P-glycoprotein expression in lamina propria lymphocytes of duodenal biopsy samples in dogs with chronic idiopathic enteropathies

被引:26
作者
Ahenspach, K [1 ]
Bergman, PJ
Sauter, S
Gröne, A
Doherr, MG
Gaschen, F
机构
[1] Univ Bern, Dept Clin Vet Med, Bern, Switzerland
[2] Univ Bern, Inst Anim Genet Nutr & Housing, Bern, Switzerland
[3] Univ Bern, Inst Anim Pathol, Vetsuisse Fac, Bern, Switzerland
[4] Anim Med Ctr, Donaldson Alwood Canc Clin, New York, NY USA
[5] Anim Med Ctr, Flaherty Comparat Oncol Lab, New York, NY USA
关键词
chronic enteropathies; corticosteroids; dog; p-glycoprotein;
D O I
10.1016/j.jcpa.2005.06.003
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
P-glycoprotein (p-gp) is a transmembrane protein functioning as a drug-efflux pump in the intestinal epithelium. Human patients with inflammatory bowel disease (IBD) who fail to respond to treatment with steroids express high levels of p-gp in lamina propria lymphocytes. The purpose of this study was to investigate p-gp expression in duodenal biopsy samples of dogs with chronic enteropathies and to evaluate the expression of p-gp after treatment with a known inducer of p-gp (prednisolone). Duodenal biopsy samples from 48 dogs were evaluated inummohistochemically with the mouse monoclonal antibody C219 for expression of p-gp in lamina propria lymphocytes. Biopsy samples were available from 15 dogs after treatment with prednisolone and 16 dogs after dietary therapy alone ("elimination diet"). Treatment with prednisolone resulted in an increase in p-gp expression (P=0.005). In contrast, dietary treatment alone produced no significant change in p-gp expression (P=0.59). A low p-gp score before initiation of steroid treatment was significantly associated with a positive response to treatment (P=0.01). These results indicate that lamina propria lymphocyte expression of p-gp is upregulated after prednisolone treatment in dogs with IBD, and that mucosal expression of p-gp may be of volue in predicting the response to therapy. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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