Inhibition by antidepressant drugs of cyclic AMP response element-binding protein/cyclic AMP response element-directed gene transcription
Clinical observations agree that antidepressant drugs are effective only after a lag phase of 1-3 weeks. This delay could be explained at the molecular level by an action on gene transcription. Transcription of many genes is directed by the cAMP/Ca(2+)-responsive element (CRE) and its cognate transc...
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Veröffentlicht in: | Molecular pharmacology 1995-06, Vol.47 (6), p.1112-1118 |
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creator | Schwaninger, M Schöfl, C Blume, R Rössig, L Knepel, W |
description | Clinical observations agree that antidepressant drugs are effective only after a lag phase of 1-3 weeks. This delay could
be explained at the molecular level by an action on gene transcription. Transcription of many genes is directed by the cAMP/Ca(2+)-responsive
element (CRE) and its cognate transcription factor CRE-binding protein (CREB). Membrane depolarization and cAMP induce the
phosphorylation of CREB at Ser-119 and thereby stimulate the transcriptional activity of CREB. The effect of antidepressant
drugs on CREB/CRE-directed gene transcription was investigated using transient transfections of reporter fusion genes in HIT
and PC-12 cells. Clomipramine, imipramine, fluoxetine, doxepin, desipramine, amitriptyline, maprotiline, mianserin, and trazodone
inhibited CRE-directed gene transcription that was stimulated by membrane depolarization, with IC50 values between 70 nM and
1.73 microM. Desipramine had no effect on transcription after stimulation by cAMP but blocked the synergistic effect of cAMP
and membrane depolarization to the level of stimulation by cAMP alone. Upon membrane depolarization, desipramine reduced the
phosphorylation of CREB at Ser-119 and also blocked the depolarization-induced increase in the intracellular free Ca2+ concentration
in HIT cells. Thus, by interfering with the depolarization-induced activation of the transcription factor CREB, antidepressant
drugs can inhibit CRE-directed gene transcription, which could underlie the pharmacological effects of these clinically important
drugs. |
format | Article |
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be explained at the molecular level by an action on gene transcription. Transcription of many genes is directed by the cAMP/Ca(2+)-responsive
element (CRE) and its cognate transcription factor CRE-binding protein (CREB). Membrane depolarization and cAMP induce the
phosphorylation of CREB at Ser-119 and thereby stimulate the transcriptional activity of CREB. The effect of antidepressant
drugs on CREB/CRE-directed gene transcription was investigated using transient transfections of reporter fusion genes in HIT
and PC-12 cells. Clomipramine, imipramine, fluoxetine, doxepin, desipramine, amitriptyline, maprotiline, mianserin, and trazodone
inhibited CRE-directed gene transcription that was stimulated by membrane depolarization, with IC50 values between 70 nM and
1.73 microM. Desipramine had no effect on transcription after stimulation by cAMP but blocked the synergistic effect of cAMP
and membrane depolarization to the level of stimulation by cAMP alone. Upon membrane depolarization, desipramine reduced the
phosphorylation of CREB at Ser-119 and also blocked the depolarization-induced increase in the intracellular free Ca2+ concentration
in HIT cells. Thus, by interfering with the depolarization-induced activation of the transcription factor CREB, antidepressant
drugs can inhibit CRE-directed gene transcription, which could underlie the pharmacological effects of these clinically important
drugs.</description><identifier>ISSN: 0026-895X</identifier><identifier>EISSN: 1521-0111</identifier><identifier>PMID: 7603449</identifier><language>eng</language><publisher>United States: American Society for Pharmacology and Experimental Therapeutics</publisher><subject>Animals ; Antidepressive Agents - pharmacology ; Base Sequence ; Calcium - metabolism ; Cricetinae ; Cyclic AMP Response Element-Binding Protein - antagonists & inhibitors ; Cyclic AMP Response Element-Binding Protein - physiology ; Desipramine - pharmacology ; DNA ; Ion Transport - drug effects ; Molecular Sequence Data ; PC12 Cells ; Phosphorylation ; Rats ; Regulatory Sequences, Nucleic Acid - drug effects ; Transcription, Genetic - drug effects ; Transcription, Genetic - physiology ; Tumor Cells, Cultured</subject><ispartof>Molecular pharmacology, 1995-06, Vol.47 (6), p.1112-1118</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7603449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwaninger, M</creatorcontrib><creatorcontrib>Schöfl, C</creatorcontrib><creatorcontrib>Blume, R</creatorcontrib><creatorcontrib>Rössig, L</creatorcontrib><creatorcontrib>Knepel, W</creatorcontrib><title>Inhibition by antidepressant drugs of cyclic AMP response element-binding protein/cyclic AMP response element-directed gene transcription</title><title>Molecular pharmacology</title><addtitle>Mol Pharmacol</addtitle><description>Clinical observations agree that antidepressant drugs are effective only after a lag phase of 1-3 weeks. This delay could
