Ischaemia is the final common pathway of brain cell death following a varie
ty of insults. We consider the effect of cerebral ischaemia on gene express
ion, concentrating on immediate early genes, those encoding heat shock prot
eins, growth factors, cytokines, adhesion molecules, nitric oxide synthase
and proteins involved in programmed cell death. We conclude that the change
s in gene expression resulting from ischaemia are important determinants of
neuronal and glial survival. In the future it may become possible to manip
ulate gene expression to limit the extent of damage arising from cerebral i
schaemia.