Mesopontine median raphe regulates hippocampal ripple oscillation and memory consolidation
It has been suggested that hippocampal sharp-wave ripples (SWR) are important for memory consolidation. Here, the authors found that the activation of a non-serotoninergic subpopulation of median raphe neurons suppresses hippocampal sharp-wave ripples and impairs memory consolidation. These findings...
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description | It has been suggested that hippocampal sharp-wave ripples (SWR) are important for memory consolidation. Here, the authors found that the activation of a non-serotoninergic subpopulation of median raphe neurons suppresses hippocampal sharp-wave ripples and impairs memory consolidation. These findings uncover a new brainstem influence on SWR and hippocampal memory function.
Sharp wave–associated field oscillations (∼200 Hz) of the hippocampus, referred to as ripples, are believed to be important for consolidation of explicit memory. Little is known about how ripples are regulated by other brain regions. We found that the median raphe region (MnR) is important for regulating hippocampal ripple activity and memory consolidation. We performed
in vivo
simultaneous recording in the MnR and hippocampus of mice and found that, when a group of MnR neurons was active, ripples were absent. Consistently, optogenetic stimulation of MnR neurons suppressed ripple activity and inhibition of these neurons increased ripple activity. Notably, using a fear conditioning procedure, we found that photostimulation of MnR neurons interfered with memory consolidation. Our results demonstrate a critical role of the MnR in regulating ripples and memory consolidation. |
doi_str_mv | 10.1038/nn.3998 |
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Sharp wave–associated field oscillations (∼200 Hz) of the hippocampus, referred to as ripples, are believed to be important for consolidation of explicit memory. Little is known about how ripples are regulated by other brain regions. We found that the median raphe region (MnR) is important for regulating hippocampal ripple activity and memory consolidation. We performed
in vivo
simultaneous recording in the MnR and hippocampus of mice and found that, when a group of MnR neurons was active, ripples were absent. Consistently, optogenetic stimulation of MnR neurons suppressed ripple activity and inhibition of these neurons increased ripple activity. Notably, using a fear conditioning procedure, we found that photostimulation of MnR neurons interfered with memory consolidation. Our results demonstrate a critical role of the MnR in regulating ripples and memory consolidation.</description><identifier>ISSN: 1097-6256</identifier><identifier>EISSN: 1546-1726</identifier><identifier>DOI: 10.1038/nn.3998</identifier><identifier>PMID: 25867120</identifier><identifier>CODEN: NANEFN</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>13/51 ; 38/32 ; 631/378/1595/1554 ; 631/378/1595/2638 ; 64/60 ; Animal Genetics and Genomics ; Animals ; Avoidance Learning - physiology ; Behavioral Sciences ; Biological Clocks ; Biological Techniques ; Biomedicine ; Brain Mapping ; Brain research ; Brain Waves - physiology ; CA1 Region, Hippocampal - physiology ; Conditioning, Classical - physiology ; Fear ; GABAergic Neurons - physiology ; Hippocampus (Brain) ; Hippocampus - physiology ; Male ; Memory ; Memory - physiology ; Memory consolidation ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neurobiology ; Neurons ; Neurosciences ; Optogenetics ; Photic Stimulation ; Psychological aspects ; Random Allocation ; Raphe Nuclei - physiology ; Serotonergic Neurons - physiology ; Serotonin</subject><ispartof>Nature neuroscience, 2015-05, Vol.18 (5), p.728-735</ispartof><rights>Springer Nature America, Inc. 2015</rights><rights>COPYRIGHT 2015 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group May 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c634t-d1606eb25f34e9c5fe7dedec4756ca1d731fa2b13cbefeef4b0e7e3f8ccabee83</citedby><cites>FETCH-LOGICAL-c634t-d1606eb25f34e9c5fe7dedec4756ca1d731fa2b13cbefeef4b0e7e3f8ccabee83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25867120$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Dong V</creatorcontrib><creatorcontrib>Yau, Hau-Jie</creatorcontrib><creatorcontrib>Broker, Carl J</creatorcontrib><creatorcontrib>Tsou, Jen-Hui</creatorcontrib><creatorcontrib>Bonci, Antonello</creatorcontrib><creatorcontrib>Ikemoto, Satoshi</creatorcontrib><title>Mesopontine median raphe regulates hippocampal ripple oscillation and memory consolidation</title><title>Nature neuroscience</title><addtitle>Nat Neurosci</addtitle><addtitle>Nat Neurosci</addtitle><description>It has been suggested that hippocampal sharp-wave ripples (SWR) are important for memory consolidation. Here, the authors found that the activation of a non-serotoninergic subpopulation of median raphe neurons suppresses hippocampal sharp-wave ripples and impairs memory consolidation. These findings uncover a new brainstem influence on SWR and hippocampal memory function.
