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J Appl Physiol 107: 921-927, 2009. First published July 23, 2009; doi:10.1152/japplphysiol.00275.2009
8750-7587/09 $8.00
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Three-dimensional alignment of the aggregated myocytes in the normal and hypertrophic murine heart

Boris Schmitt,1 Katsiaryna Fedarava,1 Jan Falkenberg,1 Kai Rothaus,2 Narendra K. Bodhey,1 Carolin Reischauer,3 Sebastian Kozerke,3 Bernhard Schnackenburg,4 Dirk Westermann,5 Paul P. Lunkenheimer,6 Robert H. Anderson,7 Felix Berger,1 and Titus Kuehne1

1Unit of Cardiovascular Imaging—Department for Congenital Heart Disease and Pediatric Cardiology, German Heart Institute Berlin, 2Institute for Informatics, University of Münster, Germany; 3Institute for Biomedical Engineering, Swiss Federal Institute of Technology (ETH) Zurich and University Zurich, Switzerland; 4 Phillips Medical Systems, Hamburg, 5Institute of Cardiology, Charité, Campus Benjamin Franklin, Berlin, 6Department of Thoracic and Cardiovascular Surgery, University Hospital Münster, Germany; and 7Cardiac Unit, Institute of Child Health, University College, London, United Kingdom

Submitted 13 March 2009 ; accepted in final form 16 July 2009

Several observations suggest that the transmission of myocardial forces is influenced in part by the spatial arrangement of the myocytes aggregated together within ventricular mass. Our aim was to assess, using diffusion tensor magnetic resonance imaging (DT-MRI), any differences in the three-dimensional arrangement of these myocytes in the normal heart compared with the hypertrophic murine myocardium. We induced ventricular hypertrophy in seven mice by infusion of angiotensin II through a subcutaneous pump, with seven other mice serving as controls. DT-MRI of explanted hearts was performed at 3.0 Tesla. We used the primary eigenvector in each voxel to determine the three-dimensional orientation of aggregated myocytes in respect to their helical angles and their transmural courses (intruding angles). Compared with controls, the hypertrophic hearts showed significant increases in myocardial mass and the outer radius of the left ventricular chamber (P < 0.05). In both groups, a significant change was noted from positive intruding angles at the base to negative angles at the ventricular apex (P < 0.01). Compared with controls, the hypertrophied hearts had significantly larger intruding angles of the aggregated myocytes, notably in the apical and basal slices (P < 0.001). In both groups, the helical angles were greatest in midventricular sections, albeit with significantly smaller angles in the mice with hypertrophied myocardium (P < 0.01). The use of DT-MRI revealed significant differences in helix and intruding angles of the myocytes in the mice with hypertrophied myocardium.

hypertrophy; orientation; magnetic resonance imaging; diffusion tensor imaging



Address for reprint requests and other correspondence: T. Kuehne, Unit of Cardiovascular Imaging—Dept. of Congenital Heart Disease and Pediatric Cardiology, German Heart Institute Berlin, Germany (e-mail: kuehne{at}dhzb.de)







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