Ethanol consumption in the female Long–Evans rat: a modulatory role of estradiol
The examination of various gonadal hormone manipulations on ethanol intake in human subjects and in rodent models has resulted in disparate findings. In the present study, we examined the effects of ovariectomy and subsequent estradiol (E 2) replacement on ethanol intake in a within-subject design,...
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Veröffentlicht in: | Alcohol (Fayetteville, N.Y.) N.Y.), 2002-02, Vol.26 (2), p.103-113 |
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creator | Ford, Matthew M. Eldridge, J.Charles Samson, Herman H. |
description | The examination of various gonadal hormone manipulations on ethanol intake in human subjects and in rodent models has resulted in disparate findings. In the present study, we examined the effects of ovariectomy and subsequent estradiol (E
2) replacement on ethanol intake in a within-subject design, as well as assessed the relevance of reproductive status on the efficacy of an E
2 stimulus in eliciting consumption. Female Long–Evans rats (
n = 24) were given access to 10% ethanol and water in a continuous-access paradigm. After establishment of baseline intake values, rats were divided into four groups: sham/placebo (Shm+P), sham/estradiol (Shm+E
2), ovariectomized/placebo (Ovx+P), and ovariectomized/estradiol (Ovx+E
2). Rats in the Ovx+P group were found to have a large and permanent decline in ethanol intake that persisted more than 3 months postsurgery. Administration of E
2 to Ovx+E
2 rats was associated with restoration of ethanol consumption to baseline levels. When Shm+E
2 and Ovx+E
2 groups were compared, reproductive status was found to be a determining factor in the efficacy of E
2 to elicit ethanol intake. Together, these findings provide evidence that ovarian hormones, particularly estradiol, exert activational effects on estrogen-responsive substrates to modulate ethanol consumption in the adult female rat. |
doi_str_mv | 10.1016/S0741-8329(01)00203-8 |
format | Article |
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2) replacement on ethanol intake in a within-subject design, as well as assessed the relevance of reproductive status on the efficacy of an E
2 stimulus in eliciting consumption. Female Long–Evans rats (
n = 24) were given access to 10% ethanol and water in a continuous-access paradigm. After establishment of baseline intake values, rats were divided into four groups: sham/placebo (Shm+P), sham/estradiol (Shm+E
2), ovariectomized/placebo (Ovx+P), and ovariectomized/estradiol (Ovx+E
2). Rats in the Ovx+P group were found to have a large and permanent decline in ethanol intake that persisted more than 3 months postsurgery. Administration of E
2 to Ovx+E
2 rats was associated with restoration of ethanol consumption to baseline levels. When Shm+E
2 and Ovx+E
2 groups were compared, reproductive status was found to be a determining factor in the efficacy of E
2 to elicit ethanol intake. Together, these findings provide evidence that ovarian hormones, particularly estradiol, exert activational effects on estrogen-responsive substrates to modulate ethanol consumption in the adult female rat.</description><identifier>ISSN: 0741-8329</identifier><identifier>EISSN: 1873-6823</identifier><identifier>DOI: 10.1016/S0741-8329(01)00203-8</identifier><identifier>PMID: 12007585</identifier><identifier>CODEN: ALCOEX</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Alcohol Drinking - metabolism ; Alcohol Drinking - physiopathology ; Alcoholism and acute alcohol poisoning ; Animals ; Biological and medical sciences ; Body Weight - drug effects ; Body Weight - physiology ; Continuous access ; Dose-Response Relationship, Drug ; Drug Implants - metabolism ; Estradiol - administration & dosage ; Estradiol - metabolism ; Estradiol - pharmacology ; Estradiol - physiology ; Estradiol replacement ; Estrogen Replacement Therapy - statistics & numerical data ; Ethanol self-administration ; Female ; Female rat ; Medical sciences ; Ovariectomy ; Ovariectomy - statistics & numerical data ; Rats ; Rats, Long-Evans ; Toxicology</subject><ispartof>Alcohol (Fayetteville, N.Y.), 2002-02, Vol.26 (2), p.103-113</ispartof><rights>2002 Elsevier Science Inc.