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The neuroscience of sadness: A multidisciplinary synthesis and collaborative review
•Sadness involves reduction of cortical control over evolutionarily ancient brain systems.•Basic emotion theorists have identified a SADNESS circuit, based on animal research.•Psychological constructionists have identified patterns of activity that dependent on context.•Competing models may relate t...
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Published in: | Neuroscience and biobehavioral reviews 2020-04, Vol.111, p.199-228 |
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creator | Arias, Juan A. Williams, Claire Raghvani, Rashmi Aghajani, Moji Baez, Sandra Belzung, Catherine Booij, Linda Busatto, Geraldo Chiarella, Julian Fu, Cynthia HY Ibanez, Agustin Liddell, Belinda J. Lowe, Leroy Penninx, Brenda W.J.H. Rosa, Pedro Kemp, Andrew H. |
description | •Sadness involves reduction of cortical control over evolutionarily ancient brain systems.•Basic emotion theorists have identified a SADNESS circuit, based on animal research.•Psychological constructionists have identified patterns of activity that dependent on context.•Competing models may relate to different levels on a phylogenetic hierarchy.•Dedicated funding to facilitate collaborative and transdisciplinary opportunities is needed.
Sadness is typically characterized by raised inner eyebrows, lowered corners of the mouth, reduced walking speed, and slumped posture. Ancient subcortical circuitry provides a neuroanatomical foundation, extending from dorsal periaqueductal grey to subgenual anterior cingulate, the latter of which is now a treatment target in disorders of sadness. Electrophysiological studies further emphasize a role for reduced left relative to right frontal asymmetry in sadness, underpinning interest in the transcranial stimulation of left dorsolateral prefrontal cortex as an antidepressant target. Neuroimaging studies – including meta-analyses – indicate that sadness is associated with reduced cortical activation, which may contribute to reduced parasympathetic inhibitory control over medullary cardioacceleratory circuits. Reduced cardiac control may – in part – contribute to epidemiological reports of reduced life expectancy in affective disorders, effects equivalent to heavy smoking. We suggest that the field may be moving toward a theoretical consensus, in which different models relating to basic emotion theory and psychological constructionism may be considered as complementary, working at different levels of the phylogenetic hierarchy. |
doi_str_mv | 10.1016/j.neubiorev.2020.01.006 |
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Sadness is typically characterized by raised inner eyebrows, lowered corners of the mouth, reduced walking speed, and slumped posture. Ancient subcortical circuitry provides a neuroanatomical foundation, extending from dorsal periaqueductal grey to subgenual anterior cingulate, the latter of which is now a treatment target in disorders of sadness. Electrophysiological studies further emphasize a role for reduced left relative to right frontal asymmetry in sadness, underpinning interest in the transcranial stimulation of left dorsolateral prefrontal cortex as an antidepressant target. Neuroimaging studies – including meta-analyses – indicate that sadness is associated with reduced cortical activation, which may contribute to reduced parasympathetic inhibitory control over medullary cardioacceleratory circuits. Reduced cardiac control may – in part – contribute to epidemiological reports of reduced life expectancy in affective disorders, effects equivalent to heavy smoking. We suggest that the field may be moving toward a theoretical consensus, in which different models relating to basic emotion theory and psychological constructionism may be considered as complementary, working at different levels of the phylogenetic hierarchy.