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Optogenetic activation of CA1 pyramidal neurons at the dorsal and ventral hippocampus evokes distinct brain-wide responses revealed by mouse fMRI
The dorsal and ventral hippocampal regions (dHP and vHP) are proposed to have distinct functions. Electrophysiological studies have revealed intra-hippocampal variances along the dorsoventral axis. Nevertheless, the extra-hippocampal influences of dHP and vHP activities remain unclear. In this study...
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Published in: | PloS one 2015-03, Vol.10 (3), p.e0121417-e0121417 |
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description | The dorsal and ventral hippocampal regions (dHP and vHP) are proposed to have distinct functions. Electrophysiological studies have revealed intra-hippocampal variances along the dorsoventral axis. Nevertheless, the extra-hippocampal influences of dHP and vHP activities remain unclear. In this study, we compared the spatial distribution of brain-wide responses upon dHP or vHP activation and further estimate connection strengths between the dHP and the vHP with corresponding extra-hippocampal areas. To achieve this, we first investigated responses of local field potential (LFP) and multi unit activities (MUA) upon light stimulation in the hippocampus of an anesthetized transgenic mouse, whose CA1 pyramidal neurons expressed a step-function opsin variant of channelrhodopsin-2 (ChR2). Optogenetic stimulation increased hippocampal LFP power at theta, gamma, and ultra-fast frequency bands, and augmented MUA, indicating light-induced activation of CA1 pyramidal neurons. Brain-wide responses examined using fMRI revealed that optogenetic activation at the dHP or vHP caused blood oxygenation level-dependent (BOLD) fMRI signals in situ. Although activation at the dHP induced BOLD responses at the vHP, the opposite was not observed. Outside the hippocampal formation, activation at the dHP, but not the vHP, evoked BOLD responses at the retrosplenial cortex (RSP), which is in line with anatomical evidence. In contrast, BOLD responses at the lateral septum (LS) were induced only upon vHP activation, even though both dHP and vHP send axonal fibers to the LS. Our findings suggest that the primary targets of dHP and vHP activation are distinct, which concurs with attributed functions of the dHP and RSP in spatial memory, as well as of the vHP and LS in emotional responses. |
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Electrophysiological studies have revealed intra-hippocampal variances along the dorsoventral axis. Nevertheless, the extra-hippocampal influences of dHP and vHP activities remain unclear. In this study, we compared the spatial distribution of brain-wide responses upon dHP or vHP activation and further estimate connection strengths between the dHP and the vHP with corresponding extra-hippocampal areas. To achieve this, we first investigated responses of local field potential (LFP) and multi unit activities (MUA) upon light stimulation in the hippocampus of an anesthetized transgenic mouse, whose CA1 pyramidal neurons expressed a step-function opsin variant of channelrhodopsin-2 (ChR2). Optogenetic stimulation increased hippocampal LFP power at theta, gamma, and ultra-fast frequency bands, and augmented MUA, indicating light-induced activation of CA1 pyramidal neurons. Brain-wide responses examined using fMRI revealed that optogenetic activation at the dHP or vHP caused blood oxygenation level-dependent (BOLD) fMRI signals in situ. Although activation at the dHP induced BOLD responses at the vHP, the opposite was not observed. Outside the hippocampal formation, activation at the dHP, but not the vHP, evoked BOLD responses at the retrosplenial cortex (RSP), which is in line with anatomical evidence. In contrast, BOLD responses at the lateral septum (LS) were induced only upon vHP activation, even though both dHP and vHP send axonal fibers to the LS. Our findings suggest that the primary targets of dHP and vHP activation are distinct, which concurs with attributed functions of the dHP and RSP in spatial memory, as well as of the vHP and LS in emotional responses.