Circadian Regulation of Hippocampal Long-Term Potentiation
The goal of this study is to investigate the possible circadian regulation of hippocampal excitability and long-term potentiation (LTP) measured by stimulating the Schaffer collaterals (SC) and recording the field excitatory postsynaptic potential (fEPSP) from the CA1 dendritic layer or the populati...
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Veröffentlicht in: | Journal of biological rhythms 2005-06, Vol.20 (3), p.225-236 |
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description | The goal of this study is to investigate the possible circadian regulation of hippocampal excitability and long-term potentiation (LTP) measured by stimulating the Schaffer collaterals (SC) and recording the field excitatory postsynaptic potential (fEPSP) from the CA1 dendritic layer or the population spike (PS) from the soma in brain slices of C3H and C57 mice. These 2 strains of mice were of interest because the C3H mice secrete melatonin rhythmically while the C57 mice do not. The authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from night slices compared to day slices of both C3H and C57 mice. They also found significant diurnal variation in the decay of LTP measured with fEPSPs, with the decay slower during the night in both strains of mice. There was evidence for a diurnal rhythm in the input/output function of pyramidal neurons measured at the soma in C57 but not C3H mice. Furthermore, LTP in the PS, measured in slices prepared during the day but recorded during the night, had a profile remarkably similar to the night group. Finally, PS recordings were carried out in slices from C3H mice maintained in constant darkness prior to experimentation. Again, the authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from subjective night slices compared to subjective day slices. These results provide the 1st evidence that an endogenous circadian oscillator modulates synaptic plasticity in the hippocampus. |
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These 2 strains of mice were of interest because the C3H mice secrete melatonin rhythmically while the C57 mice do not. The authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from night slices compared to day slices of both C3H and C57 mice. They also found significant diurnal variation in the decay of LTP measured with fEPSPs, with the decay slower during the night in both strains of mice. There was evidence for a diurnal rhythm in the input/output function of pyramidal neurons measured at the soma in C57 but not C3H mice. Furthermore, LTP in the PS, measured in slices prepared during the day but recorded during the night, had a profile remarkably similar to the night group. Finally, PS recordings were carried out in slices from C3H mice maintained in constant darkness prior to experimentation. Again, the authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from subjective night slices compared to subjective day slices. These results provide the 1st evidence that an endogenous circadian oscillator modulates synaptic plasticity in the hippocampus.</description><identifier>ISSN: 0748-7304</identifier><identifier>EISSN: 1552-4531</identifier><identifier>DOI: 10.1177/0748730405276352</identifier><identifier>PMID: 15851529</identifier><identifier>CODEN: JBRHEE</identifier><language>eng</language><publisher>Thousand Oaks, CA: Sage Publications</publisher><subject>Animals ; Brain ; Circadian rhythm ; Circadian Rhythm - physiology ; Circadian rhythms ; Darkness ; Dendrites - physiology ; Electrophysiology ; Excitatory Postsynaptic Potentials - physiology ; Hippocampus (Brain) ; Hippocampus - physiology ; In Vitro Techniques ; Long-Term Potentiation - physiology ; Male ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Neurons ; Neuroplasticity ; Rodents</subject><ispartof>Journal of biological rhythms, 2005-06, Vol.20 (3), p.225-236</ispartof><rights>COPYRIGHT 2005 Sage Publications, Inc.</rights><rights>Copyright SAGE PUBLICATIONS, INC. Jun 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c619t-21bcc32d2b79cc077142fd01bcaa82eebd0aa67ddf354d0f5e7aabd241e717273</citedby><cites>FETCH-LOGICAL-c619t-21bcc32d2b79cc077142fd01bcaa82eebd0aa67ddf354d0f5e7aabd241e717273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0748730405276352$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0748730405276352$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,780,784,885,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15851529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chaudhury, Dipesh</creatorcontrib><creatorcontrib>Wang, Louisa M</creatorcontrib><creatorcontrib>Colwell, Christopher S</creatorcontrib><title>Circadian Regulation of Hippocampal Long-Term Potentiation</title><title>Journal of biological rhythms</title><addtitle>J Biol Rhythms</addtitle><description>The goal of this study is to investigate the possible circadian regulation of hippocampal excitability and long-term potentiation (LTP) measured by stimulating the Schaffer collaterals (SC) and recording the field excitatory postsynaptic potential (fEPSP) from the CA1 dendritic layer or the population spike (PS) from the soma in brain slices of C3H and C57 mice. These 2 strains of mice were of interest because the C3H mice secrete melatonin rhythmically while the C57 mice do not. The authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from night slices compared to day slices of both C3H and C57 mice. They also found significant diurnal variation in the decay of LTP measured with fEPSPs, with the decay slower during the night in both strains of mice. There was evidence for a diurnal rhythm in the input/output function of pyramidal neurons measured at the soma in C57 but not C3H mice. Furthermore, LTP in the PS, measured in slices prepared during the day but recorded during the night, had a profile remarkably similar to the night group. Finally, PS recordings were carried out in slices from C3H mice maintained in constant darkness prior to experimentation. Again, the authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from subjective night slices compared to subjective day slices. These results provide the 1st evidence that an endogenous circadian oscillator modulates synaptic plasticity in the hippocampus.