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Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.

(AxT6)F1 hybrid mice received s.c. transplants from (AxT6)F1 mammary carcinomas. At 1, 2 or 4 weeks after tumour transplantation, the mice were bled to obtain plasma and then challenged with 25 micron E. coli lipopolysaccharide (LPS) endotoxin i.v. The mice were killed 24 hr later, further plasma wa...

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Autores principales: Bradfield, J. W., Whitmarsh-Everiss, T., Palmer, D. B., Payne, R., Symes, M. O.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1980
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010591/
https://www.ncbi.nlm.nih.gov/pubmed/7459224
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author Bradfield, J. W.
Whitmarsh-Everiss, T.
Palmer, D. B.
Payne, R.
Symes, M. O.
author_facet Bradfield, J. W.
Whitmarsh-Everiss, T.
Palmer, D. B.
Payne, R.
Symes, M. O.
author_sort Bradfield, J. W.
collection PubMed
description (AxT6)F1 hybrid mice received s.c. transplants from (AxT6)F1 mammary carcinomas. At 1, 2 or 4 weeks after tumour transplantation, the mice were bled to obtain plasma and then challenged with 25 micron E. coli lipopolysaccharide (LPS) endotoxin i.v. The mice were killed 24 hr later, further plasma was obtained and their liver ratios and spleen ratios were determined. A similar procedure was carried out on non-tumour-bearing mice. Progressive tumour growth was associated with an increase in the liver ratio. In parallel, mice with 4-week tumour transplant showed increased uptake of colloidal carbon particles and 51Cr-labelled sheep red blood cells in the liver. The plasma amino aspartate transaminase (AST) and the ornithine carbamoyl transferase (OCT) showed a constant rise in all groups of mice after LPS injection. However, at 24 hr after LPS injection, the AST level showed the greatest rise in mice with 4-week tumour transplants. By contrast, OCT, which is liberated only from hepatocytes, showed the greatest rise in non-tumour-bearing mice. IMAGES:
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spelling pubmed-20105912009-09-10 Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice. Bradfield, J. W. Whitmarsh-Everiss, T. Palmer, D. B. Payne, R. Symes, M. O. Br J Cancer Research Article (AxT6)F1 hybrid mice received s.c. transplants from (AxT6)F1 mammary carcinomas. At 1, 2 or 4 weeks after tumour transplantation, the mice were bled to obtain plasma and then challenged with 25 micron E. coli lipopolysaccharide (LPS) endotoxin i.v. The mice were killed 24 hr later, further plasma was obtained and their liver ratios and spleen ratios were determined. A similar procedure was carried out on non-tumour-bearing mice. Progressive tumour growth was associated with an increase in the liver ratio. In parallel, mice with 4-week tumour transplant showed increased uptake of colloidal carbon particles and 51Cr-labelled sheep red blood cells in the liver. The plasma amino aspartate transaminase (AST) and the ornithine carbamoyl transferase (OCT) showed a constant rise in all groups of mice after LPS injection. However, at 24 hr after LPS injection, the AST level showed the greatest rise in mice with 4-week tumour transplants. By contrast, OCT, which is liberated only from hepatocytes, showed the greatest rise in non-tumour-bearing mice. IMAGES: Nature Publishing Group 1980-12 /pmc/articles/PMC2010591/ /pubmed/7459224 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Bradfield, J. W.
Whitmarsh-Everiss, T.
Palmer, D. B.
Payne, R.
Symes, M. O.
Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
title Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
title_full Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
title_fullStr Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
title_full_unstemmed Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
title_short Hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
title_sort hyperphagocytosis and the effect of lipopolysaccharide injection in tumour-bearing mice.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010591/
https://www.ncbi.nlm.nih.gov/pubmed/7459224
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