PKA drives an increase in AMPA receptor unitary conductance during LTP in the hippocampus
Pojeong ParkiD, John GeorgiouiD, Thomas M. SandersoniD, Kwanghee KoiD, Heather KangiD, Ji‐il KimiD, Clarrisa A. BradleyiD, Zuner Assis BortolottoiD, Min ZhuoiD, Bong‐Kiun KaangiD, Graham L. CollingridgeiD
Abstract
Long-term potentiation (LTP) at hippocampal CA1 synapses can be expressed by an increase either in the number (N) of AMPA (-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid) receptors or in their single channel conductance ({gamma}). Here we have established how these distinct synaptic processes contribute to the expression of LTP in hippocampal slices obtained from young adult rodents. LTP induced by compressed theta burst stimulation (TBS), with a 10 s inter-episode interval, involved purely an increase in N (LTPN). In contrast, either a spaced TBS, with a 10 min inter-episode interval, or a single TBS, delivered when PKA was activated, resulted in LTP that was associated with a transient increase in {gamma} (LTP{gamma}). This {gamma} increase was due to the insertion of calcium-permeable (CP)-AMPA receptors. Activation of CaMKII was necessary and sufficient for LTPN whilst PKA was additionally required for LTP{gamma}. Thus, two mechanistically distinct forms of LTP co-exist at these synapses.
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