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Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys
The hippocampus plays an important role in learning and memory. Synaptic plasticity in the hippocampus, short-term and long-term, is postulated to be a neural substrate of memory trace. Paired-pulse stimulation is a standard technique for evaluating a form of short-term synaptic plasticity in rodent...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098860/ https://www.ncbi.nlm.nih.gov/pubmed/21625444 http://dx.doi.org/10.1371/journal.pone.0020006 |
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author | Tamura, Ryoi Nishida, Hiroshi Eifuku, Satoshi Nagao, Kaoru Fushiki, Hiroaki Watanabe, Yukio Ono, Taketoshi |
author_facet | Tamura, Ryoi Nishida, Hiroshi Eifuku, Satoshi Nagao, Kaoru Fushiki, Hiroaki Watanabe, Yukio Ono, Taketoshi |
author_sort | Tamura, Ryoi |
collection | PubMed |
description | The hippocampus plays an important role in learning and memory. Synaptic plasticity in the hippocampus, short-term and long-term, is postulated to be a neural substrate of memory trace. Paired-pulse stimulation is a standard technique for evaluating a form of short-term synaptic plasticity in rodents. However, evidence is lacking for paired-pulse responses in the primate hippocampus. In the present study, we recorded paired-pulse responses in the dentate gyrus of monkeys while stimulating to the medial part of the perforant path at several inter-pulse intervals (IPIs) using low and high stimulus intensities. When the stimulus intensity was low, the first pulse produced early strong depression (at IPIs of 10–30 ms) and late slight depression (at IPIs of 100–1000 ms) of field excitatory postsynaptic potentials (fEPSPs) generated by the second pulse, interposing no depression IPIs (50–70 ms). When the stimulus intensity was high, fEPSPs generated by the second pulse were depressed by the first pulse at all IPIs except for the longest one (2000 ms). Population spikes (PSs) generated by the second pulse were completely blocked or strongly depressed at shorter IPIs (10–100 or 200 ms, respectively), while no depression or slight facilitation occurred at longer IPIs (500–2000 ms). Administration of diazepam slightly increased fEPSPs, while it decreased PSs produced by the first pulse. It also enhanced the facilitation of PSs produced by the second stimulation at longer IPIs. The present results, in comparison with previous studies using rodents, indicate that paired-pulse responses of fEPSPs in the monkey are basically similar to those of rodents, although paired-pulse responses of PSs in the monkey are more delayed than those in rodents and have a different sensitivity to diazepam. |
format | Text |
id | pubmed-3098860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30988602011-05-27 Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys Tamura, Ryoi Nishida, Hiroshi Eifuku, Satoshi Nagao, Kaoru Fushiki, Hiroaki Watanabe, Yukio Ono, Taketoshi PLoS One Research Article The hippocampus plays an important role in learning and memory. Synaptic plasticity in the hippocampus, short-term and long-term, is postulated to be a neural substrate of memory trace. Paired-pulse stimulation is a standard technique for evaluating a form of short-term synaptic plasticity in rodents. However, evidence is lacking for paired-pulse responses in the primate hippocampus. In the present study, we recorded paired-pulse responses in the dentate gyrus of monkeys while stimulating to the medial part of the perforant path at several inter-pulse intervals (IPIs) using low and high stimulus intensities. When the stimulus intensity was low, the first pulse produced early strong depression (at IPIs of 10–30 ms) and late slight depression (at IPIs of 100–1000 ms) of field excitatory postsynaptic potentials (fEPSPs) generated by the second pulse, interposing no depression IPIs (50–70 ms). When the stimulus intensity was high, fEPSPs generated by the second pulse were depressed by the first pulse at all IPIs except for the longest one (2000 ms). Population spikes (PSs) generated by the second pulse were completely blocked or strongly depressed at shorter IPIs (10–100 or 200 ms, respectively), while no depression or slight facilitation occurred at longer IPIs (500–2000 ms). Administration of diazepam slightly increased fEPSPs, while it decreased PSs produced by the first pulse. It also enhanced the facilitation of PSs produced by the second stimulation at longer IPIs. The present results, in comparison with previous studies using rodents, indicate that paired-pulse responses of fEPSPs in the monkey are basically similar to those of rodents, although paired-pulse responses of PSs in the monkey are more delayed than those in rodents and have a different sensitivity to diazepam. Public Library of Science 2011-05-20 /pmc/articles/PMC3098860/ /pubmed/21625444 http://dx.doi.org/10.1371/journal.pone.0020006 Text en Tamura et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tamura, Ryoi Nishida, Hiroshi Eifuku, Satoshi Nagao, Kaoru Fushiki, Hiroaki Watanabe, Yukio Ono, Taketoshi Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys |
title | Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys |
title_full | Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys |
title_fullStr | Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys |
title_full_unstemmed | Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys |
title_short | Short-Term Synaptic Plasticity in the Dentate Gyrus of Monkeys |
title_sort | short-term synaptic plasticity in the dentate gyrus of monkeys |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098860/ https://www.ncbi.nlm.nih.gov/pubmed/21625444 http://dx.doi.org/10.1371/journal.pone.0020006 |
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