The Dorsomedial Striatum Mediates Pavlovian Appetitive Conditioning and Food Consumption
The dorsomedial striatum (DMS) is an important sensorimotor region mediating the acquisition of goal-directed instrumental reward learning and behavioral flexibility. However, whether the DMS also regulates Pavlovian cue-food learning is less clear. The current study used excitotoxic lesions to dete...
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Veröffentlicht in: | Behavioral neuroscience 2017-12, Vol.131 (6), p.447-453 |
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description | The dorsomedial striatum (DMS) is an important sensorimotor region mediating the acquisition of goal-directed instrumental reward learning and behavioral flexibility. However, whether the DMS also regulates Pavlovian cue-food learning is less clear. The current study used excitotoxic lesions to determine whether the DMS is critical in Pavlovian appetitive learning and behavior, using discriminative conditioning and reversal paradigms. The results showed that DMS lesions transiently retarded cue-food learning and subsequent reversal of this learning. Rats with DMS lesions selectively attenuated responding to a food cue but not a control cue, early in training, suggesting the DMS is involved when initial associations are formed. Similarly, initial reversal learning was attenuated in rats with DMS lesions, which suggests impaired flexibility to adjust behavior when the cue meaning is reversed. We also examined the effect of DMS lesions on food intake during tests with access to a highly palatable food along with standard chow diet. Rats with DMS lesions showed an altered pattern of intake, with an initial reduction in high-fat diet followed by an increase in chow consumption. These results demonstrate that the DMS has a role in mediating cue-food learning and its subsequent reversal, as well as changes in food intake when a choice is provided. Together, these results demonstrate the DMS is involved in reward associative learning and reward consumption, when behavioral flexibility is needed to adjust responding or consumption to match the current value. |
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However, whether the DMS also regulates Pavlovian cue-food learning is less clear. The current study used excitotoxic lesions to determine whether the DMS is critical in Pavlovian appetitive learning and behavior, using discriminative conditioning and reversal paradigms. The results showed that DMS lesions transiently retarded cue-food learning and subsequent reversal of this learning. Rats with DMS lesions selectively attenuated responding to a food cue but not a control cue, early in training, suggesting the DMS is involved when initial associations are formed. Similarly, initial reversal learning was attenuated in rats with DMS lesions, which suggests impaired flexibility to adjust behavior when the cue meaning is reversed. We also examined the effect of DMS lesions on food intake during tests with access to a highly palatable food along with standard chow diet. Rats with DMS lesions showed an altered pattern of intake, with an initial reduction in high-fat diet followed by an increase in chow consumption. These results demonstrate that the DMS has a role in mediating cue-food learning and its subsequent reversal, as well as changes in food intake when a choice is provided. Together, these results demonstrate the DMS is involved in reward associative learning and reward consumption, when behavioral flexibility is needed to adjust responding or consumption to match the current value.</description><identifier>ISSN: 0735-7044</identifier><identifier>EISSN: 1939-0084</identifier><identifier>DOI: 10.1037/bne0000216</identifier><identifier>PMID: 29189017</identifier><language>eng</language><publisher>United States: American Psychological Association</publisher><subject>Animal ; Animal behavior ; Animal cognition ; Animal Feeding Behavior ; Animal Learning ; Animals ; Appetitive conditioning ; Associative learning ; Behavior, Animal - physiology ; Classical Conditioning ; Conditioning ; Conditioning, Classical - physiology ; Conditioning, Operant - physiology ; Corpus Striatum - physiology ; Cues ; Diet, High-Fat ; Excitotoxicity ; Extinction, Psychological - physiology ; Food consumption ; Food intake ; High fat diet ; Lesions ; Male ; Motor ability ; Neostriatum ; Rats ; Rats, Long-Evans ; Reinforcement ; Reversal learning ; Reversal Learning - physiology ; Reward ; Rodents ; Sensorimotor system ; Striatum</subject><ispartof>Behavioral neuroscience, 2017-12, Vol.131 (6), p.447-453</ispartof><rights>2017 American Psychological Association</rights><rights>(c) 2017 APA, all rights reserved).</rights><rights>2017, American Psychological Association</rights><rights>Copyright American Psychological Association Dec 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a471t-cead7b4e05963500c110afe5d27f9aaf8a3cd8808453d8e2d0b0abe70e954f2c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29189017$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Burwell, Rebecca D</contributor><creatorcontrib>Cole, Sindy</creatorcontrib><creatorcontrib>Stone, Andrew D</creatorcontrib><creatorcontrib>Petrovich, Gorica D</creatorcontrib><title>The Dorsomedial Striatum Mediates Pavlovian Appetitive Conditioning and Food Consumption</title><title>Behavioral neuroscience</title><addtitle>Behav Neurosci</addtitle><description>The dorsomedial striatum (DMS) is an important sensorimotor region mediating the acquisition of goal-directed instrumental reward learning and behavioral flexibility. However, whether the DMS also regulates Pavlovian cue-food learning is less clear. The current study used excitotoxic lesions to determine whether the DMS is critical in Pavlovian appetitive learning and behavior, using discriminative conditioning and reversal paradigms. The results showed that DMS lesions transiently retarded cue-food learning and subsequent reversal of this learning. Rats with DMS lesions selectively attenuated responding to a food cue but not a control cue, early in training, suggesting the DMS is involved when initial associations are formed. Similarly, initial reversal learning was attenuated in rats with DMS lesions, which suggests impaired flexibility to adjust behavior when the cue meaning is reversed. We also examined the effect of DMS lesions on food intake during tests with access to a highly palatable food along with standard chow diet. Rats with DMS lesions showed an altered pattern of intake, with an initial reduction in high-fat diet followed by an increase in chow consumption. These results demonstrate that the DMS has a role in mediating cue-food learning and its subsequent reversal, as well as changes in food intake when a choice is provided. Together, these results demonstrate the DMS is involved in reward associative learning and reward consumption, when behavioral flexibility is needed to adjust responding or consumption to match the current value.</description><subject>Animal</subject><subject>Animal behavior</subject><subject>Animal cognition</subject><subject>Animal Feeding Behavior</subject><subject>Animal Learning</subject><subject>Animals</subject><subject>Appetitive conditioning</subject><subject>Associative learning</subject><subject>Behavior, Animal - physiology</subject><subject>Classical Conditioning</subject><subject>Conditioning</subject><subject>Conditioning, Classical - physiology</subject><subject>Conditioning, Operant - physiology</subject><subject>Corpus Striatum - physiology</subject><subject>Cues</subject><subject>Diet, High-Fat</subject><subject>Excitotoxicity</subject><subject>Extinction, Psychological - physiology</subject><subject>Food consumption</subject><subject>Food intake</subject><subject>High fat diet</subject><subject>Lesions</subject><subject>Male</subject><subject>Motor ability</subject><subject>Neostriatum</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Reinforcement</subject><subject>Reversal learning</subject><subject>Reversal Learning - physiology</subject><subject>Reward</subject><subject>Rodents</subject><subject>Sensorimotor system</subject><subject>Striatum</subject><issn>0735-7044</issn><issn>1939-0084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2L1TAUhoMoznV04w-QghsRqydN2jQbYbg6KowoOIK7cJqezmToTTpJe2H-vSl3HD8WZpPk5OElDy9jTzm85iDUm84T5FXx5h7bcC10CdDK-2wDStSlAimP2KOUrjIjQdYP2VGleauBqw37cX5JxbsQU9hR73Asvs3R4bzsis_rfaZUfMX9GPYOfXEyTTS72e2p2Abf51Pwzl8U6PviNIR-naZlN63zx-zBgGOiJ7f7Mft--v58-7E8-_Lh0_bkrESp-Fxawl51kqDWjagBLOeAA9V9pQaNOLQobN-22acWfUtVDx1gRwpI13KorDhmbw-509JlBUt-jjiaKbodxhsT0Jm_X7y7NBdhb2pVNVKoHPDiNiCG64XSbHYuWRpH9BSWZLhW0IgGZJPR5_-gV2GJPutlqq24anTb_p9SUGnV1JCplwfKxpBSpOHuyxzMWqv5XWuGn_0peYf-6jEDrw4ATmimdGMxzs6OlOwSYxZfwwwX3DRGSiV-Ap5NrhU</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Cole, Sindy</creator><creator>Stone, Andrew D</creator><creator>Petrovich, Gorica D</creator><general>American Psychological Association</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>7RZ</scope><scope>PSYQQ</scope><scope>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201712</creationdate><title>The Dorsomedial Striatum Mediates Pavlovian Appetitive Conditioning and Food Consumption</title><author>Cole, Sindy ; Stone, Andrew D ; Petrovich, Gorica D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a471t-cead7b4e05963500c110afe5d27f9aaf8a3cd8808453d8e2d0b0abe70e954f2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animal</topic><topic>Animal behavior</topic><topic>Animal cognition</topic><topic>Animal Feeding Behavior</topic><topic>Animal Learning</topic><topic>Animals</topic><topic>Appetitive conditioning</topic><topic>Associative learning</topic><topic>Behavior, Animal - physiology</topic><topic>Classical Conditioning</topic><topic>Conditioning</topic><topic>Conditioning, Classical - physiology</topic><topic>Conditioning, Operant - physiology</topic><topic>Corpus Striatum - physiology</topic><topic>Cues</topic><topic>Diet, High-Fat</topic><topic>Excitotoxicity</topic><topic>Extinction, Psychological - physiology</topic><topic>Food consumption</topic><topic>Food intake</topic><topic>High fat diet</topic><topic>Lesions</topic><topic>Male</topic><topic>Motor ability</topic><topic>Neostriatum</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Reinforcement</topic><topic>Reversal learning</topic><topic>Reversal Learning - physiology</topic><topic>Reward</topic><topic>Rodents</topic><topic>Sensorimotor system</topic><topic>Striatum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cole, Sindy</creatorcontrib><creatorcontrib>Stone, Andrew D</creatorcontrib><creatorcontrib>Petrovich, Gorica D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Access via APA PsycArticles® (ProQuest)</collection><collection>ProQuest One Psychology</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Behavioral neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cole, Sindy</au><au>Stone, Andrew D</au><au>Petrovich, Gorica D</au><au>Burwell, Rebecca D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Dorsomedial Striatum Mediates Pavlovian Appetitive Conditioning and Food Consumption</atitle><jtitle>Behavioral neuroscience</jtitle><addtitle>Behav Neurosci</addtitle><date>2017-12</date><risdate>2017</risdate><volume>131</volume><issue>6</issue><spage>447</spage><epage>453</epage><pages>447-453</pages><issn>0735-7044</issn><eissn>1939-0084</eissn><abstract>The dorsomedial striatum (DMS) is an important sensorimotor region mediating the acquisition of goal-directed instrumental reward learning and behavioral flexibility. However, whether the DMS also regulates Pavlovian cue-food learning is less clear. The current study used excitotoxic lesions to determine whether the DMS is critical in Pavlovian appetitive learning and behavior, using discriminative conditioning and reversal paradigms. The results showed that DMS lesions transiently retarded cue-food learning and subsequent reversal of this learning. Rats with DMS lesions selectively attenuated responding to a food cue but not a control cue, early in training, suggesting the DMS is involved when initial associations are formed. Similarly, initial reversal learning was attenuated in rats with DMS lesions, which suggests impaired flexibility to adjust behavior when the cue meaning is reversed. We also examined the effect of DMS lesions on food intake during tests with access to a highly palatable food along with standard chow diet. Rats with DMS lesions showed an altered pattern of intake, with an initial reduction in high-fat diet followed by an increase in chow consumption. These results demonstrate that the DMS has a role in mediating cue-food learning and its subsequent reversal, as well as changes in food intake when a choice is provided. Together, these results demonstrate the DMS is involved in reward associative learning and reward consumption, when behavioral flexibility is needed to adjust responding or consumption to match the current value.</abstract><cop>United States</cop><pub>American Psychological Association</pub><pmid>29189017</pmid><doi>10.1037/bne0000216</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal Animal behavior Animal cognition Animal Feeding Behavior Animal Learning Animals Appetitive conditioning Associative learning Behavior, Animal - physiology Classical Conditioning Conditioning Conditioning, Classical - physiology Conditioning, Operant - physiology Corpus Striatum - physiology Cues Diet, High-Fat Excitotoxicity Extinction, Psychological - physiology Food consumption Food intake High fat diet Lesions Male Motor ability Neostriatum Rats Rats, Long-Evans Reinforcement Reversal learning Reversal Learning - physiology Reward Rodents Sensorimotor system Striatum |
title | The Dorsomedial Striatum Mediates Pavlovian Appetitive Conditioning and Food Consumption |
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