Literature DB >> 15640640

Exacerbation of intestinal permeability in rats after a two-hit injury: burn and Enterococcus faecalis infection.

Victoria A Samonte1, Masakatsu Goto, Thyyar M Ravindranath, Nadeem Fazal, Vallie M Holloway, Amit Goyal, Richard L Gamelli, Mohammed M Sayeed.   

Abstract

OBJECTIVE: To determine alterations in intestinal epithelial permeability to solutes in burn injured rats with and without Enterococcus faecalis infection and the role of neutrophils in the intestinal permeability changes.
DESIGN: Prospective sham-controlled animal study.
SETTING: University research laboratory.
SUBJECTS: Male Sprague-Dawley rats.
INTERVENTIONS: Rats were subjected to 30% total body surface burn (B group), E. faecalis infection (EF group) induced via intra-abdominal implantation of bacterial pellet, or combination of burn injury and E. faecalis infection (B+EF group).
MEASUREMENTS AND MAIN RESULTS: In vivo measurements of intestinal permeability were carried out after intraluminal injection of H lactulose and C mannitol in the ileum of sham, B, EF, and B+EF groups of rats, 1 and 2 days after injury. Lactulose permeability was increased in the injured rat groups (B, EF, B+EF) on day 1 postinjury compared with sham. The combined injury group (B+EF) had the highest level of lactulose permeability. Although a significant change in lactulose permeability from day 1 to day 2 postinjury could not be demonstrated in the B and EF groups, lactulose permeability in the B+EF group on day 2 postinjury markedly decreased from day 1 but was still significantly higher than that in the sham group. Mannitol permeability was increased in all injured rat groups on day 1 postinjury; on day 2 it remained elevated post-B, decreased post-EF, and further increased after B+EF. Ex vivo measurements of lactulose movements across intestinal epithelial monolayers (IEC-18) were carried out in the presence of blood neutrophils from sham, B, EF, or B+EF rats. We also measured ex vivo transepithelial migration of neutrophils from sham, B, EF, or B+EF rat groups. Neither the transepithelial lactulose movement in the presence of neutrophils from, nor neutrophil migration in, the B or EF rats was significantly different from sham. However, a significant increase in transepithelial lactulose movement and neutrophil migration occurred in the B+EF group. Immunoblot analyses and in situ histochemical localizations of intestinal tight junction proteins, occludin and claudin-3, showed decreases in the distribution of occludin but not claudin-3 in the B, EF, and B+EF groups.
CONCLUSIONS: Alterations in intestinal solute permeability and disruption of tight junction integrity after a two-hit injury with burn and E. faecalis infection, but not after individual injuries of burn or E. faecalis infection, are likely associated with heightened neutrophil flux across the intestinal epithelium.

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Year:  2004        PMID: 15640640     DOI: 10.1097/01.ccm.0000145579.66001.05

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  14 in total

1.  Disorders of the immune system in severely burned patients.

Authors:  A D Fayazov; S I Shukurov; B I Shukurov; B C Sultanov; A N Namazov; D A Ruzimuratov
Journal:  Ann Burns Fire Disasters       Date:  2009-09-30

2.  Early apoptosis of monocytes contributes to the pathogenesis of systemic inflammatory response and of bacterial translocation in an experimental model of multiple trauma.

Authors:  N Efstathopoulos; T Tsaganos; E J Giamarellos-Bourboulis; P Kaldis; V Nicolaou; A Papalois; P Koutoukas; G Papachristou; H Giamarellou
Journal:  Clin Exp Immunol       Date:  2006-07       Impact factor: 4.330

3.  Burn-induced gut barrier injury is attenuated by phosphodiesterase inhibition: effects on tight junction structural proteins.

Authors:  Todd W Costantini; William H Loomis; James G Putnam; Dana Drusinsky; Jessica Deree; Sunghyuk Choi; Paul Wolf; Andrew Baird; Brian Eliceiri; Vishal Bansal; Raul Coimbra
Journal:  Shock       Date:  2009-04       Impact factor: 3.454

4.  The Immune Response to Skin Trauma Is Dependent on the Etiology of Injury in a Mouse Model of Burn and Excision.

Authors:  Samantha M Valvis; Jason Waithman; Fiona M Wood; Mark W Fear; Vanessa S Fear
Journal:  J Invest Dermatol       Date:  2015-05-07       Impact factor: 8.551

Review 5.  Topical antimicrobials for burn wound infections.

Authors:  T Dai; Y Y Huang; S K Sharma; J T Hashmi; D B Kurup; M R Hamblin
Journal:  Recent Pat Antiinfect Drug Discov       Date:  2010-06

Review 6.  Leukocyte-epithelial interactions and mucosal homeostasis.

Authors:  Jason D Matthews; Caroline M Weight; Charles A Parkos
Journal:  Toxicol Pathol       Date:  2013-11-27       Impact factor: 1.902

Review 7.  The role of intestinal microbiota in the development and severity of chemotherapy-induced mucositis.

Authors:  Michel J van Vliet; Hermie J M Harmsen; Eveline S J M de Bont; Wim J E Tissing
Journal:  PLoS Pathog       Date:  2010-05-27       Impact factor: 6.823

8.  Anti-IL-6 antibody treatment but not IL-6 knockout improves intestinal barrier function and reduces inflammation after binge ethanol exposure and burn injury.

Authors:  Anita Zahs; Melanie D Bird; Luis Ramirez; Mashkoor A Choudhry; Elizabeth J Kovacs
Journal:  Shock       Date:  2013-04       Impact factor: 3.454

Review 9.  Aging and animal models of systemic insult: trauma, burn, and sepsis.

Authors:  Vanessa Nomellini; Christian R Gomez; Richard L Gamelli; Elizabeth J Kovacs
Journal:  Shock       Date:  2009-01       Impact factor: 3.454

10.  Severe sepsis facilitates intestinal colonization by extended-spectrum-β-lactamase-producing Klebsiella pneumoniae and transfer of the SHV-18 resistance gene to Escherichia coli during antimicrobial treatment.

Authors:  Jun Guan; Shaoze Liu; Zhaofen Lin; Wenfang Li; Xuefeng Liu; Dechang Chen
Journal:  Antimicrob Agents Chemother       Date:  2013-11-25       Impact factor: 5.191

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