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Angiotensin II subtype 1 receptor blockade inhibits Clostridium difficile toxin A-induced intestinal secretion in a rabbit model.
Alcantara, Cirle S; Jin, Xiao-Hong; Brito, Gerly Anne C; Carneiro-Filho, Benedito A; Barrett, Leah J; Carey, Robert M; Guerrant, Richard L.
Afiliação
  • Alcantara CS; Center for Global Health, Division of Infectious Disease and International Health, University of Virginia, Charlottesville, Virginia 22903, USA.
J Infect Dis ; 191(12): 2090-6, 2005 Jun 15.
Article em En | MEDLINE | ID: mdl-15897995
ABSTRACT
Angiotensin II (ANG II) has been described in the regulation of intestinal secretion and absorption via angiotensin subtype 1 (AT(1)) and AT(2) receptors, respectively, in rats. We investigated the role that ANG II plays in the rabbit ileal-loop model of Clostridium difficile infection. Expression of AT(1), the more abundant ANG II receptor, was demonstrated in ileal loops, and an AT(1) receptor blocker, losartan, inhibited hypersecretion induced by C. difficile toxin A (mean volume length ratio, 0.27+/-0.06 vs. 0.60+/-0.06 mL/cm in controls). Losartan also decreased production of ANG II in the ileum (0.48+/-0.06 vs. 0.87+/-0.12 pg/mg in controls), raising the possibility that ANG II may participate in a positive feedback loop involving the hypersecretory response. Our findings suggest that ANG II plays a significant role in the pathogenesis of C. difficile toxin-induced diarrhea.
Assuntos
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Base de dados: MEDLINE Assunto principal: Toxinas Bacterianas / Losartan / Bloqueadores do Receptor Tipo 1 de Angiotensina II / Enterotoxinas / Mucosa Intestinal Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Infect Dis Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Base de dados: MEDLINE Assunto principal: Toxinas Bacterianas / Losartan / Bloqueadores do Receptor Tipo 1 de Angiotensina II / Enterotoxinas / Mucosa Intestinal Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Infect Dis Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Estados Unidos