Ventrolateral Striatal Medium Spiny Neurons Positively Regulate Food-Incentive, Goal-Directed Behavior Independently of D1 and D2 Selectivity
The ventral striatum is involved in motivated behavior. Akin to the dorsal striatum, the ventral striatum contains two parallel pathways: the striatomesencephalic pathway consisting of dopamine receptor Type 1-expressing medium spiny neurons (D1-MSNs) and the striatopallidal pathway consisting of D2...
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creator | Natsubori, Akiyo Tsutsui-Kimura, Iku Nishida, Hiroshi Bouchekioua, Youcef Sekiya, Hiroshi Uchigashima, Motokazu Watanabe, Masahiko de Kerchove d'Exaerde, Alban Mimura, Masaru Takata, Norio Tanaka, Kenji F |
description | The ventral striatum is involved in motivated behavior. Akin to the dorsal striatum, the ventral striatum contains two parallel pathways: the striatomesencephalic pathway consisting of dopamine receptor Type 1-expressing medium spiny neurons (D1-MSNs) and the striatopallidal pathway consisting of D2-MSNs. These two genetically identified pathways are thought to encode opposing functions in motivated behavior. It has also been reported that D1/D2 genetic selectivity is not attributed to the anatomical discrimination of two pathways. We wanted to determine whether D1- and D2-MSNs in the ventral striatum functioned in an opposing manner as previous observations claimed, and whether D1/D2 selectivity corresponded to a functional segregation in motivated behavior of mice. To address this question, we focused on the lateral portion of ventral striatum as a region implicated in food-incentive, goal-directed behavior, and recorded D1 or D2-MSN activity by using a gene-encoded ratiometric Ca
indicator and by constructing a fiberphotometry system, and manipulated their activities via optogenetic inhibition during ongoing behaviors. We observed concurrent event-related compound Ca
elevations in ventrolateral D1- and D2-MSNs, especially at trial start cue-related and first lever press-related times. D1 or D2 selective optogenetic inhibition just after the trial start cue resulted in a reduction of goal-directed behavior, indicating a shared coding of motivated behavior by both populations at this time. Only D1-selective inhibition just after the first lever press resulted in the reduction of behavior, indicating D1-MSN-specific coding at that specific time. Our data did not support opposing encoding by both populations in food-incentive, goal-directed behavior.
An opposing role of dopamine receptor Type 1 or Type 2-expressing medium spiny neurons (D1-MSNs or D2-MSNs) on striatum-mediated behaviors has been widely accepted. However, this idea has been questioned by recent reports. In the present study, we measured concurrent Ca
activity patterns of D1- and D2-MSNs in the ventrolateral striatum during food-incentive, goal-directed behavior in mice. According to Ca
activity patterns, we conducted timing-specific optogenetic inhibition of each type of MSN. We demonstrated that both D1- and D2-MSNs in the ventrolateral striatum commonly and positively encoded action initiation, whereas only D1-MSNs positively encoded sustained motivated behavior. These findings led us to r |
doi_str_mv | 10.1523/JNEUROSCI.3377-16.2017 |
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indicator and by constructing a fiberphotometry system, and manipulated their activities via optogenetic inhibition during ongoing behaviors. We observed concurrent event-related compound Ca
elevations in ventrolateral D1- and D2-MSNs, especially at trial start cue-related and first lever press-related times. D1 or D2 selective optogenetic inhibition just after the trial start cue resulted in a reduction of goal-directed behavior, indicating a shared coding of motivated behavior by both populations at this time. Only D1-selective inhibition just after the first lever press resulted in the reduction of behavior, indicating D1-MSN-specific coding at that specific time. Our data did not support opposing encoding by both populations in food-incentive, goal-directed behavior.
