Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol
This study investigated whether transcutaneous auricular vagus nerve stimulation (taVNS) enhances reversal learning and augments noradrenergic biomarkers (i.e., pupil size, cortisol, and salivary alpha‐amylase [sAA]). We also explored the effect of taVNS on respiratory rate and cardiac vagal activit...
Gespeichert in:
Veröffentlicht in: | Psychophysiology 2021-10, Vol.58 (10), p.e13885-n/a |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | n/a |
---|---|
container_issue | 10 |
container_start_page | e13885 |
container_title | Psychophysiology |
container_volume | 58 |
creator | D’Agostini, Martina Burger, Andreas M. Franssen, Mathijs Claes, Nathalie Weymar, Mathias Leupoldt, Andreas Van Diest, Ilse |
description | This study investigated whether transcutaneous auricular vagus nerve stimulation (taVNS) enhances reversal learning and augments noradrenergic biomarkers (i.e., pupil size, cortisol, and salivary alpha‐amylase [sAA]). We also explored the effect of taVNS on respiratory rate and cardiac vagal activity (CVA). Seventy‐one participants received stimulation of either the cymba concha (taVNS) or the earlobe (sham) of the left ear. After learning a series of cue‐outcome associations, the stimulation was applied before and throughout a reversal phase in which cue‐outcome associations were changed for some (reversal), but not for other (distractor) cues. Tonic pupil size, salivary cortisol, sAA, respiratory rate, and CVA were assessed at different time points. Contrary to our hypothesis, taVNS was not associated with an overall improvement in performance on the reversal task. Compared to sham, the taVNS group performed worse for distractor than reversal cues. taVNS did not increase tonic pupil size and sAA. Only post hoc analyses indicated that the cortisol decline was steeper in the sham compared to the taVNS group. Exploratory analyses showed that taVNS decreased respiratory rate but did not affect CVA. The weak and unexpected effects found in this study might relate to the lack of parameters optimization for taVNS and invite to further investigate the effect of taVNS on cortisol and respiratory rate.
Contrary to our hypotheses, we did not observe enhancing effects of transcutaneous auricular vagus nerve stimulation (taVNS) on reversal learning and noradrenergic markers. Our findings question whether a commonly used parameter‐setup of taVNS can activate the vagus nerve and modulate noradrenergic activity. These results add to a growing body of zero findings and call for more basic taVNS research regarding optimal stimulation parameters and locations. |
doi_str_mv | 10.1111/psyp.13885 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2568550669</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2568550669</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4145-abd30a11681cd38c842f1980a5081cb8fe51099b4550a4491159f258df00da5e3</originalsourceid><addsrcrecordid>eNp9kE1LBSEUhiWKun1s-gEhtIumdEYnXUb0BUFBtWg1nOtoGV6ddObGbdW6Vb-xX5J1q2VyQHzPc145L0KblOzRfPa7NOv2aCUEX0AjympZCCnqRTQihImCHxyUK2g1pUdCiKRluYxWKlYyzmo6Qm_HxmjVJxwM7iP4pIYevA5DwjBEqwYHEU_hPr-9jlONU28nWext8DhX1FMdEzjsNERv_f0u7oO3CndDZx1O9kXv4ty3U4gzDK57gI_Xd5jMHKTcAd9iFWJvU3DraMmAS3rj515DtyfHN0dnxcXl6fnR4UWhGGW8gHFbEaC0FlS1lVCClYZKQYCTrIyF0ZwSKceMcwKMSUq5NCUXrSGkBa6rNbQ99-1ieBp06pvHMESfv2xKXos8VtcyUztzSsWQUtSm6aKd5CUaSpqv2Juv2Jvv2DO89WM5jCe6_UN_c84AnQPP1unZP1bN1fXd1dz0E63jkRU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2568550669</pqid></control><display><type>article</type><title>Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>D’Agostini, Martina ; Burger, Andreas M. ; Franssen, Mathijs ; Claes, Nathalie ; Weymar, Mathias ; Leupoldt, Andreas ; Van Diest, Ilse</creator><creatorcontrib>D’Agostini, Martina ; Burger, Andreas M. ; Franssen, Mathijs ; Claes, Nathalie ; Weymar, Mathias ; Leupoldt, Andreas ; Van Diest, Ilse</creatorcontrib><description>This study investigated whether transcutaneous auricular vagus nerve stimulation (taVNS) enhances reversal learning and augments noradrenergic biomarkers (i.e., pupil size, cortisol, and salivary alpha‐amylase [sAA]). We also explored the effect of taVNS on respiratory rate and cardiac vagal activity (CVA). Seventy‐one participants received stimulation of either the cymba concha (taVNS) or the earlobe (sham) of the left ear. After learning a series of cue‐outcome associations, the stimulation was applied before and throughout a reversal phase in which cue‐outcome associations were changed for some (reversal), but not for other (distractor) cues. Tonic pupil size, salivary cortisol, sAA, respiratory rate, and CVA were assessed at different time points. Contrary to our hypothesis, taVNS was not associated with an overall improvement in performance on the reversal task. Compared to sham, the taVNS group performed worse for distractor than reversal cues. taVNS did not increase tonic pupil size and sAA. Only post hoc analyses indicated that the cortisol decline was steeper in the sham compared to the taVNS group. Exploratory analyses showed that taVNS decreased respiratory rate but did not affect CVA. The weak and unexpected effects found in this study might relate to the lack of parameters optimization for taVNS and invite to further investigate the effect of taVNS on cortisol and respiratory rate.