Sharp wave–associated field oscillations (∼200 Hz) of the hippocampus, referred to as ripples, are believed to be important for consolidation of explicit memory. Little is known about how ripples are regulated by other brain regions. We found that the median raphe region (MnR) is important for regulating hippocampal ripple activity and memory consolidation. We performed
in vivo
simultaneous recording in the MnR and hippocampus of mice and found that, when a group of MnR neurons was active, ripples were absent. Consistently, optogenetic stimulation of MnR neurons suppressed ripple activity and inhibition of these neurons increased ripple activity. Notably, using a fear conditioning procedure, we found that photostimulation of MnR neurons interfered with memory consolidation. Our results demonstrate a critical role of the MnR in regulating ripples and memory consolidation.</description><subject>13/51</subject><subject>38/32</subject><subject>631/378/1595/1554</subject><subject>631/378/1595/2638</subject><subject>64/60</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Avoidance Learning - physiology</subject><subject>Behavioral Sciences</subject><subject>Biological Clocks</subject><subject>Biological Techniques</subject><subject>Biomedicine</subject><subject>Brain Mapping</subject><subject>Brain research</subject><subject>Brain Waves - physiology</subject><subject>CA1 Region, Hippocampal - physiology</subject><subject>Conditioning, Classical - physiology</subject><subject>Fear</subject><subject>GABAergic Neurons - physiology</subject><subject>Hippocampus (Brain)</subject><subject>Hippocampus - physiology</subject><subject>Male</subject><subject>Memory</subject><subject>Memory - physiology</subject><subject>Memory consolidation</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Neurobiology</subject><subject>Neurons</subject><subject>Neurosciences</subject><subject>Optogenetics</subject><subject>Photic Stimulation</subject><subject>Psychological aspects</subject><subject>Random Allocation</subject><subject>Raphe Nuclei - 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physiology</topic><topic>Behavioral Sciences</topic><topic>Biological Clocks</topic><topic>Biological Techniques</topic><topic>Biomedicine</topic><topic>Brain Mapping</topic><topic>Brain research</topic><topic>Brain Waves - physiology</topic><topic>CA1 Region, Hippocampal - physiology</topic><topic>Conditioning, Classical - physiology</topic><topic>Fear</topic><topic>GABAergic Neurons - physiology</topic><topic>Hippocampus (Brain)</topic><topic>Hippocampus - physiology</topic><topic>Male</topic><topic>Memory</topic><topic>Memory - physiology</topic><topic>Memory consolidation</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Neurobiology</topic><topic>Neurons</topic><topic>Neurosciences</topic><topic>Optogenetics</topic><topic>Photic Stimulation</topic><topic>Psychological aspects</topic><topic>Random Allocation</topic><topic>Raphe Nuclei - physiology</topic><topic>Serotonergic Neurons - physiology</topic><topic>Serotonin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Dong V</creatorcontrib><creatorcontrib>Yau, Hau-Jie</creatorcontrib><creatorcontrib>Broker, Carl J</creatorcontrib><creatorcontrib>Tsou, Jen-Hui</creatorcontrib><creatorcontrib>Bonci, Antonello</creatorcontrib><creatorcontrib>Ikemoto, Satoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Dong V</au><au>Yau, Hau-Jie</au><au>Broker, Carl J</au><au>Tsou, Jen-Hui</au><au>Bonci, Antonello</au><au>Ikemoto, Satoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesopontine median raphe regulates hippocampal ripple oscillation and memory consolidation</atitle><jtitle>Nature neuroscience</jtitle><stitle>Nat Neurosci</stitle><addtitle>Nat Neurosci</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>18</volume><issue>5</issue><spage>728</spage><epage>735</epage><pages>728-735</pages><issn>1097-6256</issn><eissn>1546-1726</eissn><coden>NANEFN</coden><abstract>It has been suggested that hippocampal sharp-wave ripples (SWR) are important for memory consolidation. Here, the authors found that the activation of a non-serotoninergic subpopulation of median raphe neurons suppresses hippocampal sharp-wave ripples and impairs memory consolidation. These findings uncover a new brainstem influence on SWR and hippocampal memory function.
Sharp wave–associated field oscillations (∼200 Hz) of the hippocampus, referred to as ripples, are believed to be important for consolidation of explicit memory. Little is known about how ripples are regulated by other brain regions. We found that the median raphe region (MnR) is important for regulating hippocampal ripple activity and memory consolidation. We performed
in vivo
simultaneous recording in the MnR and hippocampus of mice and found that, when a group of MnR neurons was active, ripples were absent. Consistently, optogenetic stimulation of MnR neurons suppressed ripple activity and inhibition of these neurons increased ripple activity. Notably, using a fear conditioning procedure, we found that photostimulation of MnR neurons interfered with memory consolidation. Our results demonstrate a critical role of the MnR in regulating ripples and memory consolidation.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>25867120</pmid><doi>10.1038/nn.3998</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/51 38/32 631/378/1595/1554 631/378/1595/2638 64/60 Animal Genetics and Genomics Animals Avoidance Learning - physiology Behavioral Sciences Biological Clocks Biological Techniques Biomedicine Brain Mapping Brain research Brain Waves - physiology CA1 Region, Hippocampal - physiology Conditioning, Classical - physiology Fear GABAergic Neurons - physiology Hippocampus (Brain) Hippocampus - physiology Male Memory Memory - physiology Memory consolidation Mice Mice, Inbred C57BL Mice, Transgenic Neurobiology Neurons Neurosciences Optogenetics Photic Stimulation Psychological aspects Random Allocation Raphe Nuclei - physiology Serotonergic Neurons - physiology Serotonin |
title | Mesopontine median raphe regulates hippocampal ripple oscillation and memory consolidation |
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