</description><subject>Animals</subject><subject>Brain</subject><subject>Circadian rhythm</subject><subject>Circadian Rhythm - physiology</subject><subject>Circadian rhythms</subject><subject>Darkness</subject><subject>Dendrites - physiology</subject><subject>Electrophysiology</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Hippocampus (Brain)</subject><subject>Hippocampus - physiology</subject><subject>In Vitro Techniques</subject><subject>Long-Term Potentiation - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Inbred C57BL</subject><subject>Neurons</subject><subject>Neuroplasticity</subject><subject>Rodents</subject><issn>0748-7304</issn><issn>1552-4531</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS0EokvhzgkiDtxS_BknHJCqVaFIK4GgPVsT2wmuEjvYCRL_fR2yotADyAdLM795ejMPoecEnxEi5RsseS0Z5lhQWTFBH6AdEYKWXDDyEO3Wdrn2T9CTlG4wxlXD2WN0QkQtiKDNDr3du6jBOPDFF9svA8wu-CJ0xaWbpqBhnGAoDsH35ZWNY_E5zNbP7hf1FD3qYEj22fE_RdfvL672l-Xh04eP-_NDqSvSzCUlrdaMGtrKRmssJeG0MzhXAWpqbWswQCWN6ZjgBnfCSoDWUE6sJJJKdorebbrT0o7W6GwgwqCm6EaIP1UAp_7uePdN9eGHoqImXK4Cr48CMXxfbJrV6JK2wwDehiWpSsqaMIL_C1JCMZeMZvDVPfAmLNHnK6hMVDkaVmfobIN6GKxyvgvZnc7P2NHp4G3ncv2ccCwbXjWrKt4GdAwpRdv93pFgteat7uedR178eZu7gWPAGSg3IEFv71z-Q_DlxncQFPTRJXX9lWLCMG4aSWvKbgG3_btF</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Chaudhury, Dipesh</creator><creator>Wang, Louisa M</creator><creator>Colwell, Christopher S</creator><general>Sage Publications</general><general>Sage Publications, Inc</general><general>SAGE PUBLICATIONS, INC</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20050601</creationdate><title>Circadian Regulation of Hippocampal Long-Term Potentiation</title><author>Chaudhury, Dipesh ; Wang, Louisa M ; Colwell, Christopher S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c619t-21bcc32d2b79cc077142fd01bcaa82eebd0aa67ddf354d0f5e7aabd241e717273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Brain</topic><topic>Circadian rhythm</topic><topic>Circadian Rhythm - physiology</topic><topic>Circadian rhythms</topic><topic>Darkness</topic><topic>Dendrites - physiology</topic><topic>Electrophysiology</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Hippocampus (Brain)</topic><topic>Hippocampus - physiology</topic><topic>In Vitro Techniques</topic><topic>Long-Term Potentiation - physiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Mice, Inbred C57BL</topic><topic>Neurons</topic><topic>Neuroplasticity</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chaudhury, Dipesh</creatorcontrib><creatorcontrib>Wang, Louisa M</creatorcontrib><creatorcontrib>Colwell, Christopher S</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of biological rhythms</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chaudhury, Dipesh</au><au>Wang, Louisa M</au><au>Colwell, Christopher S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circadian Regulation of Hippocampal Long-Term Potentiation</atitle><jtitle>Journal of biological rhythms</jtitle><addtitle>J Biol Rhythms</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>20</volume><issue>3</issue><spage>225</spage><epage>236</epage><pages>225-236</pages><issn>0748-7304</issn><eissn>1552-4531</eissn><coden>JBRHEE</coden><abstract>The goal of this study is to investigate the possible circadian regulation of hippocampal excitability and long-term potentiation (LTP) measured by stimulating the Schaffer collaterals (SC) and recording the field excitatory postsynaptic potential (fEPSP) from the CA1 dendritic layer or the population spike (PS) from the soma in brain slices of C3H and C57 mice. These 2 strains of mice were of interest because the C3H mice secrete melatonin rhythmically while the C57 mice do not. The authors found that the magnitude of the enhancement of the PS was significantly greater in LTP recorded from night slices compared to day slices of both C3H and C57 mice. They also found significant diurnal variation in the decay of LTP measured with fEPSPs, with the decay slower during the night in both strains of mice. There was evidence for a diurnal rhythm in the input/output function of pyramidal neurons measured at the soma in C57 but not C3H mice. Furthermore, LTP in the PS, measured in slices prepared during the day but recorded during the night, had a profile remarkably similar to the night group. Finally, PS recordings were carried out in slices from C3H mice maintained in constant darkness prior to experimentation. 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subjects | Animals Brain Circadian rhythm Circadian Rhythm - physiology Circadian rhythms Darkness Dendrites - physiology Electrophysiology Excitatory Postsynaptic Potentials - physiology Hippocampus (Brain) Hippocampus - physiology In Vitro Techniques Long-Term Potentiation - physiology Male Mice Mice, Inbred C3H Mice, Inbred C57BL Neurons Neuroplasticity Rodents |
title | Circadian Regulation of Hippocampal Long-Term Potentiation |
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