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Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels

Both host carbogen (95% oxygen/5% carbon dioxide) breathing and nicotinamide administration enhance tumour radiotherapeutic response and are being re-evaluated in the clinic. Non-invasive magnetic resonance imaging (MRI) and (31)P magnetic resonance spectroscopy (MRS) methods have been used to give...

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Autores principales: Robinson, S P, Howe, F A, Stubbs, M, Griffiths, J R
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363252/
https://www.ncbi.nlm.nih.gov/pubmed/10864210
http://dx.doi.org/10.1054/bjoc.2000.1144
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author Robinson, S P
Howe, F A
Stubbs, M
Griffiths, J R
author_facet Robinson, S P
Howe, F A
Stubbs, M
Griffiths, J R
author_sort Robinson, S P
collection PubMed
description Both host carbogen (95% oxygen/5% carbon dioxide) breathing and nicotinamide administration enhance tumour radiotherapeutic response and are being re-evaluated in the clinic. Non-invasive magnetic resonance imaging (MRI) and (31)P magnetic resonance spectroscopy (MRS) methods have been used to give information on the effects of nicotinamide alone and in combination with host carbogen breathing on transplanted rat GH3 prolactinomas. Gradient recalled echo (GRE) MRI, sensitive to blood oxygenation changes, and spin echo (SE) MRI, sensitive to perfusion/flow, showed large signal intensity increases with carbogen breathing. Nicotinamide, thought to act by suppressing the transient closure of small blood vessels that cause intermittent tumour hypoxia, induced a small increase in blood oxygenation but no detectable change in perfusion/flow. Carbogen combined with nicotinamide was no more effective than carbogen alone. Both carbogen and nicotinamide caused significant increases in the nucleoside triphosphate/inorganic phosphate (βNTP/P (i)) ratio, implying that the tumour cells normally receive sub-optimal substrate supply, and is consistent with either increased glycolysis and/or a switch to more oxidative metabolism. The most striking observation was the marked increase in blood glucose (twofold) induced by both nicotinamide and carbogen. Whether this may play a role in tumour radiosensitivity has yet to be determined. Copyright 2000 Cancer Research Campaign© 2000 Cancer Research Campaign
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spelling pubmed-23632522009-09-10 Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels Robinson, S P Howe, F A Stubbs, M Griffiths, J R Br J Cancer Regular Article Both host carbogen (95% oxygen/5% carbon dioxide) breathing and nicotinamide administration enhance tumour radiotherapeutic response and are being re-evaluated in the clinic. Non-invasive magnetic resonance imaging (MRI) and (31)P magnetic resonance spectroscopy (MRS) methods have been used to give information on the effects of nicotinamide alone and in combination with host carbogen breathing on transplanted rat GH3 prolactinomas. Gradient recalled echo (GRE) MRI, sensitive to blood oxygenation changes, and spin echo (SE) MRI, sensitive to perfusion/flow, showed large signal intensity increases with carbogen breathing. Nicotinamide, thought to act by suppressing the transient closure of small blood vessels that cause intermittent tumour hypoxia, induced a small increase in blood oxygenation but no detectable change in perfusion/flow. Carbogen combined with nicotinamide was no more effective than carbogen alone. Both carbogen and nicotinamide caused significant increases in the nucleoside triphosphate/inorganic phosphate (βNTP/P (i)) ratio, implying that the tumour cells normally receive sub-optimal substrate supply, and is consistent with either increased glycolysis and/or a switch to more oxidative metabolism. The most striking observation was the marked increase in blood glucose (twofold) induced by both nicotinamide and carbogen. Whether this may play a role in tumour radiosensitivity has yet to be determined. Copyright 2000 Cancer Research Campaign© 2000 Cancer Research Campaign Nature Publishing Group 2000-06 2000-05-18 /pmc/articles/PMC2363252/ /pubmed/10864210 http://dx.doi.org/10.1054/bjoc.2000.1144 Text en Copyright © 2000 Cancer Research Campaign 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 Regular Article
Robinson, S P
Howe, F A
Stubbs, M
Griffiths, J R
Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
title Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
title_full Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
title_fullStr Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
title_full_unstemmed Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
title_short Effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
title_sort effects of nicotinamide and carbogen on tumour oxygenation, blood flow, energetics and blood glucose levels
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363252/
https://www.ncbi.nlm.nih.gov/pubmed/10864210
http://dx.doi.org/10.1054/bjoc.2000.1144
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