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Endogenous corticosteroids modulate Clostridium difficile toxin A-induced enteritis in rats.
Castagliuolo, I; Karalis, K; Valenick, L; Pasha, A; Nikulasson, S; Wlk, M; Pothoulakis, C.
Afiliación
  • Castagliuolo I; Division of Gastroenterology, Beth Israel Deaconess Medical Center, Massachusetts, Boston 02215, USA.
Am J Physiol Gastrointest Liver Physiol ; 280(4): G539-45, 2001 Apr.
Article en En | MEDLINE | ID: mdl-11254479
We examined the role of glucocorticoids in acute inflammatory diarrhea mediated by Clostridium difficile toxin A. Toxin A (5 microg) or buffer was injected in rat ileal loops, and intestinal responses were measured after 30 min to 4 h. Ileal toxin A administration increased plasma glucocorticoids after 1 h, at which time the toxin-stimulated secretion was not significant. Administration of the glucocorticoid analog dexamethasone inhibited toxin A-induced intestinal secretion and inflammation and downregulated toxin A-mediated increase of macrophage inflammatory protein-2. Adrenalectomy followed by replacement with glucocorticoids at various doses suggested that intestinal responses to toxin A were related to circulating levels of glucocorticoids. Administration of the glucocorticoid receptor antagonist RU-486 enhanced toxin A-mediated intestinal secretion and inflammation. We conclude that C. difficile toxin A causes increased secretion of endogenous glucocorticoids, which diminish the intestinal secretory and inflammatory effects of toxin A.
Asunto(s)
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Bases de datos: MEDLINE Asunto principal: Toxinas Bacterianas / Enteritis / Enterotoxinas / Glucocorticoides Límite: Animals Idioma: En Revista: Am J Physiol Gastrointest Liver Physiol Asunto de la revista: FISIOLOGIA / GASTROENTEROLOGIA Año: 2001 Tipo del documento: Article País de afiliación: Estados Unidos
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Bases de datos: MEDLINE Asunto principal: Toxinas Bacterianas / Enteritis / Enterotoxinas / Glucocorticoides Límite: Animals Idioma: En Revista: Am J Physiol Gastrointest Liver Physiol Asunto de la revista: FISIOLOGIA / GASTROENTEROLOGIA Año: 2001 Tipo del documento: Article País de afiliación: Estados Unidos