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0121417</identifier><identifier>PMID: 25793741</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Action Potentials - physiology ; Activation ; Anesthesia ; Animals ; Axon guidance ; Brain ; Brain mapping ; CA1 Region, Hippocampal - physiology ; Channelrhodopsins ; Comparative analysis ; Connectivity ; Electric Stimulation ; Electrophysiological recording ; Fibers ; Frequencies ; Functional magnetic resonance imaging ; Genetic engineering ; Hippocampus ; Implants, Experimental ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Medical research ; Medicine ; Memory tasks ; Mice, Transgenic ; Neurons ; Neurophysiology ; NMR ; Nuclear magnetic resonance ; Optical Fibers ; Optogenetics - methods ; Oxygen - blood ; Oxygenation ; Physiology ; Pyramidal cells ; Pyramidal Cells - physiology ; Rodents ; Septum ; Spatial analysis ; Spatial distribution ; Spatial memory ; Stimulation ; Theta rhythms ; Transgenic mice</subject><ispartof>PloS one, 2015-03, Vol.10 (3), p.e0121417-e0121417</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Takata et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Takata et al 2015 Takata et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-ec4e791c2f25b4881c5f16dd21cf527615b73860c79c81734ccdb80c7fd828b03</citedby><cites>FETCH-LOGICAL-c758t-ec4e791c2f25b4881c5f16dd21cf527615b73860c79c81734ccdb80c7fd828b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1669475278/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1669475278?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25793741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Schwarz, Adam J</contributor><creatorcontrib>Takata, Norio</creatorcontrib><creatorcontrib>Yoshida, Keitaro</creatorcontrib><creatorcontrib>Komaki, Yuji</creatorcontrib><creatorcontrib>Xu, Ming</creatorcontrib><creatorcontrib>Sakai, Yuki</creatorcontrib><creatorcontrib>Hikishima, Keigo</creatorcontrib><creatorcontrib>Mimura, Masaru</creatorcontrib><creatorcontrib>Okano, Hideyuki</creatorcontrib><creatorcontrib>Tanaka, Kenji F</creatorcontrib><title>Optogenetic activation of CA1 pyramidal neurons at the dorsal and ventral hippocampus evokes distinct brain-wide responses revealed by mouse fMRI</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The dorsal and ventral hippocampal regions (dHP and vHP) are proposed to have distinct functions. 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methods</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Memory tasks</subject><subject>Mice, Transgenic</subject><subject>Neurons</subject><subject>Neurophysiology</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Optical Fibers</subject><subject>Optogenetics - methods</subject><subject>Oxygen - blood</subject><subject>Oxygenation</subject><subject>Physiology</subject><subject>Pyramidal cells</subject><subject>Pyramidal Cells - physiology</subject><subject>Rodents</subject><subject>Septum</subject><subject>Spatial analysis</subject><subject>Spatial distribution</subject><subject>Spatial memory</subject><subject>Stimulation</subject><subject>Theta rhythms</subject><subject>Transgenic mice</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9uO0zAQhiMEYpeFN0BgCQnBRUvsOKcbpKriUGnRSsvh1nLsceuS2MF2Cn0M3hiXZlcN2guUi9jjb_6xf3uS5ClO5zgr8ZutHZzh7by3BuYpJpji8l5yjuuMzAqSZvdPxmfJI--3aZpnVVE8TM5IXtZZSfF58vuqD3YNBoIWiIugdzxoa5BVaLnAqN873mnJW2RgcNZ4xAMKG0DSOh-j3Ei0AxNcHG9031vBu37wCHb2O3gktQ_aiIAax7WZ_dQSkAMft-zjqoMd8BYkavaos4MHpD5drx4nDxRvPTwZ_xfJ1_fvviw_zi6vPqyWi8uZKPMqzEBQKGssiCJ5Q6sKi1zhQkqChcpJWeC8KeNpU1HWosJlRoWQTRWnSlakatLsInl-1O1b69nopme4KGpaRoUqEqsjIS3fst7pjrs9s1yzvwHr1oy76FsLTPGmVJQ2JJOKCl43NFbkvCINJSTnOGq9HasNTQdSHD2biE5XjN6wtd0xmhUVSQ8Cr0YBZ38M4APrtBfQttxA9O6w74LUOc3qiL74B737dCO1jnfAtFE21hUHUbagJKvy-qg1v4OKn4ROi_j0lI7xScLrSUJkAvwKaz54z1afr_-fvfo2ZV-esJv4cMLG23Y4vFY_BekRFM5670DdmoxTduicGzfYoXPY2Dkx7dnpBd0m3bRK9gdgqRXT</recordid><startdate>20150320</startdate><enddate>20150320</enddate><creator>Takata, Norio</creator><creator>Yoshida, Keitaro</creator><creator>Komaki, Yuji</creator><creator>Xu, Ming</creator><creator>Sakai, Yuki</creator><creator>Hikishima, Keigo</creator><creator>Mimura, Masaru</creator><creator>Okano, Hideyuki</creator><creator>Tanaka, Kenji