Elevated prodynorphin expression associated with ethanol withdrawal convulsions
The hypothesis that κ-opioid system activity may in part mediate convulsions exhibited during ethanol withdrawal was tested by exposing Withdrawal Seizure-Prone (WSP) and Withdrawal Seizure-Resistant (WSR) mice to chronic ethanol. Whole brain was harvested for RNA isolation and prodynorphin mRNA ste...
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Veröffentlicht in: | Neurochemistry international 2000-11, Vol.37 (5), p.463-472 |
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description | The hypothesis that κ-opioid system activity may in part mediate convulsions exhibited during ethanol withdrawal was tested by exposing Withdrawal Seizure-Prone (WSP) and Withdrawal Seizure-Resistant (WSR) mice to chronic ethanol. Whole brain was harvested for RNA isolation and prodynorphin mRNA steady-state levels in whole brain were examined using Northern blot analysis. The data revealed significantly increased levels of prodynorphin mRNA expression in mice susceptible to ethanol withdrawal convulsions after withdrawal, with no corresponding increase in prodynorphin steady-state levels in mice resistant to ethanol withdrawal convulsions. These findings were not due to basal differences in prodynorphin expression between the WSP and WSR mice. To verify that the differences observed were not due to an ethanol-induced global alteration in gene transcription, mRNA levels of the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase were measured. Glyceraldehyde-3-phosphate dehydrogenase expression was unchanged following both chronic exposure to ethanol and chronic exposure followed by withdrawal. These results extend our understanding of prodynorphin’s role in generalized seizure activity to include ethanol withdrawal-induced convulsions. Our findings suggest that prodynorphin expression is modulated during ethanol withdrawal convulsions, or alternatively, prodynorphin may mediate the severity of ethanol withdrawal convulsions. |
doi_str_mv | 10.1016/S0197-0186(00)00056-5 |
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Whole brain was harvested for RNA isolation and prodynorphin mRNA steady-state levels in whole brain were examined using Northern blot analysis. The data revealed significantly increased levels of prodynorphin mRNA expression in mice susceptible to ethanol withdrawal convulsions after withdrawal, with no corresponding increase in prodynorphin steady-state levels in mice resistant to ethanol withdrawal convulsions. These findings were not due to basal differences in prodynorphin expression between the WSP and WSR mice. To verify that the differences observed were not due to an ethanol-induced global alteration in gene transcription, mRNA levels of the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase were measured. Glyceraldehyde-3-phosphate dehydrogenase expression was unchanged following both chronic exposure to ethanol and chronic exposure followed by withdrawal. These results extend our understanding of prodynorphin’s role in generalized seizure activity to include ethanol withdrawal-induced convulsions. Our findings suggest that prodynorphin expression is modulated during ethanol withdrawal convulsions, or alternatively, prodynorphin may mediate the severity of ethanol withdrawal convulsions.</description><identifier>ISSN: 0197-0186</identifier><identifier>EISSN: 1872-9754</identifier><identifier>DOI: 10.1016/S0197-0186(00)00056-5</identifier><identifier>PMID: 10871698</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Administration, Inhalation ; Animals ; Aversion ; Convulsions ; Disease Susceptibility ; Enkephalins - metabolism ; Ethanol ; Ethanol - administration & dosage ; Ethanol - adverse effects ; Genetics ; Glyceraldehyde-3-Phosphate Dehydrogenases - genetics ; Male ; Mice ; Mice, Inbred Strains ; Prodynorphin ; Protein Precursors - metabolism ; RNA, Messenger - metabolism ; Seizures - chemically induced ; Seizures - metabolism ; Selected lines ; Substance Withdrawal Syndrome - metabolism ; Withdrawal ; κ-Opioid receptors</subject><ispartof>Neurochemistry international, 2000-11, Vol.37 (5), p.463-472</ispartof><rights>2000 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-af63c7f6ea89de8824cb0092e04ae8a13239d29e00ef94a8bc8c59ba1e7ef1ee3</citedby><cites>FETCH-LOGICAL-c392t-af63c7f6ea89de8824cb0092e04ae8a13239d29e00ef94a8bc8c59ba1e7ef1ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0197-0186(00)00056-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10871698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beadles-Bohling, A.S.</creatorcontrib><creatorcontrib>Crabbe, J.C.</creatorcontrib><creatorcontrib>Wiren, K.M.</creatorcontrib><title>Elevated prodynorphin expression associated with ethanol withdrawal convulsions</title><title>Neurochemistry international</title><addtitle>Neurochem Int</addtitle><description>The hypothesis that κ-opioid system activity may in part mediate convulsions exhibited during ethanol withdrawal was tested by exposing Withdrawal Seizure-Prone (WSP) and Withdrawal Seizure-Resistant (WSR) mice to chronic ethanol. Whole brain was harvested for RNA isolation and prodynorphin mRNA steady-state levels in whole brain were examined using Northern blot analysis. The data revealed significantly increased levels of prodynorphin mRNA expression in mice susceptible to ethanol withdrawal convulsions after withdrawal, with no corresponding increase in prodynorphin steady-state levels in mice resistant to ethanol withdrawal convulsions. These findings were not due to basal differences in prodynorphin expression between the WSP and WSR mice. To verify that the differences observed were not due to an ethanol-induced global alteration in gene transcription, mRNA levels of the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase were measured. Glyceraldehyde-3-phosphate dehydrogenase expression was unchanged following both chronic exposure to ethanol and chronic exposure followed by withdrawal. These results extend our understanding of prodynorphin’s role in generalized seizure activity to include ethanol withdrawal-induced convulsions. Our findings suggest that prodynorphin expression is modulated during ethanol withdrawal convulsions, or alternatively, prodynorphin may mediate the severity of ethanol withdrawal convulsions.