Gadolinium-DTPA-Enhanced Magnetic Resonance Imaging of the Isolated Rat Heart after Ischemia and Reperfusion

The objective of this study was to assess the potential of gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA) to identify myocardial ischemia and reperfusion in the isolated rat heart model. Ischemia was induced by reducing the perfusion pressure from 80 to 30 mm Hg for 2 hours. Hearts were no...

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Veröffentlicht in:Investigative radiology 1991-12, Vol.26 (12), p.1060-1064
Hauptverfasser: ROOS, ALBERT DE, MOHANLAL, RAMON W, van VAALS, JOOP J, BERGMAN, ANTHONIE H, DOORNBOS, JOOST, MATHEIJSSEN, NIELS A.A, Van, ERNST E, WALL, DER, DER LARSE, ADMOIin VAN
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Sprache:eng
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Zusammenfassung:The objective of this study was to assess the potential of gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA) to identify myocardial ischemia and reperfusion in the isolated rat heart model. Ischemia was induced by reducing the perfusion pressure from 80 to 30 mm Hg for 2 hours. Hearts were not reperfused, or were reperfused for 20 minutes or for 2 hours. Perfusion was performed with Evans blue dye and/or Gd-DTPA for 3 minutes. Twenty isolated rat hearts were perfused according to the Langendorff method, and divided into five groups according to the perfusion status and the use of Gd-DTPA and/or Evans blue as perfusion markers. The Evans blue distribution in the hearts was assessed by point-counting volumetry. The Gd-DTPA distribution was assessed by magnetic resonance microimaging at 6.3 T field strength. Evans blue staining clearly identified areas with "no flow" or "no reflow." Perfusion with Gd-DTPA enhanced signal intensity significantly, both in ischemic and reperfused myocardium. Signal intensity in hearts reperfused for 2 hours was increased significantly compared to nonreperfused ischemic hearts, but not to ischemic hearts reperfused for 20 minutes. Magnetic resonance imaging with the aid of Gd-DTPA can identify ischemia and reperfusion in the isolated rat heart, dependent on residual perfusion.
ISSN:0020-9996
1536-0210
DOI:10.1097/00004424-199112000-00005