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Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation

Sex differences in spatial memory have long been observed in humans, non-human primates and rodents, but the underlying cellular and molecular mechanisms responsible for these differences remain obscure. In the present study we found that adolescent male rats outperformed female rats in 7 d and 28 d...

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Autores principales: Qi, Xiaoqiang, Zhang, Ke, Xu, Ting, Yamaki, Vitor Nagai, Wei, Zhisheng, Huang, Mingfa, Rose, Gregory M., Cai, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091894/
https://www.ncbi.nlm.nih.gov/pubmed/27806108
http://dx.doi.org/10.1371/journal.pone.0165891
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author Qi, Xiaoqiang
Zhang, Ke
Xu, Ting
Yamaki, Vitor Nagai
Wei, Zhisheng
Huang, Mingfa
Rose, Gregory M.
Cai, Xiang
author_facet Qi, Xiaoqiang
Zhang, Ke
Xu, Ting
Yamaki, Vitor Nagai
Wei, Zhisheng
Huang, Mingfa
Rose, Gregory M.
Cai, Xiang
author_sort Qi, Xiaoqiang
collection PubMed
description Sex differences in spatial memory have long been observed in humans, non-human primates and rodents, but the underlying cellular and molecular mechanisms responsible for these differences remain obscure. In the present study we found that adolescent male rats outperformed female rats in 7 d and 28 d retention probes, but not in learning trials and immediate probes, in the Morris water maze task. Male rats also had larger long-term potentiation (LTP) at hippocampal temproammonic-CA1 (TA-CA1) synapses, which have been implicated to play a key role in place field and memory consolidation, when protocols designed to elicit late-stage LTP (LLTP) were used. Interestingly, the ratio of evoked AMPA/NMDA currents was found to be smaller at TA-CA1 synapses in male rats compared to female rats. Protein biotinylation experiments showed that male rats expressed more surface GluN1 receptors in hippocampal CA1 stratum lacunosum-moleculare (SLM) than female rats, although GluA1 expression was also slightly higher in male rats. Taken together, our results suggest that differences in the expression of AMPA and NMDA receptors may affect LTP expression at TA-CA1 synapses in adolescent male and female rats, and thus possibly contribute to the observed sex difference in spatial memory.
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spelling pubmed-50918942016-11-15 Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation Qi, Xiaoqiang Zhang, Ke Xu, Ting Yamaki, Vitor Nagai Wei, Zhisheng Huang, Mingfa Rose, Gregory M. Cai, Xiang PLoS One Research Article Sex differences in spatial memory have long been observed in humans, non-human primates and rodents, but the underlying cellular and molecular mechanisms responsible for these differences remain obscure. In the present study we found that adolescent male rats outperformed female rats in 7 d and 28 d retention probes, but not in learning trials and immediate probes, in the Morris water maze task. Male rats also had larger long-term potentiation (LTP) at hippocampal temproammonic-CA1 (TA-CA1) synapses, which have been implicated to play a key role in place field and memory consolidation, when protocols designed to elicit late-stage LTP (LLTP) were used. Interestingly, the ratio of evoked AMPA/NMDA currents was found to be smaller at TA-CA1 synapses in male rats compared to female rats. Protein biotinylation experiments showed that male rats expressed more surface GluN1 receptors in hippocampal CA1 stratum lacunosum-moleculare (SLM) than female rats, although GluA1 expression was also slightly higher in male rats. Taken together, our results suggest that differences in the expression of AMPA and NMDA receptors may affect LTP expression at TA-CA1 synapses in adolescent male and female rats, and thus possibly contribute to the observed sex difference in spatial memory. Public Library of Science 2016-11-02 /pmc/articles/PMC5091894/ /pubmed/27806108 http://dx.doi.org/10.1371/journal.pone.0165891 Text en © 2016 Qi 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Qi, Xiaoqiang
Zhang, Ke
Xu, Ting
Yamaki, Vitor Nagai
Wei, Zhisheng
Huang, Mingfa
Rose, Gregory M.
Cai, Xiang
Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation
title Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation
title_full Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation
title_fullStr Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation
title_full_unstemmed Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation
title_short Sex Differences in Long-Term Potentiation at Temporoammonic-CA1 Synapses: Potential Implications for Memory Consolidation
title_sort sex differences in long-term potentiation at temporoammonic-ca1 synapses: potential implications for memory consolidation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091894/
https://www.ncbi.nlm.nih.gov/pubmed/27806108
http://dx.doi.org/10.1371/journal.pone.0165891
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