The broad goal of this project is to develop a protocol for quantifying the time course and amplitude of skeletal muscle perfusion and metabolic demand in the same volume of tissue in response to a standardized stress test. Our research plan is based on 3 key innovations: (1) the use of FAWSETS, an MR-based arterial spin labeling (ASL) technique we have developed specifically to overcome the limitations of other ASL techniques when they are used in skeletal muscle, (2) enhancement of FAWSETS through the use of custom- built gradients to reduce acquisition times and reduce SAR effects, and (3) the combination of gradient- enhanced FAWSETS with 31-P MR spectroscopy to examine the mechanistic links between local blood flow and cellular energetics during metabolic perturbation. All of our previous developmental work has been conducted in rat skeletal muscle. In SA#1 we will design and build the hardware and develop the protocols necessary to implement gradient-enhanced FAWSETS in human leg. In SA#2 we will combine our perfusion measurements with 31-P spectroscopy and test the ability of these tools to assess the cellular impact of impaired skeletal muscle perfusion in patients suffering from peripheral artery disease (PAD). Impaired skeletal muscle perfusion is observed in a variety of diseases, including insulin resistance and diabetes, congestive heart failure, compartment syndrome, PAD and systemic sclerosis. These diseases are serious public health issues that increase medical costs and reduce the quality of life for tens of millions of Americans. Currently, there is a nearly complete lack of accurate noninvasive methods for quantifying capillary-level perfusion in muscle, so the mechanistic links between impaired perfusion and exercise intolerance are poorly defined and not well understood. As a result, effective therapeutic interventions are limited and too often inadequate. Successful completion of this project will provide researchers and clinicians with a more detailed perspective from which to view these diseases and will have a major impact on the development of improved diagnostic techniques and therapies. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21EB005250-02
Application #
7268090
Study Section
Biomedical Imaging Technology Study Section (BMIT)
Program Officer
Mclaughlin, Alan Charles
Project Start
2006-07-04
Project End
2009-12-31
Budget Start
2007-07-01
Budget End
2009-12-31
Support Year
2
Fiscal Year
2007
Total Cost
$189,345
Indirect Cost
Name
University of Washington
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Marro, Kenneth I; Lee, Donghoon; Shankland, Eric G et al. (2011) Synthetic signal injection using a single radiofrequency channel. J Magn Reson Imaging 34:1414-21
Khokhlova, Tatiana D; Canney, Michael S; Lee, Donghoon et al. (2009) Magnetic resonance imaging of boiling induced by high intensity focused ultrasound. J Acoust Soc Am 125:2420-31
Marro, Kenneth I; Lee, Donghoon; Shankland, Eric G et al. (2008) Synthetic signal injection using inductive coupling. J Magn Reson 194:67-75
Marro, Kenneth I; Lee, Donghoon; Hyyti, Outi M (2007) Nonlinear magnetic field gradients can reduce SAR in flow-driven arterial spin labeling measurements. J Magn Reson 185:94-102