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Misonidazole reduces blood flow in two experimental murine tumours.

The effects of single doses of misonidazole (MISO) on blood flow and vascular volume in the SaFA and CaNT tumours and normal tissues of the mouse have been studied. MISO was administered in the dose range 250-1,000 mg kg-1 and blood flow measured at different times after MISO by the 86RbCl extractio...

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Autores principales: Murray, J. C., Randhawa, V. S.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246764/
https://www.ncbi.nlm.nih.gov/pubmed/3166901
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author Murray, J. C.
Randhawa, V. S.
author_facet Murray, J. C.
Randhawa, V. S.
author_sort Murray, J. C.
collection PubMed
description The effects of single doses of misonidazole (MISO) on blood flow and vascular volume in the SaFA and CaNT tumours and normal tissues of the mouse have been studied. MISO was administered in the dose range 250-1,000 mg kg-1 and blood flow measured at different times after MISO by the 86RbCl extraction technique. Vascular volume was assessed by the distribution of 51Cr-labelled red blood cells. MISO at doses of 500 mg kg-1 or greater decreased flow in both tumours by up to 60% within 2 h. Flow remained reduced for up to 24 h. Similar but less profound changes were seen in the skin, although flow had recovered by 24 h. Only slight changes were seen in muscle, and none in kidney. The apparent loss of flow in tumours seen after large single doses of MISO may have important implications for its use as a chemosensitizer.
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spelling pubmed-22467642009-09-10 Misonidazole reduces blood flow in two experimental murine tumours. Murray, J. C. Randhawa, V. S. Br J Cancer Research Article The effects of single doses of misonidazole (MISO) on blood flow and vascular volume in the SaFA and CaNT tumours and normal tissues of the mouse have been studied. MISO was administered in the dose range 250-1,000 mg kg-1 and blood flow measured at different times after MISO by the 86RbCl extraction technique. Vascular volume was assessed by the distribution of 51Cr-labelled red blood cells. MISO at doses of 500 mg kg-1 or greater decreased flow in both tumours by up to 60% within 2 h. Flow remained reduced for up to 24 h. Similar but less profound changes were seen in the skin, although flow had recovered by 24 h. Only slight changes were seen in muscle, and none in kidney. The apparent loss of flow in tumours seen after large single doses of MISO may have important implications for its use as a chemosensitizer. Nature Publishing Group 1988-08 /pmc/articles/PMC2246764/ /pubmed/3166901 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
Murray, J. C.
Randhawa, V. S.
Misonidazole reduces blood flow in two experimental murine tumours.
title Misonidazole reduces blood flow in two experimental murine tumours.
title_full Misonidazole reduces blood flow in two experimental murine tumours.
title_fullStr Misonidazole reduces blood flow in two experimental murine tumours.
title_full_unstemmed Misonidazole reduces blood flow in two experimental murine tumours.
title_short Misonidazole reduces blood flow in two experimental murine tumours.
title_sort misonidazole reduces blood flow in two experimental murine tumours.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246764/
https://www.ncbi.nlm.nih.gov/pubmed/3166901
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