We assessed cytochrome oxidase (CytOx) staining in sham-operated contr
ol piglets and in piglets subjected to 30 minutes of cerebral hypoxia-
ischemia (H-I) plus 4 hours of reperfusion (REP). The I-day-old piglet
s were sedated, anesthetized, and ventilated. Cerebral blood flows (CB
Fs) were quantitated using microspheres. H-I was induced by a combinat
ion of phlebotomy and cervical tourniquet; the brain was reperfused fo
r four hours after 30 minutes of H-I. CBF was reduced during ischemia
in experimental animals from 42+13 to 12+5 ml/min/100g. CytOx staining
of hippocampal sections from 3 control and 3 experimental animals was
compared. The staining of the stratum pyramidale neurons of the same
portion of the CA1 sector in a single high power field was assessed in
a blinded fashion in 4 corresponding sections from each animal, and g
raded from 0=no staining to 3=heavy staining. The results were compare
d using one-way analysis of variance. Cells with grade 3 staining were
significantly more numerous in controls compared to H-I/REP animals (
p=0.03). There were significantly more cells with no CytOx staining in
the experimental animals (p=0.01). These findings suggest that CytOx
staining in newborn piglet CA1 is a reliable method of assessing cell
dysfunction after H-I.