Memory trace in feeding neural circuitry underlying conditioned taste aversion in Lymnaea
The pond snail Lymnaea stagnalis can maintain a conditioned taste aversion (CTA) as a long-term memory. Previous studies have shown that the inhibitory postsynaptic potential (IPSP) evoked in the neuron 1 medial (N1M) cell by activation of the cerebral giant cell (CGC) in taste aversion-trained snai...
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description | The pond snail Lymnaea stagnalis can maintain a conditioned taste aversion (CTA) as a long-term memory. Previous studies have shown that the inhibitory postsynaptic potential (IPSP) evoked in the neuron 1 medial (N1M) cell by activation of the cerebral giant cell (CGC) in taste aversion-trained snails was larger and lasted longer than that in control snails. The N1M cell is one of the interneurons in the feeding central pattern generator (CPG), and the CGC is a key regulatory neuron for the feeding CPG.
Previous studies have suggested that the neural circuit between the CGC and the N1M cell consists of two synaptic connections: (1) the excitatory connection from the CGC to the neuron 3 tonic (N3t) cell and (2) the inhibitory connection from the N3t cell to the N1M cell. However, because the N3t cell is too small to access consistently by electrophysiological methods, in the present study the synaptic inputs from the CGC to the N3t cell and those from the N3t cell to the N1M cell were monitored as the monosynaptic excitatory postsynaptic potential (EPSP) recorded in the large B1 and B3 motor neurons, respectively. The evoked monosynaptic EPSPs of the B1 motor neurons in the brains isolated from the taste aversion-trained snails were identical to those in the control snails, whereas the spontaneous monosynaptic EPSPs of the B3 motor neurons were significantly enlarged.
These results suggest that, after taste aversion training, the monosynaptic inputs from the N3t cell to the following neurons including the N1M cell are specifically facilitated. That is, one of the memory traces for taste aversion remains as an increase in neurotransmitter released from the N3t cell. We thus conclude that the N3t cell suppresses the N1M cell in the feeding CPG, in response to the conditioned stimulus in Lymnaea CTA. |
doi_str_mv | 10.1371/journal.pone.0043151 |
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Previous studies have suggested that the neural circuit between the CGC and the N1M cell consists of two synaptic connections: (1) the excitatory connection from the CGC to the neuron 3 tonic (N3t) cell and (2) the inhibitory connection from the N3t cell to the N1M cell. However, because the N3t cell is too small to access consistently by electrophysiological methods, in the present study the synaptic inputs from the CGC to the N3t cell and those from the N3t cell to the N1M cell were monitored as the monosynaptic excitatory postsynaptic potential (EPSP) recorded in the large B1 and B3 motor neurons, respectively. The evoked monosynaptic EPSPs of the B1 motor neurons in the brains isolated from the taste aversion-trained snails were identical to those in the control snails, whereas the spontaneous monosynaptic EPSPs of the B3 motor neurons were significantly enlarged.
These results suggest that, after taste aversion training, the monosynaptic inputs from the N3t cell to the following neurons including the N1M cell are specifically facilitated. That is, one of the memory traces for taste aversion remains as an increase in neurotransmitter released from the N3t cell. We thus conclude that the N3t cell suppresses the N1M cell in the feeding CPG, in response to the conditioned stimulus in Lymnaea CTA.