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State-Dependent TMS over Prefrontal Cortex Disrupts Fear-Memory Reconsolidation and Prevents the Return of Fear
Erasing maladaptive memories has been a challenge for years. A way to change fear memories is to target the process of reconsolidation, during which a retrieved memory transiently returns to a labile state, amenable to modification [1, 2]. Disruption of human fear-memory reconsolidation has been cla...
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Published in: | Current biology 2020-09, Vol.30 (18), p.3672-3679.e4 |
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description | Erasing maladaptive memories has been a challenge for years. A way to change fear memories is to target the process of reconsolidation, during which a retrieved memory transiently returns to a labile state, amenable to modification [1, 2]. Disruption of human fear-memory reconsolidation has been classically attempted with pharmacological [3] or behavioral (e.g., extinction) [4] treatments that, however, do not clarify the underlying brain mechanism. To address this issue, in 84 healthy humans submitted to six experiments, here, we combined a differential fear conditioning paradigm with repetitive transcranial magnetic stimulation (rTMS) administered in a state-dependent manner. In a critical condition, we stimulated the dorsolateral prefrontal cortex (dlPFC) 10 min after a reminder cue that reactivated a fear memory acquired 1 day before. At testing, 24 h after rTMS, participants exhibited decreased physiological expression of fear, as shown by their skin conductance response. Similar reductions were observed when targeting the left and the right dlPFC. In contrast, no decrease was observed in participants tested immediately after dlPFC-rTMS or in participants receiving either control rTMS (i.e., active control site and sham stimulations) or dlPFC-rTMS without preceding fear-memory reactivation, thus showing both the site and time specificity and state dependency of our rTMS intervention. Expression of fear was indeed reduced only when dlPFC-rTMS was administered within the reconsolidation time window. Moreover, dlPFC-rTMS prevented subsequent return of fear after extinction training. These findings highlight the causal role of dlPFC in fear-memory reconsolidation and suggest that rTMS can be used in humans to prevent the return of fear.
•Post-retrieval rTMS over dlPFC reduces physiological responding to learned fear•Post-retrieval rTMS over dlPFC prevents the return of fear after reinstatement•Post-retrieval rTMS over dlPFC disrupts fear responses, not declarative memory•The dlPFC plays a key role in fear-memory reconsolidation
Borgomaneri et al. show that the noninvasive stimulation of the prefrontal cortex after memory reactivation disrupts physiological responding to learned fear and argue in favor of a critical role of the dlPFC in the neural network that mediates the reconsolidation of fear memories in humans. |
doi_str_mv | 10.1016/j.cub.2020.06.091 |
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•Post-retrieval rTMS over dlPFC reduces physiological responding to learned fear•Post-retrieval rTMS over dlPFC prevents the return of fear after reinstatement•Post-retrieval rTMS over dlPFC disrupts fear responses, not declarative memory•The dlPFC plays a key role in fear-memory reconsolidation
Borgomaneri et al. show that the noninvasive stimulation of the prefrontal cortex after memory reactivation disrupts physiological responding to learned fear and argue in favor of a critical role of the dlPFC in the neural network that mediates the reconsolidation of fear memories in humans.