Stroke, Vol 16, 121-125, Copyright © 1985 by American Heart Association
B Jeynes
This study was undertaken to examine some of the quantitative and
qualitative changes which might occur in the cerebral granular pericyte
population when comparing control and embolically stressed animals. Eight
animals, male NZW 2-2.5 kg rabbits, were given intracarotid sublethal
injections of human atheroma concentrated at 125 mg/ml. Eight others
received 1 cc of sterile saline. Two hours after injection the brains were
fixed with either neutral buffered formalin or 3% buffered glutaraldehyde
by cardiac perfusion at 110 mmHg pressure. The brains were removed and
sliced, anteroposteriorly, in 3 mm slices. Each slice from five brains for
each condition was then processed for paraffin sectioning and staining with
Hematoxylin and PAS. Two animals for each condition underwent the same
treatments and were processed for frozen sectioning and staining with Oil
Red O. One animal for each condition had each brain slice sectioned by
vibratome (40 micrometers) and was processed appropriately and examined by
either fluorescence microscopy, standard electron microscopy or acid
phosphatase electron microscopy. In the groups stained with Hematoxylin and
PAS, granular pericytes were counted for each of the first five levels of
each brain for both the control and experimental conditions. The results of
this study reconfirmed that these cells were granular pericytes; that is,
they were autofluorescent and PAS positive; were surrounded by a basement
membrane, were acid phosphatase positive and contained a heterogenous
granular cytoplasmic inclusion population. Further, after ischemic insult,
the number of granular pericytes increased significantly at two hours. It
was also shown that these cells appeared capable of accumulating lipid
components of the injected atheroma from the vessel lumen.
ARTICLES
Reactions of granular pericytes in a rabbit cerebrovascular ischemia model
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