Loading…
Genetic analysis of the psychomotor stimulant effect of ethanol
Genetic influences on the psychomotor stimulant effect of ethanol may be a key feature of abuse liability. While earlier work has shown the activational effects of ethanol to be under the influence of a relatively uncomplicated additive genetic system, preliminary data from our laboratory suggested...
Saved in:
Published in: | Genes, brain and behavior brain and behavior, 2003-06, Vol.2 (3), p.140-151 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Request full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53 |
---|---|
cites | cdi_FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53 |
container_end_page | 151 |
container_issue | 3 |
container_start_page | 140 |
container_title | Genes, brain and behavior |
container_volume | 2 |
creator | Downing, C. Rodd‐Henricks, K. K. Flaherty, L. Dudek, B. C. |
description | Genetic influences on the psychomotor stimulant effect of ethanol may be a key feature of abuse liability. While earlier work has shown the activational effects of ethanol to be under the influence of a relatively uncomplicated additive genetic system, preliminary data from our laboratory suggested the possibility of nonadditive genetic variance. In the present study, a full Mendelian cross was conducted to further characterize gene action and search for quantitative trait loci (QTL) influencing the psychomotor stimulant properties of ethanol. We tested 3062 mice of the six Mendelian cross genotypes (P1, P2, F1, F2, BC1 and BC2) derived from a cross between the C57BL/6J (B6) and C3H/HeJ (C3H) inbred strains of mice. On day 1, mice were injected with saline, put in a holding cage for 5 min, then placed in an activity monitor for 5 min. On day 2, mice were injected with 1.5 g/kg ethanol, and activity again monitored for 5 min. Analysis showed the expected activation in the C3H strain and little activation in the B6 strain, with no effect of sex. Biometrical genetic analysis showed a best‐fit model that included the mean (m), additive effect (a), and an epistatic parameter (i = homozygote by homozygote interaction). Analysis showed good evidence for QTL on chromosomes 1 (logarithm of odds (LOD) 3.4–7.5, 88–100 cM), 6 (LOD 9.1–10.4, 46–50 cM) and 15 (LOD 7.3–8.8, 28–32 cM). While the regions on chromosomes 1 and 6 have previously been implicated in several different ethanol‐related phenotypes, this is the first report of a QTL influencing the psychomotor stimulant properties of ethanol on chromosome 15. Other studies have identified QTL in this region of chromosome 15 mediating locomotor activation caused by other psychostimulants, including cocaine, amphetamine and phencyclidine. |
doi_str_mv | 10.1034/j.1601-183X.2003.00022.x |
format | article |
fullrecord | <record><control><sourceid>proquest_24P</sourceid><recordid>TN_cdi_proquest_miscellaneous_73578304</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73578304</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53</originalsourceid><addsrcrecordid>eNqNkE1Lw0AQhhdRbK3-BcnJW-LO7ia7AUFs0SoUvPTgbUk2szQlHzWbYPPvTWypRz3NC_PMBw8hHtAAKBf32wAiCj4o_hEwSnlAKWUs2J-R6alxfspCTciVc1tKQXIFl2QCLOYglZySxyVW2ObGS6qk6F3uvNp67Qa9nevNpi7rtm481-ZlVyRV66G1aNqRwXaTVHVxTS5sUji8OdYZWb88rxev_up9-bZ4WvlGiJD5AngqIVaKs1AZFJmNEisF41EqwKICGcWhYhlaSW1sGYtMmKSAJlMhmJDPyN1h7a6pPzt0rS5zZ7AYnsK6c1ryUCpOxZ8gKCWjKB5BdQBNUzvXoNW7Ji-TptdA9ShZb_XoT48u9ShZ_0jW-2H09nijS0vMfgePVgfg4QB85QX2_16sl_P5EPg3qfGKIg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18876694</pqid></control><display><type>article</type><title>Genetic analysis of the psychomotor stimulant effect of ethanol</title><source>Wiley Open Access</source><creator>Downing, C. ; Rodd‐Henricks, K. K. ; Flaherty, L. ; Dudek, B. C.</creator><creatorcontrib>Downing, C. ; Rodd‐Henricks, K. K. ; Flaherty, L. ; Dudek, B. C.