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-1f6f99e0e04c848c3bd24656461311642d64ff9be9683706e66af716b7d0a9ca3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0741-8329(01)00203-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13633898$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12007585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ford, Matthew M.</creatorcontrib><creatorcontrib>Eldridge, J.Charles</creatorcontrib><creatorcontrib>Samson, Herman H.</creatorcontrib><title>Ethanol consumption in the female Long–Evans rat: a modulatory role of estradiol</title><title>Alcohol (Fayetteville, N.Y.)</title><addtitle>Alcohol</addtitle><description>The examination of various gonadal hormone manipulations on ethanol intake in human subjects and in rodent models has resulted in disparate findings. In the present study, we examined the effects of ovariectomy and subsequent estradiol (E
2) replacement on ethanol intake in a within-subject design, as well as assessed the relevance of reproductive status on the efficacy of an E
2 stimulus in eliciting consumption. Female Long–Evans rats (
n = 24) were given access to 10% ethanol and water in a continuous-access paradigm. After establishment of baseline intake values, rats were divided into four groups: sham/placebo (Shm+P), sham/estradiol (Shm+E
2), ovariectomized/placebo (Ovx+P), and ovariectomized/estradiol (Ovx+E
2). Rats in the Ovx+P group were found to have a large and permanent decline in ethanol intake that persisted more than 3 months postsurgery. Administration of E
2 to Ovx+E
2 rats was associated with restoration of ethanol consumption to baseline levels. When Shm+E
2 and Ovx+E
2 groups were compared, reproductive status was found to be a determining factor in the efficacy of E
2 to elicit ethanol intake. Together, these findings provide evidence that ovarian hormones, particularly estradiol, exert activational effects on estrogen-responsive substrates to modulate ethanol consumption in the adult female rat.</description><subject>Alcohol Drinking - metabolism</subject><subject>Alcohol Drinking - physiopathology</subject><subject>Alcoholism and acute alcohol poisoning</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Body Weight - physiology</subject><subject>Continuous access</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Implants - metabolism</subject><subject>Estradiol - administration & dosage</subject><subject>Estradiol - metabolism</subject><subject>Estradiol - pharmacology</subject><subject>Estradiol - physiology</subject><subject>Estradiol replacement</subject><subject>Estrogen Replacement Therapy - statistics & numerical data</subject><subject>Ethanol self-administration</subject><subject>Female</subject><subject>Female rat</subject><subject>Medical sciences</subject><subject>Ovariectomy</subject><subject>Ovariectomy - statistics & numerical data</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Toxicology</subject><issn>0741-8329</issn><issn>1873-6823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0d9KHDEUBvBQlLpqH6GSG8VeTE0ms_njjciytcJCQdvrkM2caMpMsk1mFrzrO_iGPolxXdtLr5LAjxO-8yH0mZKvlFB-dktEQyvJanVK6BdCasIq-QFNqBSs4rJmO2jyj-yh_Zx_E0KEEOoj2qN1uU7ldIJu5sO9CbHDNoY89qvBx4B9wMM9YAe96QAvYrh7-vs4X5uQcTLDOTa4j-3YmSGmB5xiMdFhyEMyrY_dIdp1psvwaXseoF_f5j9n36vFj6vr2eWiskzwoaKOO6WAAGmsbKRly7Zu-JQ3nDJKeVO3vHFOLUFxyQThwLlxgvKlaIlR1rADdPI6d5Xin7F8r3ufLXSdCRDHrIuVJWfzLqSSqVryusCjLRyXPbR6lXxv0oN-W1cBx1tgsjWdSyZYn_87xhmTShZ38eqg5F97SDpbD8FC6xPYQbfRa0r0S5F6U6R-aUkTqjdFltczxWeOQQ</recordid><startdate>20020201</startdate><enddate>20020201</enddate><creator>Ford, Matthew M.</creator><creator>Eldridge, J.Charles</creator><creator>Samson, Herman H.