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J Neurophysiol 100: 2605-2614, 2008. First published September 17, 2008; doi:10.1152/jn.90476.2008
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AMPA Silencing Is a Prerequisite for Developmental Long-Term Potentiation in the Hippocampal CA1 Region

Therése Abrahamsson, Bengt Gustafsson and Eric Hanse

Department of Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

Submitted 17 August 2008; accepted in final form 9 September 2008

AMPA ({alpha}-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) unsilencing is an often proposed expression mechanism both for developmental long-term potentiation (LTP), involved in circuitry refinement during brain development, and for mature LTP, involved in learning and memory. In the hippocampal CA3–CA1 connection naïve (nonstimulated) synapses are AMPA signaling and AMPA-silent synapses are created from naïve AMPA-signaling (AMPA-labile) synapses by test-pulse synaptic activation (AMPA silencing). To investigate to what extent LTPs at different developmental stages are explained by AMPA unsilencing, the amount of LTP obtained at these different developmental stages was related to the amount of AMPA silencing that preceded the induction of LTP. When examined in the second postnatal week Hebbian induction was found to produce no more stable potentiation than that causing a return to the naïve synaptic strength existing prior to the AMPA silencing. Moreover, in the absence of a preceding AMPA silencing Hebbian induction produced no stable potentiation above the naïve synaptic strength. Thus this early, or developmental, LTP is nothing more than an unsilencing (dedepression) and stabilization of the AMPA signaling that was lost by the prior AMPA silencing. This dedepression and stabilization of AMPA signaling was mimicked by the presence of the protein kinase A activator forskolin. As the relative degree of AMPA silencing decreased with development, LTP manifested itself more and more as a "genuine" potentiation (as opposed to a dedepression) not explained by unsilencing and stabilization of AMPA-labile synapses. This "genuine," or mature, LTP rose from close to nothing of total LTP prior to postnatal day (P)13, to about 70% of total LTP at P16, and to about 90% of total LTP at P30. Developmental LTP, by stabilization of AMPA-labile synapses, thus seems adapted to select synaptic connections to the growing synaptic network. Mature LTP, by instead strengthening existing stable connections between cells, may then create functionally tightly connected cell assemblies within this network.


Address for reprint requests and other correspondence: T. Abrahamsson, University of Gothenburg, Department of Physiology, Box 432, Medicinaregatan 11, 405 30 Gothenburg, Sweden ( E-mail: Therese.Abrahamsson{at}physiol.gu.se)




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J. Strandberg, P. Wasling, and B. Gustafsson
Modulation of Low-Frequency-Induced Synaptic Depression in the Developing CA3-CA1 Hippocampal Synapses by NMDA and Metabotropic Glutamate Receptor Activation
J Neurophysiol, May 1, 2009; 101(5): 2252 - 2262.
[Abstract] [Full Text] [PDF]




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