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2-Vessel Occlusion/Hypotension: A Rat Model of Global Brain Ischemia
Published on: June 22, 2013
Interrelations between nuclear-factor kappa B activation, glial response and neuronal apoptosis in gerbil hippocampus
K Domańska-Janik1, A Bronisz-Kowalczyk, H Zajac
1Laboratory of Molecular Neuropathology, Medical Research Centre, Polish Academy of Sciences, 5 Pawiński St., 02-106 Warsaw, Poland. kd-j@cmdik.pan.pl.
Abstract:
Spatial and temporal relations between transcriptional factor NF kappa B activation and glia reaction in gerbil hippocampus after transient cerebral ischemia has been studied. Activation of protein binding to NF kappa B consensus oligonucleotide was determined by electrophoretic mobility gel shift assay (EMSA) in homogenates from dorsal (DP- an equivalent of CA1 sector) and abdominal (AbP- containing CA2-4 and gyrus dentatus) parts of hippocampus. A significant activation of NF kappa B binding was observed exclusively in DP as early as 3 h after ischemia and at this time that response preceded any other morphological signs of postischemic tissue injury. This early enhancement of NF kappa B binding was followed by microglia activation visualized in CA1 pyramidal region at 24 h of recovery by histochemical staining with lectin from Ricinus communis (RCA-120). Simultaneously, only a moderate increase of immunostaining against glial fibrillary acidic protein (GFAP) was observed homogeneously in all parts of hippocampus. This uniform pattern of astrogliosis was preserved until postischemic day 3-4, when apoptotic DNA fragmentation in CA1 pyramidal neurons had been clearly documented by TUNEL staining. At this period however, continuous elevation of NF kappa B binding in DP corresponded with similar response manifested also in AbP of the hippocampus. These results evidence a preferential NF kappa B involvement in an early microglia activation in the apoptogenic CA1 sector, although its role in a later astrocytic response to ischemia could not be neglected too.

