Background: Considering the increased activity of hypothalamic orexinergic neurons due to morphine administration, and its extensive projections to the hippocampus, it is probable that morphine effect on CA1 neuronal function is mediated by orexinergic system. So the effect of hippocampal orexin-1 receptors (OX1R) blockade on CA1 baseline synaptic response and short term synaptic plasticity was investigated.

Materials and Methods: In this experimental study, animals received morphine 10 mg/kg/12h/(SC) for 10 days. SB-334867-A, OX1R antagonist (0.5&mug/0.5 &mul), was microinjected intrahippcampally for OX1R inhibition before each morphine injection. Baseline synaptic response and short term synaptic plasticity were evaluated by field potential recording. fEPSP was recorded from CA1 following Schaffer collaterals stimulation. After Input/Output construction, short term synaptic plasticity was induced by paired pulse stimulations.

Results: Chronic use of morphine did not affect the baseline synaptic response (p>0.05). SB- 334867-A microinjection in CA1 did not have any effect on baseline synaptic response in morphine dependent rats. Morphine increased paired pulse index (PPI) at 80 ms inter pulse interval (IPI, p<0.05). SB-334867-A pretreatment did not affect this morphine induced PPI change.

Conclusion: The results suggest that orexin-1 receptors (OX1R) do not mediate the effect of morphine on baseline synaptic response and short term synaptic plasticity in CA1 area of the hippocampus.

Background: Environmental signals have a crucial role in development of brain’s structure and function during critical period of brain development. Gt was valuated the devebpmental effeck in developmental effect of visual deprivation on synaptic plasticity of Dentate Gyrus neurons was evaluated.

Materials and Methods: This experimental study was carried on 2 groups (n=48) rats kept in standard 12-hour light/dark condition (Light Reared-LR) or in complete darkness (Dark Reared-DR) since birth throughout the study. Each group, in turn, was divided into 3 groups of 2, 6 and 10 weeks old subgroup (n=8 for each). Stimulating the perforant path, field potentials were recorded in the Dentate Gyrus area for 30 minutes. Then, the tetanic stimulation was applied to the Schaffer collaterals and the field potentials were pooled for 120 minutes post-tetanus in all animals.

Results: The basic responses of the LR animals decreased and the amplitude of the DR rats increased, across aging. After the LTP induction, amplitude of responses increased in all groups but the amount and stability of them were lower dark reared in animals than the LR ones.

Conclusion: Change in environmental visual signals impairs basic response and LTP induction in neurons of Dentate Gyrus area of hippocampus.