An opposing role of dopamine receptor Type 1 or Type 2-expressing medium spiny neurons (D1-MSNs or D2-MSNs) on striatum-mediated behaviors has been widely accepted. However, this idea has been questioned by recent reports. In the present study, we measured concurrent Ca
activity patterns of D1- and D2-MSNs in the ventrolateral striatum during food-incentive, goal-directed behavior in mice. According to Ca
activity patterns, we conducted timing-specific optogenetic inhibition of each type of MSN. We demonstrated that both D1- and D2-MSNs in the ventrolateral striatum commonly and positively encoded action initiation, whereas only D1-MSNs positively encoded sustained motivated behavior. These findings led us to reconsider the prevailing notion of a functional segregation of MSN activity in the ventral striatum.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.3377-16.2017</identifier><identifier>PMID: 28167674</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Animals ; Behavior, Animal - physiology ; Corpus Striatum - physiology ; Feedback, Psychological - physiology ; Feeding Behavior - physiology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Motivation - physiology ; Nerve Net - physiology ; Neurons - physiology ; Receptors, Dopamine - metabolism ; Reward</subject><ispartof>The Journal of neuroscience, 2017-03, Vol.37 (10), p.2723-2733</ispartof><rights>Copyright © 2017 the authors 0270-6474/17/372724-11$15.00/0.</rights><rights>Copyright © 2017 the authors 0270-6474/17/372724-11$15.00/0 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c566t-444d62ac3c6b4b382cad2ee43c667a6ed8c4bedbf4d4d23eeb5d1805a0481da63</citedby><cites>FETCH-LOGICAL-c566t-444d62ac3c6b4b382cad2ee43c667a6ed8c4bedbf4d4d23eeb5d1805a0481da63</cites><orcidid>0000-0001-5037-7138 ; 0000-0002-0682-5877 ; 0000-0003-2511-0057</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596637/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596637/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28167674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Natsubori, Akiyo</creatorcontrib><creatorcontrib>Tsutsui-Kimura, Iku</creatorcontrib><creatorcontrib>Nishida, Hiroshi</creatorcontrib><creatorcontrib>Bouchekioua, Youcef</creatorcontrib><creatorcontrib>Sekiya, Hiroshi</creatorcontrib><creatorcontrib>Uchigashima, Motokazu</creatorcontrib><creatorcontrib>Watanabe, Masahiko</creatorcontrib><creatorcontrib>de Kerchove d'Exaerde, Alban</creatorcontrib><creatorcontrib>Mimura, Masaru</creatorcontrib><creatorcontrib>Takata, Norio</creatorcontrib><creatorcontrib>Tanaka, Kenji F</creatorcontrib><title>Ventrolateral Striatal Medium Spiny Neurons Positively Regulate Food-Incentive, Goal-Directed Behavior Independently of D1 and D2 Selectivity</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>The ventral striatum is involved in motivated behavior. Akin to the dorsal striatum, the ventral striatum contains two parallel pathways: the striatomesencephalic pathway consisting of dopamine receptor Type 1-expressing medium spiny neurons (D1-MSNs) and the striatopallidal pathway consisting of D2-MSNs. These two genetically identified pathways are thought to encode opposing functions in motivated behavior. It has also been reported that D1/D2 genetic selectivity is not attributed to the anatomical discrimination of two pathways. We wanted to determine whether D1- and D2-MSNs in the ventral striatum functioned in an opposing manner as previous observations claimed, and whether D1/D2 selectivity corresponded to a functional segregation in motivated behavior of mice. To address this question, we focused on the lateral portion of ventral striatum as a region implicated in food-incentive, goal-directed behavior, and recorded D1 or D2-MSN activity by using a gene-encoded ratiometric Ca
indicator and by constructing a fiberphotometry system, and manipulated their activities via optogenetic inhibition during ongoing behaviors. We observed concurrent event-related compound Ca
elevations in ventrolateral D1- and D2-MSNs, especially at trial start cue-related and first lever press-related times. D1 or D2 selective optogenetic inhibition just after the trial start cue resulted in a reduction of goal-directed behavior, indicating a shared coding of motivated behavior by both populations at this time. Only D1-selective inhibition just after the first lever press resulted in the reduction of behavior, indicating D1-MSN-specific coding at that specific time. Our data did not support opposing encoding by both populations in food-incentive, goal-directed behavior.
