Future behavioral studies may help differentiate effects on memory versus emotional function

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mg/kg Apalutamide rapamycin shown reduced quantity of crossings (A), 649735-46-6 increased fecal pellets (B), retention time in the central spot (C) and freezing time (D). n = 15 rats/ group.We also assessed the effect of rapamycin treatment on the development of late progenitors (DCX-expressing cells) after 4 weeks of rapamycin treatment. Similar to other findings in the present study, rapamycin at the dose of 0.3 mg /kg had no obvious effect on the DCX-positive cells, whereas 1.0 and 3.0 mg/kg rapamycin markedly decreased the DCX-positive cells in dentate gyrus in hippocampus (Fig 8). Therefore treatment with rapamycin at an early age decreased the development of late progenitor cells, which may exert adverse effects on development and subsequently affect cognition.Fig 7. Long-term treatment with rapamycin results in decrease in cellular immune factors. Rats of 2 weeks of age were administrated different doses of rapamycin for 4 weeks and sacrificed. Cortical brain tissue (A, C, E, G) and blood (B, D, F, H) were collected and used for ELISA examination of Il-1, IL-2, IFN- and TNF-. No obvious change was noted among different groups in Il-1 both in brain and blood (A,B). IL-2 was decreased with 1.0 and 3.0 mg/kg rapamycin treatment both in brain and blood (C, D). IFN- was only decreased with 3.0 mg/kg rapamycin treatment both in brain and blood (E, F). All rapamycin-treated groups exhibited a decrease in TNF- in brain (G), while the decrease was only shown in 3.0 mg/kg of rapamycin treatment in blood (H). p

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