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Muramyl peptides confer hepatoprotection against murine viral hepatitis

The hepatoprotection induced by synthetic muramyl peptides was investigated using a model of lethal murine mouse hepatitis MHV-3 virus infection. MDP and a nonpyrogenic analog, Murametide, inhibited the steep elevation of serum transaminases induced by MHV-3 irrespective of whether the immunomodulat...

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Detalles Bibliográficos
Autores principales: Masihi, K.Noel, Kröger, Hans, Lange, Werner, Chedid, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173131/
https://www.ncbi.nlm.nih.gov/pubmed/2559041
http://dx.doi.org/10.1016/0192-0561(89)90109-4
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author Masihi, K.Noel
Kröger, Hans
Lange, Werner
Chedid, Louis
author_facet Masihi, K.Noel
Kröger, Hans
Lange, Werner
Chedid, Louis
author_sort Masihi, K.Noel
collection PubMed
description The hepatoprotection induced by synthetic muramyl peptides was investigated using a model of lethal murine mouse hepatitis MHV-3 virus infection. MDP and a nonpyrogenic analog, Murametide, inhibited the steep elevation of serum transaminases induced by MHV-3 irrespective of whether the immunomodulators were administered before or after the infection. A significant proportion of MDP or Murametide-treated animals, in contrast to controls, survived the MHV-3 infection. The histopathological examination of the liver revealed marked necrosis of the hepatic parenchymal cells and infiltration of the inflammatory cells in controls but not in MDP-treated animals.
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spelling pubmed-71731312020-04-22 Muramyl peptides confer hepatoprotection against murine viral hepatitis Masihi, K.Noel Kröger, Hans Lange, Werner Chedid, Louis Int J Immunopharmacol Article The hepatoprotection induced by synthetic muramyl peptides was investigated using a model of lethal murine mouse hepatitis MHV-3 virus infection. MDP and a nonpyrogenic analog, Murametide, inhibited the steep elevation of serum transaminases induced by MHV-3 irrespective of whether the immunomodulators were administered before or after the infection. A significant proportion of MDP or Murametide-treated animals, in contrast to controls, survived the MHV-3 infection. The histopathological examination of the liver revealed marked necrosis of the hepatic parenchymal cells and infiltration of the inflammatory cells in controls but not in MDP-treated animals. Published by Elsevier Ltd. 1989 2006-03-15 /pmc/articles/PMC7173131/ /pubmed/2559041 http://dx.doi.org/10.1016/0192-0561(89)90109-4 Text en Copyright © 1989 Published by Elsevier Ltd. 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
Masihi, K.Noel
Kröger, Hans
Lange, Werner
Chedid, Louis
Muramyl peptides confer hepatoprotection against murine viral hepatitis
title Muramyl peptides confer hepatoprotection against murine viral hepatitis
title_full Muramyl peptides confer hepatoprotection against murine viral hepatitis
title_fullStr Muramyl peptides confer hepatoprotection against murine viral hepatitis
title_full_unstemmed Muramyl peptides confer hepatoprotection against murine viral hepatitis
title_short Muramyl peptides confer hepatoprotection against murine viral hepatitis
title_sort muramyl peptides confer hepatoprotection against murine viral hepatitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173131/
https://www.ncbi.nlm.nih.gov/pubmed/2559041
http://dx.doi.org/10.1016/0192-0561(89)90109-4
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