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Clock genes × stress × reward interactions in alcohol and substance use disorders
Abstract Adverse life events and highly stressful environments have deleterious consequences for mental health. Those environmental factors can potentiate alcohol and drug abuse in vulnerable individuals carrying specific genetic risk factors, hence producing the final risk for alcohol- and substanc...
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Published in: | Alcohol (Fayetteville, N.Y.) N.Y.), 2015-06, Vol.49 (4), p.351-357 |
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description | Abstract Adverse life events and highly stressful environments have deleterious consequences for mental health. Those environmental factors can potentiate alcohol and drug abuse in vulnerable individuals carrying specific genetic risk factors, hence producing the final risk for alcohol- and substance-use disorders development. The nature of these genes remains to be fully determined, but studies indicate their direct or indirect relation to the stress hypothalamo-pituitary-adrenal (HPA) axis and/or reward systems. Over the past decade, clock genes have been revealed to be key-players in influencing acute and chronic alcohol/drug effects. In parallel, the influence of chronic stress and stressful life events in promoting alcohol and substance use and abuse has been demonstrated. Furthermore, the reciprocal interaction of clock genes with various HPA-axis components, as well as the evidence for an implication of clock genes in stress-induced alcohol abuse, have led to the idea that clock genes, and Period genes in particular, may represent key genetic factors to consider when examining gene × environment interaction in the etiology of addiction. The aim of the present review is to summarize findings linking clock genes, stress, and alcohol and substance abuse, and to propose potential underlying neurobiological mechanisms. |
doi_str_mv | 10.1016/j.alcohol.2015.04.003 |
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Those environmental factors can potentiate alcohol and drug abuse in vulnerable individuals carrying specific genetic risk factors, hence producing the final risk for alcohol- and substance-use disorders development. The nature of these genes remains to be fully determined, but studies indicate their direct or indirect relation to the stress hypothalamo-pituitary-adrenal (HPA) axis and/or reward systems. Over the past decade, clock genes have been revealed to be key-players in influencing acute and chronic alcohol/drug effects. In parallel, the influence of chronic stress and stressful life events in promoting alcohol and substance use and abuse has been demonstrated. Furthermore, the reciprocal interaction of clock genes with various HPA-axis components, as well as the evidence for an implication of clock genes in stress-induced alcohol abuse, have led to the idea that clock genes, and Period genes in particular, may represent key genetic factors to consider when examining gene × environment interaction in the etiology of addiction. The aim of the present review is to summarize findings linking clock genes, stress, and alcohol and substance abuse, and to propose potential underlying neurobiological mechanisms.</description><identifier>ISSN: 0741-8329</identifier><identifier>EISSN: 1873-6823</identifier><identifier>DOI: 10.1016/j.alcohol.2015.04.003</identifier><identifier>PMID: 25943583</identifier><identifier>CODEN: ALCOEX</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alcohol ; Alcoholism - metabolism ; Animals ; Central Nervous System Depressants - pharmacology ; Circadian clock ; Circadian Clocks - drug effects ; Circadian Clocks - genetics ; Circadian rhythm ; Circadian Rhythm Signaling Peptides and Proteins - drug effects ; Circadian Rhythm Signaling Peptides and Proteins - genetics ; Cocaine ; Cocaine - pharmacology ; Dopamine Uptake Inhibitors - pharmacology ; Ethanol - pharmacology ; Gene-Environment Interaction ; HPA axis ; Humans ; Hypothalamo-Hypophyseal System - drug effects ; Hypothalamo-Hypophyseal System - metabolism ; Kinases ; Metabolic disorders ; Nicotine ; Nicotine - pharmacology ; Nicotinic Agonists - pharmacology ; Period genes ; Pituitary-Adrenal System - drug effects ; Pituitary-Adrenal System - metabolism ; Psychiatry ; Reward ; Rodents ; Sleep ; Stress, Psychological - metabolism ; Substance-Related Disorders - metabolism</subject><ispartof>Alcohol (Fayetteville, N.Y.), 2015-06, Vol.49 (4), p.351-357</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited 2015</rights><rights>2015 Published by Elsevier Inc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4983-affdd880d962471c4e9a538f5e4bc7de429b27dfa8cad31eaab43036923fcfb23</citedby><cites>FETCH-LOGICAL-c4983-affdd880d962471c4e9a538f5e4bc7de429b27dfa8cad31eaab43036923fcfb23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1684208981/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1684208981?