Relaxin-3 mRNA levels in nucleus incertus correlate with alcohol and sucrose intake in rats

Abstract Background Chronic alcohol intake produces multiple neuroadaptive changes, including up- and down-regulation of neuropeptides and receptors. There are widespread projections of relaxin-3 containing neurons to, and abundant relaxin family peptide 3 receptor (RXFP3) expression within, brain r...

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Veröffentlicht in:Drug and alcohol dependence 2014-07, Vol.140, p.8-16
Hauptverfasser: Ryan, P.J, Krstew, E.V, Sarwar, M, Gundlach, A.L, Lawrence, A.J
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creator Ryan, P.J
Krstew, E.V
Sarwar, M
Gundlach, A.L
Lawrence, A.J
description Abstract Background Chronic alcohol intake produces multiple neuroadaptive changes, including up- and down-regulation of neuropeptides and receptors. There are widespread projections of relaxin-3 containing neurons to, and abundant relaxin family peptide 3 receptor (RXFP3) expression within, brain regions involved in modulating alcohol intake. Recently we demonstrated the involvement of relaxin-3/RXFP3 signalling in alcohol-seeking in rats; therefore in this study we examined whether relaxin-3 and/or RXFP3 expression were altered by chronic alcohol intake in alcohol-preferring iP rats. Methods Expression of relaxin-3 mRNA in the hindbrain nucleus incertus and RXFP3 radioligand binding levels in discrete forebrain regions were investigated following voluntary intake of alcohol or sucrose for 12 weeks, with a 2 day washout, using quantitative in situ hybridisation histochemistry and in vitro receptor autoradiography, respectively, in cohorts of adult, male iP rats. Results Levels of relaxin-3 mRNA in the hindbrain nucleus incertus were positively correlated with the level of intake of both alcohol ( r (12) = 0.59, p = 0.03) and sucrose ( r (7) = 0.70, p = 0.04) in iP rats. Dense binding of the RXFP3-selective radioligand, [125 ]-R3/I5, was detected in hypothalamic and extrahypothalamic sites, but no significant changes in the density of RXFP3 were observed in the brain regions quantified following chronic sucrose or ethanol intake. Conclusions Our findings suggest high endogenous relaxin-3 expression may be associated with higher intake of rewarding substances, rather than its expression being regulated in response to their intake, consistent with an active role for the relaxin-3/RXFP3 system in modulating ingestive and alcohol-related behaviours.
doi_str_mv 10.1016/j.drugalcdep.2014.04.017
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There are widespread projections of relaxin-3 containing neurons to, and abundant relaxin family peptide 3 receptor (RXFP3) expression within, brain regions involved in modulating alcohol intake. Recently we demonstrated the involvement of relaxin-3/RXFP3 signalling in alcohol-seeking in rats; therefore in this study we examined whether relaxin-3 and/or RXFP3 expression were altered by chronic alcohol intake in alcohol-preferring iP rats. Methods Expression of relaxin-3 mRNA in the hindbrain nucleus incertus and RXFP3 radioligand binding levels in discrete forebrain regions were investigated following voluntary intake of alcohol or sucrose for 12 weeks, with a 2 day washout, using quantitative in situ hybridisation histochemistry and in vitro receptor autoradiography, respectively, in cohorts of adult, male iP rats. Results Levels of relaxin-3 mRNA in the hindbrain nucleus incertus were positively correlated with the level of intake of both alcohol ( r (12) = 0.59, p = 0.03) and sucrose ( r (7) = 0.70, p = 0.04) in iP rats. Dense binding of the RXFP3-selective radioligand, [125 ]-R3/I5, was detected in hypothalamic and extrahypothalamic sites, but no significant changes in the density of RXFP3 were observed in the brain regions quantified following chronic sucrose or ethanol intake. Conclusions Our findings suggest high endogenous relaxin-3 expression may be associated with higher intake of rewarding substances, rather than its expression being regulated in response to their intake, consistent with an active role for the relaxin-3/RXFP3 system in modulating ingestive and alcohol-related behaviours.