A New EPR Oximetry Protocol to Estimate the Tissue Oxygen Consumption In Vivo

被引:20
作者
Diepart, Caroline [1 ]
Jordan, Benedicte F. [1 ]
Gallez, Bernard [1 ]
机构
[1] Catholic Univ Louvain, Lab Biomed Magnet Resonance, B-1200 Brussels, Belgium
关键词
ELECTRON-PARAMAGNETIC-RESONANCE; TUMOR OXYGENATION; OXIDATIVE DAMAGE; REDOX STATUS; BLOOD-FLOW; MECHANISM; DECREASE; THERAPY; HYPOXIA; GLUCOSE;
D O I
10.1667/RR1448.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The oxygen consumption rate in tumors affects tumor oxygenation and response to therapies. A new EPR method was developed to measure tissue oxygen consumption non-invasively. The protocol was based on the measurement of pO(2) during a carbogen challenge. The following sequence was used: (1) basal value during air breathing; (2) saturation of tissue with oxygen by carbogen breathing; (3) switch back to air breathing. The assumption was that the kinetics of the return to the basal value after oxygen saturation would be governed mainly by tissue oxygen consumption. This challenge was applied in hyperthyroid mice (generated by chronic treatment with L-thyroxine) and control mice because hyperthyroidism is known to dramatically affect the oxygen consumption rate of tumor and muscle cells. Muscle and tumor cells from the hyperthyroid mice consumed oxygen faster than muscle and tumor cells from the control mice, which is consistent with the results of in vitro studies. Tumor perfusion was not affected by the treatment with L-thyroxine. This method gives an index that may reasonably be ascribed to the local oxygen consumption and has the unique advantage of being adaptable to in vivo studies. (C) 2009 by Radiation Research Society
引用
收藏
页码:220 / 225
页数:6
相关论文
共 24 条
[1]  
Ansiaux R, 2005, CLIN CANCER RES, V11, P743
[2]   Mechanism of reoxygenation after antianglogenic therapy using SU5416 and its importance for guiding combined antitumor therapy [J].
Ansiaux, Reginald ;
Baudelet, Christine ;
Jordan, Benedicte F. ;
Crokart, Nathalie ;
Martinive, Philippe ;
DeWever, Julie ;
Gregoire, Vincent ;
Feron, Olivier ;
Gallez, Bernard .
CANCER RESEARCH, 2006, 66 (19) :9698-9704
[3]   MIBG inhibits respiration: Potential for radio- and hyperthermic sensitization [J].
Biaglow, JE ;
Manevich, Y ;
Leeper, D ;
Chance, B ;
Dewhirst, MW ;
Jenkins, WT ;
Tuttle, SW ;
Wroblewski, K ;
Glickson, JD ;
Stevens, C ;
Evans, SM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 42 (04) :871-876
[4]   Tumor radiosensitization by anti inflammatory drugs:: Evidence for a new mechanism involving the oxygen effect [J].
Crokart, N ;
Radermacher, K ;
Jordan, BF ;
Baudelet, C ;
Cron, GO ;
Grégoire, V ;
Beghein, N ;
Bouzin, C ;
Feron, O ;
Gallez, B .
CANCER RESEARCH, 2005, 65 (17) :7911-7916
[5]   Glucocorticoids modulate tumor radiation response through a decrease in tumor oxygen consumption [J].
Crokart, Nathalie ;
Jordan, Benedicte F. ;
Baudelet, Christine ;
Cron, Gregory O. ;
Hotton, Julie ;
Radermacher, Kim ;
Gregoire, Vincent ;
Beghein, Nelson ;
Martinive, Philippe ;
Bouzin, Caroline ;
Feron, Olivier ;
Gallez, Bernard .
CLINICAL CANCER RESEARCH, 2007, 13 (02) :630-635
[6]  
Dewhirst MW, 1996, BRIT J CANCER, V74, pS241
[7]  
DEWHIRST MW, 1964, CANCER RES, V54, P3333
[8]  
Gallez B, 1999, MAGN RESON MED, V42, P627, DOI 10.1002/(SICI)1522-2594(199910)42:4<627::AID-MRM2>3.0.CO
[9]  
2-M
[10]   Assessment of tumor oxygenation by electron paramagnetic resonance: principles and applications [J].
Gallez, B ;
Baudelet, C ;
Jordan, BF .
NMR IN BIOMEDICINE, 2004, 17 (05) :240-262