</description><identifier>ISSN: 0149-7634</identifier><identifier>EISSN: 1873-7528</identifier><identifier>DOI: 10.1016/j.neubiorev.2020.01.006</identifier><identifier>PMID: 32001274</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Affective neuroscience ; Autonomic Nervous System - metabolism ; Autonomic Nervous System - physiopathology ; Basic emotions ; Cerebral Cortex - metabolism ; Cerebral Cortex - physiopathology ; Epigenesis, Genetic - physiology ; Genetics ; GENIAL model ; Health and wellbeing ; Heart rate variability ; Humans ; Interoception - physiology ; Major depressive disorder ; Mood Disorders - genetics ; Mood Disorders - metabolism ; Mood Disorders - physiopathology ; Nerve Net - metabolism ; Nerve Net - physiopathology ; Neuroimaging ; Neurosciences ; Psychological constructionism ; Psychological Theory ; Psychophysiology ; Sadness ; Sadness - physiology ; Vagal function</subject><ispartof>Neuroscience and biobehavioral reviews, 2020-04, Vol.111, p.199-228</ispartof><rights>2020 The Authors</rights><rights>Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-e10582fba81d40cdab1a651f04bd83f1aa9d76e6cc90adfca6a4d69fce022ec73</citedby><cites>FETCH-LOGICAL-c420t-e10582fba81d40cdab1a651f04bd83f1aa9d76e6cc90adfca6a4d69fce022ec73</cites><orcidid>0000-0003-4313-3500 ; 0000-0003-1146-3791 ; 0000-0002-3355-6393</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32001274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arias, Juan A.</creatorcontrib><creatorcontrib>Williams, Claire</creatorcontrib><creatorcontrib>Raghvani, Rashmi</creatorcontrib><creatorcontrib>Aghajani, Moji</creatorcontrib><creatorcontrib>Baez, Sandra</creatorcontrib><creatorcontrib>Belzung, Catherine</creatorcontrib><creatorcontrib>Booij, Linda</creatorcontrib><creatorcontrib>Busatto, Geraldo</creatorcontrib><creatorcontrib>Chiarella, Julian</creatorcontrib><creatorcontrib>Fu, Cynthia HY</creatorcontrib><creatorcontrib>Ibanez, Agustin</creatorcontrib><creatorcontrib>Liddell, Belinda J.</creatorcontrib><creatorcontrib>Lowe, Leroy</creatorcontrib><creatorcontrib>Penninx, Brenda W.J.H.</creatorcontrib><creatorcontrib>Rosa, Pedro</creatorcontrib><creatorcontrib>Kemp, Andrew H.</creatorcontrib><title>The neuroscience of sadness: A multidisciplinary synthesis and collaborative review</title><title>Neuroscience and biobehavioral reviews</title><addtitle>Neurosci Biobehav Rev</addtitle><description>•Sadness involves reduction of cortical control over evolutionarily ancient brain systems.•Basic emotion theorists have identified a SADNESS circuit, based on animal research.•Psychological constructionists have identified patterns of activity that dependent on context.•Competing models may relate to different levels on a phylogenetic hierarchy.•Dedicated funding to facilitate collaborative and transdisciplinary opportunities is needed.
Sadness is typically characterized by raised inner eyebrows, lowered corners of the mouth, reduced walking speed, and slumped posture. Ancient subcortical circuitry provides a neuroanatomical foundation, extending from dorsal periaqueductal grey to subgenual anterior cingulate, the latter of which is now a treatment target in disorders of sadness. Electrophysiological studies further emphasize a role for reduced left relative to right frontal asymmetry in sadness, underpinning interest in the transcranial stimulation of left dorsolateral prefrontal cortex as an antidepressant target. Neuroimaging studies – including meta-analyses – indicate that sadness is associated with reduced cortical activation, which may contribute to reduced parasympathetic inhibitory control over medullary cardioacceleratory circuits. Reduced cardiac control may – in part – contribute to epidemiological reports of reduced life expectancy in affective disorders, effects equivalent to heavy smoking. We suggest that the field may be moving toward a theoretical consensus, in which different models relating to basic emotion theory and psychological constructionism may be considered as complementary, working at different levels of the phylogenetic hierarchy.