Literature DB >> 3129330

Effect of immunologic reactions on rat intestinal epithelium. Correlation of increased permeability to chromium 51-labeled ethylenediaminetetraacetic acid and ovalbumin during acute inflammation and anaphylaxis.

J K Ramage1, A Stanisz, R Scicchitano, R H Hunt, M H Perdue.   

Abstract

In these studies we compared jejunal permeability to two probes--chromium 51-labeled ethylenediaminetetraacetic acid (51Cr-EDTA) (mol wt, 360) and ovalbumin (mol wt, 45,000)--under control conditions, during acute intestinal inflammation, and in response to systemic anaphylaxis. Acute inflammation was produced after infection with Nippostrongylus brasiliensis and rats were studied at day 0 (control), day 4 (early), day 10 (acute), and day 35 (postinfection). At the latter stage, immune rats were also studied during anaphylaxis induced by i.v. N. brasiliensis antigen. In each study, blood and urine were sampled over 5 h after the probes were simultaneously injected into ligated loops in anesthetized rats. In controls, small quantities (less than 0.04% and 0.002% of the administered dose for 51Cr-EDTA and ovalbumin, respectively) appeared in the circulation and plateaued at 1 h. During acute inflammation, the appearance of both probes continued to increase with time. Compared with controls, 5-h values for 51Cr-EDTA and ovalbumin were (a) significantly elevated at day 4 (p less than 0.005), (b) increased approximately 20-fold at day 10 (p less than 0.005 and less than 0.01, respectively), and (c) normal at day 35. Urinary recovery of 51Cr-EDTA followed the same pattern. During anaphylaxis, appearance of the probes in the circulation increased at 1 h to values approximately 10-fold those in controls (p less than 0.001 and less than 0.01, for 51Cr-EDTA and ovalbumin, respectively), and then declined. Urinary recovery of 51Cr-EDTA over 5 h was also significantly increased. We conclude that epithelial barrier function becomes impaired during both acute inflammation and anaphylaxis. In this rat model, gut permeability changes to 51Cr-EDTA reflect gut permeability changes to macromolecular antigens. If similar conditions exist in humans, urinary recovery of 51Cr-EDTA may be useful in monitoring intestinal abnormalities associated with inflammation.

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Year:  1988        PMID: 3129330

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  19 in total

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Authors:  E J Hall; R M Batt
Journal:  Gut       Date:  1991-07       Impact factor: 23.059

2.  Role of T lymphocytes in intestinal mucosal injury. Inflammatory changes in athymic nude rats.

Authors:  R D'Inca; P Ernst; R H Hunt; M H Perdue
Journal:  Dig Dis Sci       Date:  1992-01       Impact factor: 3.199

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Journal:  Gut       Date:  1999-02       Impact factor: 23.059

Review 4.  Helminths and intestinal barrier function.

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Authors: 
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6.  Intestinal mucosal injury is associated with mast cell activation and leukotriene generation during Nippostrongylus-induced inflammation in the rat.

Authors:  M H Perdue; J K Ramage; D Burget; J Marshall; S Masson
Journal:  Dig Dis Sci       Date:  1989-05       Impact factor: 3.199

7.  Divalent hapten-induced intestinal anaphylaxis in the mouse: uptake and characterization of a bystander protein.

Authors:  R E Kleinman; P R Harmatz; R A Hatz; M Brown; P D Ariniello; W A Walker; K J Bloch
Journal:  Immunology       Date:  1989-12       Impact factor: 7.397

8.  Interferon-gamma expression by intraepithelial lymphocytes results in a loss of epithelial barrier function in a mouse model of total parenteral nutrition.

Authors:  Hua Yang; Irfan Kiristioglu; Yongyi Fan; Benjamin Forbush; D Keith Bishop; Paul A Antony; Hong Zhou; Daniel H Teitelbaum
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9.  Animal model of gluten induced enteropathy in mice.

Authors:  R Troncone; A Ferguson
Journal:  Gut       Date:  1991-08       Impact factor: 23.059

10.  Alterations in regional blood flow in rats following sensitization to the nematode Nippostrongylus brasiliensis: effects of PAF antagonists.

Authors:  R Mathison; C Rimmer; J S Davison; J L Wallace; A D Befus
Journal:  Br J Pharmacol       Date:  1990-09       Impact factor: 8.739

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