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Detection of Microregional Fluctuations in Erythrocyte Flow Using Laser Doppler Microprobes

  • S. A. Hill
  • D. J. Chaplin
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 388)

Abstract

It is well established that experimental tumours develop microregions of nutrient-deprived and oxygen-deficient cells as a consequence of their heterogeneous vascular supply. Spatial heterogeneity can lead to the existence of chronically hypoxic cells at a distance from blood vessels, as originally described by Thomlinson and Gray (1955). However, it has also been suggested that a temporal heterogeneity in perfusion could lead to a transient, potentially reversible, acute hypoxia (Brown, 1979). Evidence for temporary non-perfusion of vessels has been provided by direct observation of ‘sandwich’ tumour preparations (Reinhold et al., 1977) as well as by histological techniques which involve the injection of two fluorescent markers, separated in time (Trotter et al., 1989). These perfusion markers have provided evidence of intermittent blood flow in a number of different experimental murine tumours, but they do have limitations; in some systems the dyes themselves are vasoactive, the techniques are not clinically applicable and they provide no kinetic information on the duration of vessel non-perfusion.

Keywords

Hypoxic Cell Acute Hypoxia Temporal Heterogeneity Tumour Blood Flow Trace Direction 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Brown, J.M. Evidence for acutely hypoxic cells in mouse tumours and a possible mechanism for reoxygeneration. Br. J. Radiol, 52, 650–656, 1979.PubMedCrossRefGoogle Scholar
  2. Chaplin, D.J., Horstman, M.R. and Trotter, M.J. Effect of nicotinamide on the microregional heterogeneity of oxygen delivery within a murine tumour. JNCI, 82, 672–676, 1990.PubMedGoogle Scholar
  3. Reinhold, H.S., Blachiwiecz, B. and Blok, A. Oxygenation and reoxygenation in “sandwich” tumours. Bibl Anat., 15, 270–272, 1977.PubMedGoogle Scholar
  4. Thomlinson, R.H. and Gray, L.H. The histological structure of some human lung cancers and the possible implications for radiotherapy. Br. J. Cancer, 9, 539–549, 1955.PubMedCrossRefGoogle Scholar
  5. Trotter, M.J., Chaplin, D.J., Durand, R.E. and Olive, RL. The use of fluorescent probes to identify regions of transient perfusion in murine tumors. Int. J. Radiat. Oncol. Biol Phys., 16, 931–934, 1989.PubMedCrossRefGoogle Scholar

Copyright information

© Plenum Press, New York 1996

Authors and Affiliations

  • S. A. Hill
    • 1
  • D. J. Chaplin
    • 1
  1. 1.CRC Gray LaboratoryMount Vernon HospitalMiddlesexUK

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