</description><subject>Affective neuroscience</subject><subject>Autonomic Nervous System - metabolism</subject><subject>Autonomic Nervous System - physiopathology</subject><subject>Basic emotions</subject><subject>Cerebral Cortex - metabolism</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Epigenesis, Genetic - physiology</subject><subject>Genetics</subject><subject>GENIAL model</subject><subject>Health and wellbeing</subject><subject>Heart rate variability</subject><subject>Humans</subject><subject>Interoception - physiology</subject><subject>Major depressive disorder</subject><subject>Mood Disorders - genetics</subject><subject>Mood Disorders - metabolism</subject><subject>Mood Disorders - physiopathology</subject><subject>Nerve Net - metabolism</subject><subject>Nerve Net - physiopathology</subject><subject>Neuroimaging</subject><subject>Neurosciences</subject><subject>Psychological constructionism</subject><subject>Psychological Theory</subject><subject>Psychophysiology</subject><subject>Sadness</subject><subject>Sadness - physiology</subject><subject>Vagal function</subject><issn>0149-7634</issn><issn>1873-7528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EoqXwC-Alm4SxkzgJuwrxkiqxoKwtx56orvIodlLUv8dVS7esvPCZmXsPIXcMYgZMPKzjDsfK9g63MQcOMbAYQJyRKSvyJMozXpyTKbC0jHKRpBNy5f0aIJBJdkkmCQdgPE-n5HO5Qhp2ud5ri51G2tfUK9Oh9490TtuxGayx4XPT2E65HfW7bliht56qzlDdN42qeqcGu0Ua4lj8uSYXtWo83hzfGfl6eV4-vUWLj9f3p_ki0imHIUIGWcHrShXMpKCNqpgSGashrUyR1Eyp0uQChdYlKFNrJVRqRFlrBM5R58mM3B_2blz_PaIfZBuCYgjUYT96yZMMoCgz2KP5AdWhqHdYy42zbagjGci9UbmWJ6Nyb1QCk8FomLw9HhmrFs1p7k9hAOYHAEPVUN_Jo0ljHepBmt7-e-QX6M-OMA</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Arias, Juan A.</creator><creator>Williams, Claire</creator><creator>Raghvani, Rashmi</creator><creator>Aghajani, Moji</creator><creator>Baez, Sandra</creator><creator>Belzung, Catherine</creator><creator>Booij, Linda</creator><creator>Busatto, Geraldo</creator><creator>Chiarella, Julian</creator><creator>Fu, Cynthia HY</creator><creator>Ibanez, Agustin</creator><creator>Liddell, Belinda J.</creator><creator>Lowe, Leroy</creator><creator>Penninx, Brenda W.J.H.</creator><creator>Rosa, Pedro</creator><creator>Kemp, Andrew H.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><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><orcidid>https://orcid.org/0000-0003-4313-3500</orcidid><orcidid>https://orcid.org/0000-0003-1146-3791</orcidid><orcidid>https://orcid.org/0000-0002-3355-6393</orcidid></search><sort><creationdate>202004</creationdate><title>The neuroscience of sadness: A multidisciplinary synthesis and collaborative review</title><author>Arias, Juan A. ; Williams, Claire ; Raghvani, Rashmi ; Aghajani, Moji ; Baez, Sandra ; Belzung, Catherine ; Booij, Linda ; Busatto, Geraldo ; Chiarella, Julian ; Fu, Cynthia HY ; Ibanez, Agustin ; Liddell, Belinda J. ; Lowe, Leroy ; Penninx, Brenda W.J.H. ; Rosa, Pedro ; Kemp, Andrew H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-e10582fba81d40cdab1a651f04bd83f1aa9d76e6cc90adfca6a4d69fce022ec73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Affective neuroscience</topic><topic>Autonomic Nervous System - metabolism</topic><topic>Autonomic Nervous System - physiopathology</topic><topic>Basic emotions</topic><topic>Cerebral Cortex - metabolism</topic><topic>Cerebral Cortex - physiopathology</topic><topic>Epigenesis, Genetic - physiology</topic><topic>Genetics</topic><topic>GENIAL model</topic><topic>Health and wellbeing</topic><topic>Heart rate variability</topic><topic>Humans</topic><topic>Interoception - physiology</topic><topic>Major depressive disorder</topic><topic>Mood Disorders - genetics</topic><topic>Mood Disorders - metabolism</topic><topic>Mood Disorders - physiopathology</topic><topic>Nerve Net - metabolism</topic><topic>Nerve Net - physiopathology</topic><topic>Neuroimaging</topic><topic>Neurosciences</topic><topic>Psychological constructionism</topic><topic>Psychological Theory</topic><topic>Psychophysiology</topic><topic>Sadness</topic><topic>Sadness - physiology</topic><topic>Vagal function</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arias, Juan A.</creatorcontrib><creatorcontrib>Williams, Claire</creatorcontrib><creatorcontrib>Raghvani, Rashmi</creatorcontrib><creatorcontrib>Aghajani, Moji</creatorcontrib><creatorcontrib>Baez, Sandra</creatorcontrib><creatorcontrib>Belzung, Catherine</creatorcontrib><creatorcontrib>Booij, Linda</creatorcontrib><creatorcontrib>Busatto, Geraldo</creatorcontrib><creatorcontrib>Chiarella, Julian</creatorcontrib><creatorcontrib>Fu, Cynthia HY</creatorcontrib><creatorcontrib>Ibanez, Agustin</creatorcontrib><creatorcontrib>Liddell, Belinda J.