An opposing role of dopamine receptor Type 1 or Type 2-expressing medium spiny neurons (D1-MSNs or D2-MSNs) on striatum-mediated behaviors has been widely accepted. However, this idea has been questioned by recent reports. In the present study, we measured concurrent Ca
activity patterns of D1- and D2-MSNs in the ventrolateral striatum during food-incentive, goal-directed behavior in mice. According to Ca
activity patterns, we conducted timing-specific optogenetic inhibition of each type of MSN. We demonstrated that both D1- and D2-MSNs in the ventrolateral striatum commonly and positively encoded action initiation, whereas only D1-MSNs positively encoded sustained motivated behavior. These findings led us to reconsider the prevailing notion of a functional segregation of MSN activity in the ventral striatum.</description><subject>Animals</subject><subject>Behavior, Animal - physiology</subject><subject>Corpus Striatum - physiology</subject><subject>Feedback, Psychological - physiology</subject><subject>Feeding Behavior - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Motivation - physiology</subject><subject>Nerve Net - physiology</subject><subject>Neurons - physiology</subject><subject>Receptors, Dopamine - metabolism</subject><subject>Reward</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1uEzEUhS0EoqHwCpWXLJjU9vhnukGCpC1BpUUNZWt5xjet0cRObU-kPATvjEdto7Lrxj863zm6VwehI0qmVLD6-Pvl6c311XK2mNa1UhWVU0aoeoUmRT2pGCf0NZoQpkglueIH6F1KfwghqkBv0QFrqFRS8Qn6-xt8jqE3GaLp8TJHZ3J5_ADrhjVebpzf4UsYYvAJ_wzJZbeFfoev4XYYTfgsBFstfFdiivIJnwfTV3MXoctg8Ve4M1sXIl54Cxsoh8_FHVZ4TrHxFs8ZXkJfYLd1efcevVmZPsGHx_sQ3Zyd_pp9qy6uzhezLxdVJ6TMFefcSma6upMtb-uGdcYyAF7-UhkJtul4C7ZdccstqwFaYWlDhCG8odbI-hB9fsjdDO0a7Dh82V5volubuNPBOP2_4t2dvg1bLcWJlLUqAR8fA2K4HyBlvXapg743HsKQNG0aqoSghL8AlaJhQkhSUPmAdjGkFGG1n4gSPdau97XrsXZNpR5rL8aj5_vsbU891_8Arp6tvQ</recordid><startdate>20170308</startdate><enddate>20170308</enddate><creator>Natsubori, Akiyo</creator><creator>Tsutsui-Kimura, Iku</creator><creator>Nishida, Hiroshi</creator><creator>Bouchekioua, Youcef</creator><creator>Sekiya, Hiroshi</creator><creator>Uchigashima, Motokazu</creator><creator>Watanabe, Masahiko</creator><creator>de Kerchove d'Exaerde, Alban</creator><creator>Mimura, Masaru</creator><creator>Takata, Norio</creator><creator>Tanaka, Kenji F</creator><general>Society for Neuroscience</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>7X8</scope><scope>7QG</scope><scope>7TK</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5037-7138</orcidid><orcidid>https://orcid.org/0000-0002-0682-5877</orcidid><orcidid>https://orcid.org/0000-0003-2511-0057</orcidid></search><sort><creationdate>20170308</creationdate><title>Ventrolateral Striatal Medium Spiny Neurons Positively Regulate Food-Incentive, Goal-Directed Behavior Independently of D1 and D2 Selectivity</title><author>Natsubori, Akiyo ; Tsutsui-Kimura, Iku ; Nishida, Hiroshi ; Bouchekioua, Youcef ; Sekiya, Hiroshi ; Uchigashima, Motokazu ; Watanabe, Masahiko ; de Kerchove d'Exaerde, Alban ; Mimura, Masaru ; Takata, Norio ; Tanaka, Kenji F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c566t-444d62ac3c6b4b382cad2ee43c667a6ed8c4bedbf4d4d23eeb5d1805a0481da63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Behavior, Animal - physiology</topic><topic>Corpus Striatum - physiology</topic><topic>Feedback, Psychological - physiology</topic><topic>Feeding Behavior - physiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Motivation - physiology</topic><topic>Nerve Net - physiology</topic><topic>Neurons - physiology</topic><topic>Receptors, Dopamine - metabolism</topic><topic>Reward</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Natsubori, Akiyo</creatorcontrib><creatorcontrib>Tsutsui-Kimura, Iku</creatorcontrib><creatorcontrib>Nishida, Hiroshi</creatorcontrib><creatorcontrib>Bouchekioua, Youcef</creatorcontrib><creatorcontrib>Sekiya, Hiroshi</creatorcontrib><creatorcontrib>Uchigashima, Motokazu</creatorcontrib><creatorcontrib>Watanabe, Masahiko</creatorcontrib><creatorcontrib>de Kerchove d'Exaerde, Alban</creatorcontrib><creatorcontrib>Mimura, Masaru</creatorcontrib><creatorcontrib>Takata, Norio</creatorcontrib><creatorcontrib>Tanaka, Kenji