Intracellular tetanization with hyperpolarizing currents potentiates synapses formed by mossy fibers on pyramidal cells in hippocampal field CA3 in rats.

Studies on living rat hippocampal slices using point recording in the whole cell configuration addressed the efficiency of the synaptic responses of pyramidal neurons in field CA3 in conditions of minimal stimulation of mossy fibers. Paired-pulse responses were recorded before and after intracellular tetanizing hyperpolarization of pyramidal neurons. In these conditions, potentiation of excitatory synaptic transmission lasting at least 20 min was seen.

[Intracellular tetanization by the hyperpolarizing current potentiates synapses formed by mossy fibers on the pyramidal cells of the CA3 hyppocampal area of the rat].

Whole-cell recordings of excitatory postsynaptic potentials evoked by the minimum stimulation of mossy fiber inputs were performed in CA3pyramidal neurons in rat hippocampal slices. Paired responses were recorded before and after intracellular hyperpolarization tetanization. This procedure produced an increase in excitatory postsynaptic potentials at least for 20-min recording period.

Studies of the synaptic plasticity of field CA3 of the hippocampus during tetanization of the perforant path.

Studies on living slices of hippocampus-entorhinal cortex formation from adult rats were performed to investigate changes in responses in field CA3 to stimulation of mossy fibers in conditions of perforant path tetanization with different parameters. Tetanization of the perforant path at frequencies of 10 and 100 Hz induced depression of responses in CA3 on testing of this same path. Tetanization of the perforant path at a frequency of 10 Hz and an amplitude subthreshold for potentiating mossy fiber synapses in CA3 became threshold if preceded by tetanization of the perforant path at a frequency of 100 Hz.

Stimulation of the lateral hypothalamus provokes the initiation of robust long-term potentiation of the thalamo-cortical input to the barrel field of the adult, freely moving rat.

Long-term potentiation in the thalamo-cortical input to the somatosensory cortex barrel field has been reported to be inducible in vitro only during a narrow critical period of the first postnatal week. Here we explored whether this is due to inability of adult synapses to express LTP or lack of appropriate conditions for LTP induction in slice preparations. We recorded thalamo-cortical field potentials (FPs) from the barrel field of chronically prepared adult rats.