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0043151</identifier><identifier>PMID: 22900097</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animal behavior ; Animals ; Biology ; Cell activation ; Central pattern generator ; Central Pattern Generators ; Cerebrum ; Circuits ; Computer simulation ; Conditioned stimulus ; Conditioning ; Conditioning, Classical ; Excitatory postsynaptic potentials ; Excitatory Postsynaptic Potentials - physiology ; Feeding ; Feeding Behavior ; Gene expression ; Inhibitory postsynaptic potentials ; Interneurons ; Laboratories ; Learning ; Long term memory ; Lymnaea ; Lymnaea - physiology ; Lymnaea stagnalis ; Medicine ; Memory ; Memory, Long-Term ; Mollusks ; Motor neurons ; Motor Neurons - physiology ; Nervous system ; Neural circuitry ; Neural networks ; Neural Networks (Computer) ; Neurons ; Pharmaceutical sciences ; Rodents ; Snails ; Social and Behavioral Sciences ; Synapses ; Taste ; Taste - physiology ; Taste aversion</subject><ispartof>PloS one, 2012-08, Vol.7 (8), p.e43151-e43151</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Ito et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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>2012 Ito et al 2012 Ito et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-d63a9d405144128ec6116d3d3c67b1a57f371e05947ef2c161b810bbaf6124db3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3416747/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3416747/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22900097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Sakakibara, Manabu</contributor><creatorcontrib>Ito, Etsuro</creatorcontrib><creatorcontrib>Otsuka, Emi</creatorcontrib><creatorcontrib>Hama, Noriyuki</creatorcontrib><creatorcontrib>Aonuma, Hitoshi</creatorcontrib><creatorcontrib>Okada, Ryuichi</creatorcontrib><creatorcontrib>Hatakeyama, Dai</creatorcontrib><creatorcontrib>Fujito, Yutaka</creatorcontrib><creatorcontrib>Kobayashi, Suguru</creatorcontrib><title>Memory trace in feeding neural circuitry underlying conditioned taste aversion in Lymnaea</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The pond snail Lymnaea stagnalis can maintain a conditioned taste aversion (CTA) as a long-term memory. Previous studies have shown that the inhibitory postsynaptic potential (IPSP) evoked in the neuron 1 medial (N1M) cell by activation of the cerebral giant cell (CGC) in taste aversion-trained snails was larger and lasted longer than that in control snails. The N1M cell is one of the interneurons in the feeding central pattern generator (CPG), and the CGC is a key regulatory neuron for the feeding CPG.
Previous studies have suggested that the neural circuit between the CGC and the N1M cell consists of two synaptic connections: (1) the excitatory connection from the CGC to the neuron 3 tonic (N3t) cell and (2) the inhibitory connection from the N3t cell to the N1M cell. However, because the N3t cell is too small to access consistently by electrophysiological methods, in the present study the synaptic inputs from the CGC to the N3t cell and those from the N3t cell to the N1M cell were monitored as the monosynaptic excitatory postsynaptic potential (EPSP) recorded in the large B1 and B3 motor neurons, respectively. The evoked monosynaptic EPSPs of the B1 motor neurons in the brains isolated from the taste aversion-trained snails were identical to those in the control snails, whereas the spontaneous monosynaptic EPSPs of the B3 motor neurons were significantly enlarged.
These results suggest that, after taste aversion training, the monosynaptic inputs from the N3t cell to the following neurons including the N1M cell are specifically facilitated. That is, one of the memory traces for taste aversion remains as an increase in neurotransmitter released from the N3t cell. We thus conclude that the N3t cell suppresses the N1M cell in the feeding CPG, in response to the conditioned stimulus in Lymnaea CTA.</description><subject>Animal behavior</subject><subject>Animals</subject><subject>Biology</subject><subject>Cell activation</subject><subject>Central pattern generator</subject><subject>Central Pattern Generators</subject><subject>Cerebrum</subject><subject>Circuits</subject><subject>Computer simulation</subject><subject>Conditioned stimulus</subject><subject>Conditioning</subject><subject>Conditioning, Classical</subject><subject>Excitatory postsynaptic potentials</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Feeding</subject><subject>Feeding Behavior</subject><subject>Gene expression</subject><subject>Inhibitory postsynaptic