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Accelerated dual-contrast first-pass perfusion MRI of the mouse heart: development and application to diet-induced obese mice.

Authors :
Naresh NK
Chen X
Roy RJ
Antkowiak PF
Annex BH
Epstein FH
Source :
Magnetic resonance in medicine [Magn Reson Med] 2015 Mar; Vol. 73 (3), pp. 1237-45. Date of Electronic Publication: 2014 Apr 23.
Publication Year :
2015

Abstract

Purpose: Gene-modified mice may be used to elucidate molecular mechanisms underlying abnormal myocardial blow flow (MBF). We sought to develop a quantitative myocardial perfusion imaging technique for mice and to test the hypothesis that myocardial perfusion reserve (MPR) is reduced in a mouse model of diet-induced obesity (DIO).<br />Methods: A dual-contrast saturation-recovery sequence with ky -t undersampling and a motion-compensated compressed sensing reconstruction algorithm was developed for first-pass MRI on a small-bore 7 Tesla system. Control mice were imaged at rest and with the vasodilators ATL313 and Regadenoson (n = 6 each). In addition, we imaged mice fed a high-fat diet (HFD) for 24 weeks.<br />Results: In control mice, MBF was 5.7 ± 0.8 mL/g/min at rest and it increased to 11.8 ± 0.6 mL/g/min with ATL313 and to 10.4 ± 0.3 mL/g/min with Regadenoson. In HFD mice, we detected normal resting MBF (5.6 ± 0.4 versus 5.0 ± 0.3 on control diet), low MBF at stress (7.7 ± 0.4 versus 10.4 ± 0.3 on control diet, P < 0.05), and reduced MPR (1.4 ± 0.2 versus 2.0 ± 0.3 on control diet, P < 0.05).<br />Conclusion: Accelerated dual-contrast first-pass MRI with motion-compensated compressed sensing provides spatiotemporal resolution suitable for measuring MBF in free-breathing mice, and detected reduced MPR in DIO mice. These techniques may be used to study molecular mechanisms that underlie abnormal myocardial perfusion.<br /> (© 2014 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1522-2594
Volume :
73
Issue :
3
Database :
MEDLINE
Journal :
Magnetic resonance in medicine
Publication Type :
Academic Journal
Accession number :
24760707
Full Text :
https://doi.org/10.1002/mrm.25238