Ea. Irving et al., Decreased nuclear factor-kappa B DNA binding activity following permanent focal cerebral ischaemia in the rat, NEUROSCI L, 288(1), 2000, pp. 45-48
Many factors implicated in the pathogenesis of cerebral ischaemia such as g
lutamate, tumour necrosis factor and interleukin-1 have a Iso been shown to
activate nuclear factor-kappa B (NF-kappa B). In the present study we have
investigated NF-kappa B activity at various times following permanent foca
l cerebral ischaemia in rats using immunohistochemistry, western blotting a
nd electrophoretic mobility sh ift assay (EMSA). Three hours following midd
le cerebral artery occlusion nuclear translocation of NF-kappa B was detect
ed using immunohistochemical and western blotting techniques. This was refl
ected in a trend towards increased NF-kappa B binding activity (EMSA) in th
e ischaemic cortex compared to histologically normal tissue. In contrast ho
wever, from 6 to 48 h post-occlusion nuclear translocation and NF-kappa B b
inding activity was decreased in the ischaemic cortex. Decreased NF-kappa B
binding activity detected in degenerating neurones, suggests that decrease
d NF-kappa B activity may exacerbate ischaemia induced neuronal cell death.
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