1 Department of Neurosurgery and Physiology, University of Wisconsin, Madison, Wisconsin; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts 02114
The intracranial blood volume and hematocrit of the isolated perfused dog brain preparation were determined with Cr51-labeIed erythrocytes. The intracranial blood volume was determined to be 8.6 ml/100 gm brain (SE±1.2 ml). Over the range of perfusing hematocrits studied, the relationship of perfusing hematocrit (HctPR) to intracranial hematocrit (HctIC) was found to be a linear function (HctIC = 5.44 + 0.702 HctPR). At a peripheral hematocrit of 20% the HctIC/HctPR With increasing perfusing hematocrits the carotid artery pressure rose markedly and there was flattening of the EEG. Since the isolated dog brain is a closed system void of extracranial anastomoses, high viscosity blood cannot circumvent the cerebral circulation but must follow the high resistance networks of the deep cerebral vasculature until sludging of the erythrocytes becomes sufficient to cause anoxia and loss of autoregulation. In the intact erythrocythemic animal, however, increases in arteriolar pressure can be reflected downstream to the large cerebral and meningeal vessels with extracranial shunting of high hematocrit (high viscosity) blood from the brain.
© 1970 American Heart Association, Inc.
Blood Volume, Hematocrit and Pressure Relationships in the Isolated Perfused Dog Brain
2 University of Wisconsin Medical School, Madison, Wisconsin, 53706
1.0, whereas at hematocrits of 50 to 55% this ratio dropped to 0.87.
Key Words: erythrocythemia isotope-labeled erythrocytes extracranial shunts increased carotid artery pressure
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