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Investigating Cardiac Metabolism in the Isolated Perfused Mouse Heart with Hyperpolarized [1-13C]Pyruvate and 13C/31P NMR Spectroscopy
Published on: April 21, 2023
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Cardiac metabolic imaging using hyperpolarized [1-13 C]lactate as a substrate
Angus Z Lau1,2, Albert P Chen3, Charles H Cunningham1,2
1Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
NMR in Biomedicine
|May 8, 2021
Summary
Hyperpolarized (HP) [1-13 C]lactate shows promise for cardiac metabolism imaging in large animals, similar to HP [1-13 C]pyruvate. While lactate yielded lower signal-to-noise ratios, its potential for human heart imaging was demonstrated.
Area of Science:
- Medical Imaging
- Metabolic Imaging
- Cardiovascular Research
Background:
- Hyperpolarized (HP) [1-13 C]lactate is a potential alternative to [1-13 C]pyruvate for cardiac metabolism studies.
- HP lactate can be safely administered at higher doses and polarized effectively.
- Previous HP lactate cardiac studies were limited to small animal models.
Purpose of the Study:
- To evaluate HP [1-13 C]lactate as a substrate for cardiac metabolism imaging in a large animal model.
- To compare the performance of HP [1-13 C]lactate with HP [1-13 C]pyruvate in porcine hearts.
Main Methods:
- Utilized dynamic nuclear polarization for substrate polarization.
- Acquired 13 C metabolic images in porcine hearts following injections of HP [1-13 C]lactate and HP [1-13 C]pyruvate.
- Employed hardware and data acquisition methods similar to the first human HP 13 C cardiac study.
Main Results:
- 13 C bicarbonate signal was localized to the myocardium with both substrates.
- No 13 C pyruvate signal was detected after HP 13 C lactate injection.
- HP lactate showed a signal-to-noise ratio of 88% compared to pyruvate.
- Bicarbonate signal SNR was 52% with lactate versus pyruvate, likely due to lactate's shorter T1 and an extra metabolic step.
Conclusions:
- HP [1-13 C]lactate can be successfully used for cardiac metabolism imaging in a large animal model.
- Despite lower SNR, HP lactate demonstrates potential as a clinical substrate for human heart metabolic imaging.
- Further optimization may be needed to overcome SNR limitations for clinical translation.

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