.

Authors:  Y Tazuke; R A Drongowski; D H Teitelbaum; A G Coran
Journal:  Pediatr Surg Int       Date:  2003-05-06       Impact factor: 1.827

3.  Post-pyloric enteral nutrition in septic patients: effects on hepato-splanchnic hemodynamics and energy status.

Authors:  Richard Rokyta; Martin Matejovic; Ales Krouzecky; Vaclav Senft; Ladislav Trefil; Ivan Novak
Journal:  Intensive Care Med       Date:  2004-02-06       Impact factor: 17.440

4.  Modulation of HSP27 alters hypoxia-induced endothelial permeability and related signaling pathways.

Authors:  Tiegang Liu; Oscar E Guevara; Rod R Warburton; Nicholas S Hill; Matthias Gaestel; Usamah S Kayyali
Journal:  J Cell Physiol       Date:  2009-09       Impact factor: 6.384

  4 in total

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