Norepinephrine-induced interleukin-6 increase in rat hearts: differential signal transduction in myocytes and non-myocytes
Continuous i.v. infusion of norepinephrine in rats has been shown to induce early interleukin (IL)-6 mRNA expression in the left ventricle (LV) which was followed by hypertrophy and fibrosis. In this study, two approaches were used. In the first, NE (0.1 mg/kg per hour) was infused i.v. in rats for...
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description | Continuous i.v. infusion of norepinephrine in rats has been shown to induce early interleukin (IL)-6 mRNA expression in the left ventricle (LV) which was followed by hypertrophy and fibrosis. In this study, two approaches were used. In the first, NE (0.1 mg/kg per hour) was infused i.v. in rats for several time periods, and freshly obtained ventricular myocardium was dissociated into myocyte (MC) and non-myocyte (NMC) fractions. Second, isolated adult MCs and fibroblasts were treated with NE (10 microM). NE infusion (4 h, in vivo) caused an 11-fold increase in IL-6 mRNA in both cell populations. In vitro treatment of isolated adult MCs for 2 h and of fibroblasts for 1 h with NE induced a 3.5- and 23-fold maximum increase, respectively, in IL-6 mRNA. After in vivo NE treatment, the expression of the mRNA of the transcriptional factor of IL-6, C/EBP-beta, was elevated earlier (after 45 min of NE infusion) than IL-6 mRNA (after 4 h) and was seen in MCs and NMCs. The mRNAs of both receptors of IL-6, the soluble IL6R and gp130, were increased subsequently to IL-6 mRNA. Gp130 was elevated after 24 h and, like IL6R, predominantly in NMCs. In contrast, the IL6R protein and the downstream regulator STAT3 were increased only in MCs after 24 h of NE infusion. The mRNA of C/EBP-delta, which is regulated by STAT3, was elevated only in myocytes. |
doi_str_mv | 10.1007/s00424-003-1043-x |
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In this study, two approaches were used. In the first, NE (0.1 mg/kg per hour) was infused i.v. in rats for several time periods, and freshly obtained ventricular myocardium was dissociated into myocyte (MC) and non-myocyte (NMC) fractions. Second, isolated adult MCs and fibroblasts were treated with NE (10 microM). NE infusion (4 h, in vivo) caused an 11-fold increase in IL-6 mRNA in both cell populations. In vitro treatment of isolated adult MCs for 2 h and of fibroblasts for 1 h with NE induced a 3.5- and 23-fold maximum increase, respectively, in IL-6 mRNA. After in vivo NE treatment, the expression of the mRNA of the transcriptional factor of IL-6, C/EBP-beta, was elevated earlier (after 45 min of NE infusion) than IL-6 mRNA (after 4 h) and was seen in MCs and NMCs. The mRNAs of both receptors of IL-6, the soluble IL6R and gp130, were increased subsequently to IL-6 mRNA. Gp130 was elevated after 24 h and, like IL6R, predominantly in NMCs. In contrast, the IL6R protein and the downstream regulator STAT3 were increased only in MCs after 24 h of NE infusion. The mRNA of C/EBP-delta, which is regulated by STAT3, was elevated only in myocytes.</description><identifier>ISSN: 0031-6768</identifier><identifier>EISSN: 1432-2013</identifier><identifier>DOI: 10.1007/s00424-003-1043-x</identifier><identifier>PMID: 12733076</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Adrenergic alpha-Agonists - pharmacology ; Animals ; Antigens, CD - genetics ; CCAAT-Enhancer-Binding Proteins - genetics ; CCAAT-Enhancer-Binding Proteins - metabolism ; Cytokine Receptor gp130 ; DNA-Binding Proteins - metabolism ; Female ; Fibroblasts - physiology ; Gene Expression - drug effects ; Interleukin-6 - genetics ; Interleukin-6 - metabolism ; Membrane Glycoproteins - genetics ; Myocytes, Cardiac - physiology ; Norepinephrine - pharmacology ; Phosphorylation ; Rats ; Rats, Sprague-Dawley ; Receptors, Interleukin-6 - genetics ; Receptors, Interleukin-6 - metabolism ; RNA, Messenger - analysis ; Signal transduction ; Signal Transduction - drug effects ; STAT3 Transcription Factor ; Trans-Activators - metabolism</subject><ispartof>Pflügers Archiv, 2003-07, Vol.446 (4), p.437-446</ispartof><rights>Springer-Verlag 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c324t-94a602b853cc58c91404bdf992c95260a598b480609be898ada5679280aca72e3</citedby><cites>FETCH-LOGICAL-c324t-94a602b853cc58c91404bdf992c95260a598b480609be898ada5679280aca72e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12733076$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Briest, W</creatorcontrib><creatorcontrib>Rassler, B</creatorcontrib><creatorcontrib>Deten, A</creatorcontrib><creatorcontrib>Leicht, M</creatorcontrib><creatorcontrib>Morwinski, R</creatorcontrib><creatorcontrib>Neichel, D</creatorcontrib><creatorcontrib>Wallukat, G</creatorcontrib><creatorcontrib>Ziegelhöffer, T</creatorcontrib><creatorcontrib>Zimmer, H-G</creatorcontrib><title>Norepinephrine-induced interleukin-6 increase in rat hearts: differential signal transduction in myocytes and non-myocytes</title><title>Pflügers Archiv</title><addtitle>Pflugers Arch</addtitle><description>Continuous i.v. infusion of norepinephrine in rats has been shown to induce early interleukin (IL)-6 mRNA expression in the left ventricle (LV) which was followed by hypertrophy and fibrosis. In this study, two approaches were used. In the first, NE (0.1 mg/kg per hour) was infused i.v. in rats for several time periods, and freshly obtained ventricular myocardium was dissociated into myocyte (MC) and non-myocyte (NMC) fractions. Second, isolated adult MCs and fibroblasts were treated with NE (10 microM). NE infusion (4 h, in vivo) caused an 11-fold increase in IL-6 mRNA in both cell populations. In vitro treatment of isolated adult MCs for 2 h and of fibroblasts for 1 h with NE induced a 3.5- and 23-fold maximum increase, respectively, in IL-6 mRNA. After in vivo NE treatment, the expression of the mRNA of the transcriptional factor of IL-6, C/EBP-beta, was elevated earlier (after 45 min of NE infusion) than IL-6 mRNA (after 4 h) and was seen in MCs and NMCs. The mRNAs of both receptors of IL-6, the soluble IL6R and gp130, were increased subsequently to IL-6 mRNA. Gp130 was elevated after 24 h and, like IL6R, predominantly in NMCs. In contrast, the IL6R protein and the downstream regulator STAT3 were increased only in MCs after 24 h of NE infusion. The mRNA of C/EBP-delta, which is regulated by STAT3, was elevated only in myocytes.</description><subject>Adrenergic alpha-Agonists - pharmacology</subject><subject>Animals</subject><subject>Antigens, CD - genetics</subject><subject>CCAAT-Enhancer-Binding Proteins - genetics</subject><subject>CCAAT-Enhancer-Binding Proteins - metabolism</subject><subject>Cytokine Receptor gp130</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Female</subject><subject>Fibroblasts - physiology</subject><subject>Gene Expression - drug effects</subject><subject>Interleukin-6 - genetics</subject><subject>Interleukin-6 - metabolism</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Myocytes, Cardiac - physiology</subject><subject>Norepinephrine - pharmacology</subject><subject>Phosphorylation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Interleukin-6 - genetics</subject><subject>Receptors, Interleukin-6 - metabolism</subject><subject>RNA, Messenger - 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pharmacology</topic><topic>Animals</topic><topic>Antigens, CD - genetics</topic><topic>CCAAT-Enhancer-Binding Proteins - genetics</topic><topic>CCAAT-Enhancer-Binding Proteins - metabolism</topic><topic>Cytokine Receptor gp130</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Female</topic><topic>Fibroblasts - physiology</topic><topic>Gene Expression - drug effects</topic><topic>Interleukin-6 - genetics</topic><topic>Interleukin-6 - metabolism</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Myocytes, Cardiac - physiology</topic><topic>Norepinephrine - pharmacology</topic><topic>Phosphorylation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Interleukin-6 - genetics</topic><topic>Receptors, Interleukin-6 - metabolism</topic><topic>RNA, Messenger - analysis</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>STAT3 Transcription Factor</topic><topic>Trans-Activators - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Briest, W</creatorcontrib><creatorcontrib>Rassler, B</creatorcontrib><creatorcontrib>Deten, A</creatorcontrib><creatorcontrib>Leicht, M</creatorcontrib><creatorcontrib>Morwinski, R</creatorcontrib><creatorcontrib>Neichel, D</creatorcontrib><creatorcontrib>Wallukat, G</creatorcontrib><creatorcontrib>Ziegelhöffer, T</creatorcontrib><creatorcontrib>Zimmer, H-G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Pflügers Archiv</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Briest, W</au><au>Rassler, B</au><au>Deten, A</au><au>Leicht, M</au><au>Morwinski, R</au><au>Neichel, D</au><au>Wallukat, G</au><au>Ziegelhöffer, T</au><au>Zimmer, H-G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Norepinephrine-induced interleukin-6 increase in rat hearts: differential signal transduction in myocytes and non-myocytes</atitle><jtitle>Pflügers Archiv</jtitle><addtitle>Pflugers Arch</addtitle><date>2003-07</date><risdate>2003</risdate><volume>446</volume><issue>4</issue><spage>437</spage><epage>446</epage><pages>437-446</pages><issn>0031-6768</issn><eissn>1432-2013</eissn><abstract>Continuous i.v. infusion of norepinephrine in rats has been shown to induce early interleukin (IL)-6 mRNA expression in the left ventricle (LV) which was followed by hypertrophy and fibrosis. In this study, two approaches were used. In the first, NE (0.1 mg/kg per hour) was infused i.v. in rats for several time periods, and freshly obtained ventricular myocardium was dissociated into myocyte (MC) and non-myocyte (NMC) fractions. Second, isolated adult MCs and fibroblasts were treated with NE (10 microM). NE infusion (4 h, in vivo) caused an 11-fold increase in IL-6 mRNA in both cell populations. In vitro treatment of isolated adult MCs for 2 h and of fibroblasts for 1 h with NE induced a 3.5- and 23-fold maximum increase, respectively, in IL-6 mRNA. After in vivo NE treatment, the expression of the mRNA of the transcriptional factor of IL-6, C/EBP-beta, was elevated earlier (after 45 min of NE infusion) than IL-6 mRNA (after 4 h) and was seen in MCs and NMCs. The mRNAs of both receptors of IL-6, the soluble IL6R and gp130, were increased subsequently to IL-6 mRNA. Gp130 was elevated after 24 h and, like IL6R, predominantly in NMCs. In contrast, the IL6R protein and the downstream regulator STAT3 were increased only in MCs after 24 h of NE infusion. The mRNA of C/EBP-delta, which is regulated by STAT3, was elevated only in myocytes.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>12733076</pmid><doi>10.1007/s00424-003-1043-x</doi><tpages>10</tpages></addata></record> |
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subjects | Adrenergic alpha-Agonists - pharmacology Animals Antigens, CD - genetics CCAAT-Enhancer-Binding Proteins - genetics CCAAT-Enhancer-Binding Proteins - metabolism Cytokine Receptor gp130 DNA-Binding Proteins - metabolism Female Fibroblasts - physiology Gene Expression - drug effects Interleukin-6 - genetics Interleukin-6 - metabolism Membrane Glycoproteins - genetics Myocytes, Cardiac - physiology Norepinephrine - pharmacology Phosphorylation Rats Rats, Sprague-Dawley Receptors, Interleukin-6 - genetics Receptors, Interleukin-6 - metabolism RNA, Messenger - analysis Signal transduction Signal Transduction - drug effects STAT3 Transcription Factor Trans-Activators - metabolism |
title | Norepinephrine-induced interleukin-6 increase in rat hearts: differential signal transduction in myocytes and non-myocytes |
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