Divergence in the Expression of Molecular Markers of Neuronal Activation in the Parvocellular Paraventricular Nucleus of the Hypothalamus Evoked by Alcohol Administration via Different Routes
Immediate early gene (IEG) expression has been routinely used by neuroscientists as an index of neuronal activation. In the case of the hypothalamic-pituitary-adrenal axis, induction of c-fos and/or NGFI-B mRNAs in the parvocellular paraventricular nucleus (pPVN) has been documented after a variety...
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description | Immediate early gene (IEG) expression has been routinely used by neuroscientists as an index of neuronal activation. In the case of the hypothalamic-pituitary-adrenal axis, induction of c-fos and/or NGFI-B mRNAs in the parvocellular paraventricular nucleus (pPVN) has been documented after a variety of stimuli that increase adrenocorticotropin (ACTH) in the systemic circulation. However, the functional relationship between expression of IEGs and transcription of the genes for the ACTH secretagogues corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) is not clear. While investigating the neuroendocrine correlates of alcohol administration via different routes (intraperitoneal vs intragastric), we noted a difference in the time course of NGFI-B mRNA expression in the pPVN, despite comparable dynamics in ACTH secretion. By comparing the temporal cascade of transcriptional events in vivo after alcohol injection via either route, we sought to determine functional relationships between IEGs and the induction of CRF and AVP heteronuclear RNAs (hnRNAs). One advantage of our paradigm is the use of the same stimulus (systemic alcohol injection) in which access to the CNS does not differ between the groups to be compared. Intraperitoneal administration of the drug resulted in significant increases in c-fos mRNA, Fos protein, CRF hnRNA, and AVP hnRNA. In contrast, intragastric treatment evoked a brief, modest elevation in c-fos mRNA and Fos protein, increased AVP hnRNA, and caused no detectable change in CRF hnRNA. These data indicate that robust increases in CRF hnRNA are closely linked to full expression of c-fos mRNA and Fos protein. In addition, the expression of NGFI-B after both routes of administration is indicative of cellular activation within the pPVN in parallel with secretion of ACTH. |
doi_str_mv | 10.1523/jneurosci.18-11-04344.1998 |
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In the case of the hypothalamic-pituitary-adrenal axis, induction of c-fos and/or NGFI-B mRNAs in the parvocellular paraventricular nucleus (pPVN) has been documented after a variety of stimuli that increase adrenocorticotropin (ACTH) in the systemic circulation. However, the functional relationship between expression of IEGs and transcription of the genes for the ACTH secretagogues corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) is not clear. While investigating the neuroendocrine correlates of alcohol administration via different routes (intraperitoneal vs intragastric), we noted a difference in the time course of NGFI-B mRNA expression in the pPVN, despite comparable dynamics in ACTH secretion. By comparing the temporal cascade of transcriptional events in vivo after alcohol injection via either route, we sought to determine functional relationships between IEGs and the induction of CRF and AVP heteronuclear RNAs (hnRNAs). One advantage of our paradigm is the use of the same stimulus (systemic alcohol injection) in which access to the CNS does not differ between the groups to be compared. Intraperitoneal administration of the drug resulted in significant increases in c-fos mRNA, Fos protein, CRF hnRNA, and AVP hnRNA. In contrast, intragastric treatment evoked a brief, modest elevation in c-fos mRNA and Fos protein, increased AVP hnRNA, and caused no detectable change in CRF hnRNA. These data indicate that robust increases in CRF hnRNA are closely linked to full expression of c-fos mRNA and Fos protein. In addition, the expression of NGFI-B after both routes of administration is indicative of cellular activation within the pPVN in parallel with secretion of ACTH.