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Biomedical subjects

J E Guinane

Publications and source records attributed to J E Guinane.

3 recordsLinked to original sources

Why does hydrocephalus progress?

Experimental results in rabbits support the hypothesis that occlusion of the cerebral subarachnoid space, resulting in an increased strain-stress ratio in the ventricular wall, is the mechanical basis of chronic progressive hydrocephalus within a rigid skull. When the cerebral subarachnoid space was drained through an artificial low-resistance fluid pathway, the wall of the olfactory ventricle showed edema that was indistinguishable from the edema of kaolin hydrocephalus. Increased CSF pressure did not produce edema of this grade when the cerebral subarachnoid space was patent. When the subarachnoid space surrounding the right olfactory bulb was occluded with silicone rubber, the right but not the left olfactory ventricle enlarged; resistance to cerebrospinal fluid absorption remained normal.

Animals

Cerebrospinal fluid pressure in mannitol-treated rabbits.

Equations describing the response of cerebrospinal fluid (CSF) pressure to a rapid intravenous injection of mannitol were developed by combining equations of membrane transport with equations of CSF hydrodynamics. The physiologic variables appearing in these equations were measured in anesthetized rabbits as brain water volume = 7.9 cm3, plasma osmolality = 308 mmol/kg, fractional total body water content = 0.62, time constant of blood-brain osmotic flow = 32 min, resistance to CSF absorption = 1.92 TPa-s/m3 and brain compliance = 0.173 mm3/Pa. Mannitol (5.5-27.5 mmol/kg) was administered intravenously to anesthetized rabbits while Elliott's B solution was infused (0.13-1.27 mm3/sec) into a lateral ventricle to simulate formation of CSF. Measured CSF pressure changes corresponded closely with those predicted by theory.

Animals

Cerebrospinal fluid pulse pressure and brain compliance in adult cats.

Cerebrospinal fluid (CSF) pulse pressure was inversely proportional to a brain compliance determined from artificial CSF pulsations generated by an external pump. Brain compliance was 0.71 cu mm/mm H2O at steady-state CSF mean pressure and decreased 50 percent for each 240 mm H2O increase in CSF mean pressure (mean results of duplicate experiments on 10 adult cats). Both CSF pulse pressure and the time course of transient changes in CSF mean pressure could be described in terms of a model of the CSF circulation consisting of a constant resistance to CSF absorption in parallel with a pressure-dependent brain compliance.

Animals