Background and Purpose: Our purpose was to characterize the surface ar
ea of the infarct and the surface area at risk of infarction as define
d spatially by arterial anastomoses to determine whether position, siz
e, or shape of the infarct and the area at risk were related in stroke
-prone rats or hybrid rats. Methods: Stroke-prone rats (n=18; mean+/-S
EM blood pressure, 182+/-8 mm Hg) and hybrid rats (n=18; mean+/-SEM bl
ood pressure, 147+/-6 mm Hg; p<0.05) were anesthetized and the left mi
ddle cerebral artery was occluded with a ligature. The rats were kille
d 7 days later, arterial anastomoses were made visible with latex, the
brains were fixed in formalin, and film recorded the infarct and anas
tomoses. Anastomoses and infarcts were digitized for measurements of r
isk area, luminal width, and infarct area. Results: Mean risk area was
similar in size, length, width, and variability in stroke-prone rats
(area, 85+/-5 mm2) and hybrid rats (area, 84+/-7 mm2; p>0.05), whereas
mean infarct area was larger, longer, wider, and less variable in str
oke-prone rats (area, 53+/-6 mm2) than in hybrid rats (area, 15+/-11 m
m2; p<0.05). Infarct length was appreciably greater than infarct width
in both groups, indicating that infarct shape was not amorphous. Spat
ial overlap maps indicated that the infarct area common to all stroke-
prone rats was positioned centrally in the risk area and was surrounde
d by a variable infarct area, which indicated that the likelihood of i
nfarction increased with distance from the anastomoses. Shape factors
for both risk area and infarct area were significantly different withi
n each rat group, which indicated that infarct shape did not uniformly
parallel the anastomotic sites that determined risk area shape (p<0.0
5). Risk area anastomoses and border zone width were linearly correlat
ed in size and both were significantly wider in hybrid rats than in st
roke-prone rats (p<0.05), which suggests that the narrower border zone
tissue was perfused by narrower anastomoses. Conclusions: We conclude
that the position of the infarct within the risk area relates to lumi
nal widths of conterminous anastomoses that define the risk area, but
not to the size or shape of the area at risk of infarction defined spa
tially by the anastomoses.