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The effects of hyperoxic and hypercarbic gases on tumour blood flow
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  • Published: 26 March 1999

The effects of hyperoxic and hypercarbic gases on tumour blood flow

  • T J Dunn1,
  • R D Braun1,
  • W E Rhemus1,
  • G L Rosner2,
  • T W Secomb3,
  • G M Tozer4,
  • D J Chaplin4 &
  • …
  • M W Dewhirst1 

British Journal of Cancer volume 80, pages 117–126 (1999)Cite this article

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Abstract

Carbogen (95% O2 and 5% CO2) has been used in preference to 100% oxygen (O2) as a radiosensitizer, because it is believed that CO2 blocks O2-induced vasoconstriction. However, recent work suggests that both normal and tumour arterioles of dorsal flap window chambers exhibit the opposite: no vasoconstriction vs constriction for O2 vs carbogen breathing respectively. We hypothesized that CO2 content might cause vasoconstriction and investigated the effects of three O2–CO2 breathing mixtures on tumour arteriolar diameter (TAD) and blood flow (TBF). Fischer 344 rats with R3230Ac tumours transplanted into window chambers breathed either 1%, 5%, or 10% CO2 + O2. Intravital microscopy and laser Doppler flowmetry were used to measure TAD and TBF respectively. Animals breathing 1% CO2 had increased mean arterial pressure (MAP), no change in heart rate (HR), transient reduction in TAD and no change in TBF. Rats breathing 5% CO2 (carbogen) had transiently increased MAP, decreased HR, reduced TAD and a sustained 25% TBF decrease. Animals exposed to 10% CO2 experienced a transient decrease in MAP, no HR change, reduced TAD and a 30–40% transient TBF decrease. The effects on MAP, HR, TAD and TBF were not CO2 dose-dependent, suggesting that complex physiologic mechanisms are involved. Nevertheless, when ≥ 5% CO2 was breathed, there was clear vasoconstriction and TBF reduction in this model. This suggests that the effects of hypercarbic gases on TBF are site-dependent and that use of carbogen as a radiosensitizer may be counterproductive in certain situations.

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Departments of Radiation Oncology, Duke University Medical Center, PO Box 3455, Durham, 27710, NC, USA

    T J Dunn, R D Braun, W E Rhemus & M W Dewhirst

  2. Departments of Biometry and Medical Informatics, Duke University Medical Center, Durham, 27710, NC, USA

    G L Rosner

  3. Department of Physiology, Arizona Health Sciences Center, University of Arizona, Tucson, 85724, AZ, USA

    T W Secomb

  4. Tumour Microcirculation Group, Gray Laboratory Cancer Research Trust, Northwood, Middlesex, HA6 2RJ, UK

    G M Tozer & D J Chaplin

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Dunn, T., Braun, R., Rhemus, W. et al. The effects of hyperoxic and hypercarbic gases on tumour blood flow. Br J Cancer 80, 117–126 (1999). https://doi.org/10.1038/sj.bjc.6690330

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  • Received: 16 January 1998

  • Revised: 17 August 1998

  • Accepted: 18 August 1998

  • Published: 26 March 1999

  • Issue date: 01 April 1999

  • DOI: https://doi.org/10.1038/sj.bjc.6690330

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Keywords

  • tumour
  • blood flow
  • arteriolar diameter
  • carbogen
  • carbon dioxide

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