</description><identifier>ISSN: 0960-9822</identifier><identifier>EISSN: 1879-0445</identifier><identifier>DOI: 10.1016/j.cub.2020.06.091</identifier><identifier>PMID: 32735813</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>dorsolateral prefrontal cortex ; fear conditioning ; memory reconsolidation ; reinstatement ; state dependency ; transcranial magnetic stimulation</subject><ispartof>Current biology, 2020-09, Vol.30 (18), p.3672-3679.e4</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c348t-ebcc58e91e585f0b1ee3bd9304f901b16ca8b6c569246afae14879ca1a869db23</cites><orcidid>0000-0002-6023-2802 ; 0000-0003-1139-9996 ; 0000-0001-7080-4758 ; 0000-0003-4133-654X ; 0000-0003-4959-6442</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32735813$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borgomaneri, Sara</creatorcontrib><creatorcontrib>Battaglia, Simone</creatorcontrib><creatorcontrib>Garofalo, Sara</creatorcontrib><creatorcontrib>Tortora, Francesco</creatorcontrib><creatorcontrib>Avenanti, Alessio</creatorcontrib><creatorcontrib>di Pellegrino, Giuseppe</creatorcontrib><title>State-Dependent TMS over Prefrontal Cortex Disrupts Fear-Memory Reconsolidation and Prevents the Return of Fear</title><title>Current biology</title><addtitle>Curr Biol</addtitle><description>Erasing maladaptive memories has been a challenge for years. A way to change fear memories is to target the process of reconsolidation, during which a retrieved memory transiently returns to a labile state, amenable to modification [1, 2]. Disruption of human fear-memory reconsolidation has been classically attempted with pharmacological [3] or behavioral (e.g., extinction) [4] treatments that, however, do not clarify the underlying brain mechanism. To address this issue, in 84 healthy humans submitted to six experiments, here, we combined a differential fear conditioning paradigm with repetitive transcranial magnetic stimulation (rTMS) administered in a state-dependent manner. In a critical condition, we stimulated the dorsolateral prefrontal cortex (dlPFC) 10 min after a reminder cue that reactivated a fear memory acquired 1 day before. At testing, 24 h after rTMS, participants exhibited decreased physiological expression of fear, as shown by their skin conductance response. Similar reductions were observed when targeting the left and the right dlPFC. In contrast, no decrease was observed in participants tested immediately after dlPFC-rTMS or in participants receiving either control rTMS (i.e., active control site and sham stimulations) or dlPFC-rTMS without preceding fear-memory reactivation, thus showing both the site and time specificity and state dependency of our rTMS intervention. Expression of fear was indeed reduced only when dlPFC-rTMS was administered within the reconsolidation time window. Moreover, dlPFC-rTMS prevented subsequent return of fear after extinction training. These findings highlight the causal role of dlPFC in fear-memory reconsolidation and suggest that rTMS can be used in humans to prevent the return of fear.
•Post-retrieval rTMS over dlPFC reduces physiological responding to learned fear•Post-retrieval rTMS over dlPFC prevents the return of fear after reinstatement•Post-retrieval rTMS over dlPFC disrupts fear responses, not declarative memory•The dlPFC plays a key role in fear-memory reconsolidation
Borgomaneri et al. show that the noninvasive stimulation of the prefrontal cortex after memory reactivation disrupts physiological responding to learned fear and argue in favor of a critical role of the dlPFC in the neural network that mediates the reconsolidation of fear memories in humans.</description><subject>dorsolateral prefrontal cortex</subject><subject>fear conditioning</subject><subject>memory reconsolidation</subject><subject>reinstatement</subject><subject>state dependency</subject><subject>transcranial magnetic stimulation</subject><issn>0960-9822</issn><issn>1879-0445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kMFO3DAURS3UqkyhH8Cm8rKbpM9O4rHFqhqgIIFaAV1bjvOiepSxp7Yzgr_H04Euu7qbc690DyFnDGoGTHxd13buaw4cahA1KHZEFkwuVQVt270jC1ACKiU5PyYfU1oDMC6V-ECOG75sOsmaBQkP2WSsLnCLfkCf6ePdAw07jPRnxDEGn81EVyFmfKIXLsV5mxO9QhOrO9yE-Ezv0QafwuQGk13w1PhhX92VrUTzbyxAnqOnYfxbOyXvRzMl_PSaJ-TX1eXj6rq6_fH9ZvXttrJNK3OFvbWdRMWwk90IPUNs-kE10I4KWM-ENbIXthOKt8KMBllbflvDjBRq6HlzQr4cdrcx_JkxZb1xyeI0GY9hTpq3XC0lLLkqKDugNoaUymu9jW5j4rNmoPee9VoXz3rvWYPQxXPpfH6dn_sNDv8ab2ILcH4AsJzcOYw6WYfe4uAi2qyH4P4z_wIW1o8k</recordid><startdate>20200921</startdate><enddate>20200921</enddate><creator>Borgomaneri, Sara</creator><creator>Battaglia, Simone</creator><creator>Garofalo, Sara</creator><creator>Tortora, Francesco</creator><creator>Avenanti, Alessio</creator><creator>di