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Regulation of oxidative stress in the intestine of piglets after enterotoxigenic Escherichia coli (ETEC) infection.
Jin, Shunshun; Xu, Haoxiang; Yang, Chengbo; O, Karmin.
Afiliación
  • Jin S; Department of Animal Science, University of Manitoba, Canada; St. Boniface Hospital Research Centre, Canada.
  • Xu H; Department of Animal Science, University of Manitoba, Canada.
  • Yang C; Department of Animal Science, University of Manitoba, Canada.
  • O K; Department of Animal Science, University of Manitoba, Canada; St. Boniface Hospital Research Centre, Canada; Department of Physiology and Pathophysiology, University of Manitoba, Canada. Electronic address: karmino@sbrc.ca.
Biochim Biophys Acta Mol Cell Res ; 1871(5): 119711, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38574824
ABSTRACT
Enterotoxigenic Escherichia coli (ETEC) is recognized globally as a major gastrointestinal pathogen that impairs intestinal function. ETEC infection can lead to oxidative stress and disruption of intestinal integrity. The present study investigated the mechanism of increased oxidative stress and whether restoration of antioxidant defense could improve intestinal integrity in a piglet model with ETEC infection. Weaned piglets were divided into three groups control, ETEC-infection and ETEC-infection with antibiotic supplementation. The infection caused a significant elevation of serum diamine oxidase activity and D-lactate levels coupled with a reduced intestinal (mid-jejunum) tight-junction protein expression, suggesting increased intestinal permeability and impaired gut function. The infection also inhibited nuclear factor erythroid 2-related factor 2 (Nrf2) activation, decreased the expression of glutathione synthesizing enzymes, superoxide dismutase-1 (SOD1), and heme oxygenase-1 (HO-1) in the intestine. This led to a decreased antioxidant glutathione level and an increased lipid peroxidation in the intestine and serum, indicating oxidative stress. The infection stimulated the expression of pro-inflammatory cytokines (IL-6, TNF-α). Antibiotic supplementation attenuated oxidative stress, in part, through restoration of glutathione levels and antioxidant enzyme expression in the intestine. Such a treatment enhanced tight-junction protein expression and improved intestinal function. Furthermore, induction of oxidative stress in Caco2 cells by hydrogen peroxide inhibited tight-junction protein expression and stimulated inflammatory cytokine expression. Glutathione supplementation effectively attenuated oxidative stress and restored tight-junction protein expression. These results suggest that downregulation of Nrf2 activation may weaken antioxidant defense and increase oxidative stress in the intestine. Mitigation of oxidative stress can improve intestinal function after infection.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estrés Oxidativo / Infecciones por Escherichia coli / Escherichia coli Enterotoxigénica / Mucosa Intestinal Límite: Animals / Humans Idioma: En Revista: Biochim Biophys Acta Mol Cell Res Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estrés Oxidativo / Infecciones por Escherichia coli / Escherichia coli Enterotoxigénica / Mucosa Intestinal Límite: Animals / Humans Idioma: En Revista: Biochim Biophys Acta Mol Cell Res Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Países Bajos