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                <text>Two components of long-term potentiation induced by different patterns of afferent activation.</text>
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                <text>2-Amino-5-phosphonovalerate/*pharmacology; Afferent Pathways/physiology; Animals; Calcium/*physiology; Hippocampus/*physiology; In Vitro Techniques; Membrane Potentials; Memory/*physiology; N-Methyl-D-Aspartate/*physiology; Neuronal Plasticity; Receptors; Synaptic Transmission; Time Factors</text>
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                <text>Grover L M; Teyler T J</text>
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                <text>Long-term potentiation (LTP) of excitatory synaptic transmission could be a mechanism underlying memory. Induction of LTP requires Ca2+ influx into postsynaptic neurons through ion channels gated by NMDA (N-methyl-D-aspartate) receptors in hippocampus (area CA1 and dentate gyrus) and neocortex. Here we report that a component of LTP not requiring the activation of NMDA receptors can be induced in area CA1. The component is dependent on tetanus frequency, requires increases in postsynaptic intracellular Ca2+ concentrations, and is suppressed by an antagonist of voltage-dependent Ca2+ channels.</text>
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              <text>&lt;a href="http://doi.org/10.1002/hipo.450040602" target="_blank" rel="noreferrer noopener"&gt;http://doi.org/10.1002/hipo.450040602&lt;/a&gt;</text>
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                <text>Multideterminant role of calcium in hippocampal synaptic plasticity.</text>
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                <text>Hippocampal CA1 cells possess several varieties of long-lasting synaptic plasticity: two different forms of long-term potentiation (LTP) and at least one form of long-term depression (LTD). All forms of synaptic plasticity are induced by afferent activation, all involve Ca2+ influx, all can be blocked by Ca2+ chelators, and all activate Ca(2+)-dependent mechanisms. The question arises as how different physiological responses can be initiated by activation of the same second messenger. We consider two hypotheses which could account for these phenomena: voltage-dependent differences in cytosolic Ca2+ concentration acting upon Ca2+ substrates of differing Ca2+ affinities and compartmentalization of the Ca2+ and its substrates.</text>
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                <text>&lt;a href="http://doi.org/10.1002/hipo.450040602" target="_blank" rel="noreferrer noopener"&gt;10.1002/hipo.450040602&lt;/a&gt;</text>
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