</description><identifier>ISSN: 0376-8716</identifier><identifier>EISSN: 1879-0046</identifier><identifier>DOI: 10.1016/j.drugalcdep.2014.04.017</identifier><identifier>PMID: 24837581</identifier><identifier>CODEN: DADEDV</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Alcohol ; Alcohol Drinking - genetics ; Alcohol Drinking - psychology ; Alcohol related ; Animals ; Brain ; Drinking - physiology ; Eating - genetics ; Ethyl alcohol ; Male ; mRNA ; Neurons ; Neuropeptides ; Nucleus incertus ; Psychiatry ; Raphe Nuclei - metabolism ; Rats ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - metabolism ; Receptors, Peptide - genetics ; Receptors, Peptide - metabolism ; Relaxin-3 ; Rhombencephalon - drug effects ; Rhombencephalon - metabolism ; RNA, Messenger - biosynthesis ; RXFP3 ; Sucrose ; Sucrose - pharmacology</subject><ispartof>Drug and alcohol dependence, 2014-07, Vol.140, p.8-16</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2014 Elsevier Ireland Ltd</rights><rights>Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c582t-4c68085285c39a580ae368fb3e74ddfe69bbd680d7a041c25e74d44a26e17cd83</citedby><cites>FETCH-LOGICAL-c582t-4c68085285c39a580ae368fb3e74ddfe69bbd680d7a041c25e74d44a26e17cd83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0376871614008436$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,30977,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24837581$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ryan, P.J</creatorcontrib><creatorcontrib>Krstew, E.V</creatorcontrib><creatorcontrib>Sarwar, M</creatorcontrib><creatorcontrib>Gundlach, A.L</creatorcontrib><creatorcontrib>Lawrence, A.J</creatorcontrib><title>Relaxin-3 mRNA levels in nucleus incertus correlate with alcohol and sucrose intake in rats</title><title>Drug and alcohol dependence</title><addtitle>Drug Alcohol Depend</addtitle><description>Abstract Background Chronic alcohol intake produces multiple neuroadaptive changes, including up- and down-regulation of neuropeptides and receptors. There are widespread projections of relaxin-3 containing neurons to, and abundant relaxin family peptide 3 receptor (RXFP3) expression within, brain regions involved in modulating alcohol intake. Recently we demonstrated the involvement of relaxin-3/RXFP3 signalling in alcohol-seeking in rats; therefore in this study we examined whether relaxin-3 and/or RXFP3 expression were altered by chronic alcohol intake in alcohol-preferring iP rats. Methods Expression of relaxin-3 mRNA in the hindbrain nucleus incertus and RXFP3 radioligand binding levels in discrete forebrain regions were investigated following voluntary intake of alcohol or sucrose for 12 weeks, with a 2 day washout, using quantitative in situ hybridisation histochemistry and in vitro receptor autoradiography, respectively, in cohorts of adult, male iP rats. Results Levels of relaxin-3 mRNA in the hindbrain nucleus incertus were positively correlated with the level of intake of both alcohol ( r (12) = 0.59, p = 0.03) and sucrose ( r (7) = 0.70, p = 0.04) in iP rats. Dense binding of the RXFP3-selective radioligand, [125 ]-R3/I5, was detected in hypothalamic and extrahypothalamic sites, but no significant changes in the density of RXFP3 were observed in the brain regions quantified following chronic sucrose or ethanol intake. Conclusions Our findings suggest high endogenous relaxin-3 expression may be associated with higher intake of rewarding substances, rather than its expression being regulated in response to their intake, consistent with an active role for the relaxin-3/RXFP3 system in modulating ingestive and alcohol-related behaviours.</description><subject>Alcohol</subject><subject>Alcohol Drinking - genetics</subject><subject>Alcohol Drinking - psychology</subject><subject>Alcohol related</subject><subject>Animals</subject><subject>Brain</subject><subject>Drinking - physiology</subject><subject>Eating - genetics</subject><subject>Ethyl alcohol</subject><subject>Male</subject><subject>mRNA</subject><subject>Neurons</subject><subject>Neuropeptides</subject><subject>Nucleus incertus</subject><subject>Psychiatry</subject><subject>Raphe Nuclei - metabolism</subject><subject>Rats</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Receptors, Peptide - genetics</subject><subject>Receptors, Peptide - metabolism</subject><subject>Relaxin-3</subject><subject>Rhombencephalon - drug effects</subject><subject>Rhombencephalon - metabolism</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RXFP3</subject><subject>Sucrose</subject><subject>Sucrose - pharmacology</subject><issn>0376-8716</issn><issn>1879-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNkt9rHCEQxyW0NNe0_0LwMS97HVdX3ZdAEvoLQgtp-9QH8XQu8eLtXnU3bf77Kpek0KfIwAzycb74nSGEMlgyYPLdZunTfG2j87hbtsDEEkowdUAWTKu-ARDyBVkAV7LRislD8jrnDZQje3hFDluhueo0W5CfVxjtnzA0nG6vvpzRiHcYMw0DHWYXca6lwzSVwo0pFXhC-jtMN7SojzdjpHbwNM8ujRkLO9nbmmiyU35DXq5tzPj2IR-RHx_ef7_41Fx-_fj54uyycZ1up0Y4qUF3re4c722nwSKXer3iqIT3a5T9auUL4pUFwVzb1XshbCuRKec1PyIn-767NP6aMU9mG7LDGO2A45wN6zrotQClnoFyoXrZSl5QvUfr13LCtdmlsLXp3jAwdQpmY_5NwdQpGCjBqsrxg8q82qJ_evhoewHO90DxGu8CJpNdwGK0DwndZPwYnqNy-l8TF8MQnI23eI95M85pKLYbZnJrwHyr21CXgQkALbjkfwFTmbJM</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Ryan, P.J</creator><creator>Krstew, E.V</creator><creator>Sarwar, M</creator><creator>Gundlach, A.L</creator><creator>Lawrence, A.J</creator><general>Elsevier Ireland Ltd</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>7X8</scope><scope>7QJ</scope></search><sort><creationdate>20140701</creationdate><title>Relaxin-3 mRNA levels in nucleus incertus correlate with alcohol and sucrose intake in rats</title><author>Ryan, P.J ; Krstew, E.V ; Sarwar, M ; Gundlach, A.L ; Lawrence, A.