L. Covolan et Leam. Mello, Temporal profile of neuronal injury following pilocarpine or kainic acid-induced status epilepticus, EPILEPSY R, 39(2), 2000, pp. 133-152
Systemic administration of pilocarpine and kainic acid (KA) has been extens
ively used to model temporal lobe epilepsy in rats. Here the regional distr
ibution of selectively vulnerable neurons and the temporal evolution of suc
h neuronal injury after status epilepticus (SE) are compared in both models
. Using the silver staining technique of Gallyas, argyrophilic neurons were
measured on a 0-3 (least-most) scale in 53 different brain areas. Few neur
ons were silver-stained 2.5 h after kainate-induced SE, but many silver-sta
ined cells could be seen in most neocortical, hippocampal, amygdaloid and h
ypothalamic structures for pilocarpine group. In general, 8 or 24 h interva
ls between SE onset and perfusion times yielded the most intense neuronal s
ilver-impregnation. Pilocarpine-induced neuronal silver impregnation was mo
re prominent than that induced by kainate treatment for many areas in corte
x, hippocampus. endopiriform nucleus, amygdaloid complex and hypothalamus.
On the other hand, in the thalamus, some cortical areas, claustrum, lateral
septum and caudoputamen, kainate-induced neuronal silver staining was also
prominent, but occurred later than in pilocarpine-treated animals. Neurona
l injury was found in almost the same brain areas in both models of SE but
with different intensity levels and time course profiles. It was suggested
that such differences in the temporal profile of cell damage should be take
n into account when searching for neuroprotective agents. (C) 2000 Elsevier
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