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.18-11-04344.1998</identifier><identifier>PMID: 9592111</identifier><language>eng</language><publisher>United States: Soc Neuroscience</publisher><subject>Animals ; Arginine Vasopressin - genetics ; Biomarkers ; Central Nervous System Depressants - administration & dosage ; Central Nervous System Depressants - pharmacology ; Corticotropin-Releasing Hormone - metabolism ; DNA-Binding Proteins - analysis ; DNA-Binding Proteins - genetics ; Ethanol - administration & dosage ; Ethanol - pharmacology ; Gene Expression - drug effects ; Genes, Immediate-Early - drug effects ; Genes, Immediate-Early - physiology ; Hypothalamo-Hypophyseal System - cytology ; Hypothalamo-Hypophyseal System - drug effects ; Injections, Intraperitoneal ; Instillation, Drug ; Male ; Neurons - chemistry ; Neurons - drug effects ; Neurons - physiology ; Nuclear Receptor Subfamily 4, Group A, Member 1 ; Paraventricular Hypothalamic Nucleus - cytology ; Paraventricular Hypothalamic Nucleus - drug effects ; Pituitary-Adrenal System - cytology ; Pituitary-Adrenal System - drug effects ; Proto-Oncogene Proteins c-fos - analysis ; Proto-Oncogene Proteins c-fos - genetics ; Rats ; Rats, Sprague-Dawley ; Receptors, Cytoplasmic and Nuclear ; Receptors, Steroid - analysis ; Receptors, Steroid - genetics ; RNA, Heterogeneous Nuclear - analysis ; RNA, Heterogeneous Nuclear - genetics ; Stomach ; Transcription Factors - analysis ; Transcription Factors - genetics</subject><ispartof>The Journal of neuroscience, 1998-06, Vol.18 (11), p.4344-4352</ispartof><rights>Copyright © 1998 Society for Neuroscience 1998</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-e58a0974bede48170ee7e53c24421c7d56a8b74b6b177d4983a9bcbe2bf4da853</citedby><cites>FETCH-LOGICAL-c484t-e58a0974bede48170ee7e53c24421c7d56a8b74b6b177d4983a9bcbe2bf4da853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792808/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792808/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9592111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogilvie, Kathleen M</creatorcontrib><creatorcontrib>Lee, Soon</creatorcontrib><creatorcontrib>Rivier, Catherine</creatorcontrib><title>Divergence in the Expression of Molecular Markers of Neuronal Activation in the Parvocellular Paraventricular Nucleus of the Hypothalamus Evoked by Alcohol Administration via Different Routes</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Immediate early gene (IEG) expression has been routinely used by neuroscientists as an index of neuronal activation. In the case of the hypothalamic-pituitary-adrenal axis, induction of c-fos and/or NGFI-B mRNAs in the parvocellular paraventricular nucleus (pPVN) has been documented after a variety of stimuli that increase adrenocorticotropin (ACTH) in the systemic circulation. However, the functional relationship between expression of IEGs and transcription of the genes for the ACTH secretagogues corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) is not clear. While investigating the neuroendocrine correlates of alcohol administration via different routes (intraperitoneal vs intragastric), we noted a difference in the time course of NGFI-B mRNA expression in the pPVN, despite comparable dynamics in ACTH secretion. By comparing the temporal cascade of transcriptional events in vivo after alcohol injection via either route, we sought to determine functional relationships between IEGs and the induction of CRF and AVP heteronuclear RNAs (hnRNAs). One advantage of our paradigm is the use of the same stimulus (systemic alcohol injection) in which access to the CNS does not differ between the groups to be compared. Intraperitoneal administration of the drug resulted in significant increases in c-fos mRNA, Fos protein, CRF hnRNA, and AVP hnRNA. In contrast, intragastric treatment evoked a brief, modest elevation in c-fos mRNA and Fos protein, increased AVP hnRNA, and caused no detectable change in CRF hnRNA. These data indicate that robust increases in CRF hnRNA are closely linked to full expression of c-fos mRNA and Fos protein. In addition, the expression of NGFI-B after both routes of administration is indicative of cellular activation within the pPVN in parallel with secretion of ACTH.