</creatorcontrib><creatorcontrib>Lowe, Leroy</creatorcontrib><creatorcontrib>Penninx, Brenda W.J.H.</creatorcontrib><creatorcontrib>Rosa, Pedro</creatorcontrib><creatorcontrib>Kemp, Andrew H.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><jtitle>Neuroscience and biobehavioral reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arias, Juan A.</au><au>Williams, Claire</au><au>Raghvani, Rashmi</au><au>Aghajani, Moji</au><au>Baez, Sandra</au><au>Belzung, Catherine</au><au>Booij, Linda</au><au>Busatto, Geraldo</au><au>Chiarella, Julian</au><au>Fu, Cynthia HY</au><au>Ibanez, Agustin</au><au>Liddell, Belinda J.</au><au>Lowe, Leroy</au><au>Penninx, Brenda W.J.H.</au><au>Rosa, Pedro</au><au>Kemp, Andrew H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The neuroscience of sadness: A multidisciplinary synthesis and collaborative review</atitle><jtitle>Neuroscience and biobehavioral reviews</jtitle><addtitle>Neurosci Biobehav Rev</addtitle><date>2020-04</date><risdate>2020</risdate><volume>111</volume><spage>199</spage><epage>228</epage><pages>199-228</pages><issn>0149-7634</issn><eissn>1873-7528</eissn><abstract>•Sadness involves reduction of cortical control over evolutionarily ancient brain systems.•Basic emotion theorists have identified a SADNESS circuit, based on animal research.•Psychological constructionists have identified patterns of activity that dependent on context.•Competing models may relate to different levels on a phylogenetic hierarchy.•Dedicated funding to facilitate collaborative and transdisciplinary opportunities is needed.
Sadness is typically characterized by raised inner eyebrows, lowered corners of the mouth, reduced walking speed, and slumped posture. Ancient subcortical circuitry provides a neuroanatomical foundation, extending from dorsal periaqueductal grey to subgenual anterior cingulate, the latter of which is now a treatment target in disorders of sadness. Electrophysiological studies further emphasize a role for reduced left relative to right frontal asymmetry in sadness, underpinning interest in the transcranial stimulation of left dorsolateral prefrontal cortex as an antidepressant target. Neuroimaging studies – including meta-analyses – indicate that sadness is associated with reduced cortical activation, which may contribute to reduced parasympathetic inhibitory control over medullary cardioacceleratory circuits. Reduced cardiac control may – in part – contribute to epidemiological reports of reduced life expectancy in affective disorders, effects equivalent to heavy smoking. We suggest that the field may be moving toward a theoretical consensus, in which different models relating to basic emotion theory and psychological constructionism may be considered as complementary, working at different levels of the phylogenetic hierarchy.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>32001274</pmid><doi>10.1016/j.neubiorev.2020.01.006</doi><tpages>30</tpages><orcidid>https://orcid.org/0000-0003-4313-3500</orcidid><orcidid>https://orcid.org/0000-0003-1146-3791</orcidid><orcidid>https://orcid.org/0000-0002-3355-6393</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Affective neuroscience Autonomic Nervous System - metabolism Autonomic Nervous System - physiopathology Basic emotions Cerebral Cortex - metabolism Cerebral Cortex - physiopathology Epigenesis, Genetic - physiology Genetics GENIAL model Health and wellbeing Heart rate variability Humans Interoception - physiology Major depressive disorder Mood Disorders - genetics Mood Disorders - metabolism Mood Disorders - physiopathology Nerve Net - metabolism Nerve Net - physiopathology Neuroimaging Neurosciences Psychological constructionism Psychological Theory Psychophysiology Sadness Sadness - physiology Vagal function |
title | The neuroscience of sadness: A multidisciplinary synthesis and collaborative review |
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