Figure 5
From: Selection of reference genes for quantitative real-time PCR in a rat asphyxial cardiac arrest model
Immunofluorescence staining of the hippocampus. In sham-operated animals (A), the hippocampus appeared intact on NeuN immunostaining 21 day post insult. Asphyxia-exposed animals (B), however, showed a significant decrease of NeuN immunopositive cells, particularly prominent in the CA1 and dentate gyrus regions. In parallel, OX42-immunocytostaining (red) revealed a massive microgliosis in the CA1 region (D) when compared to sham-operated animals (C). C, D: MAP2 counter stained, bar = 400 μm.