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      Histo-anatomical structure of the living isolated rat heart in two contraction states assessed by diffusion tensor MRI

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          Abstract

          Deformation and wall-thickening of ventricular myocardium are essential for cardiac pump function. However, insight into the histo-anatomical basis for cardiac tissue re-arrangement during contraction is limited. In this report, we describe dynamic changes in regionally prevailing cardiomyocyte (fibre) and myolaminar (sheet) orientations, using Diffusion Tensor Imaging (DTI) of ventricles in the same living heart in two different mechanical states. Hearts, isolated from Sprague–Dawley rats, were Langendorff-perfused and imaged, initially in their slack state during cardioplegic arrest, then during lithium-induced contracture. Regional fibre- and sheet-orientations were derived from DTI-data on a voxel-wise basis. Contraction was accompanied with a decrease in left-handed helical fibres (handedness relative to the baso-apical direction) in basal, equatorial, and apical sub-epicardium (by 14.0%, 17.3%, 15.8% respectively; p < 0.001), and an increase in right-handed helical fibres of the sub-endocardium (by 11.0%, 12.1% and 16.1%, respectively; p < 0.001). Two predominant sheet-populations were observed, with sheet-angles of either positive ( β+) or negative ( β−) polarity relative to a ‘chamber-horizontal plane’ (defined as normal to the left ventricular long-axis). In contracture, mean ‘intersection’-angle (geometrically quantifiable intersection of sheet-angle projections) between β+ and β− sheet-populations increased from 86.2 ± 5.5° (slack) to 108.3 ± 5.4° ( p < 0.001). Subsequent high-resolution DTI of fixed myocardium, and histological sectioning, reconfirmed the existence of alternating sheet-plane populations. Our results suggest that myocardial tissue layers in alternating sheet-populations align into a more chamber-horizontal orientation during contraction. This re-arrangement occurs via an accordion-like mechanism that, combined with inter-sheet slippage, can significantly contribute to ventricular deformation, including wall-thickening in a predominantly centripetal direction and baso-apical shortening.

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          Most cited references23

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          Estimation of the effective self-diffusion tensor from the NMR spin echo.

          The diagonal and off-diagonal elements of the effective self-diffusion tensor, Deff, are related to the echo intensity in an NMR spin-echo experiment. This relationship is used to design experiments from which Deff is estimated. This estimate is validated using isotropic and anisotropic media, i.e., water and skeletal muscle. It is shown that significant errors are made in diffusion NMR spectroscopy and imaging of anisotropic skeletal muscle when off-diagonal elements of Deff are ignored, most notably the loss of information needed to determine fiber orientation. Estimation of Deff provides the theoretical basis for a new MRI modality, diffusion tensor imaging, which provides information about tissue microstructure and its physiologic state not contained in scalar quantities such as T1, T2, proton density, or the scalar apparent diffusion constant.
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            Histological validation of myocardial microstructure obtained from diffusion tensor magnetic resonance imaging.

            Diffusion tensor magnetic resonance imaging (MRI) is a possible new means of elucidating the anatomic structure of the myocardium. It enjoys several advantages over traditional histological approaches, including the ability to rapidly measure fiber organization in isolated, perfused, arrested hearts, thereby avoiding fixation and sectioning of artifacts. However, quantitative validation of this MRI method has been lacking. Here, fiber orientations estimated in the same locations in the same heart using both diffusion tensor MRI and histology are compared in a total of two perfused rabbit hearts. Fiber orientations were statistically similar for both methods and differed on average by 12 degrees at any single location. This is similar to the 10 degrees uncertainty in fiber orientation achieved with histology. In addition, imaging studies performed in a total of seven hearts support a level of organization beyond the myofiber, the recently described laminar organization of the ventricular myocardium.
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              Magnetic resonance myocardial fiber-orientation mapping with direct histological correlation.

              Functional properties of the myocardium are mediated by the tissue structure. Consequently, proper physiological studies and modeling necessitate a precise knowledge of the fiber orientation. Magnetic resonance (MR) diffusion tensor imaging techniques have been used as a nondestructive means to characterize tissue fiber structure; however, the descriptions so far have been mostly qualitative. This study presents a direct, quantitative comparison of high-resolution MR fiber mapping and histology measurements in a block of excised canine myocardium. Results show an excellent correspondence of the measured fiber angles not only on a point-by-point basis (average difference of -2.30 +/- 0.98 degrees, n = 239) but also in the transmural rotation of the helix angles (average correlation coefficient of 0.942 +/- 0.008 with average false-positive probability of 0.004 +/- 0.001, n = 24). These data strongly support the hypothesis that the eigenvector of the largest MR diffusion tensor eigenvalue coincides with the orientation of the local myocardial fibers and underscore the potential of MR imaging as a noninvasive, three-dimensional modality to characterize tissue fiber architecture.
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                Author and article information

                Journal
                Prog Biophys Mol Biol
                Prog. Biophys. Mol. Biol
                Progress in Biophysics and Molecular Biology
                Pergamon Press
                0079-6107
                1873-1732
                October 2012
                October 2012
                : 110
                : 2-3
                : 319-330
                Affiliations
                [a ]Department of Cardiovascular Medicine, University of Oxford, Oxford OX3 7BN, UK
                [b ]National Heart and Lung Institute, Imperial College London, London UB9 6JH, UK
                [c ]Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK
                [d ]Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK
                [e ]Department of Computer Science, University of Oxford, Oxford OX1 3QD, UK
                Author notes
                []Corresponding author. Imaging and Biophysics Unit, UCL Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK. Tel.: +44 (0) 20 79052192; fax: +44 (0) 20 79052358. p.hales@ 123456ucl.ac.uk
                [1]

                Both authors contributed equally to this work.

                Article
                JPBM809
                10.1016/j.pbiomolbio.2012.07.014
                3526796
                23043978
                37a03ef9-e0a2-44ae-b5a0-24130efb0451
                © 2012 Elsevier Ltd.

                This document may be redistributed and reused, subject to certain conditions.

                History
                Categories
                Original Research

                Biophysics
                idl, interactive data language,diffusion tensor imaging,lhf/rhf, left/right-handed helical fibre,myolaminae,fa, fractional anisotropy,myocardial histo-architecture,nmr, nuclear magnetic resonance,adc, apparent diffusion coefficient,3d, three-dimensional,fov, field of view,dti, diffusion tensor imaging,lv, left ventricle,cardiac magnetic resonance imaging,mri, magnetic resonance imaging,cardiac contraction,cf, circumferential fibre,2d, two-dimensional

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