Pellegrino, Giuseppe</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6023-2802</orcidid><orcidid>https://orcid.org/0000-0003-1139-9996</orcidid><orcidid>https://orcid.org/0000-0001-7080-4758</orcidid><orcidid>https://orcid.org/0000-0003-4133-654X</orcidid><orcidid>https://orcid.org/0000-0003-4959-6442</orcidid></search><sort><creationdate>20200921</creationdate><title>State-Dependent TMS over Prefrontal Cortex Disrupts Fear-Memory Reconsolidation and Prevents the Return of Fear</title><author>Borgomaneri, Sara ; Battaglia, Simone ; Garofalo, Sara ; Tortora, Francesco ; Avenanti, Alessio ; di Pellegrino, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-ebcc58e91e585f0b1ee3bd9304f901b16ca8b6c569246afae14879ca1a869db23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>dorsolateral prefrontal cortex</topic><topic>fear conditioning</topic><topic>memory reconsolidation</topic><topic>reinstatement</topic><topic>state dependency</topic><topic>transcranial magnetic stimulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borgomaneri, Sara</creatorcontrib><creatorcontrib>Battaglia, Simone</creatorcontrib><creatorcontrib>Garofalo, Sara</creatorcontrib><creatorcontrib>Tortora, Francesco</creatorcontrib><creatorcontrib>Avenanti, Alessio</creatorcontrib><creatorcontrib>di Pellegrino, Giuseppe</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borgomaneri, Sara</au><au>Battaglia, Simone</au><au>Garofalo, Sara</au><au>Tortora, Francesco</au><au>Avenanti, Alessio</au><au>di Pellegrino, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>State-Dependent TMS over Prefrontal Cortex Disrupts Fear-Memory Reconsolidation and Prevents the Return of Fear</atitle><jtitle>Current biology</jtitle><addtitle>Curr Biol</addtitle><date>2020-09-21</date><risdate>2020</risdate><volume>30</volume><issue>18</issue><spage>3672</spage><epage>3679.e4</epage><pages>3672-3679.e4</pages><issn>0960-9822</issn><eissn>1879-0445</eissn><abstract>Erasing maladaptive memories has been a challenge for years. A way to change fear memories is to target the process of reconsolidation, during which a retrieved memory transiently returns to a labile state, amenable to modification [1, 2]. Disruption of human fear-memory reconsolidation has been classically attempted with pharmacological [3] or behavioral (e.g., extinction) [4] treatments that, however, do not clarify the underlying brain mechanism. To address this issue, in 84 healthy humans submitted to six experiments, here, we combined a differential fear conditioning paradigm with repetitive transcranial magnetic stimulation (rTMS) administered in a state-dependent manner. In a critical condition, we stimulated the dorsolateral prefrontal cortex (dlPFC) 10 min after a reminder cue that reactivated a fear memory acquired 1 day before. At testing, 24 h after rTMS, participants exhibited decreased physiological expression of fear, as shown by their skin conductance response. Similar reductions were observed when targeting the left and the right dlPFC. In contrast, no decrease was observed in participants tested immediately after dlPFC-rTMS or in participants receiving either control rTMS (i.e., active control site and sham stimulations) or dlPFC-rTMS without preceding fear-memory reactivation, thus showing both the site and time specificity and state dependency of our rTMS intervention. Expression of fear was indeed reduced only when dlPFC-rTMS was administered within the reconsolidation time window. Moreover, dlPFC-rTMS prevented subsequent return of fear after extinction training. These findings highlight the causal role of dlPFC in fear-memory reconsolidation and suggest that rTMS can be used in humans to prevent the return of fear.
•Post-retrieval rTMS over dlPFC reduces physiological responding to learned fear•Post-retrieval rTMS over dlPFC prevents the return of fear after reinstatement•Post-retrieval rTMS over dlPFC disrupts fear responses, not declarative memory•The dlPFC plays a key role in fear-memory reconsolidation
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subjects | dorsolateral prefrontal cortex fear conditioning memory reconsolidation reinstatement state dependency transcranial magnetic stimulation |
title | State-Dependent TMS over Prefrontal Cortex Disrupts Fear-Memory Reconsolidation and Prevents the Return of Fear |
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