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The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats

The wound healing process and production of tumour necrosis factor alpha (TNF-α) by peritoneal cells of 7-day and 14-day obstructive jaundice (OJ) and sham-operated rats were investigated. In the study the skin wound breaking strength was measured, In addition such histological and biochemical param...

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Autores principales: Dawiskiba, Janusz, Kwiatkowska, Danuta, Zimecki, Michał, Kornafel, Pawel, Tyran, Wanda, Czapiiska, Elżbieta, Woźniak, Zdzisław
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423987/
https://www.ncbi.nlm.nih.gov/pubmed/10674746
http://dx.doi.org/10.1155/2000/82905
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author Dawiskiba, Janusz
Kwiatkowska, Danuta
Zimecki, Michał
Kornafel, Pawel
Tyran, Wanda
Czapiiska, Elżbieta
Woźniak, Zdzisław
author_facet Dawiskiba, Janusz
Kwiatkowska, Danuta
Zimecki, Michał
Kornafel, Pawel
Tyran, Wanda
Czapiiska, Elżbieta
Woźniak, Zdzisław
author_sort Dawiskiba, Janusz
collection PubMed
description The wound healing process and production of tumour necrosis factor alpha (TNF-α) by peritoneal cells of 7-day and 14-day obstructive jaundice (OJ) and sham-operated rats were investigated. In the study the skin wound breaking strength was measured, In addition such histological and biochemical parameters as fibroblast and endothelial cell proliferation, inflammatory cell infiltration and hydroxyproline content were evaluated in polyurethane sponge discs implanted subcutaneously into rats. TNF-α production by peritoneal exudate cells (PEC), both spontaneous and lipopolysaccharide (LPS)- induced was determined by a bioassay. In OJ rats the process of both early as well as late phase of healing was impaired. The breaking strength of skin wound was decreased, the fibroblast and endothelial cell proliferation and collagen deposition, as well as hydroxyproline content were diminished. In 7 day OJ the numbers of inflammatory cells in the implants were lowered with a subsequent slight increase on day 14 of OJ. The spontaneous and LPS induced TNF- α production by PEC were significantly higher in 7 day OJ as compared with sham-operated controls. On day 14 of OJ the LPS-induced TNF-α level was, in contrast, much lower and did not differ much from the spontaneous TNF-α production. We conclude that the impairment of wound healing in OJ results from disturbances in functioning of the immune system caused by systemic endotoxaemia.
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spelling pubmed-24239872008-07-08 The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats Dawiskiba, Janusz Kwiatkowska, Danuta Zimecki, Michał Kornafel, Pawel Tyran, Wanda Czapiiska, Elżbieta Woźniak, Zdzisław HPB Surg Research Article The wound healing process and production of tumour necrosis factor alpha (TNF-α) by peritoneal cells of 7-day and 14-day obstructive jaundice (OJ) and sham-operated rats were investigated. In the study the skin wound breaking strength was measured, In addition such histological and biochemical parameters as fibroblast and endothelial cell proliferation, inflammatory cell infiltration and hydroxyproline content were evaluated in polyurethane sponge discs implanted subcutaneously into rats. TNF-α production by peritoneal exudate cells (PEC), both spontaneous and lipopolysaccharide (LPS)- induced was determined by a bioassay. In OJ rats the process of both early as well as late phase of healing was impaired. The breaking strength of skin wound was decreased, the fibroblast and endothelial cell proliferation and collagen deposition, as well as hydroxyproline content were diminished. In 7 day OJ the numbers of inflammatory cells in the implants were lowered with a subsequent slight increase on day 14 of OJ. The spontaneous and LPS induced TNF- α production by PEC were significantly higher in 7 day OJ as compared with sham-operated controls. On day 14 of OJ the LPS-induced TNF-α level was, in contrast, much lower and did not differ much from the spontaneous TNF-α production. We conclude that the impairment of wound healing in OJ results from disturbances in functioning of the immune system caused by systemic endotoxaemia. Hindawi Publishing Corporation 2000-01 /pmc/articles/PMC2423987/ /pubmed/10674746 http://dx.doi.org/10.1155/2000/82905 Text en Copyright © 2000 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
Kwiatkowska, Danuta
Zimecki, Michał
Kornafel, Pawel
Tyran, Wanda
Czapiiska, Elżbieta
Woźniak, Zdzisław
The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats
title The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats
title_full The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats
title_fullStr The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats
title_full_unstemmed The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats
title_short The Impairment of Wound Healing Process is Correlated With Abnormalities of TNF-α Production by Peritoneal Exudate Cells in Obstructive Jaundiced Rats
title_sort impairment of wound healing process is correlated with abnormalities of tnf-α production by peritoneal exudate cells in obstructive jaundiced rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423987/
https://www.ncbi.nlm.nih.gov/pubmed/10674746
http://dx.doi.org/10.1155/2000/82905
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