In vivo proton T1 relaxation times of mouse myocardial metabolites at 9.4 T

Magn Reson Med. 2015 Jun;73(6):2069-74. doi: 10.1002/mrm.25340. Epub 2014 Jun 24.

Abstract

Purpose: Proton magnetic resonance spectroscopy ((1) H-MRS) for quantitative in vivo assessment of mouse myocardial metabolism requires accurate acquisition timing to minimize motion artifacts and corrections for T1 -dependent partial saturation effects. In this study, mouse myocardial water and metabolite T1 relaxation time constants were quantified.

Methods: Cardiac-triggered and respiratory-gated PRESS-localized (1) H-MRS was employed at 9.4 T to acquire signal from a 4-µL voxel in the septum of healthy mice (n = 10) while maintaining a steady state of magnetization using dummy scans during respiratory gates. Signal stability was assessed via standard deviations (SD) of zero-order phases and amplitudes of water spectra. Saturation-recovery experiments were performed to determine T1 values.

Results: Phase SD did not vary for different repetition times (TR), and was 13.1° ± 4.5°. Maximal amplitude SD was 14.2% ± 5.1% at TR = 500 ms. Myocardial T1 values (mean ± SD) were quantified for water (1.71 ± 0.25 s), taurine (2.18 ± 0.62 s), trimethylamine from choline-containing compounds and carnitine (1.67 ± 0.25 s), creatine-methyl (1.34 ± 0.19 s), triglyceride-methylene (0.60 ± 0.15 s), and triglyceride-methyl (0.90 ± 0.17 s) protons.

Conclusion: This work provides in vivo quantifications of proton T1 values for mouse myocardial water and metabolites at 9.4 T.

Keywords: 1H-MRS; PRESS; metabolite T1 relaxation; mouse heart; myocardial metabolism; saturation-recovery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiac-Gated Imaging Techniques
  • Electrocardiography
  • Mice
  • Mice, Inbred C57BL
  • Myocardium / metabolism*
  • Proton Magnetic Resonance Spectroscopy / methods*
  • Respiratory-Gated Imaging Techniques