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,777,781,882,21357,21375,27905,27906,33592,33593,33750,33751,43714,43795,73970,74059</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25943583$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perreau-Lenz, Stéphanie</creatorcontrib><creatorcontrib>Spanagel, Rainer</creatorcontrib><title>Clock genes × stress × reward interactions in alcohol and substance use disorders</title><title>Alcohol (Fayetteville, N.Y.)</title><addtitle>Alcohol</addtitle><description>Abstract Adverse life events and highly stressful environments have deleterious consequences for mental health. Those environmental factors can potentiate alcohol and drug abuse in vulnerable individuals carrying specific genetic risk factors, hence producing the final risk for alcohol- and substance-use disorders development. The nature of these genes remains to be fully determined, but studies indicate their direct or indirect relation to the stress hypothalamo-pituitary-adrenal (HPA) axis and/or reward systems. Over the past decade, clock genes have been revealed to be key-players in influencing acute and chronic alcohol/drug effects. In parallel, the influence of chronic stress and stressful life events in promoting alcohol and substance use and abuse has been demonstrated. Furthermore, the reciprocal interaction of clock genes with various HPA-axis components, as well as the evidence for an implication of clock genes in stress-induced alcohol abuse, have led to the idea that clock genes, and Period genes in particular, may represent key genetic factors to consider when examining gene × environment interaction in the etiology of addiction. The aim of the present review is to summarize findings linking clock genes, stress, and alcohol and substance abuse, and to propose potential underlying neurobiological mechanisms.</description><subject>Alcohol</subject><subject>Alcoholism - metabolism</subject><subject>Animals</subject><subject>Central Nervous System Depressants - pharmacology</subject><subject>Circadian clock</subject><subject>Circadian Clocks - drug effects</subject><subject>Circadian Clocks - genetics</subject><subject>Circadian rhythm</subject><subject>Circadian Rhythm Signaling Peptides and Proteins - drug effects</subject><subject>Circadian Rhythm Signaling Peptides and Proteins - genetics</subject><subject>Cocaine</subject><subject>Cocaine - pharmacology</subject><subject>Dopamine Uptake Inhibitors - pharmacology</subject><subject>Ethanol - pharmacology</subject><subject>Gene-Environment Interaction</subject><subject>HPA axis</subject><subject>Humans</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Kinases</subject><subject>Metabolic disorders</subject><subject>Nicotine</subject><subject>Nicotine - pharmacology</subject><subject>Nicotinic Agonists - pharmacology</subject><subject>Period genes</subject><subject>Pituitary-Adrenal System - drug effects</subject><subject>Pituitary-Adrenal System - metabolism</subject><subject>Psychiatry</subject><subject>Reward</subject><subject>Rodents</subject><subject>Sleep</subject><subject>Stress, Psychological - metabolism</subject><subject>Substance-Related Disorders - metabolism</subject><issn>0741-8329</issn><issn>1873-6823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>BGRYB</sourceid><sourceid>M0O</sourceid><recordid>eNqFUk1v1DAQjRCILoWfAIrEhUuCvxI7lyK0ooBUiQMgjpZjT1pvs3bxJEX9Jb32t5Q_hlcbCvTCybb85s2896YonlNSU0Lb15vajDaexbFmhDY1ETUh_EGxokryqlWMPyxWRApaKc66g-IJ4oYQIqXsHhcHrOkEbxRfFd_WY7Tn5SkEwNubn9e3NzglwOWe4IdJrvRhgmTs5GPA_CiXzqUJrsS5x8kEC-WMUDqPMTlI-LR4NJgR4dlyHhZfj999WX-oTj69_7h-e1JZ0SlemWFwTiniupYJSa2AzjRcDQ2I3koHgnU9k24wyhrHKRjTC0542zE-2KFn_LA42vNezP0WnIUwJTPqi-S3Jl3paLz-9yf4M30aL7UQjWyJzASvFoIUv8-Ak956tDCOJkCcUVMpWqUaptoMfXkPuolzClmepq0SjKhO0Yxq9iibImKC4W4YSvQuOr3Ri4F6F50mQufoct2Lv5XcVf3OKgPe7AGQ_bz0kDRaD9l55xPYSbvo_9vi6B6DHX3w1ozncAX4R41Gpon-vNuf3frQhhNCJee_ABRSyGw</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Perreau-Lenz, Stéphanie</creator><creator>Spanagel, Rainer</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>0-V</scope><scope>3V.