Table 1.
Brain areas | NeuN* (%) | Hoechst* (%) | HMGB1* (%) | Nissl* (%) | |
---|---|---|---|---|---|
Poorly-perfused brain | parietal cortex | 46 ± 2 | 31 ± 3 | 41 ± 5 | 36 ± 5 |
hind- and forelimb areas of cortex | 43 ± 5 | 34 ± 4 | 39 ± 6 | 32 ± 4 | |
preoptic area (medial and lateral) | 55 ± 4 | 34 ± 4 | 32 ± 5 | 36 ± 2 | |
Well-perfused brain | parietal cortex | 5 ± 1 | 1 ± 0 | 2 ± 1 | 5 ± 0 |
hind- and forelimb areas of cortex | 6 ± 1 | 2 ± 1 | 3 ± 1 | 6 ± 1 | |
preoptic area (medial and lateral) | 3 ± 1 | 2 ± 0 | 3 ± 1 | 5 ± 1 |
In one subcortical and two cortical areas the average percentage of abnormally stained donut-like nuclei are given for poorly-perfused (6 mice) and well-perfused (4 mice) brains with different markers. For Nissl staining, the numbers refer to the ratio of dysmorphic neurons surrounded by swollen astrocyte end-feet to total cell nuclei in the contralateral hemisphere embedded in paraffin. NeuN staining gives a higher ratio because it shows the proportion of donut-stained neurons to total number of neurons unlike other markers, which give the ratio of donuts to the total nuclei including glial cells. Data are expressed as mean (percentage) ± standard error of mean (SEM). *p < 0.05 when poorly- and well-perfused groups compared. Brain anatomical areas are defined at the level of the anterior commissure according to Garcia et al.2.