potentials</subject><subject>Interneurons</subject><subject>Laboratories</subject><subject>Learning</subject><subject>Long term memory</subject><subject>Lymnaea</subject><subject>Lymnaea - physiology</subject><subject>Lymnaea stagnalis</subject><subject>Medicine</subject><subject>Memory</subject><subject>Memory, Long-Term</subject><subject>Mollusks</subject><subject>Motor neurons</subject><subject>Motor Neurons - physiology</subject><subject>Nervous system</subject><subject>Neural circuitry</subject><subject>Neural networks</subject><subject>Neural Networks (Computer)</subject><subject>Neurons</subject><subject>Pharmaceutical sciences</subject><subject>Rodents</subject><subject>Snails</subject><subject>Social and Behavioral Sciences</subject><subject>Synapses</subject><subject>Taste</subject><subject>Taste - physiology</subject><subject>Taste aversion</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9-L1DAQx4so3nn6H4gWBNGHXfOrafsiHIc_FlYO_AU-hWky3c3RNntJe7j_vanbO7ZyD5KHhMlnvpOZySTJc0qWlOf03ZUbfAfNcuc6XBIiOM3og-SUlpwtJCP84dH5JHkSwhUhGS-kfJycMFYSQsr8NPn1BVvn92nvQWNqu7RGNLbbpB0OHppUW68H20di6Az6Zj_eadcZ29sY2KQ9hB5TuEEfomFUWO_bDhCeJo9qaAI-m_az5MfHD98vPi_Wl59WF-frhZYl6xdGciiNIBkVgrICtaRUGm64lnlFIcvrmCySrBQ51kxTSauCkqqCWlImTMXPkpcH3V3jgpqqEhTlTGZCUsIisToQxsGV2nnbgt8rB1b9NTi_UeB7qxtUuigAJEhSSCa0LCpCgQGLjzGFoPkY7f0UbahaNBq7WLlmJjq_6exWbdyN4oLKXORR4M0k4N31gKFXrQ0amwY6dEN8N4lkWZTFiL76B70_u4naQEzAdrUbezmKqvNMcE4kK3mklvdQcRlsbewn1jbaZw5vZw6R6fF3v4EhBLX69vX_2cufc_b1EbtFaPptcM0wfqcwB8UB1N6F4LG-KzIlapyA22qocQLUNAHR7cVxg-6cbr88_wORg__v</recordid><startdate>20120810</startdate><enddate>20120810</enddate><creator>Ito, Etsuro</creator><creator>Otsuka, Emi</creator><creator>Hama, Noriyuki</creator><creator>Aonuma, Hitoshi</creator><creator>Okada, Ryuichi</creator><creator>Hatakeyama, Dai</creator><creator>Fujito, Yutaka</creator><creator>Kobayashi, Suguru</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>AEUYN</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>20120810</creationdate><title>Memory trace in feeding neural circuitry underlying conditioned taste aversion in Lymnaea</title><author>Ito, Etsuro ; Otsuka, Emi ; Hama, Noriyuki ; Aonuma, Hitoshi ; Okada, Ryuichi ; Hatakeyama, Dai ; Fujito, Yutaka ; Kobayashi, Suguru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-d63a9d405144128ec6116d3d3c67b1a57f371e05947ef2c161b810bbaf6124db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animal behavior</topic><topic>Animals</topic><topic>Biology</topic><topic>Cell activation</topic><topic>Central pattern generator</topic><topic>Central Pattern Generators</topic><topic>Cerebrum</topic><topic>Circuits</topic><topic>Computer simulation</topic><topic>Conditioned stimulus</topic><topic>Conditioning</topic><topic>Conditioning, Classical</topic><topic>Excitatory postsynaptic potentials</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Feeding</topic><topic>Feeding Behavior</topic><topic>Gene expression</topic><topic>Inhibitory postsynaptic potentials</topic><topic>Interneurons</topic><topic>Laboratories</topic><topic>Learning</topic><topic>Long term memory</topic><topic>Lymnaea</topic><topic>Lymnaea - physiology</topic><topic>Lymnaea stagnalis</topic><topic>Medicine</topic><topic>Memory</topic><topic>Memory, Long-Term</topic><topic>Mollusks</topic><topic>Motor neurons</topic><topic>Motor Neurons - physiology</topic><topic>Nervous system</topic><topic>Neural circuitry</topic><topic>Neural networks</topic><topic>Neural Networks (Computer)</topic><topic>Neurons</topic><topic>Pharmaceutical sciences</topic><topic>Rodents</topic><topic>Snails</topic><topic>Social and Behavioral Sciences</topic><topic>Synapses</topic><topic>Taste</topic><topic>Taste - physiology</topic><topic>Taste aversion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ito, Etsuro</creatorcontrib><creatorcontrib>Otsuka, Emi</creatorcontrib><creatorcontrib>Hama, Noriyuki</creatorcontrib><creatorcontrib>Aonuma, Hitoshi</creatorcontrib><creatorcontrib>Okada, Ryuichi</creatorcontrib><creatorcontrib>Hatakeyama, Dai</creatorcontrib><creatorcontrib>Fujito, Yutaka</creatorcontrib><creatorcontrib>Kobayashi, Suguru</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: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</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>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ito, Etsuro</au><au>Otsuka, Emi</au><au>Hama, Noriyuki</au><au>Aonuma, Hitoshi</au><au>Okada, Ryuichi</au><au>Hatakeyama, Dai</au><au>Fujito, Yutaka</au><au>Kobayashi, Suguru</au><au>Sakakibara, Manabu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Memory