</scope><scope>7QG</scope><scope>7RV</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AM</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGRYB</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K7.</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0O</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20150601</creationdate><title>Clock genes × stress × reward interactions in alcohol and substance use disorders</title><author>Perreau-Lenz, Stéphanie ; Spanagel, Rainer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4983-affdd880d962471c4e9a538f5e4bc7de429b27dfa8cad31eaab43036923fcfb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alcohol</topic><topic>Alcoholism - metabolism</topic><topic>Animals</topic><topic>Central Nervous System Depressants - pharmacology</topic><topic>Circadian clock</topic><topic>Circadian Clocks - drug effects</topic><topic>Circadian Clocks - genetics</topic><topic>Circadian rhythm</topic><topic>Circadian Rhythm Signaling Peptides and Proteins - drug effects</topic><topic>Circadian Rhythm Signaling Peptides and Proteins - genetics</topic><topic>Cocaine</topic><topic>Cocaine - pharmacology</topic><topic>Dopamine Uptake Inhibitors - pharmacology</topic><topic>Ethanol - pharmacology</topic><topic>Gene-Environment Interaction</topic><topic>HPA axis</topic><topic>Humans</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Kinases</topic><topic>Metabolic disorders</topic><topic>Nicotine</topic><topic>Nicotine - pharmacology</topic><topic>Nicotinic Agonists - pharmacology</topic><topic>Period genes</topic><topic>Pituitary-Adrenal System - drug effects</topic><topic>Pituitary-Adrenal System - 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Those environmental factors can potentiate alcohol and drug abuse in vulnerable individuals carrying specific genetic risk factors, hence producing the final risk for alcohol- and substance-use disorders development. The nature of these genes remains to be fully determined, but studies indicate their direct or indirect relation to the stress hypothalamo-pituitary-adrenal (HPA) axis and/or reward systems. Over the past decade, clock genes have been revealed to be key-players in influencing acute and chronic alcohol/drug effects. In parallel, the influence of chronic stress and stressful life events in promoting alcohol and substance use and abuse has been demonstrated. Furthermore, the reciprocal interaction of clock genes with various HPA-axis components, as well as the evidence for an implication of clock genes in stress-induced alcohol abuse, have led to the idea that clock genes, and Period genes in particular, may represent key genetic factors to consider when examining gene × environment interaction in the etiology of addiction. The aim of the present review is to summarize findings linking clock genes, stress, and alcohol and substance abuse, and to propose potential underlying neurobiological mechanisms.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25943583</pmid><doi>10.1016/j.alcohol.2015.04.003</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Alcoholism - metabolism Animals Central Nervous System Depressants - pharmacology Circadian clock Circadian Clocks - drug effects Circadian Clocks - genetics Circadian rhythm Circadian Rhythm Signaling Peptides and Proteins - drug effects Circadian Rhythm Signaling Peptides and Proteins - genetics Cocaine Cocaine - pharmacology Dopamine Uptake Inhibitors - pharmacology Ethanol - pharmacology Gene-Environment Interaction HPA axis Humans Hypothalamo-Hypophyseal System - drug effects Hypothalamo-Hypophyseal System - metabolism Kinases Metabolic disorders Nicotine Nicotine - pharmacology Nicotinic Agonists - pharmacology Period genes Pituitary-Adrenal System - drug effects Pituitary-Adrenal System - metabolism Psychiatry Reward Rodents Sleep Stress, Psychological - metabolism Substance-Related Disorders - metabolism |
title | Clock genes × stress × reward interactions in alcohol and substance use disorders |
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