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. 2004 Jan 7;24(1):257–268. doi: 10.1523/JNEUROSCI.4485-03.2004

Figure 2.


Figure 2.

PGE2 is neuroprotective in cultured hippocampal neurons but not in organotypic hippocampal slices. A, PGE2 administration at submicromolar concentrations promotes protection in hippocampal cultures stimulated with glutamate (100 μm) for 24 hr (n = 4 wells per condition; *p < 0.02; **p < 0.01; representative of 3 experiments). B, Increasing concentrations of PGE2 had no effect on neuronal viability when assayed in organotypic hippocampal slices treated with 1 hr NMDA (10 μm), suggesting a negative effect of PGE2 at the level of astrocytes in neutralizing the protective effects of PGE2 on pure hippocampal cultures. Neuronal death in CA1 is measured by percentage of maximal PI fluorescence (n = 10-15 slices per condition; n = 6 experiments). Concentrations of PGE2 were used at submicromolar concentrations to avoid the cross-activation of other PG receptors at higher concentrations (Breyer et al., 2001).