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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.

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