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Stimulation of the dorsal periaqueductal gray enhances spontaneous recovery of a conditioned taste aversion
Abstract Due to its relevance to clinical practice, extinction of learned fears has been a major focus of recent research. However, less is known about the means by which conditioned fears re-emerge (i.e., spontaneously recover) as time passes or contexts change following extinction. The periaqueduc...
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Published in: | Brain research 2013-02, Vol.1493, p.27-39 |
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description | Abstract Due to its relevance to clinical practice, extinction of learned fears has been a major focus of recent research. However, less is known about the means by which conditioned fears re-emerge (i.e., spontaneously recover) as time passes or contexts change following extinction. The periaqueductal gray represents the final common pathway mediating defensive reactions to fear and we have reported previously that the dorsolateral PAG (dlPAG) exhibits a small but reliable increase in neural activity (as measured by c-fos protein immunoreactivity) when spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced. Here we extend these correlational studies to determine if inducing dlPAG c-fos expression through electrical brain stimulation could cause a reduction in SR of a CTA. Male Sprague-Dawley rats acquired a strong aversion to saccharin (conditioned stimulus; CS) and then underwent CTA extinction through multiple non-reinforced exposures to the CS. Following a 30-day latency period after asymptotic extinction was achieved; rats either received stimulation of the dorsal PAG (dPAG) or stimulation of closely adjacent structures. Sixty minutes following the stimulation, rats were again presented with the saccharin solution as we tested for SR of the CTA. The brain stimulation evoked c-fos expression around the tip of the electrodes. However, stimulation of the dPAG failed to reduce SR of the previously extinguished CTA. In fact, dPAG stimulation caused rats to significantly suppress their saccharin drinking (relative to controls) – indicating an enhanced SR. These data refute a cause-and-effect relationship between enhanced dPAG c-fos expression and a reduction in SR. However, they highlight a role for the dPAG in modulating SR of extinguished CTAs. |
doi_str_mv | 10.1016/j.brainres.2012.11.029 |
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Andrew ; Ketchesin, Kyle D ; Ramos, Linnet ; Luchsinger, Joseph R ; Rogers, Morgan M ; Wiles, Nathanael R ; Hoxha, Nita</creator><creatorcontrib>Mickley, G. Andrew ; Ketchesin, Kyle D ; Ramos, Linnet ; Luchsinger, Joseph R ; Rogers, Morgan M ; Wiles, Nathanael R ; Hoxha, Nita</creatorcontrib><description>Abstract Due to its relevance to clinical practice, extinction of learned fears has been a major focus of recent research. However, less is known about the means by which conditioned fears re-emerge (i.e., spontaneously recover) as time passes or contexts change following extinction. The periaqueductal gray represents the final common pathway mediating defensive reactions to fear and we have reported previously that the dorsolateral PAG (dlPAG) exhibits a small but reliable increase in neural activity (as measured by c-fos protein immunoreactivity) when spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced. Here we extend these correlational studies to determine if inducing dlPAG c-fos expression through electrical brain stimulation could cause a reduction in SR of a CTA. Male Sprague-Dawley rats acquired a strong aversion to saccharin (conditioned stimulus; CS) and then underwent CTA extinction through multiple non-reinforced exposures to the CS. Following a 30-day latency period after asymptotic extinction was achieved; rats either received stimulation of the dorsal PAG (dPAG) or stimulation of closely adjacent structures. Sixty minutes following the stimulation, rats were again presented with the saccharin solution as we tested for SR of the CTA. The brain stimulation evoked c-fos expression around the tip of the electrodes. However, stimulation of the dPAG failed to reduce SR of the previously extinguished CTA. In fact, dPAG stimulation caused rats to significantly suppress their saccharin drinking (relative to controls) – indicating an enhanced SR. These data refute a cause-and-effect relationship between enhanced dPAG c-fos expression and a reduction in SR. However, they highlight a role for the dPAG in modulating SR of extinguished CTAs.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2012.11.029</identifier><identifier>PMID: 23183042</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Anatomical correlates of behavior ; Animals ; Avoidance Learning - physiology ; Behavior, Animal - physiology ; Behavioral psychophysiology ; Biological and medical sciences ; brain ; c-fos ; Central gray ; Conditioned taste aversion ; Conditioning (Psychology) - physiology ; CTA ; drinking ; Electric Stimulation ; electrodes ; Electrodes, Implanted ; Extinction ; Extinction, Psychological - physiology ; Fundamental and applied biological sciences. Psychology ; Male ; Neurology ; Olfactory system and olfaction. Gustatory system and gustation ; PAG ; Periaqueductal gray ; Periaqueductal Gray - physiology ; Psychology. Psychoanalysis. Psychiatry ; Psychology. Psychophysiology ; Rats ; Rats, Sprague-Dawley ; Saccharin ; Spontaneous recovery ; taste ; Taste - physiology ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research, 2013-02, Vol.1493, p.27-39</ispartof><rights>Elsevier B.V.