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  4. Mucosal pathophysiology and inflammatory changes in the late phase of the intestinal allergic reaction in the rat
 
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Mucosal pathophysiology and inflammatory changes in the late phase of the intestinal allergic reaction in the rat

Journal
American Journal of Pathology
Journal Volume
158
Journal Issue
2
Pages
681-690
Date Issued
2001
Author(s)
Yang P.-C.
Berin M.C.
LINDA CHIA-HUI YU  
Perdue M.H.
DOI
10.1016/S0002-9440(10)64010-2
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035132174&doi=10.1016%2fS0002-9440%2810%2964010-2&partnerID=40&md5=4e014f15783b0e98ac982fb48aae610c
https://scholars.lib.ntu.edu.tw/handle/123456789/507319
Abstract
Relatively little information exists concerning the late phase of the allergic reaction in the gastrointestinal tract. Here, we characterized jejunal mucosal pathophysiology and inflammation after oral antigen challenge of sensitized rats, and examined the role of mast cells in events after challenge. Sprague-Dawley rats, mast cell-deficient (Ws/Ws), and +/+ control rats were sensitized to horseradish peroxidase, and challenged intragastrically with antigen 14 days later. Jejunal segments were obtained at 0.5 to 72 hours after challenge for functional assessment in Ussing chambers and for morphological assessment by light and electron microscopy. Intestine from sensitized Sprague-Dawley rats demonstrated enhanced ion secretion and permeability at all times after challenge. Electron microscopy revealed abnormal mitochondria within enterocytes and disruption of the epithelial basement membrane associated with influx into the mucosa of mast cells, eosinophils, neutrophils, and mononuclear cells. Many inflammatory cells appeared activated. In contrast, antigen-challenged Ws/Ws rats demonstrated no functional changes or inflammatory cell infiltrate. We conclude that oral antigen challenge of sensitized rats induces sustained epithelial dysfunction. Mast cells mediate both epithelial pathophysiology and recruitment of additional inflammatory cells that may contribute to persistent pathophysiology and symptoms.
SDGs

[SDGs]SDG3

Publisher
American Society for Investigative Pathology Inc.
Type
journal article

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