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Effects of hyperoxia on T   2 * and resonance frequency weighted magnetic resonance images of rodent tumours
Author(s) -
Karczmar G. S.,
River J. N.,
Li J.,
Vijayakumar S.,
Goldman Z.,
Lewis M. Z.
Publication year - 1994
Publication title -
nmr in biomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 114
eISSN - 1099-1492
pISSN - 0952-3480
DOI - 10.1002/nbm.1940070103
Subject(s) - hyperoxia , nuclear magnetic resonance , magnetic resonance imaging , chemistry , pulse (music) , oxygen , voxel , pulse sequence , resonance (particle physics) , nuclear medicine , medicine , physics , atomic physics , optics , radiology , organic chemistry , detector
Experiments were performed to determine whether T   2 *and resonance frequency weighted MR images are sensitive to effects of hyperoxia on model tumors. Hyperoxia can increase tumor oxygen tension and thus affect T   2 *and/or the average resonance frequency within each image voxel due to the paramagnetism of oxygen itself or through modulation of the oxidation state of hemoglobin. Alternatively, changes in T   2 *during hyperoxia may reflect changes in tumor water content due to changes in systemic blood pressure. Mammary adenocarcinomas implanted in the flanks of rats were studied. Imaging sequences were preceded by two 90° pulses separated by an evolution period of 50 or 75 ms and followed by a crusher gradient to eliminate transverse magnetization. This pulse sequence produced images which were sensitized to both T   2 *and the average resonance frequency of each voxel. Images were produced at 2 T using a gradient echo imaging method with a TR of 3 s. Images obtained during inhalation of air and 100% O 2 were compared. Significant increases in image intensity were observed in most tumors during hyperoxia, particularly at the tumor center. The increase was accentuated when the evolution period was increased and greatly reduced when a 180° refocusing pulse was placed at the center of the evolution period. These results suggest that hyperoxia reduces local magnetic susceptibility gradients leading to an increase in T   2 *or causes a shift in resonance frequency. The magnitude of this change may be a function of the rate at which oxygen is delivered to and metabolized by tumors and may also reflect tumor oxygen tension under normoxic conditions. Therefore, response to hyperoxia may provide useful contrast in MR images which could aid identification and characterization of tumors and provide an indirect measure of tumor blood flow and oxygenation.

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