</rights><rights>2012 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><rights>2012 Elsevier B.V. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c679t-e2d5d29992611fb1ea5045ce95d4ae8e982688532236578dc43b132cc47e5063</citedby><cites>FETCH-LOGICAL-c679t-e2d5d29992611fb1ea5045ce95d4ae8e982688532236578dc43b132cc47e5063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26803194$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23183042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mickley, G. Andrew</creatorcontrib><creatorcontrib>Ketchesin, Kyle D</creatorcontrib><creatorcontrib>Ramos, Linnet</creatorcontrib><creatorcontrib>Luchsinger, Joseph R</creatorcontrib><creatorcontrib>Rogers, Morgan M</creatorcontrib><creatorcontrib>Wiles, Nathanael R</creatorcontrib><creatorcontrib>Hoxha, Nita</creatorcontrib><title>Stimulation of the dorsal periaqueductal gray enhances spontaneous recovery of a conditioned taste aversion</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Abstract Due to its relevance to clinical practice, extinction of learned fears has been a major focus of recent research. However, less is known about the means by which conditioned fears re-emerge (i.e., spontaneously recover) as time passes or contexts change following extinction. The periaqueductal gray represents the final common pathway mediating defensive reactions to fear and we have reported previously that the dorsolateral PAG (dlPAG) exhibits a small but reliable increase in neural activity (as measured by c-fos protein immunoreactivity) when spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced. Here we extend these correlational studies to determine if inducing dlPAG c-fos expression through electrical brain stimulation could cause a reduction in SR of a CTA. Male Sprague-Dawley rats acquired a strong aversion to saccharin (conditioned stimulus; CS) and then underwent CTA extinction through multiple non-reinforced exposures to the CS. Following a 30-day latency period after asymptotic extinction was achieved; rats either received stimulation of the dorsal PAG (dPAG) or stimulation of closely adjacent structures. Sixty minutes following the stimulation, rats were again presented with the saccharin solution as we tested for SR of the CTA. The brain stimulation evoked c-fos expression around the tip of the electrodes. However, stimulation of the dPAG failed to reduce SR of the previously extinguished CTA. In fact, dPAG stimulation caused rats to significantly suppress their saccharin drinking (relative to controls) – indicating an enhanced SR. These data refute a cause-and-effect relationship between enhanced dPAG c-fos expression and a reduction in SR. However, they highlight a role for the dPAG in modulating SR of extinguished CTAs.</description><subject>Anatomical correlates of behavior</subject><subject>Animals</subject><subject>Avoidance Learning - physiology</subject><subject>Behavior, Animal - physiology</subject><subject>Behavioral psychophysiology</subject><subject>Biological and medical sciences</subject><subject>brain</subject><subject>c-fos</subject><subject>Central gray</subject><subject>Conditioned taste aversion</subject><subject>Conditioning (Psychology) - physiology</subject><subject>CTA</subject><subject>drinking</subject><subject>Electric Stimulation</subject><subject>electrodes</subject><subject>Electrodes, Implanted</subject><subject>Extinction</subject><subject>Extinction, Psychological - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Neurology</subject><subject>Olfactory system and olfaction. Gustatory system and gustation</subject><subject>PAG</subject><subject>Periaqueductal gray</subject><subject>Periaqueductal Gray - physiology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Saccharin</subject><subject>Spontaneous recovery</subject><subject>taste</subject><subject>Taste - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkk2P0zAQhiMEYsvCX1hyQeLS4o84sS8r0IovaSUOXc6Wa09ad1O72E6l_nsmanf5uMApcvzM6xk9U1VXlCwooe277WKVjA8J8oIRyhaULghTT6oZlR2bt6whT6sZIaSdS6X4RfUi5y0eOVfkeXXBOJWcNGxW3S-L342DKT6GOvZ12UDtYspmqPeQvPkxghttweM6mWMNYWOChVznfQzFBIhjrhPYeIB0nOpNbWNwfooDVxeTC9QGLzP-eFk9682Q4dX5e1ndffp4d_Nlfvvt89ebD7dz23aqzIE54ZhSirWU9isKRpBGWFDCNQYkKMlaKQVnjLeik842fEU5s7bpQJCWX1bXp9j9uNqBsxBKMoPeJ78z6aij8frPm-A3eh0PmoumEUJgwNtzQIo4fy5657OFYTjNqynrOBNEie5_UNYRITuJaHtCbYo5J-gfO6JET071Vj841ZNTTalGp1h49fs8j2UPEhF4cwZMtmboEyry-RfXSsKpapB7feJ6E7VZJ2S-L_ElgYuhGkkn4v2JANRz8JB0th5QuPMouWgX_b-7vf4rwg4-eOzrHo6Qt3FMAeVrqjPTRC-nHZ1WlGKIZFzxn8di41k</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Mickley, G. Andrew</creator><creator>Ketchesin, Kyle D</creator><creator>Ramos, Linnet</creator><creator>Luchsinger, Joseph R</creator><creator>Rogers, Morgan M</creator><creator>Wiles, Nathanael R</creator><creator>Hoxha, Nita</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</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>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>20130201</creationdate><title>Stimulation