We developed a sequence by which T1- and T2*-weighted images can be acquire
d simultaneously and demonstrated its validity for assessing myocardial inj
ury. The interleaved T1-T2* imaging sequence consisted of one preparatory p
ulse (a 90 degrees pulse) and a gradient-echo imaging sequence with a dynam
ically variable echo time varying between 4.2 msec for T1-weighted imaging
and 15 msec for T2*-weighted imaging. The sequence was tested and validated
on isolated blood-perfused pig hearts (n = 4). We found that contrast agen
t-induced T1 and T2* effects,were clearly delineated during the first pass
and steady-state periods of a contrast agent (gadolinium diethylenetriamino
pentaacetic acid). With a bolus injection of contrast agent, the maximum ch
anges in T2* signal intensity occur significantly earlier than the changes
in T1 signal. We also found that the maximum change in T1 signal intensity
during the first pass of contrast agent was significantly gl-eater in a rep
erfused-infarcted region than in normal regions. The suppression of T2* sig
nal was similar in both regions. Ar steady state of contrast agent, T2* sig
nal intensities gradually recovered to a significantly higher- level in the
reperfused-infarcted region than in normal regions. This suggests that the
contrast agent diffused into the intracellular space, indicating the loss
of cell membrane integrity. As a result, T1 signal intensity was also highe
r- in the reperfused-infarcted myocardium than in normal myocardium. T1-and
T2*-weighted images can be acquired simultaneously. The interleaved T1-T2*
sequence is useful in assessing myocardial injury.