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c582t-4c68085285c39a580ae368fb3e74ddfe69bbd680d7a041c25e74d44a26e17cd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Alcohol</topic><topic>Alcohol Drinking - genetics</topic><topic>Alcohol Drinking - psychology</topic><topic>Alcohol related</topic><topic>Animals</topic><topic>Brain</topic><topic>Drinking - physiology</topic><topic>Eating - genetics</topic><topic>Ethyl alcohol</topic><topic>Male</topic><topic>mRNA</topic><topic>Neurons</topic><topic>Neuropeptides</topic><topic>Nucleus incertus</topic><topic>Psychiatry</topic><topic>Raphe Nuclei - metabolism</topic><topic>Rats</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Receptors, Peptide - genetics</topic><topic>Receptors, Peptide - metabolism</topic><topic>Relaxin-3</topic><topic>Rhombencephalon - drug effects</topic><topic>Rhombencephalon - metabolism</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RXFP3</topic><topic>Sucrose</topic><topic>Sucrose - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ryan, P.J</creatorcontrib><creatorcontrib>Krstew, E.V</creatorcontrib><creatorcontrib>Sarwar, M</creatorcontrib><creatorcontrib>Gundlach, A.L</creatorcontrib><creatorcontrib>Lawrence, A.J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><jtitle>Drug and alcohol dependence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ryan, P.J</au><au>Krstew, E.V</au><au>Sarwar, M</au><au>Gundlach, A.L</au><au>Lawrence, A.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relaxin-3 mRNA levels in nucleus incertus correlate with alcohol and sucrose intake in rats</atitle><jtitle>Drug and alcohol dependence</jtitle><addtitle>Drug Alcohol Depend</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>140</volume><spage>8</spage><epage>16</epage><pages>8-16</pages><issn>0376-8716</issn><eissn>1879-0046</eissn><coden>DADEDV</coden><abstract>Abstract Background Chronic alcohol intake produces multiple neuroadaptive changes, including up- and down-regulation of neuropeptides and receptors. There are widespread projections of relaxin-3 containing neurons to, and abundant relaxin family peptide 3 receptor (RXFP3) expression within, brain regions involved in modulating alcohol intake. Recently we demonstrated the involvement of relaxin-3/RXFP3 signalling in alcohol-seeking in rats; therefore in this study we examined whether relaxin-3 and/or RXFP3 expression were altered by chronic alcohol intake in alcohol-preferring iP rats. Methods Expression of relaxin-3 mRNA in the hindbrain nucleus incertus and RXFP3 radioligand binding levels in discrete forebrain regions were investigated following voluntary intake of alcohol or sucrose for 12 weeks, with a 2 day washout, using quantitative in situ hybridisation histochemistry and in vitro receptor autoradiography, respectively, in cohorts of adult, male iP rats. Results Levels of relaxin-3 mRNA in the hindbrain nucleus incertus were positively correlated with the level of intake of both alcohol ( r (12) = 0.59, p = 0.03) and sucrose ( r (7) = 0.70, p = 0.04) in iP rats. Dense binding of the RXFP3-selective radioligand, [125 ]-R3/I5, was detected in hypothalamic and extrahypothalamic sites, but no significant changes in the density of RXFP3 were observed in the brain regions quantified following chronic sucrose or ethanol intake. Conclusions Our findings suggest high endogenous relaxin-3 expression may be associated with higher intake of rewarding substances, rather than its expression being regulated in response to their intake, consistent with an active role for the relaxin-3/RXFP3 system in modulating ingestive and alcohol-related behaviours.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>24837581</pmid><doi>10.1016/j.drugalcdep.2014.04.017</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source Applied Social Sciences Index & Abstracts (ASSIA); MEDLINE; Elsevier ScienceDirect Journals
subjects Alcohol
Alcohol Drinking - genetics
Alcohol Drinking - psychology
Alcohol related
Animals
Brain
Drinking - physiology
Eating - genetics
Ethyl alcohol
Male
mRNA
Neurons
Neuropeptides
Nucleus incertus
Psychiatry
Raphe Nuclei - metabolism
Rats
Receptors, G-Protein-Coupled - genetics
Receptors, G-Protein-Coupled - metabolism
Receptors, Peptide - genetics
Receptors, Peptide - metabolism
Relaxin-3
Rhombencephalon - drug effects
Rhombencephalon - metabolism
RNA, Messenger - biosynthesis
RXFP3
Sucrose
Sucrose - pharmacology
title Relaxin-3 mRNA levels in nucleus incertus correlate with alcohol and sucrose intake in rats
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