</description><subject>Animals</subject><subject>Arginine Vasopressin - genetics</subject><subject>Biomarkers</subject><subject>Central Nervous System Depressants - administration & dosage</subject><subject>Central Nervous System Depressants - pharmacology</subject><subject>Corticotropin-Releasing Hormone - metabolism</subject><subject>DNA-Binding Proteins - analysis</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Ethanol - administration & dosage</subject><subject>Ethanol - pharmacology</subject><subject>Gene Expression - drug effects</subject><subject>Genes, Immediate-Early - drug effects</subject><subject>Genes, Immediate-Early - physiology</subject><subject>Hypothalamo-Hypophyseal System - cytology</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Injections, Intraperitoneal</subject><subject>Instillation, Drug</subject><subject>Male</subject><subject>Neurons - chemistry</subject><subject>Neurons - drug effects</subject><subject>Neurons - physiology</subject><subject>Nuclear Receptor Subfamily 4, Group A, Member 1</subject><subject>Paraventricular Hypothalamic Nucleus - cytology</subject><subject>Paraventricular Hypothalamic Nucleus - drug effects</subject><subject>Pituitary-Adrenal System - cytology</subject><subject>Pituitary-Adrenal System - drug effects</subject><subject>Proto-Oncogene Proteins c-fos - analysis</subject><subject>Proto-Oncogene Proteins c-fos - genetics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Cytoplasmic and Nuclear</subject><subject>Receptors, Steroid - analysis</subject><subject>Receptors, Steroid - genetics</subject><subject>RNA, Heterogeneous Nuclear - analysis</subject><subject>RNA, Heterogeneous Nuclear - genetics</subject><subject>Stomach</subject><subject>Transcription Factors - analysis</subject><subject>Transcription Factors - genetics</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFktFu0zAUhiMEGmPwCEgRF3CVYidObHOBVHWFDW0dGuzacpyT1psTd3aS0qfj1XCaaoIrriyf_z_f8bH-KHqH0QznafbxvoXeWa_0DLME4wSRjJAZ5pw9i06DgycpQfh5dIpSipKCUPIyeuX9PUKIIkxPohOe8xRjfBr9PtcDuDW0CmLdxt0G4uWvrQPvtW1jW8fX1oDqjXTxtXQP4PxYXI3zW2niuer0ILvRe-z-Lt1gFRhz6Ak3OUDbOT0xVr0y0B8Yo_liv7XdRhrZhNpysA9QxeU-nhtlNzbQq0a32ndumjBoGZ_rugYXiPGt7Tvwr6MXtTQe3hzPs-juy_Ln4iK5uvl6uZhfJYow0iWQM4k4JSVUQBimCIBCnqmUkBQrWuWFZGWQixJTWhHOMslLVUJa1qSSLM_Oos8Td9uXDVRq3EkasXW6kW4vrNTiX6XVG7G2gygoTxliAfD-CHD2sQffiUb78Z9kC7b3gnJGCUfov0ZcZBwVjAbjp8moQha8g_rpNRiJMSfi22p5d3vzY3EpMBMYi0NOxJiT0Pz2732eWo_BCPqHSd_o9WanHQjfSGOCG4vdbjfxRlz2B6Lw0BY</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>Ogilvie, Kathleen M</creator><creator>Lee, Soon</creator><creator>Rivier, Catherine</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19980601</creationdate><title>Divergence in the Expression of Molecular Markers of Neuronal Activation in the Parvocellular Paraventricular Nucleus of the Hypothalamus Evoked by Alcohol Administration via Different Routes</title><author>Ogilvie, Kathleen M ; Lee, Soon ; Rivier, Catherine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-e58a0974bede48170ee7e53c24421c7d56a8b74b6b177d4983a9bcbe2bf4da853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Arginine Vasopressin - genetics</topic><topic>Biomarkers</topic><topic>Central Nervous System Depressants - administration & dosage</topic><topic>Central Nervous System Depressants - pharmacology</topic><topic>Corticotropin-Releasing Hormone - metabolism</topic><topic>DNA-Binding Proteins - analysis</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Ethanol - administration & dosage</topic><topic>Ethanol - pharmacology</topic><topic>Gene Expression - drug effects</topic><topic>Genes, Immediate-Early - drug effects</topic><topic>Genes, Immediate-Early - physiology</topic><topic>Hypothalamo-Hypophyseal System - cytology</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Injections, Intraperitoneal</topic><topic>Instillation, Drug</topic><topic>Male</topic><topic>Neurons - chemistry</topic><topic>Neurons - drug effects</topic><topic>Neurons - physiology</topic><topic>Nuclear Receptor Subfamily 4, Group A, Member 1</topic><topic>Paraventricular Hypothalamic Nucleus - cytology</topic><topic>Paraventricular Hypothalamic Nucleus - drug effects</topic><topic>Pituitary-Adrenal System - cytology</topic><topic>Pituitary-Adrenal System - drug effects</topic><topic>Proto-Oncogene Proteins c-fos - analysis</topic><topic>Proto-Oncogene Proteins c-fos - genetics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Cytoplasmic and Nuclear</topic><topic>Receptors, Steroid - analysis</topic><topic>Receptors, Steroid - genetics</topic><topic>RNA, Heterogeneous Nuclear - analysis</topic><topic>RNA, Heterogeneous Nuclear - genetics</topic><topic>Stomach</topic><topic>Transcription Factors - analysis</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogilvie, Kathleen M</creatorcontrib><creatorcontrib>Lee, Soon</creatorcontrib><creatorcontrib>Rivier, Catherine</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogilvie, Kathleen M</au><au>Lee, Soon</au><au>Rivier, Catherine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergence in the Expression of Molecular Markers of Neuronal Activation in the Parvocellular Paraventricular Nucleus of the Hypothalamus Evoked by Alcohol Administration via Different Routes</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>18</volume><issue>11</issue><spage>4344</spage><epage>4352</epage><pages>4344-4352</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>Immediate early gene (IEG) expression has been routinely used by neuroscientists as an index of neuronal activation. In the case of the hypothalamic-pituitary-adrenal axis, induction of c-fos and/or NGFI-B mRNAs in the parvocellular paraventricular nucleus (pPVN) has been documented after a variety of stimuli that increase adrenocorticotropin (ACTH) in the systemic circulation. However, the functional relationship between expression of IEGs and transcription of the genes for the ACTH secretagogues corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) is not clear. While investigating the neuroendocrine correlates of alcohol administration via different routes (intraperitoneal vs intragastric), we noted a difference in the time course of NGFI-B mRNA expression in the pPVN, despite comparable dynamics in ACTH secretion. By comparing the temporal cascade of transcriptional events in vivo after alcohol injection via either route, we sought to determine functional relationships between IEGs and the induction of CRF and AVP heteronuclear RNAs (hnRNAs). One advantage of our paradigm is the use of the same stimulus (systemic alcohol injection) in which access to the CNS does not differ between the groups to be compared. Intraperitoneal administration of the drug resulted in significant increases in c-fos mRNA, Fos protein, CRF hnRNA, and AVP hnRNA. In contrast, intragastric treatment evoked a brief, modest elevation in c-fos mRNA and Fos protein, increased AVP hnRNA, and caused no detectable change in CRF hnRNA. These data indicate that robust increases in CRF hnRNA are closely linked to full expression of c-fos mRNA and Fos protein. In addition, the expression of NGFI-B after both routes of administration is indicative of cellular activation within the pPVN in parallel with secretion of ACTH.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>9592111</pmid><doi>10.1523/jneurosci.18-11-04344.1998</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Arginine Vasopressin - genetics Biomarkers Central Nervous System Depressants - administration & dosage Central Nervous System Depressants - pharmacology Corticotropin-Releasing Hormone - metabolism DNA-Binding Proteins - analysis DNA-Binding Proteins - genetics Ethanol - administration & dosage Ethanol - pharmacology Gene Expression - drug effects Genes, Immediate-Early - drug effects Genes, Immediate-Early - physiology Hypothalamo-Hypophyseal System - cytology Hypothalamo-Hypophyseal System - drug effects Injections, Intraperitoneal Instillation, Drug Male Neurons - chemistry Neurons - drug effects Neurons - physiology Nuclear Receptor Subfamily 4, Group A, Member 1 Paraventricular Hypothalamic Nucleus - cytology Paraventricular Hypothalamic Nucleus - drug effects Pituitary-Adrenal System - cytology Pituitary-Adrenal System - drug effects Proto-Oncogene Proteins c-fos - analysis Proto-Oncogene Proteins c-fos - genetics Rats Rats, Sprague-Dawley Receptors, Cytoplasmic and Nuclear Receptors, Steroid - analysis Receptors, Steroid - genetics RNA, Heterogeneous Nuclear - analysis RNA, Heterogeneous Nuclear - genetics Stomach Transcription Factors - analysis Transcription Factors - genetics |
title | Divergence in the Expression of Molecular Markers of Neuronal Activation in the Parvocellular Paraventricular Nucleus of the Hypothalamus Evoked by Alcohol Administration via Different Routes |
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