Contrary to our hypotheses, we did not observe enhancing effects of transcutaneous auricular vagus nerve stimulation (taVNS) on reversal learning and noradrenergic markers. Our findings question whether a commonly used parameter‐setup of taVNS can activate the vagus nerve and modulate noradrenergic activity. These results add to a growing body of zero findings and call for more basic taVNS research regarding optimal stimulation parameters and locations.</description><identifier>ISSN: 0048-5772</identifier><identifier>EISSN: 1469-8986</identifier><identifier>EISSN: 1540-5958</identifier><identifier>DOI: 10.1111/psyp.13885</identifier><identifier>PMID: 34245461</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adult ; Association Learning - physiology ; Autonomic Nervous System - physiology ; Cortisol ; Ear Auricle ; Female ; Heart rate ; Heart Rate - physiology ; Hormones ; Humans ; Hydrocortisone - metabolism ; Male ; noradrenaline ; Norepinephrine ; Pupil - physiology ; pupillometry ; Respiration ; Respiratory Rate - physiology ; Reversal learning ; Reversal Learning - physiology ; Salivary alpha-Amylases - metabolism ; salivary alpha‐amylase ; transcutaneous auricular vagus nerve stimulation ; Transcutaneous Electric Nerve Stimulation ; Vagus nerve ; Vagus Nerve Stimulation ; Young Adult</subject><ispartof>Psychophysiology, 2021-10, Vol.58 (10), p.e13885-n/a</ispartof><rights>2021 Society for Psychophysiological Research</rights><rights>2021 Society for Psychophysiological Research.</rights><rights>Copyright © 2021 by the Society for Psychophysiological Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4145-abd30a11681cd38c842f1980a5081cb8fe51099b4550a4491159f258df00da5e3</citedby><cites>FETCH-LOGICAL-c4145-abd30a11681cd38c842f1980a5081cb8fe51099b4550a4491159f258df00da5e3</cites><orcidid>0000-0003-1383-7638 ; 0000-0002-3968-9656 ; 0000-0002-0048-774X ; 0000-0002-5727-1130</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpsyp.13885$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpsyp.13885$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34245461$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>D’Agostini, Martina</creatorcontrib><creatorcontrib>Burger, Andreas M.</creatorcontrib><creatorcontrib>Franssen, Mathijs</creatorcontrib><creatorcontrib>Claes, Nathalie</creatorcontrib><creatorcontrib>Weymar, Mathias</creatorcontrib><creatorcontrib>Leupoldt, Andreas</creatorcontrib><creatorcontrib>Van Diest, Ilse</creatorcontrib><title>Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol</title><title>Psychophysiology</title><addtitle>Psychophysiology</addtitle><description>This study investigated whether transcutaneous auricular vagus nerve stimulation (taVNS) enhances reversal learning and augments noradrenergic biomarkers (i.e., pupil size, cortisol, and salivary alpha‐amylase [sAA]). We also explored the effect of taVNS on respiratory rate and cardiac vagal activity (CVA). Seventy‐one participants received stimulation of either the cymba concha (taVNS) or the earlobe (sham) of the left ear. After learning a series of cue‐outcome associations, the stimulation was applied before and throughout a reversal phase in which cue‐outcome associations were changed for some (reversal), but not for other (distractor) cues. Tonic pupil size, salivary cortisol, sAA, respiratory rate, and CVA were assessed at different time points. Contrary to our hypothesis, taVNS was not associated with an overall improvement in performance on the reversal task. Compared to sham, the taVNS group performed worse for distractor than reversal cues. taVNS did not increase tonic pupil size and sAA. Only post hoc analyses indicated that the cortisol decline was steeper in the sham compared to the taVNS group. Exploratory analyses showed that taVNS decreased respiratory rate but did not affect CVA. The weak and unexpected effects found in this study might relate to the lack of parameters optimization for taVNS and invite to further investigate the effect of taVNS on cortisol and respiratory rate.
