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The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats

In rats with 2-week obstructive jaundice the sensitivity to endotoxin was studied and the effect of a single dose of endotoxin on histological development in the kidney, liver and spleen was also investigated. We were tested the effect on accumulation and distribution within organs, of fibrinogen la...

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Detalles Bibliográficos
Autor principal: Dawiskiba, Janusz
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423827/
https://www.ncbi.nlm.nih.gov/pubmed/9187546
http://dx.doi.org/10.1155/1996/85863
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author Dawiskiba, Janusz
author_facet Dawiskiba, Janusz
author_sort Dawiskiba, Janusz
collection PubMed
description In rats with 2-week obstructive jaundice the sensitivity to endotoxin was studied and the effect of a single dose of endotoxin on histological development in the kidney, liver and spleen was also investigated. We were tested the effect on accumulation and distribution within organs, of fibrinogen labelled with radioactive iodine 125. We showed an increased sensitivity to endotoxin in obstructive jaundice. The cause of death in most rats was acute circulatory failure during the course of endotoxic shock, without clinical features of disseminated intravascular coagulation. In the isotope study, after endotoxin administration there was a specific dynamic increase of fibrinogen accumulation in the kidneys of rats with obstructive jaundice. We proposed, that the cause of the kidney changes during the course of obstructive jaundice could be the local activation of intrarenal coagulation.
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spelling pubmed-24238272008-07-08 The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats Dawiskiba, Janusz HPB Surg Research Article In rats with 2-week obstructive jaundice the sensitivity to endotoxin was studied and the effect of a single dose of endotoxin on histological development in the kidney, liver and spleen was also investigated. We were tested the effect on accumulation and distribution within organs, of fibrinogen labelled with radioactive iodine 125. We showed an increased sensitivity to endotoxin in obstructive jaundice. The cause of death in most rats was acute circulatory failure during the course of endotoxic shock, without clinical features of disseminated intravascular coagulation. In the isotope study, after endotoxin administration there was a specific dynamic increase of fibrinogen accumulation in the kidneys of rats with obstructive jaundice. We proposed, that the cause of the kidney changes during the course of obstructive jaundice could be the local activation of intrarenal coagulation. Hindawi Publishing Corporation 1996 /pmc/articles/PMC2423827/ /pubmed/9187546 http://dx.doi.org/10.1155/1996/85863 Text en Copyright © 1996 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dawiskiba, Janusz
The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats
title The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats
title_full The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats
title_fullStr The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats
title_full_unstemmed The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats
title_short The Role of Endotoxaemia in the development of Renal Disorders Experimental Obstructive Jaundice in Rats
title_sort role of endotoxaemia in the development of renal disorders experimental obstructive jaundice in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423827/
https://www.ncbi.nlm.nih.gov/pubmed/9187546
http://dx.doi.org/10.1155/1996/85863
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