Lipid-induced abnormalities in myocardial function have been implicate
d in a number of ischemic events including the accumulation of lipids
in human myocardium following myocardial infarction. Although animal m
odels have shown the source of these lipids to be triglycerides, the s
pecific species involved has not been identified. In order to better u
nderstand the mechanism(s) defining this lipid accumulation, it follow
s that the identification of the lipids involved may be important in a
chieving this aim. Therefore, this study examined the use of NMR probe
s for delineating the biochemical makeup of the increased H-1 NMR obse
rved lipid signal following myocardial infarction. Specifically, the p
resent study demonstrated the utility of the spin-echo pulse sequence
for the study of alterations in myocardial lipids following ischemic i
njury. Spin-echo spectra allowed the analysis of subsets of lipids wit
hin the large lipid pool inherent in most myocardium. The analyses of
the chemical shifts of the lipid resonances provided a simple yet powe
rful means for deducing lipid class associated with the ischemic injur
y and suggested the species arises predominantly from saturated lipids
. The examination of the CH2/CH3 NMR ratio provided additional informa
tion regarding the species involved, however, because the spin-echo te
chnique was utilized, which may distort certain signal intensities, ca
ution must be exercised in interpreting the specific species involved.
With this in mind, a tentative assignment has been given to octanoic
acid. Finally, a temperature dependence of the lipid signals was noted
and determined to be unique for spin-echo lipid. Although this depend
ence did not provide the necessary information regarding the gel-to-li
quid crystal phase transition temperature which might aid in understan
ding the origin of the lipid species, it did determine that the specie
s involved was only the spin-echo observed lipid and that the dependen
ce was reversible. Finally, the increase in signal intensity associate
d with the spin-echo lipid signal at physiologic temperature may provi
de the necessary means to observe such species utilizing chemical shif
t imaging methods.