Objective: Ischemic lesions seen on diffusion-weighted imaging (DWI) are re
versible if reperfusion is performed within minutes after the onset of isch
emia. This study was designed to determine whether acute reversibility of D
WI abnormalities is transient following brief temporary focal brain ischemi
a and to characterize the temporal evolution of in vivo ischemic lesions. M
et hods: Eight rats were subjected to 30 minutes of temporary middle cerebr
al artery occlusion and underwent diffusion-, perfusion-, and T2-weighted M
RI during occlusion; immediately after reperfusion; 30, 60, and 90 minutes
after reperfusion; and 12, 24, 48, and 72 hours after reperfusion. Average
apparent diffusion coefficient (ADC(av)) values and the cerebral blood flow
index (CBFi) ratio were calculated in both the lateral caudoputamen and ov
erlying cortex at each time point. The size of the in vivo ischemic abnorma
lities was calculated from the ADC(av) and the T2 maps. Postmortem tripheny
ltetrazolium chloride (TTC) staining was used to verify ischemic injury. Re
sults: Both the CBFi ratio and ADC(av) values declined significantly in the
two regions during occlusion. The CBFi ratio recovered immediately after r
eperfusion and remained unchanged over 72 hours. However, ADC(av) values re
turned to normal at 60 to 90 minutes and secondarily decreased at 12 hours
after reperfusion as compared with those in the contralateral hemisphere. T
he extent of the in vivo ischemic lesions maximized at 48 hours and was hig
hly correlated with TTC-derived lesion size. Conclusions: Acute recovery of
initial ADC(av)-defined lesions after reperfusion is transient, and second
ary ADC(av)-defined lesions develop in a slow and delayed fashion.