MRI and PET of delayed heavy-ion radiation injury in the rabbit brain

Magnetic resonance imaging Berkeley, CAaging (MRI) and positron emission tomography (PET) techniques were used to obtain in vivo scans of delayed (30 GyE helium ion, 230 MeV/u) radiation injury in rabbit brain. T2-weighted (T2W) MRI scans demonstrated alterations that were restricted primarily to th...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 1991-04, Vol.20 (4), p.689-696
Hauptverfasser: Lo, Eng H., Delapaz, Robert L., Frankel, Kenneth A., Poljak, Alex, Phillips, Mark H., Brennan, Kathleen M., Woodruff, Kay H., Valk, Peter E., Steinberg, Gary K., Fabrikant, Jacob I.
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Sprache:eng
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Zusammenfassung:Magnetic resonance imaging Berkeley, CAaging (MRI) and positron emission tomography (PET) techniques were used to obtain in vivo scans of delayed (30 GyE helium ion, 230 MeV/u) radiation injury in rabbit brain. T2-weighted (T2W) MRI scans demonstrated alterations that were restricted primarily to the white matter tracts and the deep perithalamic and thalamic regions. Quantitative measurements of T2 and T1 values demonstrated wide variations in absolute values. However, paired comparisons in hemibrain-irradiated rabbits revealed significant increases in T2 ( p < 0.001) and T1 ( p < 0.01) in irradiated versus unirradiated brain. Gadolinium DTPA (GdDTPA) enhanced MRI and 82Rubidium ( 82Rb) PET detected focal regions of blood-brain barrier (BBB) disruption restricted to the deep white matter and thalamic regions. Sequential GdDTPA enhanced MRI scans showed the spreading of the tracer from the initial site of contrast enhancement. 18Fluorodeoxyglucose ( 18FDG) PET studies demonstrated the markedly depressed metabolic profiles of irradiated brain. Histological findings of tissue edema and necrosis correlated well with the in vivo imaging abnormalities. These initial studies demonstrate that the irradiated rabbit brain is a suitable animal model for examining the delayed effects of radiation injury in the brain.
ISSN:0360-3016
1879-355X
DOI:10.1016/0360-3016(91)90010-2