</creatorcontrib><description>Genetic influences on the psychomotor stimulant effect of ethanol may be a key feature of abuse liability. While earlier work has shown the activational effects of ethanol to be under the influence of a relatively uncomplicated additive genetic system, preliminary data from our laboratory suggested the possibility of nonadditive genetic variance. In the present study, a full Mendelian cross was conducted to further characterize gene action and search for quantitative trait loci (QTL) influencing the psychomotor stimulant properties of ethanol. We tested 3062 mice of the six Mendelian cross genotypes (P1, P2, F1, F2, BC1 and BC2) derived from a cross between the C57BL/6J (B6) and C3H/HeJ (C3H) inbred strains of mice. On day 1, mice were injected with saline, put in a holding cage for 5 min, then placed in an activity monitor for 5 min. On day 2, mice were injected with 1.5 g/kg ethanol, and activity again monitored for 5 min. Analysis showed the expected activation in the C3H strain and little activation in the B6 strain, with no effect of sex. Biometrical genetic analysis showed a best‐fit model that included the mean (m), additive effect (a), and an epistatic parameter (i = homozygote by homozygote interaction). Analysis showed good evidence for QTL on chromosomes 1 (logarithm of odds (LOD) 3.4–7.5, 88–100 cM), 6 (LOD 9.1–10.4, 46–50 cM) and 15 (LOD 7.3–8.8, 28–32 cM). While the regions on chromosomes 1 and 6 have previously been implicated in several different ethanol‐related phenotypes, this is the first report of a QTL influencing the psychomotor stimulant properties of ethanol on chromosome 15. Other studies have identified QTL in this region of chromosome 15 mediating locomotor activation caused by other psychostimulants, including cocaine, amphetamine and phencyclidine.</description><identifier>ISSN: 1601-1848</identifier><identifier>EISSN: 1601-183X</identifier><identifier>DOI: 10.1034/j.1601-183X.2003.00022.x</identifier><identifier>PMID: 12931787</identifier><language>eng</language><publisher>Oxford, UK: Munksgaard International Publishers</publisher><subject>Alcohol ; Animals ; Central Nervous System Stimulants - pharmacology ; Crosses, Genetic ; Dose-Response Relationship, Drug ; Ethanol - pharmacology ; Female ; genetics ; Genotype ; inbred strains ; Male ; Mice ; Mice, Inbred C3H ; Motor Activity - drug effects ; Motor Activity - genetics ; psychomotor stimulation ; QTL ; Quantitative Trait Loci</subject><ispartof>Genes, brain and behavior, 2003-06, Vol.2 (3), p.140-151</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53</citedby><cites>FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1034%2Fj.1601-183X.2003.00022.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1034%2Fj.1601-183X.2003.00022.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,11561,27923,27924,46051,46475</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1034%2Fj.1601-183X.2003.00022.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12931787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Downing, C.</creatorcontrib><creatorcontrib>Rodd‐Henricks, K. K.</creatorcontrib><creatorcontrib>Flaherty, L.</creatorcontrib><creatorcontrib>Dudek, B. C.</creatorcontrib><title>Genetic analysis of the psychomotor stimulant effect of ethanol</title><title>Genes, brain and behavior</title><addtitle>Genes Brain Behav</addtitle><description>Genetic influences on the psychomotor stimulant effect of ethanol may be a key feature of abuse liability. While earlier work has shown the activational effects of ethanol to be under the influence of a relatively uncomplicated additive genetic system, preliminary data from our laboratory suggested the possibility of nonadditive genetic variance. In the present study, a full Mendelian cross was conducted to further