Stroke, Vol 9, 165-168, Copyright © 1978 by American Heart Association
BH Cook, HJ Granger, DN Granger, AE Taylor and EE Smith
Intriguing questions have recently been raised regarding the applicability
of direct observations of the pial microcirculation to the behavior of the
total cerebral microcirculation. Operating under the assumption that
arteriolar tone and, thus, cerebrovascular resistance is, to some extent,
directly related to the intrinsic energy metabolism of the arteriolar wall,
a comparative histochemical analysis of cerebral microvessels, both pial
and parenchymal, was undertaken. Reactions were chosen on the bases of
representation of substrate and of enzymes of glycolysis, the hexose
monophosphate shunt, beta- oxidation of fat, Krebs cycle, cytochrome system
and ATP hydrolysis. Three metabolically distinct segments of the cerebral
microvasculature were delineated with the pial vessels showing strong
capacities for glycolysis, beta-oxidation of fats and utilization of
glucose through the hexose monophosphate shunt. Microvessels of the gray
matter have a qualitatively similar metabolic profile but the capacities of
each pathway are lower when compared to pial arterioles. Arterioles of the
white matter demonstrate the weakest energy-yielding capacities.
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