F</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150320</creationdate><title>Optogenetic activation of CA1 pyramidal neurons at the dorsal and ventral hippocampus evokes distinct brain-wide responses revealed by mouse fMRI</title><author>Takata, Norio ; Yoshida, Keitaro ; Komaki, Yuji ; Xu, Ming ; Sakai, Yuki ; Hikishima, Keigo ; Mimura, Masaru ; Okano, Hideyuki ; Tanaka, Kenji F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-ec4e791c2f25b4881c5f16dd21cf527615b73860c79c81734ccdb80c7fd828b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Action Potentials - 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Electrophysiological studies have revealed intra-hippocampal variances along the dorsoventral axis. Nevertheless, the extra-hippocampal influences of dHP and vHP activities remain unclear. In this study, we compared the spatial distribution of brain-wide responses upon dHP or vHP activation and further estimate connection strengths between the dHP and the vHP with corresponding extra-hippocampal areas. To achieve this, we first investigated responses of local field potential (LFP) and multi unit activities (MUA) upon light stimulation in the hippocampus of an anesthetized transgenic mouse, whose CA1 pyramidal neurons expressed a step-function opsin variant of channelrhodopsin-2 (ChR2). Optogenetic stimulation increased hippocampal LFP power at theta, gamma, and ultra-fast frequency bands, and augmented MUA, indicating light-induced activation of CA1 pyramidal neurons. Brain-wide responses examined using fMRI revealed that optogenetic activation at the dHP or vHP caused blood oxygenation level-dependent (BOLD) fMRI signals in situ. Although activation at the dHP induced BOLD responses at the vHP, the opposite was not observed. Outside the hippocampal formation, activation at the dHP, but not the vHP, evoked BOLD responses at the retrosplenial cortex (RSP), which is in line with anatomical evidence. In contrast, BOLD responses at the lateral septum (LS) were induced only upon vHP activation, even though both dHP and vHP send axonal fibers to the LS. Our findings suggest that the primary targets of dHP and vHP activation are distinct, which concurs with attributed functions of the dHP and RSP in spatial memory, as well as of the vHP and LS in emotional responses.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25793741</pmid><doi>10.1371/journal.pone.0121417</doi><oa>free_for_read</oa></addata></record> |
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subjects | Action Potentials - physiology Activation Anesthesia Animals Axon guidance Brain Brain mapping CA1 Region, Hippocampal - physiology Channelrhodopsins Comparative analysis Connectivity Electric Stimulation Electrophysiological recording Fibers Frequencies Functional magnetic resonance imaging Genetic engineering Hippocampus Implants, Experimental Magnetic resonance imaging Magnetic Resonance Imaging - methods Medical research Medicine Memory tasks Mice, Transgenic Neurons Neurophysiology NMR Nuclear magnetic resonance Optical Fibers Optogenetics - methods Oxygen - blood Oxygenation Physiology Pyramidal cells Pyramidal Cells - physiology Rodents Septum Spatial analysis Spatial distribution Spatial memory Stimulation Theta rhythms Transgenic mice |
title | Optogenetic activation of CA1 pyramidal neurons at the dorsal and ventral hippocampus evokes distinct brain-wide responses revealed by mouse fMRI |
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