Contrary to our hypotheses, we did not observe enhancing effects of transcutaneous auricular vagus nerve stimulation (taVNS) on reversal learning and noradrenergic markers. Our findings question whether a commonly used parameter‐setup of taVNS can activate the vagus nerve and modulate noradrenergic activity. These results add to a growing body of zero findings and call for more basic taVNS research regarding optimal stimulation parameters and locations.</description><subject>Adult</subject><subject>Association Learning - physiology</subject><subject>Autonomic Nervous System - physiology</subject><subject>Cortisol</subject><subject>Ear Auricle</subject><subject>Female</subject><subject>Heart rate</subject><subject>Heart Rate - physiology</subject><subject>Hormones</subject><subject>Humans</subject><subject>Hydrocortisone - metabolism</subject><subject>Male</subject><subject>noradrenaline</subject><subject>Norepinephrine</subject><subject>Pupil - physiology</subject><subject>pupillometry</subject><subject>Respiration</subject><subject>Respiratory Rate - physiology</subject><subject>Reversal learning</subject><subject>Reversal Learning - physiology</subject><subject>Salivary alpha-Amylases - metabolism</subject><subject>salivary alpha‐amylase</subject><subject>transcutaneous auricular vagus nerve stimulation</subject><subject>Transcutaneous Electric Nerve Stimulation</subject><subject>Vagus nerve</subject><subject>Vagus Nerve Stimulation</subject><subject>Young Adult</subject><issn>0048-5772</issn><issn>1469-8986</issn><issn>1540-5958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LBSEUhiWKun1s-gEhtIumdEYnXUb0BUFBtWg1nOtoGV6ddObGbdW6Vb-xX5J1q2VyQHzPc145L0KblOzRfPa7NOv2aCUEX0AjympZCCnqRTQihImCHxyUK2g1pUdCiKRluYxWKlYyzmo6Qm_HxmjVJxwM7iP4pIYevA5DwjBEqwYHEU_hPr-9jlONU28nWext8DhX1FMdEzjsNERv_f0u7oO3CndDZx1O9kXv4ty3U4gzDK57gI_Xd5jMHKTcAd9iFWJvU3DraMmAS3rj515DtyfHN0dnxcXl6fnR4UWhGGW8gHFbEaC0FlS1lVCClYZKQYCTrIyF0ZwSKceMcwKMSUq5NCUXrSGkBa6rNbQ99-1ieBp06pvHMESfv2xKXos8VtcyUztzSsWQUtSm6aKd5CUaSpqv2Juv2Jvv2DO89WM5jCe6_UN_c84AnQPP1unZP1bN1fXd1dz0E63jkRU</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>D’Agostini, Martina</creator><creator>Burger, Andreas M.</creator><creator>Franssen, Mathijs</creator><creator>Claes, Nathalie</creator><creator>Weymar, Mathias</creator><creator>Leupoldt, Andreas</creator><creator>Van Diest, Ilse</creator><general>Blackwell Publishing Ltd</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>7TK</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0003-1383-7638</orcidid><orcidid>https://orcid.org/0000-0002-3968-9656</orcidid><orcidid>https://orcid.org/0000-0002-0048-774X</orcidid><orcidid>https://orcid.org/0000-0002-5727-1130</orcidid></search><sort><creationdate>202110</creationdate><title>Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol</title><author>D’Agostini, Martina ; Burger, Andreas M. ; Franssen, Mathijs ; Claes, Nathalie ; Weymar, Mathias ; Leupoldt, Andreas ; Van Diest, Ilse</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4145-abd30a11681cd38c842f1980a5081cb8fe51099b4550a4491159f258df00da5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Association Learning - physiology</topic><topic>Autonomic Nervous System - physiology</topic><topic>Cortisol</topic><topic>Ear Auricle</topic><topic>Female</topic><topic>Heart rate</topic><topic>Heart Rate - physiology</topic><topic>Hormones</topic><topic>Humans</topic><topic>Hydrocortisone - metabolism</topic><topic>Male</topic><topic>noradrenaline</topic><topic>Norepinephrine</topic><topic>Pupil - physiology</topic><topic>pupillometry</topic><topic>Respiration</topic><topic>Respiratory Rate - physiology</topic><topic>Reversal learning</topic><topic>Reversal Learning - physiology</topic><topic>Salivary alpha-Amylases - metabolism</topic><topic>salivary alpha‐amylase</topic><topic>transcutaneous auricular vagus nerve stimulation</topic><topic>Transcutaneous Electric Nerve Stimulation</topic><topic>Vagus nerve</topic><topic>Vagus Nerve Stimulation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>D’Agostini, Martina</creatorcontrib><creatorcontrib>Burger, Andreas M.</creatorcontrib><creatorcontrib>Franssen, Mathijs</creatorcontrib><creatorcontrib>Claes, Nathalie</creatorcontrib><creatorcontrib>Weymar, Mathias</creatorcontrib><creatorcontrib>Leupoldt, Andreas</creatorcontrib><creatorcontrib>Van Diest, Ilse</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Psychophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>D’Agostini, Martina</au><au>Burger, Andreas M.