F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Natsubori, Akiyo</au><au>Tsutsui-Kimura, Iku</au><au>Nishida, Hiroshi</au><au>Bouchekioua, Youcef</au><au>Sekiya, Hiroshi</au><au>Uchigashima, Motokazu</au><au>Watanabe, Masahiko</au><au>de Kerchove d'Exaerde, Alban</au><au>Mimura, Masaru</au><au>Takata, Norio</au><au>Tanaka, Kenji F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ventrolateral Striatal Medium Spiny Neurons Positively Regulate Food-Incentive, Goal-Directed Behavior Independently of D1 and D2 Selectivity</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2017-03-08</date><risdate>2017</risdate><volume>37</volume><issue>10</issue><spage>2723</spage><epage>2733</epage><pages>2723-2733</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>The ventral striatum is involved in motivated behavior. Akin to the dorsal striatum, the ventral striatum contains two parallel pathways: the striatomesencephalic pathway consisting of dopamine receptor Type 1-expressing medium spiny neurons (D1-MSNs) and the striatopallidal pathway consisting of D2-MSNs. These two genetically identified pathways are thought to encode opposing functions in motivated behavior. It has also been reported that D1/D2 genetic selectivity is not attributed to the anatomical discrimination of two pathways. We wanted to determine whether D1- and D2-MSNs in the ventral striatum functioned in an opposing manner as previous observations claimed, and whether D1/D2 selectivity corresponded to a functional segregation in motivated behavior of mice. To address this question, we focused on the lateral portion of ventral striatum as a region implicated in food-incentive, goal-directed behavior, and recorded D1 or D2-MSN activity by using a gene-encoded ratiometric Ca
indicator and by constructing a fiberphotometry system, and manipulated their activities via optogenetic inhibition during ongoing behaviors. We observed concurrent event-related compound Ca
elevations in ventrolateral D1- and D2-MSNs, especially at trial start cue-related and first lever press-related times. D1 or D2 selective optogenetic inhibition just after the trial start cue resulted in a reduction of goal-directed behavior, indicating a shared coding of motivated behavior by both populations at this time. Only D1-selective inhibition just after the first lever press resulted in the reduction of behavior, indicating D1-MSN-specific coding at that specific time. Our data did not support opposing encoding by both populations in food-incentive, goal-directed behavior.
An opposing role of dopamine receptor Type 1 or Type 2-expressing medium spiny neurons (D1-MSNs or D2-MSNs) on striatum-mediated behaviors has been widely accepted. However, this idea has been questioned by recent reports. In the present study, we measured concurrent Ca
activity patterns of D1- and D2-MSNs in the ventrolateral striatum during food-incentive, goal-directed behavior in mice. According to Ca
activity patterns, we conducted timing-specific optogenetic inhibition of each type of MSN. We demonstrated that both D1- and D2-MSNs in the ventrolateral striatum commonly and positively encoded action initiation, whereas only D1-MSNs positively encoded sustained motivated behavior. These findings led us to reconsider the prevailing notion of a functional segregation of MSN activity in the ventral striatum.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>28167674</pmid><doi>10.1523/JNEUROSCI.3377-16.2017</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-5037-7138</orcidid><orcidid>https://orcid.org/0000-0002-0682-5877</orcidid><orcidid>https://orcid.org/0000-0003-2511-0057</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Behavior, Animal - physiology Corpus Striatum - physiology Feedback, Psychological - physiology Feeding Behavior - physiology Male Mice Mice, Inbred C57BL Mice, Transgenic Motivation - physiology Nerve Net - physiology Neurons - physiology Receptors, Dopamine - metabolism Reward |
title | Ventrolateral Striatal Medium Spiny Neurons Positively Regulate Food-Incentive, Goal-Directed Behavior Independently of D1 and D2 Selectivity |
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