characterize gene action and search for quantitative trait loci (QTL) influencing the psychomotor stimulant properties of ethanol. We tested 3062 mice of the six Mendelian cross genotypes (P1, P2, F1, F2, BC1 and BC2) derived from a cross between the C57BL/6J (B6) and C3H/HeJ (C3H) inbred strains of mice. On day 1, mice were injected with saline, put in a holding cage for 5 min, then placed in an activity monitor for 5 min. On day 2, mice were injected with 1.5 g/kg ethanol, and activity again monitored for 5 min. Analysis showed the expected activation in the C3H strain and little activation in the B6 strain, with no effect of sex. Biometrical genetic analysis showed a best‐fit model that included the mean (m), additive effect (a), and an epistatic parameter (i = homozygote by homozygote interaction). Analysis showed good evidence for QTL on chromosomes 1 (logarithm of odds (LOD) 3.4–7.5, 88–100 cM), 6 (LOD 9.1–10.4, 46–50 cM) and 15 (LOD 7.3–8.8, 28–32 cM). While the regions on chromosomes 1 and 6 have previously been implicated in several different ethanol‐related phenotypes, this is the first report of a QTL influencing the psychomotor stimulant properties of ethanol on chromosome 15. Other studies have identified QTL in this region of chromosome 15 mediating locomotor activation caused by other psychostimulants, including cocaine, amphetamine and phencyclidine.</description><subject>Alcohol</subject><subject>Animals</subject><subject>Central Nervous System Stimulants - pharmacology</subject><subject>Crosses, Genetic</subject><subject>Dose-Response Relationship, Drug</subject><subject>Ethanol - pharmacology</subject><subject>Female</subject><subject>genetics</subject><subject>Genotype</subject><subject>inbred strains</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Motor Activity - drug effects</subject><subject>Motor Activity - genetics</subject><subject>psychomotor stimulation</subject><subject>QTL</subject><subject>Quantitative Trait Loci</subject><issn>1601-1848</issn><issn>1601-183X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkE1Lw0AQhhdRbK3-BcnJW-LO7ia7AUFs0SoUvPTgbUk2szQlHzWbYPPvTWypRz3NC_PMBw8hHtAAKBf32wAiCj4o_hEwSnlAKWUs2J-R6alxfspCTciVc1tKQXIFl2QCLOYglZySxyVW2ObGS6qk6F3uvNp67Qa9nevNpi7rtm481-ZlVyRV66G1aNqRwXaTVHVxTS5sUji8OdYZWb88rxev_up9-bZ4WvlGiJD5AngqIVaKs1AZFJmNEisF41EqwKICGcWhYhlaSW1sGYtMmKSAJlMhmJDPyN1h7a6pPzt0rS5zZ7AYnsK6c1ryUCpOxZ8gKCWjKB5BdQBNUzvXoNW7Ji-TptdA9ShZb_XoT48u9ShZ_0jW-2H09nijS0vMfgePVgfg4QB85QX2_16sl_P5EPg3qfGKIg</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Downing, C.</creator><creator>Rodd‐Henricks, K. K.</creator><creator>Flaherty, L.</creator><creator>Dudek, B. C.</creator><general>Munksgaard International Publishers</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200306</creationdate><title>Genetic analysis of the psychomotor stimulant effect of ethanol</title><author>Downing, C. ; Rodd‐Henricks, K. K. ; Flaherty, L. ; Dudek, B. C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Alcohol</topic><topic>Animals</topic><topic>Central Nervous System Stimulants - pharmacology</topic><topic>Crosses, Genetic</topic><topic>Dose-Response Relationship, Drug</topic><topic>Ethanol - pharmacology</topic><topic>Female</topic><topic>genetics</topic><topic>Genotype</topic><topic>inbred strains</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Motor Activity - drug effects</topic><topic>Motor Activity - genetics</topic><topic>psychomotor stimulation</topic><topic>QTL</topic><topic>Quantitative Trait Loci</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Downing, C.</creatorcontrib><creatorcontrib>Rodd‐Henricks, K. K.</creatorcontrib><creatorcontrib>Flaherty, L.</creatorcontrib><creatorcontrib>Dudek, B. C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Genes, brain and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Downing, C.