Abstract
A variety of morphological and physiological techniques have been applied to a transplantable rat glioma model in an attempt to elucidate details of vascular development and transport phenomena. Three mor-phological stages of tumour vascular development are defined. General vascularity has been quantitatively assessed using light microscopy of paraffin and resin-embedded material. Fenestrations, abnormal junctions and vesicular profiles have been counted in normal and tumour vessels to provide a quantitative assessment of these recognised ultrastructural abnormalities of glioma vasculature. Changes in the numerical density of sectioned vascular profiles and in the size of vessels have been measured in consecutive sample areas extending from brain surrounding tumour towards the tumour centre.
Intravenous and cerebral intraventricular injections of horseradish peroxidase (HRP) were used to demonstrate differences in the transport of a large hydrophilic molecule by vessels within tumours and by those of peritumoral tissue. To quantify the kinetics of transfer of a small polar molecule into tumours and adjacent brain steady plasma levels of [14C] mannitol were maintained for increasing periods of time in separate tumour-bearing and control animals. The ratio of tissue to plasma radioactivity was plotted against time and the apparent transfer constants for mannitol calculated: that for entry into tumour tissue was approximately 80 times that into normal brain.
These studies aim to solve clinical problems including those of cerebral oedema and of drug delivery to gliomas.
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© 1986 Martinas Nijhoff Publishers, Boston
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Luthert, P.J., Deane, B.R., Greenwood, J., Pratt, O.E., Lantos, P.L. (1986). The vasculature of experimental brain tumours: angiogenesis, vascular pathology and permeability studies. In: Walker, M.D., Thomas, D.G.T. (eds) Biology of Brain Tumour. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2297-9_27
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DOI: https://doi.org/10.1007/978-1-4613-2297-9_27
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