G. Ning et al., Magnetic resonance imaging during cerebral hypoxia-ischemia: T-2 increasesin 2-week-old but not 4-week-old rats, PEDIAT RES, 45(2), 1999, pp. 173-179
We investigated whether the changes detectable with magnetic resonance imag
ing techniques during and after an episode of cerebral hypoxia-ischemia dif
fer in immature and older brain. Diffusion weighted (DW) and T-2-weighted (
T2W) images were repeatedly acquired before, during, and after an episode o
f cerebral hypoxia-ischemia (unilateral carotid artery occlusion plus hypox
ia) in 2- and 4-wk-old rats lightly anesthetized with isoflurane, Areas of
increased brightness were detected in DW images from both 2- and 4-wk-old r
ats by 10-20 min after the start of hypoxia. These hyperintense areas incre
ased during hypoxia, comprising 60.8 +/- 4.9% and 30.5 +/- 2.7% of the brai
n image at the level of the thalamus in 2-wk-old and 4-wk-old animals, resp
ectively (p < 0.003). Hyperintense areas (e.g. 27.0 +/- 8.3%) also appeared
in T2W images during hypoxia-ischemia in 2-wk-old animals, but these did n
ot occur in 4-wk-old animals (p < 0.02). This observation was reflected in
T-2, which increased during hypoxia-ischemia in the 2-wk-old but not the 4-
wk-old group. By 60 min after the termination of hypoxia-ischemia in either
age group, areas of hyperintensity resolved and then reappeared 24 h later
on both DW and T2W images. Thus, irrespective of age, magnetic resonance i
maging changes during transient hypoxia-ischemia generally recover with a d
elayed or secondary increase in DW and T2W hyperintensity hours later. Imma
ture brain differs from older brain primarily with respect to some combinat
ion of hypoxic/ischemic cellular or biochemical changes, that are detectabl
e as increases in T-2 within 2-wk-old but not 4-wk-old animals.