TY - JOUR
T1 - In vivo proton T1 relaxation times of mouse myocardial metabolites at 9.4 T
AU - Bakermans, Adrianus J.
AU - Abdurrachim, Desiree
AU - Geraedts, Tom R.
AU - Houten, Sander M.
AU - Nicolay, Klaas
AU - Prompers, Jeanine J.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - Purpose Proton magnetic resonance spectroscopy (1H-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 1H-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. Magn Reson Med 73:2069-2074, 2015.
AB - Purpose Proton magnetic resonance spectroscopy (1H-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 1H-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. Magn Reson Med 73:2069-2074, 2015.
KW - <sup>1</sup>H-MRS
KW - metabolite T<inf>1</inf> relaxation
KW - mouse heart
KW - myocardial metabolism
KW - PRESS
KW - saturation-recovery
UR - http://www.scopus.com/inward/record.url?scp=84929643546&partnerID=8YFLogxK
U2 - 10.1002/mrm.25340
DO - 10.1002/mrm.25340
M3 - Article
C2 - 24962369
AN - SCOPUS:84929643546
SN - 0740-3194
VL - 73
SP - 2069
EP - 2074
JO - Magnetic Resonance in Medicine
JF - Magnetic Resonance in Medicine
IS - 6
ER -