Increased brain-derived neurotrophic factor (BDNF) expression in the ventral tegmental area during cocaine abstinence is associated with increased histone acetylation at BDNF exon I-containing promoters
J. Neurochem. (2012) 120, 202–209. Recent evidence suggests that the persistence of cocaine seeking during periods of protracted drug abstinence following chronic cocaine exposure is mediated, in part, by neuroadaptations in the mesolimbic dopamine system. Specifically, incubation of cocaine‐seeking...
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description | J. Neurochem. (2012) 120, 202–209.
Recent evidence suggests that the persistence of cocaine seeking during periods of protracted drug abstinence following chronic cocaine exposure is mediated, in part, by neuroadaptations in the mesolimbic dopamine system. Specifically, incubation of cocaine‐seeking behavior coincides with increased brain‐derived neurotrophic factor (BDNF) protein expression in the ventral tegmental area (VTA). However, the molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during cocaine abstinence are unclear. The goal of these experiments was to determine whether VTA BDNF transcript levels are altered following cocaine abstinence and identify the molecular mechanisms regulating cocaine‐induced changes in VTA BDNF transcription. Rats were allowed to self‐administer cocaine (0.25 mg/infusion, i.v.) for 14 days on a fixed‐ratio schedule of reinforcement followed by 7 days of forced drug abstinence. BDNF protein and exon I‐containing transcripts were significantly increased in the VTA of cocaine‐experienced rats following 7 days of forced drug abstinence compared to yoked saline controls. Cocaine‐induced changes in BDNF mRNA were associated with increased acetylation of histone 3 and binding of CREB‐binding protein to exon I‐containing promoters in the VTA. Taken together, these results suggest that drug abstinence following cocaine self‐administration remodels chromatin in the VTA resulting in increased expression of BDNF, which may contribute to neuroadaptations underlying cocaine craving and relapse.
Cocaine‐induced effects at specific BDNF promoters are mediated by distinct epigenetic mechanisms.
The molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during drug abstinence are not clear. Here, we show for the first time that VTA BDNF mRNA, specifically exon I‐containing transcript, is increased following 7 days of drug abstinence and that distinct epigenetic mechanisms regulate BDNF gene transcription. These results indicate that targeting specific epigenetic mechanisms that regulate VTA BDNF expression during drug abstinence may prevent cocaine craving and relapse. |
doi_str_mv | 10.1111/j.1471-4159.2011.07571.x |
format | Article |
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Recent evidence suggests that the persistence of cocaine seeking during periods of protracted drug abstinence following chronic cocaine exposure is mediated, in part, by neuroadaptations in the mesolimbic dopamine system. Specifically, incubation of cocaine‐seeking behavior coincides with increased brain‐derived neurotrophic factor (BDNF) protein expression in the ventral tegmental area (VTA). However, the molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during cocaine abstinence are unclear. The goal of these experiments was to determine whether VTA BDNF transcript levels are altered following cocaine abstinence and identify the molecular mechanisms regulating cocaine‐induced changes in VTA BDNF transcription. Rats were allowed to self‐administer cocaine (0.25 mg/infusion, i.v.) for 14 days on a fixed‐ratio schedule of reinforcement followed by 7 days of forced drug abstinence. BDNF protein and exon I‐containing transcripts were significantly increased in the VTA of cocaine‐experienced rats following 7 days of forced drug abstinence compared to yoked saline controls. Cocaine‐induced changes in BDNF mRNA were associated with increased acetylation of histone 3 and binding of CREB‐binding protein to exon I‐containing promoters in the VTA. Taken together, these results suggest that drug abstinence following cocaine self‐administration remodels chromatin in the VTA resulting in increased expression of BDNF, which may contribute to neuroadaptations underlying cocaine craving and relapse.
Cocaine‐induced effects at specific BDNF promoters are mediated by distinct epigenetic mechanisms.
The molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during drug abstinence are not clear. Here, we show for the first time that VTA BDNF mRNA, specifically exon I‐containing transcript, is increased following 7 days of drug abstinence and that distinct epigenetic mechanisms regulate BDNF gene transcription. These results indicate that targeting specific epigenetic mechanisms that regulate VTA BDNF expression during drug abstinence may prevent cocaine craving and relapse.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.2011.07571.x</identifier><identifier>PMID: 22043863</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acetylation ; Acetylation - drug effects ; addiction ; Anesthetics, Local - administration & dosage ; Animals ; Biological and medical sciences ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - genetics ; Brain-Derived Neurotrophic Factor - metabolism ; Chromatin ; Chromatin Immunoprecipitation ; chromatin remodeling ; Cocaine ; Cocaine - administration & dosage ; Cocaine-Related Disorders ; Conditioning, Operant - drug effects ; CREB-binding protein ; CREB-Binding Protein - metabolism ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Drug abuse ; Drug addiction ; Drug addictions ; Drug self-administration ; Enzyme-Linked Immunosorbent Assay - methods ; epigenetics ; Exons ; Gene Expression Regulation - drug effects ; Histones ; Histones - metabolism ; Male ; Medical sciences ; Mesolimbic system ; Molecular modelling ; Neurochemistry ; Neurology ; neurotrophic factor ; Promoter Regions, Genetic - drug effects ; Promoter Regions, Genetic - physiology ; Promoters ; psychostimulant ; Rats ; Rats, Sprague-Dawley ; Reinforcement ; Reinforcement Schedule ; RNA, Messenger - metabolism ; Self Administration ; Statistics, Nonparametric ; Substance Withdrawal Syndrome - metabolism ; Time Factors ; Toxicology ; Transcription ; Ventral Tegmental Area - drug effects ; Ventral Tegmental Area - metabolism ; Ventral tegmentum</subject><ispartof>Journal of neurochemistry, 2012-01, Vol.120 (2), p.202-209</ispartof><rights>2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry</rights><rights>2015 INIST-CNRS</rights><rights>2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5451-81bf23078d205d67b0ab2218670fdc21f6f7a2e2e8bb4de10e56b077df42c7af3</citedby><cites>FETCH-LOGICAL-c5451-81bf23078d205d67b0ab2218670fdc21f6f7a2e2e8bb4de10e56b077df42c7af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.2011.07571.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.2011.07571.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,1434,4025,27928,27929,27930,45579,45580,46414,46838</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25557061$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22043863$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmidt, Heath D.</creatorcontrib><creatorcontrib>Sangrey, Gavin R.</creatorcontrib><creatorcontrib>Darnell, Shayna B.</creatorcontrib><creatorcontrib>Schassburger, Rachel L.</creatorcontrib><creatorcontrib>Cha, Jang-Ho J.</creatorcontrib><creatorcontrib>Pierce, R. Christopher</creatorcontrib><creatorcontrib>Sadri-Vakili, Ghazaleh</creatorcontrib><title>Increased brain-derived neurotrophic factor (BDNF) expression in the ventral tegmental area during cocaine abstinence is associated with increased histone acetylation at BDNF exon I-containing promoters</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>J. Neurochem. (2012) 120, 202–209.
Recent evidence suggests that the persistence of cocaine seeking during periods of protracted drug abstinence following chronic cocaine exposure is mediated, in part, by neuroadaptations in the mesolimbic dopamine system. Specifically, incubation of cocaine‐seeking behavior coincides with increased brain‐derived neurotrophic factor (BDNF) protein expression in the ventral tegmental area (VTA). However, the molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during cocaine abstinence are unclear. The goal of these experiments was to determine whether VTA BDNF transcript levels are altered following cocaine abstinence and identify the molecular mechanisms regulating cocaine‐induced changes in VTA BDNF transcription. Rats were allowed to self‐administer cocaine (0.25 mg/infusion, i.v.) for 14 days on a fixed‐ratio schedule of reinforcement followed by 7 days of forced drug abstinence. BDNF protein and exon I‐containing transcripts were significantly increased in the VTA of cocaine‐experienced rats following 7 days of forced drug abstinence compared to yoked saline controls. Cocaine‐induced changes in BDNF mRNA were associated with increased acetylation of histone 3 and binding of CREB‐binding protein to exon I‐containing promoters in the VTA. Taken together, these results suggest that drug abstinence following cocaine self‐administration remodels chromatin in the VTA resulting in increased expression of BDNF, which may contribute to neuroadaptations underlying cocaine craving and relapse.
Cocaine‐induced effects at specific BDNF promoters are mediated by distinct epigenetic mechanisms.
The molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during drug abstinence are not clear. Here, we show for the first time that VTA BDNF mRNA, specifically exon I‐containing transcript, is increased following 7 days of drug abstinence and that distinct epigenetic mechanisms regulate BDNF gene transcription. These results indicate that targeting specific epigenetic mechanisms that regulate VTA BDNF expression during drug abstinence may prevent cocaine craving and relapse.</description><subject>Acetylation</subject><subject>Acetylation - drug effects</subject><subject>addiction</subject><subject>Anesthetics, Local - administration & dosage</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - genetics</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Chromatin</subject><subject>Chromatin Immunoprecipitation</subject><subject>chromatin remodeling</subject><subject>Cocaine</subject><subject>Cocaine - administration & dosage</subject><subject>Cocaine-Related Disorders</subject><subject>Conditioning, Operant - drug effects</subject><subject>CREB-binding protein</subject><subject>CREB-Binding Protein - metabolism</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Drug abuse</subject><subject>Drug addiction</subject><subject>Drug addictions</subject><subject>Drug self-administration</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>epigenetics</subject><subject>Exons</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Histones</subject><subject>Histones - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mesolimbic system</subject><subject>Molecular modelling</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>neurotrophic factor</subject><subject>Promoter Regions, Genetic - drug effects</subject><subject>Promoter Regions, Genetic - physiology</subject><subject>Promoters</subject><subject>psychostimulant</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reinforcement</subject><subject>Reinforcement Schedule</subject><subject>RNA, Messenger - metabolism</subject><subject>Self Administration</subject><subject>Statistics, Nonparametric</subject><subject>Substance Withdrawal Syndrome - metabolism</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>Transcription</subject><subject>Ventral Tegmental Area - drug effects</subject><subject>Ventral Tegmental Area - metabolism</subject><subject>Ventral tegmentum</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc2O0zAUhS0EYkrhFZCFhIBFiu3EcbpgwRRmpqgqPwKxtBznZuqS2sV2ZtpX5KlwaKdIrMjG18p3zrnyQQhTMqHpe72e0ELQrKB8OmGE0gkRXNDJ7h4anX7cRyNCGMtyUrAz9CiENSG0LEr6EJ0xRoq8KvMR-jW32oMK0ODaK2OzBry5STcLvXfRu-3KaNwqHZ3HL8_fLS9eYdhtPYRgnMXG4rgCfAM2etXhCNebNKZJJVPc9N7Ya6ydTs6AVR1iOq0GbAJWIThtVExZtyauktXdIisToht4DXHfqTgEqYiH8JSdLvNMu5Ri7OC-9W7jIvjwGD1oVRfgyfEco28X77_OrrLFx8v57O0i07zgNKto3bKciKphhDelqImqGaNVKUjbaEbbshWKAYOqrosGKAFe1kSIpi2YFqrNx-jFwTcl_-whRLkxQUPXKQuuD3LKiJhSnl54jJ79Q65d721aTk4pFYzmjCSoOkDauxA8tHLrzUb5vaREDm3LtRxKlUOpcmhb_mlb7pL06dG_rzfQnIR39Sbg-RFQQauu9cpqE_5ynHNBSpq4Nwfu1nSw_-8F5IflbJiSPjvoU3OwO-mV_yFLkQsuvy8vpZheLc7LL5_lp_w3SQXYaQ</recordid><startdate>201201</startdate><enddate>201201</enddate><creator>Schmidt, Heath D.</creator><creator>Sangrey, Gavin R.</creator><creator>Darnell, Shayna B.</creator><creator>Schassburger, Rachel L.</creator><creator>Cha, Jang-Ho J.</creator><creator>Pierce, R. Christopher</creator><creator>Sadri-Vakili, Ghazaleh</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>BSCLL</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>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></search><sort><creationdate>201201</creationdate><title>Increased brain-derived neurotrophic factor (BDNF) expression in the ventral tegmental area during cocaine abstinence is associated with increased histone acetylation at BDNF exon I-containing promoters</title><author>Schmidt, Heath D. ; Sangrey, Gavin R. ; Darnell, Shayna B. ; Schassburger, Rachel L. ; Cha, Jang-Ho J. ; Pierce, R. Christopher ; Sadri-Vakili, Ghazaleh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5451-81bf23078d205d67b0ab2218670fdc21f6f7a2e2e8bb4de10e56b077df42c7af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acetylation</topic><topic>Acetylation - drug effects</topic><topic>addiction</topic><topic>Anesthetics, Local - administration & dosage</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain-derived neurotrophic factor</topic><topic>Brain-Derived Neurotrophic Factor - genetics</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Chromatin</topic><topic>Chromatin Immunoprecipitation</topic><topic>chromatin remodeling</topic><topic>Cocaine</topic><topic>Cocaine - administration & dosage</topic><topic>Cocaine-Related Disorders</topic><topic>Conditioning, Operant - drug effects</topic><topic>CREB-binding protein</topic><topic>CREB-Binding Protein - metabolism</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Drug abuse</topic><topic>Drug addiction</topic><topic>Drug addictions</topic><topic>Drug self-administration</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>epigenetics</topic><topic>Exons</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Histones</topic><topic>Histones - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mesolimbic system</topic><topic>Molecular modelling</topic><topic>Neurochemistry</topic><topic>Neurology</topic><topic>neurotrophic factor</topic><topic>Promoter Regions, Genetic - drug effects</topic><topic>Promoter Regions, Genetic - physiology</topic><topic>Promoters</topic><topic>psychostimulant</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reinforcement</topic><topic>Reinforcement Schedule</topic><topic>RNA, Messenger - metabolism</topic><topic>Self Administration</topic><topic>Statistics, Nonparametric</topic><topic>Substance Withdrawal Syndrome - metabolism</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>Transcription</topic><topic>Ventral Tegmental Area - drug effects</topic><topic>Ventral Tegmental Area - metabolism</topic><topic>Ventral tegmentum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmidt, Heath D.