Flt-1 baseline level of CA1 and CA2 neurons occupied the intermediary position relative to CA3 and DG; CA1 and CA2 neurons showed quite the same baseline distribution pattern of Flt-1. In all four regions the expression of Flt-1 at basal level was visibly higher in P14 rats than in 8–10 wks rats. In Venetoclax datasheet animals of both ages i.p.-injected with PNV there was immediate upregulation of the level of Flt-1 expression in all the four hippocampal regions studied. CA1 and DG were the regions with most dramatic rise of Flt-1 expression 1 h after injection: Flt-1 level of PNV-exposed rats was upregulated by 90% in CA1, 135% in DG whereas CA2 and CA3 just showed a trend for rising. Also, it is of interest to observe
that CA1 and DG neurons of animals of both ages displayed a similar time-course changes of the VEGF’s Flt-1 receptor density of pixels (compare Fig. 4A and D). Likewise, neurons of CA2 and CA3 in animals of both ages showed quite the same pattern of time-course changes in their immunolabeling (compare Fig. 4B and C). In animals of both ages, the neurons of CA2 were the least susceptible to change the expression of Flt-1 receptor (Fig. 4B). The two-way analysis of variance showed that there was interaction between time after PNV injection versus age of animals for CA3 and DG in relation to the expression of the receptor. The Flt-1 expression was
influenced by the two variables “time after envenoming” and “age of animals” in all the four regions scanned. To investigate a potential involvement of the vascular endothelial growth factor (VEGF) in the neurotoxic effects caused by P. nigriventer venom in the hippocampus, selleck kinase inhibitor we analyzed whether the expression of VEGFR-1, also named Flt-1, was changed after i.p. administration of venom. Using immunohistochemistry for the Flt-1 it was possible to determine that neurons were the principal cells constitutively expressing the receptor and that anti-Flt-1 was immunodetected in the nucleus of neurons; by immunohistochemistry labeling the distribution
and expressional level of Flt-1 was demonstrated in all the four selected regions of the hippocampus: CA1, CA2, CA3 and DG. Nuclear location of Flt-1 has been found in the dorsal root Vitamin B12 ganglion sensory neurons ( Dhondt et al., 2011), ventral root motor neurons ( Poesen et al., 2008), and lumbar motor neurons ( Islamov et al., 2004) and others. In hippocampus, Flt-1 mRNA is restricted to pyramidal neurons of CA regions and granular neurons of DG ( Choi et al., 2007). In all these regions the upregulation of Flt-1 has been associated with neuroprotective signals mediating VEGF effects in different injury conditions. Herein, the investigation was focused on hippocampus as one of the brain regions particularly targeted by PNV as has been shown by our laboratory (Le Sueur et al., 2003; Rapôso et al., 2007; da Cruz-Höfling et al., 2009). These previous studies have shown that the i.v.
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