</description><subject>Administration, Inhalation</subject><subject>Animals</subject><subject>Aversion</subject><subject>Convulsions</subject><subject>Disease Susceptibility</subject><subject>Enkephalins - metabolism</subject><subject>Ethanol</subject><subject>Ethanol - administration & dosage</subject><subject>Ethanol - adverse effects</subject><subject>Genetics</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Prodynorphin</subject><subject>Protein Precursors - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Seizures - chemically induced</subject><subject>Seizures - metabolism</subject><subject>Selected lines</subject><subject>Substance Withdrawal Syndrome - metabolism</subject><subject>Withdrawal</subject><subject>κ-Opioid receptors</subject><issn>0197-0186</issn><issn>1872-9754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqXwCaCsECwC47xsrxCqykOq1AWwthxnohqlcbDTlv49aVIhdqxGI507j0PIJYU7CjS7fwMqWAiUZzcAtwCQZmF6RMaUsygULE2OyfgXGZEz7z87iAlIT8mIAmc0E3xMFrMKN6rFImicLXa1dc3S1AF-Nw69N7YOlPdWmx7ZmnYZYLtUta36pnBqq6pA23qzrva0Pycnpao8XhzqhHw8zd6nL-F88fw6fZyHOhZRG6oyizUrM1RcFMh5lOgcQEQIiUKuaBzFoogEAmApEsVzzXUqckWRYUkR4wm5HuZ2Z3-t0bdyZbzGqlI12rWXlLEoAs47MB1A7az3DkvZOLNSbicpyL1J2ZuUe00SQPYmZdrlrg4L1vkKiz-pQV0HPAwAdm9uDDrptcFaY2Ec6lYW1vyz4gcNb4Wl</recordid><startdate>20001101</startdate><enddate>20001101</enddate><creator>Beadles-Bohling, A.S.</creator><creator>Crabbe, J.C.</creator><creator>Wiren, K.M.</creator><general>Elsevier 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>7TK</scope></search><sort><creationdate>20001101</creationdate><title>Elevated prodynorphin expression associated with ethanol withdrawal convulsions</title><author>Beadles-Bohling, A.S. ; Crabbe, J.C. ; Wiren, K.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-af63c7f6ea89de8824cb0092e04ae8a13239d29e00ef94a8bc8c59ba1e7ef1ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Administration, Inhalation</topic><topic>Animals</topic><topic>Aversion</topic><topic>Convulsions</topic><topic>Disease Susceptibility</topic><topic>Enkephalins - metabolism</topic><topic>Ethanol</topic><topic>Ethanol - administration & dosage</topic><topic>Ethanol - adverse effects</topic><topic>Genetics</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Prodynorphin</topic><topic>Protein Precursors - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Seizures - chemically induced</topic><topic>Seizures - metabolism</topic><topic>Selected lines</topic><topic>Substance Withdrawal Syndrome - metabolism</topic><topic>Withdrawal</topic><topic>κ-Opioid receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beadles-Bohling, A.S.</creatorcontrib><creatorcontrib>Crabbe, J.C.</creatorcontrib><creatorcontrib>Wiren, K.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Neurochemistry international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beadles-Bohling, A.S.</au><au>Crabbe, J.C.</au><au>Wiren, K.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elevated prodynorphin expression associated with ethanol withdrawal convulsions</atitle><jtitle>Neurochemistry international</jtitle><addtitle>Neurochem Int</addtitle><date>2000-11-01</date><risdate>2000</risdate><volume>37</volume><issue>5</issue><spage>463</spage><epage>472</epage><pages>463-472</pages><issn>0197-0186</issn><eissn>1872-9754</eissn><abstract>The hypothesis that κ-opioid system activity may in part mediate convulsions exhibited during ethanol withdrawal was tested by exposing Withdrawal Seizure-Prone (WSP) and Withdrawal Seizure-Resistant (WSR) mice to chronic ethanol. Whole brain was harvested for RNA isolation and prodynorphin mRNA steady-state levels in whole brain were examined using Northern blot analysis. The data revealed significantly increased levels of prodynorphin mRNA expression in mice susceptible to ethanol withdrawal convulsions after withdrawal, with no corresponding increase in prodynorphin steady-state levels in mice resistant to ethanol withdrawal convulsions. These findings were not due to basal differences in prodynorphin expression between the WSP and WSR mice. To verify that the differences observed were not due to an ethanol-induced global alteration in gene transcription, mRNA levels of the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase were measured. Glyceraldehyde-3-phosphate dehydrogenase expression was unchanged following both chronic exposure to ethanol and chronic exposure followed by withdrawal. These results extend our understanding of prodynorphin’s role in generalized seizure activity to include ethanol withdrawal-induced convulsions. Our findings suggest that prodynorphin expression is modulated during ethanol withdrawal convulsions, or alternatively, prodynorphin may mediate the severity of ethanol withdrawal convulsions.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>10871698</pmid><doi>10.1016/S0197-0186(00)00056-5</doi><tpages>10</tpages></addata></record> |
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subjects | Administration, Inhalation Animals Aversion Convulsions Disease Susceptibility Enkephalins - metabolism Ethanol Ethanol - administration & dosage Ethanol - adverse effects Genetics Glyceraldehyde-3-Phosphate Dehydrogenases - genetics Male Mice Mice, Inbred Strains Prodynorphin Protein Precursors - metabolism RNA, Messenger - metabolism Seizures - chemically induced Seizures - metabolism Selected lines Substance Withdrawal Syndrome - metabolism Withdrawal κ-Opioid receptors |
title | Elevated prodynorphin expression associated with ethanol withdrawal convulsions |
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