</au><au>Rodd‐Henricks, K. K.</au><au>Flaherty, L.</au><au>Dudek, B. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic analysis of the psychomotor stimulant effect of ethanol</atitle><jtitle>Genes, brain and behavior</jtitle><addtitle>Genes Brain Behav</addtitle><date>2003-06</date><risdate>2003</risdate><volume>2</volume><issue>3</issue><spage>140</spage><epage>151</epage><pages>140-151</pages><issn>1601-1848</issn><eissn>1601-183X</eissn><abstract>Genetic influences on the psychomotor stimulant effect of ethanol may be a key feature of abuse liability. While earlier work has shown the activational effects of ethanol to be under the influence of a relatively uncomplicated additive genetic system, preliminary data from our laboratory suggested the possibility of nonadditive genetic variance. In the present study, a full Mendelian cross was conducted to further characterize gene action and search for quantitative trait loci (QTL) influencing the psychomotor stimulant properties of ethanol. We tested 3062 mice of the six Mendelian cross genotypes (P1, P2, F1, F2, BC1 and BC2) derived from a cross between the C57BL/6J (B6) and C3H/HeJ (C3H) inbred strains of mice. On day 1, mice were injected with saline, put in a holding cage for 5 min, then placed in an activity monitor for 5 min. On day 2, mice were injected with 1.5 g/kg ethanol, and activity again monitored for 5 min. Analysis showed the expected activation in the C3H strain and little activation in the B6 strain, with no effect of sex. Biometrical genetic analysis showed a best‐fit model that included the mean (m), additive effect (a), and an epistatic parameter (i = homozygote by homozygote interaction). Analysis showed good evidence for QTL on chromosomes 1 (logarithm of odds (LOD) 3.4–7.5, 88–100 cM), 6 (LOD 9.1–10.4, 46–50 cM) and 15 (LOD 7.3–8.8, 28–32 cM). While the regions on chromosomes 1 and 6 have previously been implicated in several different ethanol‐related phenotypes, this is the first report of a QTL influencing the psychomotor stimulant properties of ethanol on chromosome 15. Other studies have identified QTL in this region of chromosome 15 mediating locomotor activation caused by other psychostimulants, including cocaine, amphetamine and phencyclidine.</abstract><cop>Oxford, UK</cop><pub>Munksgaard International Publishers</pub><pmid>12931787</pmid><doi>10.1034/j.1601-183X.2003.00022.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | ISSN: 1601-1848 |
ispartof | Genes, brain and behavior, 2003-06, Vol.2 (3), p.140-151 |
issn | 1601-1848 1601-183X |
language | eng |
recordid | cdi_proquest_miscellaneous_73578304 |
source | Wiley Open Access |
subjects | Alcohol Animals Central Nervous System Stimulants - pharmacology Crosses, Genetic Dose-Response Relationship, Drug Ethanol - pharmacology Female genetics Genotype inbred strains Male Mice Mice, Inbred C3H Motor Activity - drug effects Motor Activity - genetics psychomotor stimulation QTL Quantitative Trait Loci |
title | Genetic analysis of the psychomotor stimulant effect of ethanol |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T20%3A07%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_24P&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetic%20analysis%20of%20the%20psychomotor%20stimulant%20effect%20of%20ethanol&rft.jtitle=Genes,%20brain%20and%20behavior&rft.au=Downing,%20C.&rft.date=2003-06&rft.volume=2&rft.issue=3&rft.spage=140&rft.epage=151&rft.pages=140-151&rft.issn=1601-1848&rft.eissn=1601-183X&rft_id=info:doi/10.1034/j.1601-183X.2003.00022.x&rft_dat=%3Cproquest_24P%3E73578304%3C/proquest_24P%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4452-413b719883258ce4df6af74236b41fe81769582def70f9f226c5ab1ecd851c53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=18876694&rft_id=info:pmid/12931787&rfr_iscdi=true |