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Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()

Piglets infected with transmissible gastroenteritis virus, compared to matched-fed littermates, had massive diarrhea characterized by increased quantities and concentrations of sodium, potassium, and chloride. Determinations of Na-K-ATPase in mucosal homogenates from small and large intestine reveal...

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Detalles Bibliográficos
Autores principales: Kelly, M., Butler, D.G., Hamilton, J.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Mosby, Inc. 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131288/
https://www.ncbi.nlm.nih.gov/pubmed/4260289
http://dx.doi.org/10.1016/S0022-3476(72)80003-9
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author Kelly, M.
Butler, D.G.
Hamilton, J.R.
author_facet Kelly, M.
Butler, D.G.
Hamilton, J.R.
author_sort Kelly, M.
collection PubMed
description Piglets infected with transmissible gastroenteritis virus, compared to matched-fed littermates, had massive diarrhea characterized by increased quantities and concentrations of sodium, potassium, and chloride. Determinations of Na-K-ATPase in mucosal homogenates from small and large intestine revealed decreased activity of this enzyme in the upper small bowel. Our data indicate that a defect in active sodium transport in this region may be an important factor in the pathogenesis of the diarrhea. Further studies using this model should help to define the mechanisms producing diarrhea in acute infantile gastroenteritis.
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spelling pubmed-71312882020-04-08 Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea() Kelly, M. Butler, D.G. Hamilton, J.R. J Pediatr Article Piglets infected with transmissible gastroenteritis virus, compared to matched-fed littermates, had massive diarrhea characterized by increased quantities and concentrations of sodium, potassium, and chloride. Determinations of Na-K-ATPase in mucosal homogenates from small and large intestine revealed decreased activity of this enzyme in the upper small bowel. Our data indicate that a defect in active sodium transport in this region may be an important factor in the pathogenesis of the diarrhea. Further studies using this model should help to define the mechanisms producing diarrhea in acute infantile gastroenteritis. Published by Mosby, Inc. 1972-06 2006-03-14 /pmc/articles/PMC7131288/ /pubmed/4260289 http://dx.doi.org/10.1016/S0022-3476(72)80003-9 Text en Copyright © 1972 Published by Mosby, Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kelly, M.
Butler, D.G.
Hamilton, J.R.
Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()
title Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()
title_full Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()
title_fullStr Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()
title_full_unstemmed Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()
title_short Transmissible gastroenteritis in piglets:A model of infantile viral diarrhea()
title_sort transmissible gastroenteritis in piglets:a model of infantile viral diarrhea()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131288/
https://www.ncbi.nlm.nih.gov/pubmed/4260289
http://dx.doi.org/10.1016/S0022-3476(72)80003-9
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