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QG</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20020201</creationdate><title>Ethanol consumption in the female Long–Evans rat: a modulatory role of estradiol</title><author>Ford, Matthew M. ; Eldridge, J.Charles ; Samson, Herman H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-1f6f99e0e04c848c3bd24656461311642d64ff9be9683706e66af716b7d0a9ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Alcohol Drinking - metabolism</topic><topic>Alcohol Drinking - physiopathology</topic><topic>Alcoholism and acute alcohol poisoning</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Body Weight - physiology</topic><topic>Continuous access</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Implants - metabolism</topic><topic>Estradiol - administration & dosage</topic><topic>Estradiol - metabolism</topic><topic>Estradiol - pharmacology</topic><topic>Estradiol - physiology</topic><topic>Estradiol replacement</topic><topic>Estrogen Replacement Therapy - statistics & numerical data</topic><topic>Ethanol self-administration</topic><topic>Female</topic><topic>Female rat</topic><topic>Medical sciences</topic><topic>Ovariectomy</topic><topic>Ovariectomy - statistics & numerical data</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ford, Matthew M.</creatorcontrib><creatorcontrib>Eldridge, J.Charles</creatorcontrib><creatorcontrib>Samson, Herman H.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Animal Behavior Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Alcohol (Fayetteville, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ford, Matthew M.</au><au>Eldridge, J.Charles</au><au>Samson, Herman H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ethanol consumption in the female Long–Evans rat: a modulatory role of estradiol</atitle><jtitle>Alcohol (Fayetteville, N.Y.)</jtitle><addtitle>Alcohol</addtitle><date>2002-02-01</date><risdate>2002</risdate><volume>26</volume><issue>2</issue><spage>103</spage><epage>113</epage><pages>103-113</pages><issn>0741-8329</issn><eissn>1873-6823</eissn><coden>ALCOEX</coden><abstract>The examination of various gonadal hormone manipulations on ethanol intake in human subjects and in rodent models has resulted in disparate findings. In the present study, we examined the effects of ovariectomy and subsequent estradiol (E
2) replacement on ethanol intake in a within-subject design, as well as assessed the relevance of reproductive status on the efficacy of an E
2 stimulus in eliciting consumption. Female Long–Evans rats (
n = 24) were given access to 10% ethanol and water in a continuous-access paradigm. After establishment of baseline intake values, rats were divided into four groups: sham/placebo (Shm+P), sham/estradiol (Shm+E
2), ovariectomized/placebo (Ovx+P), and ovariectomized/estradiol (Ovx+E
2). Rats in the Ovx+P group were found to have a large and permanent decline in ethanol intake that persisted more than 3 months postsurgery. Administration of E
2 to Ovx+E
2 rats was associated with restoration of ethanol consumption to baseline levels. When Shm+E
2 and Ovx+E
2 groups were compared, reproductive status was found to be a determining factor in the efficacy of E
2 to elicit ethanol intake. Together, these findings provide evidence that ovarian hormones, particularly estradiol, exert activational effects on estrogen-responsive substrates to modulate ethanol consumption in the adult female rat.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12007585</pmid><doi>10.1016/S0741-8329(01)00203-8</doi><tpages>11</tpages></addata></record> |
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subjects | Alcohol Drinking - metabolism Alcohol Drinking - physiopathology Alcoholism and acute alcohol poisoning Animals Biological and medical sciences Body Weight - drug effects Body Weight - physiology Continuous access Dose-Response Relationship, Drug Drug Implants - metabolism Estradiol - administration & dosage Estradiol - metabolism Estradiol - pharmacology Estradiol - physiology Estradiol replacement Estrogen Replacement Therapy - statistics & numerical data Ethanol self-administration Female Female rat Medical sciences Ovariectomy Ovariectomy - statistics & numerical data Rats Rats, Long-Evans Toxicology |
title | Ethanol consumption in the female Long–Evans rat: a modulatory role of estradiol |
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