</creatorcontrib><creatorcontrib>Sangrey, Gavin R.</creatorcontrib><creatorcontrib>Darnell, Shayna B.</creatorcontrib><creatorcontrib>Schassburger, Rachel L.</creatorcontrib><creatorcontrib>Cha, Jang-Ho J.</creatorcontrib><creatorcontrib>Pierce, R. Christopher</creatorcontrib><creatorcontrib>Sadri-Vakili, Ghazaleh</creatorcontrib><collection>Istex</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>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><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmidt, Heath D.</au><au>Sangrey, Gavin R.</au><au>Darnell, Shayna B.</au><au>Schassburger, Rachel L.</au><au>Cha, Jang-Ho J.</au><au>Pierce, R. Christopher</au><au>Sadri-Vakili, Ghazaleh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased brain-derived neurotrophic factor (BDNF) expression in the ventral tegmental area during cocaine abstinence is associated with increased histone acetylation at BDNF exon I-containing promoters</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2012-01</date><risdate>2012</risdate><volume>120</volume><issue>2</issue><spage>202</spage><epage>209</epage><pages>202-209</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>J. Neurochem. (2012) 120, 202–209.
Recent evidence suggests that the persistence of cocaine seeking during periods of protracted drug abstinence following chronic cocaine exposure is mediated, in part, by neuroadaptations in the mesolimbic dopamine system. Specifically, incubation of cocaine‐seeking behavior coincides with increased brain‐derived neurotrophic factor (BDNF) protein expression in the ventral tegmental area (VTA). However, the molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during cocaine abstinence are unclear. The goal of these experiments was to determine whether VTA BDNF transcript levels are altered following cocaine abstinence and identify the molecular mechanisms regulating cocaine‐induced changes in VTA BDNF transcription. Rats were allowed to self‐administer cocaine (0.25 mg/infusion, i.v.) for 14 days on a fixed‐ratio schedule of reinforcement followed by 7 days of forced drug abstinence. BDNF protein and exon I‐containing transcripts were significantly increased in the VTA of cocaine‐experienced rats following 7 days of forced drug abstinence compared to yoked saline controls. Cocaine‐induced changes in BDNF mRNA were associated with increased acetylation of histone 3 and binding of CREB‐binding protein to exon I‐containing promoters in the VTA. Taken together, these results suggest that drug abstinence following cocaine self‐administration remodels chromatin in the VTA resulting in increased expression of BDNF, which may contribute to neuroadaptations underlying cocaine craving and relapse.
Cocaine‐induced effects at specific BDNF promoters are mediated by distinct epigenetic mechanisms.
The molecular mechanisms that regulate time‐dependent changes in VTA BDNF protein expression during drug abstinence are not clear. Here, we show for the first time that VTA BDNF mRNA, specifically exon I‐containing transcript, is increased following 7 days of drug abstinence and that distinct epigenetic mechanisms regulate BDNF gene transcription. These results indicate that targeting specific epigenetic mechanisms that regulate VTA BDNF expression during drug abstinence may prevent cocaine craving and relapse.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22043863</pmid><doi>10.1111/j.1471-4159.2011.07571.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylation Acetylation - drug effects addiction Anesthetics, Local - administration & dosage Animals Biological and medical sciences Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - genetics Brain-Derived Neurotrophic Factor - metabolism Chromatin Chromatin Immunoprecipitation chromatin remodeling Cocaine Cocaine - administration & dosage Cocaine-Related Disorders Conditioning, Operant - drug effects CREB-binding protein CREB-Binding Protein - metabolism Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Drug abuse Drug addiction Drug addictions Drug self-administration Enzyme-Linked Immunosorbent Assay - methods epigenetics Exons Gene Expression Regulation - drug effects Histones Histones - metabolism Male Medical sciences Mesolimbic system Molecular modelling Neurochemistry Neurology neurotrophic factor Promoter Regions, Genetic - drug effects Promoter Regions, Genetic - physiology Promoters psychostimulant Rats Rats, Sprague-Dawley Reinforcement Reinforcement Schedule RNA, Messenger - metabolism Self Administration Statistics, Nonparametric Substance Withdrawal Syndrome - metabolism Time Factors Toxicology Transcription Ventral Tegmental Area - drug effects Ventral Tegmental Area - metabolism Ventral tegmentum |
title | Increased brain-derived neurotrophic factor (BDNF) expression in the ventral tegmental area during cocaine abstinence is associated with increased histone acetylation at BDNF exon I-containing promoters |
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