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The Journal of Neuroscience, January 15, 1998, 18(2):658-671

Stability in Synapse Number and Size at 2 Hr after Long-Term Potentiation in Hippocampal Area CA1

Karin E. Sorra and Kristen M. Harris

Program in Neuroscience, Harvard Medical School, and Division of Neuroscience in the Department of Neurology, Children's Hospital, Boston, Massachusetts 02115

Long-term potentiation (LTP) is an important model for examining synaptic mechanisms of learning and memory. A key question is whether the enhanced synaptic transmission occurring with LTP involves the addition of new synapses, the enlargement of existing synapses, or a redistribution in synaptic weight among synapses. Two experimental designs were used to address this question. In the first experimental design three conditions were evaluated across hippocampal slices maintained in vitro, including slices with LTP analyzed at 2 hr post-tetanus, slices tetanized in the presence of APV, and control slices receiving test stimulation only. In the second experimental design independent LTP and control (low-frequency stimulation) sites were examined. Synapse density was estimated by an unbiased volume sampling procedure. Synapse size was computed by three-dimensional reconstruction from serial electron microscopy (EM). Serial EM also was used to compute synapse number per unit length of dendrite. In both experimental designs there were no significant effects of LTP on total synapse number, on the distribution of different types of synapses (thin, mushroom, stubby, or branched dendritic spines and macular, perforated, or segmented postsynaptic densities), on the frequency of shaft synapses, nor on the relative proportion of single or multiple synapse axonal boutons. There was also no increase in synapse size. These results suggest that LTP does not cause an overall formation of new synapses nor an enlargement of synapses at 2 hr post-tetanus in hippocampal area CA1, and these results support the hypothesis that LTP could involve a redistribution of synaptic weights among existing synapses.

Key words: long-term potentiation; hippocampus; area CA1; serial electron microscopy; dendritic spines; postsynaptic density; disector; axonal boutons; three-dimensional reconstructions; ultrastructure; hippocampal slice; in vitro


Copyright © 1998 Society for Neuroscience  0270-6474/98/182658-14$05.00/0


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