ELECTRONIC POSTER - ismrm
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ELECTRONIC POSTER - ismrm
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15:00 3611. An Optimal Physiologic Model for Study of Murine Cardiac Function Under<br />
Inhalational Anesthesia<br />
Christakis Constantinides 1 , Richard Mean 1 , Laurence W. Hedlund 2<br />
1 Mechanical and Manufacturing Engineering, University of Cyprus, Nicosia, Cyprus; 2 Radiology, Duke<br />
University Medical Center, Durham, NC, United States<br />
While cardiac mechanical functional studies initially focused on large mammals and the human, the mouse emerged as the preferred<br />
animal species for research in recent years. Albeit evidence supports that bioenergetically and hemodynamically the mouse scales<br />
linearly with larger mammals and humans, important physiological questions still remain for the appropriateness of this model for<br />
extrapolation of conclusions to man. Since the complete characterization of the mouse and human genomes in 2002 and 2003<br />
respectively, there has been a plethora of transgenic mouse studies targeting the cardiovascular system. Equally important were noninvasive<br />
imaging studies of such animals for phenotypic and genotypic screening, often conducted under inhalational anesthesia.<br />
Anesthetics, however, are known to cause severe cardio-depression with adverse physiological effects on hormonal release, centrally<br />
to the heart and peripherally to the vasculature, at the cellular level, affecting calcium entry through L-type Ca2+ channels, the<br />
calcium binding sensitivity of the contractile proteins to calcium, and on conduction and excitability. The objective of this study was<br />
to determine the isoflurane dose in normal mice for optimal physiological status (respiration, cardiac function, and metabolism) for a<br />
period of 1-2 hours post-induction, facilitating migration of such work to the non-invasive imaging platform of MRI, with tremendous<br />
potential for future basic science towards the phenotypic screening of transgenic mice and translational research.<br />
Thursday 13:30-15:30 Computer 31<br />
13:30 3612. The Patho-Physiological Sensitivity of Cardiac MR Elastography: Preliminary<br />
Results.<br />
Thomas Elgeti 1 , Mark Beling 2 , Dieter Klatt 1 , Sebastian Papazoglou 1 , Sebastian Hirsch 1 ,<br />
Kerstin Riek 1 , Bernd Hamm 1 , Jürgen Braun 3 , Ingolf Sack 1<br />
1 Institut für Radiologie, Charité Universitätsmedizin , Berlin, Germany; 2 Klinik und Poliklinik für Kardiologie,<br />
Charité Universitätsmedizin , Berlin, Germany; 3 Institut für Medizinische Informatik und Biometrie, Charité<br />
Universitätsmedizin , Berlin, Germany<br />
MR Elastography (MRE) is capable to directly measure tissue stiffness. This is particularly interesting for cardiac applications, since<br />
the cardiac shear modulus changes over the cardiac cycle. It is known, that increasing myocardial stiffness yields decrease of wave<br />
amplitudes in MRE. Therefore, left ventricular shear wave amplitudes were measured in 11 healthy volunteers and 11 patients with<br />
relaxation abnormalities. It is observed, that shear wave amplitudes are significantly lower in the left ventricle of patients. This result<br />
indicates the sensitivity of amplitude-based cardiac MRE to identify increased myocardial stiffness.<br />
14:00 3613. Relationship Between Mitral Velocity and Mitral Flow Time-Profiles During<br />
Ventricular Filling<br />
June Cheng-Baron 1 , Jessica M. Scott 2 , Ben T. Esch 2 , Mark J. Haykowsky 2 , John V.<br />
Tyberg 3 , Richard B. Thompson 1<br />
1 Biomedical Engineering, University of Alberta, Edmonton, AB, Canada; 2 Physical Therapy, University of<br />
Alberta, Edmonton, AB, Canada; 3 Cardiac Sciences, University of Calgary, Calgary, AB, Canada<br />
It has been shown that blood velocity waveforms measured at the conventional mitral leaflet tips location do not match mitral flow<br />
waveforms. In this study we quantify the relationship between velocity profiles at several points along the inflow path and volumetric<br />
flow, illustrating the dependence of commonly derived diastolic parameters (E/A ratio, deceleration time) on the measurement<br />
approach. Velocity profiles and derived parameters vary significantly over small (1 cm) intervals and are distinct from flow profiles.<br />
Velocity-time curves above the conventional leaflet tip location (in the atrium) are less susceptible to measurement error and are most<br />
similar to flow curves.<br />
14:30 3614. Cine DENSE and Manganese-Enhanced Cardiac MRI Demonstrate That ENOS<br />
Does Not Play a Determining Role in Modulating the Effects of ß-Adrenergic Stimulation<br />
Moriel H. Vandsburger 1 , Brent A. French 1 , Xiaodong Zhong 1,2 , Christopher M. Kramer 1 ,<br />
Frederick H. Epstein 1<br />
1 University of Virginia, Charlottesville, VA, United States; 2 MR R&D Collaborations, Siemens Healthcare,<br />
Atlanta, GA, United States<br />
Dynamic manganese-enhanced MRI and cine DENSE MRI can be used to probe calcium flux and contractile function in vivo in the<br />
mouse heart. Using these methods, we sought to elucidate the role of endothelial nitric oxide synthase (eNOS) in modulating calcium<br />
flux and contractile function. Counter to the prevailing opinion, which suggests that eNOS inhibits basal calcium flux, we found that<br />
eNOS does not play a role in modulating either calcium flux or contractile function at baseline, during β-adrenergic stimulation, or<br />
during muscarinic inhibition of β-adrenergic stimulation.