of the dorsal periaqueductal gray enhances spontaneous recovery of a conditioned taste aversion</title><author>Mickley, G. Andrew ; Ketchesin, Kyle D ; Ramos, Linnet ; Luchsinger, Joseph R ; Rogers, Morgan M ; Wiles, Nathanael R ; Hoxha, Nita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c679t-e2d5d29992611fb1ea5045ce95d4ae8e982688532236578dc43b132cc47e5063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anatomical correlates of behavior</topic><topic>Animals</topic><topic>Avoidance Learning - physiology</topic><topic>Behavior, Animal - physiology</topic><topic>Behavioral psychophysiology</topic><topic>Biological and medical sciences</topic><topic>brain</topic><topic>c-fos</topic><topic>Central gray</topic><topic>Conditioned taste aversion</topic><topic>Conditioning (Psychology) - physiology</topic><topic>CTA</topic><topic>drinking</topic><topic>Electric Stimulation</topic><topic>electrodes</topic><topic>Electrodes, Implanted</topic><topic>Extinction</topic><topic>Extinction, Psychological - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Neurology</topic><topic>Olfactory system and olfaction. Gustatory system and gustation</topic><topic>PAG</topic><topic>Periaqueductal gray</topic><topic>Periaqueductal Gray - physiology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Saccharin</topic><topic>Spontaneous recovery</topic><topic>taste</topic><topic>Taste - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mickley, G. Andrew</creatorcontrib><creatorcontrib>Ketchesin, Kyle D</creatorcontrib><creatorcontrib>Ramos, Linnet</creatorcontrib><creatorcontrib>Luchsinger, Joseph R</creatorcontrib><creatorcontrib>Rogers, Morgan M</creatorcontrib><creatorcontrib>Wiles, Nathanael R</creatorcontrib><creatorcontrib>Hoxha, Nita</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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>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>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mickley, G. Andrew</au><au>Ketchesin, Kyle D</au><au>Ramos, Linnet</au><au>Luchsinger, Joseph R</au><au>Rogers, Morgan M</au><au>Wiles, Nathanael R</au><au>Hoxha, Nita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stimulation of the dorsal periaqueductal gray enhances spontaneous recovery of a conditioned taste aversion</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>1493</volume><spage>27</spage><epage>39</epage><pages>27-39</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Abstract Due to its relevance to clinical practice, extinction of learned fears has been a major focus of recent research. However, less is known about the means by which conditioned fears re-emerge (i.e., spontaneously recover) as time passes or contexts change following extinction. The periaqueductal gray represents the final common pathway mediating defensive reactions to fear and we have reported previously that the dorsolateral PAG (dlPAG) exhibits a small but reliable increase in neural activity (as measured by c-fos protein immunoreactivity) when spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced. Here we extend these correlational studies to determine if inducing dlPAG c-fos expression through electrical brain stimulation could cause a reduction in SR of a CTA. Male Sprague-Dawley rats acquired a strong aversion to saccharin (conditioned stimulus; CS) and then underwent CTA extinction through multiple non-reinforced exposures to the CS. Following a 30-day latency period after asymptotic extinction was achieved; rats either received stimulation of the dorsal PAG (dPAG) or stimulation of closely adjacent structures. Sixty minutes following the stimulation, rats were again presented with the saccharin solution as we tested for SR of the CTA. The brain stimulation evoked c-fos expression around the tip of the electrodes. However, stimulation of the dPAG failed to reduce SR of the previously extinguished CTA. In fact, dPAG stimulation caused rats to significantly suppress their saccharin drinking (relative to controls) – indicating an enhanced SR. These data refute a cause-and-effect relationship between enhanced dPAG c-fos expression and a reduction in SR. However, they highlight a role for the dPAG in modulating SR of extinguished CTAs.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23183042</pmid><doi>10.1016/j.brainres.2012.11.029</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anatomical correlates of behavior Animals Avoidance Learning - physiology Behavior, Animal - physiology Behavioral psychophysiology Biological and medical sciences brain c-fos Central gray Conditioned taste aversion Conditioning (Psychology) - physiology CTA drinking Electric Stimulation electrodes Electrodes, Implanted Extinction Extinction, Psychological - physiology Fundamental and applied biological sciences. Psychology Male Neurology Olfactory system and olfaction. Gustatory system and gustation PAG Periaqueductal gray Periaqueductal Gray - physiology Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Rats Rats, Sprague-Dawley Saccharin Spontaneous recovery taste Taste - physiology Vertebrates: nervous system and sense organs |
title | Stimulation of the dorsal periaqueductal gray enhances spontaneous recovery of a conditioned taste aversion |
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