Disturbance of calcium homeostasis and unregulated increase in intrace
llular calcium have been implicated in cell damage and cell death in t
he central nervous system in particular. To determine the specific pat
hway(s) of cerebral Ca transport of importance in a pathophysiological
situation, we have measured long term Ca flux in brain in vivo in rat
, and developed a kinetic model incorporating physiologically relevant
pathways of cerebral Ca transport Ca-45 was injected into a rail vein
in conscious rats. plasma Ca was monitored up to 4 days post-injectio
n and Ca-45 uptake determined in samples of cerebrospinal fluid (CSF)
and at several sites of brain at euthanasia. Uptake of the tracer by t
issues peaked after 1 h, isotopic equilibration taking longer. The upt
ake at hippocampus was the highest. Computer simulation of the kinetic
s of the plasma, CSF and tissue data was performed using a compartment
al model, which included two subcompartments (intra- and extra-cellula
r) and two pathways from plasma to the brain: directly across the bloo
d-brain barrier and via CSF, which included a delay. The analysis base
d on this model enabled estimation of the fractional rates of transpor
t of Ca to cerebral and noncerebral tissues across all the barriers of
the model.