</au><au>Franssen, Mathijs</au><au>Claes, Nathalie</au><au>Weymar, Mathias</au><au>Leupoldt, Andreas</au><au>Van Diest, Ilse</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol</atitle><jtitle>Psychophysiology</jtitle><addtitle>Psychophysiology</addtitle><date>2021-10</date><risdate>2021</risdate><volume>58</volume><issue>10</issue><spage>e13885</spage><epage>n/a</epage><pages>e13885-n/a</pages><issn>0048-5772</issn><eissn>1469-8986</eissn><eissn>1540-5958</eissn><abstract>This study investigated whether transcutaneous auricular vagus nerve stimulation (taVNS) enhances reversal learning and augments noradrenergic biomarkers (i.e., pupil size, cortisol, and salivary alpha‐amylase [sAA]). We also explored the effect of taVNS on respiratory rate and cardiac vagal activity (CVA). Seventy‐one participants received stimulation of either the cymba concha (taVNS) or the earlobe (sham) of the left ear. After learning a series of cue‐outcome associations, the stimulation was applied before and throughout a reversal phase in which cue‐outcome associations were changed for some (reversal), but not for other (distractor) cues. Tonic pupil size, salivary cortisol, sAA, respiratory rate, and CVA were assessed at different time points. Contrary to our hypothesis, taVNS was not associated with an overall improvement in performance on the reversal task. Compared to sham, the taVNS group performed worse for distractor than reversal cues. taVNS did not increase tonic pupil size and sAA. Only post hoc analyses indicated that the cortisol decline was steeper in the sham compared to the taVNS group. Exploratory analyses showed that taVNS decreased respiratory rate but did not affect CVA. The weak and unexpected effects found in this study might relate to the lack of parameters optimization for taVNS and invite to further investigate the effect of taVNS on cortisol and respiratory rate.
Contrary to our hypotheses, we did not observe enhancing effects of transcutaneous auricular vagus nerve stimulation (taVNS) on reversal learning and noradrenergic markers. Our findings question whether a commonly used parameter‐setup of taVNS can activate the vagus nerve and modulate noradrenergic activity. These results add to a growing body of zero findings and call for more basic taVNS research regarding optimal stimulation parameters and locations.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>34245461</pmid><doi>10.1111/psyp.13885</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0003-1383-7638</orcidid><orcidid>https://orcid.org/0000-0002-3968-9656</orcidid><orcidid>https://orcid.org/0000-0002-0048-774X</orcidid><orcidid>https://orcid.org/0000-0002-5727-1130</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0048-5772 |
ispartof | Psychophysiology, 2021-10, Vol.58 (10), p.e13885-n/a |
issn | 0048-5772 1469-8986 1540-5958 |
language | eng |
recordid | cdi_proquest_journals_2568550669 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Adult Association Learning - physiology Autonomic Nervous System - physiology Cortisol Ear Auricle Female Heart rate Heart Rate - physiology Hormones Humans Hydrocortisone - metabolism Male noradrenaline Norepinephrine Pupil - physiology pupillometry Respiration Respiratory Rate - physiology Reversal learning Reversal Learning - physiology Salivary alpha-Amylases - metabolism salivary alpha‐amylase transcutaneous auricular vagus nerve stimulation Transcutaneous Electric Nerve Stimulation Vagus nerve Vagus Nerve Stimulation Young Adult |
title | Effects of transcutaneous auricular vagus nerve stimulation on reversal learning, tonic pupil size, salivary alpha‐amylase, and cortisol |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T14%3A42%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20transcutaneous%20auricular%20vagus%20nerve%20stimulation%20on%20reversal%20learning,%20tonic%20pupil%20size,%20salivary%20alpha%E2%80%90amylase,%20and%20cortisol&rft.jtitle=Psychophysiology&rft.au=D%E2%80%99Agostini,%20Martina&rft.date=2021-10&rft.volume=58&rft.issue=10&rft.spage=e13885&rft.epage=n/a&rft.pages=e13885-n/a&rft.issn=0048-5772&rft.eissn=1469-8986&rft_id=info:doi/10.1111/psyp.13885&rft_dat=%3Cproquest_cross%3E2568550669%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2568550669&rft_id=info:pmid/34245461&rfr_iscdi=true |