The Effect of Prosopis farcta and Its Bioactive Luteolin on the Hippocampus of Mice after Induced Ischemia Reperfusion

Figure 5

Immunofluorescence staining of neuron marker. (a) (DCX), (b) NeuN, and (c) mean of the percentage of immunopositive cells. Immunofluorescence assay was performed for DAPI (A), DCX, NeuN (B), and MERGE (C) in CA1 hippocampal brain incisions in different groups on day 57 (a, b); (SH + NE) sham not exercised, (SH + E) exercised sham, (SH + EX) sham-treated with Prosopis farcta extract, (SH + LU) sham-treated with luteolin, (IS + NE) not exercised ischemia, (IS + E) exercised ischemia, (IS + EX) ischemia treated with Prosopis farcta extract, and (IS + LU) ischemia treated with luteolin. ^∗P < 0.01 vs SH + NE, ^∗∗P < 0.001 vs SH + NE.