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Modulation of Intestinal Microbiome Prevents Intestinal Ischemic Injury.
Bertacco, Alessandra; Dehner, Carina A; Caturegli, Giorgio; D'Amico, Francesco; Morotti, Raffaella; Rodriguez, Manuel I; Mulligan, David C; Kriegel, Martin A; Geibel, John P.
Afiliação
  • Bertacco A; Department of Surgery, Yale School of Medicine, Yale University, New Haven, CT, United States.
  • Dehner CA; Hepatobiliary and Liver Transplant Unit, Università di Padova, Padova, Italy.
  • Caturegli G; Department of Surgery, Yale School of Medicine, Yale University, New Haven, CT, United States.
  • D'Amico F; Department of Immunology, Yale School of Medicine, Yale University, New Haven, CT, United States.
  • Morotti R; Department of Surgery, Yale School of Medicine, Yale University, New Haven, CT, United States.
  • Rodriguez MI; Department of Surgery, Yale School of Medicine, Yale University, New Haven, CT, United States.
  • Mulligan DC; Hepatobiliary and Liver Transplant Unit, Università di Padova, Padova, Italy.
  • Kriegel MA; Department of Pathology, Yale School of Medicine, Yale University, New Haven, CT, United States.
  • Geibel JP; Department of Surgery, Yale School of Medicine, Yale University, New Haven, CT, United States.
Front Physiol ; 8: 1064, 2017.
Article em En | MEDLINE | ID: mdl-29311987
ABSTRACT

Background:

Butyrate protects against ischemic injury to the small intestine by reducing inflammation and maintaining the structure of the intestinal barrier, but is expensive, short-lived, and cannot be administered easily due to its odor. Lactate, both economical and more palatable, can be converted into butyrate by the intestinal microbiome. This study aimed to assess in a rat model whether lactate perfusion can also protect against intestinal ischemia. Materials and

Methods:

Rat intestinal segments were loaded in an in vitro bowel perfusion device, and water absorption or secretion was assessed based on fluorescence of FITC-inulin, a fluorescent marker bound to a biologically inert sugar. Change in FITC concentration was used as a measure of ischemic injury, given the tendency of ischemic cells to retain water. Hematoxylin and eosin-stained sections at light level microscopy were examined to evaluate intestinal epithelium morphology. Comparisons between the data sets were paired Student t-tests or ANOVA with p < 0.05 performed on GraphPad.

Results:

Lactate administration resulted in a protective effect against intestinal ischemia of similar magnitude to that observed with butyrate. Both exhibited approximately 1.5 times the secretion exhibited by control sections (p = 0.03). Perfusion with lactate and methoxyacetate, a specific inhibitor of lactate-butyrate conversion, abolished this effect (p = 0.09). Antibiotic treatment also eliminated this effect, rendering lactate-perfused sections similar to control sections (p = 0.72). Perfusion with butyrate and methoxyacetate did not eliminate the observed increased secretion, which indicates that ischemic protection was mediated by microbial conversion of lactate to butyrate (p = 0.71).

Conclusions:

Lactate's protective effect against intestinal ischemia due to microbial conversion to butyrate suggests possible applications in the transplant setting for reducing ischemic injury and ameliorating intestinal preservation during transport.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Physiol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Physiol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos