The Human Centromedial Amygdala Contributes to Negative Prediction Error Signaling during Appetitive and Aversive Pavlovian Gustatory Learning
Prediction error (PE) is the mismatch between a prior expectation and reality, and it lies at the core of associative learning about aversive and appetitive stimuli. Human studies on fear learning have linked the amygdala to aversive PEs. In contrast, the relationship between the amygdala and PE in...
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creator | Kolada, Emilia Bielski, Krzysztof Wilk, Mateusz Rymarczyk, Krystyna Bogorodzki, Piotr Kazulo, Paweł Kossowski, Bartosz Wypych, Marek Marchewka, Artur Kaczmarek, Leszek Knapska, Ewelina Szatkowska, Iwona |
description | Prediction error (PE) is the mismatch between a prior expectation and reality, and it lies at the core of associative learning about aversive and appetitive stimuli. Human studies on fear learning have linked the amygdala to aversive PEs. In contrast, the relationship between the amygdala and PE in appetitive settings and stimuli, unlike those that induce fear, has received less research attention. Animal studies show that the amygdala is a functionally heterogeneous structure. Nevertheless, the role of the amygdala nuclei in PE signaling remains unknown in humans. To clarify the role of two subdivisions of the human amygdala, the centromedial amygdala (CMA) and basolateral amygdala (BLA), in appetitive and aversive PE signaling, we used gustatory pavlovian learning involving eating-related naturalistic outcomes. Thirty-eight right-handed individuals (19 females) participated in the study. We found that surprise with neutral feedback when a reward is expected triggers activity within the left and right CMA. When an aversive outcome is expected, surprise with neutral feedback triggers activity only within the left CMA. Notably, the BLA was not activated by those conditions. Thus, the CMA engages in negative PE signaling during appetitive and aversive gustatory pavlovian learning, whereas the BLA is not critical for this process. In addition, PE-related activity within the left CMA during aversive learning is negatively correlated with neuroticism and positively correlated with extraversion. The findings indicate the importance of the CMA in gustatory learning when the value of outcomes changes and have implications for understanding psychological conditions that manifest perturbed processing of negative PEs.
A discrepancy between a prediction and an actual outcome (PE) plays a crucial role in learning. Learning improves when an outcome is more significant than expected (positive PE) and worsens when it is smaller than expected (negative PE). We found that the negative PE during appetitive and aversive taste learning is associated with increased activity of the CMA, which suggests that the CMA controls taste learning. Our findings may have implications for understanding psychological states associated with deficient learning from negative PEs, such as obesity and addictive behaviors. |
doi_str_mv | 10.1523/JNEUROSCI.0926-22.2023 |
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A discrepancy between a prediction and an actual outcome (PE) plays a crucial role in learning. Learning improves when an outcome is more significant than expected (positive PE) and worsens when it is smaller than expected (negative PE). We found that the negative PE during appetitive and aversive taste learning is associated with increased activity of the CMA, which suggests that the CMA controls taste learning. Our findings may have implications for understanding psychological states associated with deficient learning from negative PEs, such as obesity and addictive behaviors.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.0926-22.2023</identifier><identifier>PMID: 36963846</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Amygdala ; Amygdala - diagnostic imaging ; Animals ; Appetitive Behavior ; Associative learning ; Avoidance Learning ; Basolateral Nuclear Complex ; Conditioning, Classical ; Fear ; Feedback ; Female ; Handedness ; Heterogeneous structure ; Humans ; Learning ; Neurosis ; Signaling ; Stimuli ; Subdivisions</subject><ispartof>The Journal of neuroscience, 2023-04, Vol.43 (17), p.3176-3185</ispartof><rights>Copyright © 2023 Kolada et al.</rights><rights>Copyright Society for Neuroscience Apr 26, 2023</rights><rights>Copyright © 2023 Kolada et al. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-7baa96b3c4805f0cff9fc4dc0bfda8e4862835273ae7f16eb28f1ea1351527ab3</citedby><cites>FETCH-LOGICAL-c443t-7baa96b3c4805f0cff9fc4dc0bfda8e4862835273ae7f16eb28f1ea1351527ab3</cites><orcidid>0000-0002-3185-7336 ; 0000-0001-9319-2176</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/PMC10146448/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146448/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36963846$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kolada, Emilia</creatorcontrib><creatorcontrib>Bielski, Krzysztof</creatorcontrib><creatorcontrib>Wilk, Mateusz</creatorcontrib><creatorcontrib>Rymarczyk, Krystyna</creatorcontrib><creatorcontrib>Bogorodzki, Piotr</creatorcontrib><creatorcontrib>Kazulo, Paweł</creatorcontrib><creatorcontrib>Kossowski, Bartosz</creatorcontrib><creatorcontrib>Wypych, Marek</creatorcontrib><creatorcontrib>Marchewka, Artur</creatorcontrib><creatorcontrib>Kaczmarek, Leszek</creatorcontrib><creatorcontrib>Knapska, Ewelina</creatorcontrib><creatorcontrib>Szatkowska, Iwona</creatorcontrib><title>The Human Centromedial Amygdala Contributes to Negative Prediction Error Signaling during Appetitive and Aversive Pavlovian Gustatory Learning</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Prediction error (PE) is the mismatch between a prior expectation and reality, and it lies at the core of associative learning about aversive and appetitive stimuli. Human studies on fear learning have linked the amygdala to aversive PEs. In contrast, the relationship between the amygdala and PE in appetitive settings and stimuli, unlike those that induce fear, has received less research attention. Animal studies show that the amygdala is a functionally heterogeneous structure. Nevertheless, the role of the amygdala nuclei in PE signaling remains unknown in humans. To clarify the role of two subdivisions of the human amygdala, the centromedial amygdala (CMA) and basolateral amygdala (BLA), in appetitive and aversive PE signaling, we used gustatory pavlovian learning involving eating-related naturalistic outcomes. Thirty-eight right-handed individuals (19 females) participated in the study. We found that surprise with neutral feedback when a reward is expected triggers activity within the left and right CMA. When an aversive outcome is expected, surprise with neutral feedback triggers activity only within the left CMA. Notably, the BLA was not activated by those conditions. Thus, the CMA engages in negative PE signaling during appetitive and aversive gustatory pavlovian learning, whereas the BLA is not critical for this process. In addition, PE-related activity within the left CMA during aversive learning is negatively correlated with neuroticism and positively correlated with extraversion. The findings indicate the importance of the CMA in gustatory learning when the value of outcomes changes and have implications for understanding psychological conditions that manifest perturbed processing of negative PEs.
A discrepancy between a prediction and an actual outcome (PE) plays a crucial role in learning. Learning improves when an outcome is more significant than expected (positive PE) and worsens when it is smaller than expected (negative PE). We found that the negative PE during appetitive and aversive taste learning is associated with increased activity of the CMA, which suggests that the CMA controls taste learning. Our findings may have implications for understanding psychological states associated with deficient learning from negative PEs, such as obesity and addictive behaviors.</description><subject>Amygdala</subject><subject>Amygdala - diagnostic imaging</subject><subject>Animals</subject><subject>Appetitive Behavior</subject><subject>Associative learning</subject><subject>Avoidance Learning</subject><subject>Basolateral Nuclear Complex</subject><subject>Conditioning, Classical</subject><subject>Fear</subject><subject>Feedback</subject><subject>Female</subject><subject>Handedness</subject><subject>Heterogeneous structure</subject><subject>Humans</subject><subject>Learning</subject><subject>Neurosis</subject><subject>Signaling</subject><subject>Stimuli</subject><subject>Subdivisions</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd1u1DAQhS0EokvhFSpL3HCTrf_iJFdoFS390apFtL22JomTukrixXYi7UvwzDhtWQFXI3m-M54zB6EzStY0Zfz8-mb78OP2rrxak4LJhLE1I4y_QavYLRImCH2LVoRlJJEiEyfog_dPhJCM0Ow9OuGykDwXcoV-3T9qfDkNMOJSj8HZQTcGerwZDl0DPeDSxldTTUF7HCy-0R0EM2v83UWwDsaOeOucdfjOdCP0ZuxwM7mlbPZ7HcwzDGODN7N2_lkJc29nE3-8mHyAYN0B7zS4MYo-onct9F5_eq2n6OHb9r68THa3F1flZpfUQvCQZBVAIStei5ykLanbtmhr0dSkahvItcgly3nKMg46a6nUFctbqoHyNJ4ng4qfoq8vc_dTFR3Xi3Xo1d6ZAdxBWTDq385oHlVnZ0UJFVKIPE748jrB2Z-T9kENxte672HUdvKKZQXlMhdURvTzf-iTnVw8VqRyItM0T2kRKflC1c5673R73IYStWSujpmrJXPFmFoyj8Kzv70cZX9C5r8BeqmtBA</recordid><startdate>20230426</startdate><enddate>20230426</enddate><creator>Kolada, Emilia</creator><creator>Bielski, Krzysztof</creator><creator>Wilk, Mateusz</creator><creator>Rymarczyk, Krystyna</creator><creator>Bogorodzki, Piotr</creator><creator>Kazulo, Paweł</creator><creator>Kossowski, Bartosz</creator><creator>Wypych, Marek</creator><creator>Marchewka, Artur</creator><creator>Kaczmarek, Leszek</creator><creator>Knapska, Ewelina</creator><creator>Szatkowska, Iwona</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>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3185-7336</orcidid><orcidid>https://orcid.org/0000-0001-9319-2176</orcidid></search><sort><creationdate>20230426</creationdate><title>The Human Centromedial Amygdala Contributes to Negative Prediction Error Signaling during Appetitive and Aversive Pavlovian Gustatory Learning</title><author>Kolada, Emilia ; Bielski, Krzysztof ; Wilk, Mateusz ; Rymarczyk, Krystyna ; Bogorodzki, Piotr ; Kazulo, Paweł ; Kossowski, Bartosz ; Wypych, Marek ; Marchewka, Artur ; Kaczmarek, Leszek ; Knapska, Ewelina ; Szatkowska, Iwona</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-7baa96b3c4805f0cff9fc4dc0bfda8e4862835273ae7f16eb28f1ea1351527ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amygdala</topic><topic>Amygdala - diagnostic imaging</topic><topic>Animals</topic><topic>Appetitive Behavior</topic><topic>Associative learning</topic><topic>Avoidance Learning</topic><topic>Basolateral Nuclear Complex</topic><topic>Conditioning, Classical</topic><topic>Fear</topic><topic>Feedback</topic><topic>Female</topic><topic>Handedness</topic><topic>Heterogeneous structure</topic><topic>Humans</topic><topic>Learning</topic><topic>Neurosis</topic><topic>Signaling</topic><topic>Stimuli</topic><topic>Subdivisions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kolada, Emilia</creatorcontrib><creatorcontrib>Bielski, Krzysztof</creatorcontrib><creatorcontrib>Wilk, Mateusz</creatorcontrib><creatorcontrib>Rymarczyk, Krystyna</creatorcontrib><creatorcontrib>Bogorodzki, Piotr</creatorcontrib><creatorcontrib>Kazulo, Paweł</creatorcontrib><creatorcontrib>Kossowski, Bartosz</creatorcontrib><creatorcontrib>Wypych, Marek</creatorcontrib><creatorcontrib>Marchewka, Artur</creatorcontrib><creatorcontrib>Kaczmarek, Leszek</creatorcontrib><creatorcontrib>Knapska, Ewelina</creatorcontrib><creatorcontrib>Szatkowska, Iwona</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</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>Kolada, Emilia</au><au>Bielski, Krzysztof</au><au>Wilk, Mateusz</au><au>Rymarczyk, Krystyna</au><au>Bogorodzki, Piotr</au><au>Kazulo, Paweł</au><au>Kossowski, Bartosz</au><au>Wypych, Marek</au><au>Marchewka, Artur</au><au>Kaczmarek, Leszek</au><au>Knapska, Ewelina</au><au>Szatkowska, Iwona</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Human Centromedial Amygdala Contributes to Negative Prediction Error Signaling during Appetitive and Aversive Pavlovian Gustatory Learning</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2023-04-26</date><risdate>2023</risdate><volume>43</volume><issue>17</issue><spage>3176</spage><epage>3185</epage><pages>3176-3185</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>Prediction error (PE) is the mismatch between a prior expectation and reality, and it lies at the core of associative learning about aversive and appetitive stimuli. Human studies on fear learning have linked the amygdala to aversive PEs. In contrast, the relationship between the amygdala and PE in appetitive settings and stimuli, unlike those that induce fear, has received less research attention. Animal studies show that the amygdala is a functionally heterogeneous structure. Nevertheless, the role of the amygdala nuclei in PE signaling remains unknown in humans. To clarify the role of two subdivisions of the human amygdala, the centromedial amygdala (CMA) and basolateral amygdala (BLA), in appetitive and aversive PE signaling, we used gustatory pavlovian learning involving eating-related naturalistic outcomes. Thirty-eight right-handed individuals (19 females) participated in the study. We found that surprise with neutral feedback when a reward is expected triggers activity within the left and right CMA. When an aversive outcome is expected, surprise with neutral feedback triggers activity only within the left CMA. Notably, the BLA was not activated by those conditions. Thus, the CMA engages in negative PE signaling during appetitive and aversive gustatory pavlovian learning, whereas the BLA is not critical for this process. In addition, PE-related activity within the left CMA during aversive learning is negatively correlated with neuroticism and positively correlated with extraversion. The findings indicate the importance of the CMA in gustatory learning when the value of outcomes changes and have implications for understanding psychological conditions that manifest perturbed processing of negative PEs.
A discrepancy between a prediction and an actual outcome (PE) plays a crucial role in learning. Learning improves when an outcome is more significant than expected (positive PE) and worsens when it is smaller than expected (negative PE). We found that the negative PE during appetitive and aversive taste learning is associated with increased activity of the CMA, which suggests that the CMA controls taste learning. Our findings may have implications for understanding psychological states associated with deficient learning from negative PEs, such as obesity and addictive behaviors.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>36963846</pmid><doi>10.1523/JNEUROSCI.0926-22.2023</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3185-7336</orcidid><orcidid>https://orcid.org/0000-0001-9319-2176</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amygdala Amygdala - diagnostic imaging Animals Appetitive Behavior Associative learning Avoidance Learning Basolateral Nuclear Complex Conditioning, Classical Fear Feedback Female Handedness Heterogeneous structure Humans Learning Neurosis Signaling Stimuli Subdivisions |
title | The Human Centromedial Amygdala Contributes to Negative Prediction Error Signaling during Appetitive and Aversive Pavlovian Gustatory Learning |
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