trace in feeding neural circuitry underlying conditioned taste aversion in Lymnaea</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-08-10</date><risdate>2012</risdate><volume>7</volume><issue>8</issue><spage>e43151</spage><epage>e43151</epage><pages>e43151-e43151</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The pond snail Lymnaea stagnalis can maintain a conditioned taste aversion (CTA) as a long-term memory. Previous studies have shown that the inhibitory postsynaptic potential (IPSP) evoked in the neuron 1 medial (N1M) cell by activation of the cerebral giant cell (CGC) in taste aversion-trained snails was larger and lasted longer than that in control snails. The N1M cell is one of the interneurons in the feeding central pattern generator (CPG), and the CGC is a key regulatory neuron for the feeding CPG.
Previous studies have suggested that the neural circuit between the CGC and the N1M cell consists of two synaptic connections: (1) the excitatory connection from the CGC to the neuron 3 tonic (N3t) cell and (2) the inhibitory connection from the N3t cell to the N1M cell. However, because the N3t cell is too small to access consistently by electrophysiological methods, in the present study the synaptic inputs from the CGC to the N3t cell and those from the N3t cell to the N1M cell were monitored as the monosynaptic excitatory postsynaptic potential (EPSP) recorded in the large B1 and B3 motor neurons, respectively. The evoked monosynaptic EPSPs of the B1 motor neurons in the brains isolated from the taste aversion-trained snails were identical to those in the control snails, whereas the spontaneous monosynaptic EPSPs of the B3 motor neurons were significantly enlarged.
These results suggest that, after taste aversion training, the monosynaptic inputs from the N3t cell to the following neurons including the N1M cell are specifically facilitated. That is, one of the memory traces for taste aversion remains as an increase in neurotransmitter released from the N3t cell. We thus conclude that the N3t cell suppresses the N1M cell in the feeding CPG, in response to the conditioned stimulus in Lymnaea CTA.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22900097</pmid><doi>10.1371/journal.pone.0043151</doi><tpages>e43151</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Animal behavior Animals Biology Cell activation Central pattern generator Central Pattern Generators Cerebrum Circuits Computer simulation Conditioned stimulus Conditioning Conditioning, Classical Excitatory postsynaptic potentials Excitatory Postsynaptic Potentials - physiology Feeding Feeding Behavior Gene expression Inhibitory postsynaptic potentials Interneurons Laboratories Learning Long term memory Lymnaea Lymnaea - physiology Lymnaea stagnalis Medicine Memory Memory, Long-Term Mollusks Motor neurons Motor Neurons - physiology Nervous system Neural circuitry Neural networks Neural Networks (Computer) Neurons Pharmaceutical sciences Rodents Snails Social and Behavioral Sciences Synapses Taste Taste - physiology Taste aversion |
title | Memory trace in feeding neural circuitry underlying conditioned taste aversion in Lymnaea |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T13%3A13%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Memory%20trace%20in%20feeding%20neural%20circuitry%20underlying%20conditioned%20taste%20aversion%20in%20Lymnaea&rft.jtitle=PloS%20one&rft.au=Ito,%20Etsuro&rft.date=2012-08-10&rft.volume=7&rft.issue=8&rft.spage=e43151&rft.epage=e43151&rft.pages=e43151-e43151&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0043151&rft_dat=%3Cgale_plos_%3EA543306293%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1326546102&rft_id=info:pmid/22900097&rft_galeid=A543306293&rft_doaj_id=oai_doaj_org_article_c88aa6a608624c68b01a2a23c6d8417b&rfr_iscdi=true |