be explained at the molecular level by an action on gene transcription. Transcription of many genes is directed by the cAMP/Ca(2+)-responsive
element (CRE) and its cognate transcription factor CRE-binding protein (CREB). Membrane depolarization and cAMP induce the
phosphorylation of CREB at Ser-119 and thereby stimulate the transcriptional activity of CREB. The effect of antidepressant
drugs on CREB/CRE-directed gene transcription was investigated using transient transfections of reporter fusion genes in HIT
and PC-12 cells. Clomipramine, imipramine, fluoxetine, doxepin, desipramine, amitriptyline, maprotiline, mianserin, and trazodone
inhibited CRE-directed gene transcription that was stimulated by membrane depolarization, with IC50 values between 70 nM and
1.73 microM. Desipramine had no effect on transcription after stimulation by cAMP but blocked the synergistic effect of cAMP
and membrane depolarization to the level of stimulation by cAMP alone. Upon membrane depolarization, desipramine reduced the
phosphorylation of CREB at Ser-119 and also blocked the depolarization-induced increase in the intracellular free Ca2+ concentration
in HIT cells. Thus, by interfering with the depolarization-induced activation of the transcription factor CREB, antidepressant
drugs can inhibit CRE-directed gene transcription, which could underlie the pharmacological effects of these clinically important
drugs.</description><subject>Animals</subject><subject>Antidepressive Agents - pharmacology</subject><subject>Base Sequence</subject><subject>Calcium - metabolism</subject><subject>Cricetinae</subject><subject>Cyclic AMP Response Element-Binding Protein - antagonists & inhibitors</subject><subject>Cyclic AMP Response Element-Binding Protein - physiology</subject><subject>Desipramine - pharmacology</subject><subject>DNA</subject><subject>Ion Transport - drug effects</subject><subject>Molecular Sequence Data</subject><subject>PC12 Cells</subject><subject>Phosphorylation</subject><subject>Rats</subject><subject>Regulatory Sequences, Nucleic Acid - drug effects</subject><subject>Transcription, Genetic - drug effects</subject><subject>Transcription, Genetic - physiology</subject><subject>Tumor Cells, Cultured</subject><issn>0026-895X</issn><issn>1521-0111</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9KxDAQxoso67r6CEJO3opJ0ybNcVn8s7CiBwVvIU2mbaRNa9JF-gi-tREXvCkMzMD8-L7hm6NkSYqMpJgQcpwsMc5YWori9TQ5C-ENY5IXJV4kC84wzXOxTD63rrWVnezgUDUj5SZrYPQQQhyR8fsmoKFGetad1Wj98ITibhxcAAQd9OCmtLLOWNeg0Q8TWHf9F2usBz2BQQ04QJNXLmhvx2_78-SkVl2Ai0NfJS-3N8-b-3T3eLfdrHdpm7EyuhEloDTUMFLzqjB5phitS06MMgUXmOpcqMxwqmlZMFNlDGfKEGAQQdCUrpKrH9147_sewiR7GzR0nXIw7IPknMYq8n9BwoSgmIgIXh7AfdWDkaO3vfKzPIT8K9Tapv2ICcixVb5XeuiGZpY5l0zGf2X0CxnOifU</recordid><startdate>19950601</startdate><enddate>19950601</enddate><creator>Schwaninger, M</creator><creator>Schöfl, C</creator><creator>Blume, R</creator><creator>Rössig, L</creator><creator>Knepel, W</creator><general>American Society for Pharmacology and Experimental Therapeutics</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>19950601</creationdate><title>Inhibition by antidepressant drugs of cyclic AMP response element-binding protein/cyclic AMP response element-directed gene transcription</title><author>Schwaninger, M ; Schöfl, C ; Blume, R ; Rössig, L ; Knepel, W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h268t-b1a9e8d3d61f7b5d42a63f871dad57903c49a2d73c3856db2602ad1e6e2a6ec33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Antidepressive Agents - pharmacology</topic><topic>Base Sequence</topic><topic>Calcium - metabolism</topic><topic>Cricetinae</topic><topic>Cyclic AMP Response Element-Binding Protein - antagonists & inhibitors</topic><topic>Cyclic AMP Response Element-Binding Protein - physiology</topic><topic>Desipramine - pharmacology</topic><topic>DNA</topic><topic>Ion Transport - drug effects</topic><topic>Molecular Sequence Data</topic><topic>PC12 Cells</topic><topic>Phosphorylation</topic><topic>Rats</topic><topic>Regulatory Sequences, Nucleic Acid - drug effects</topic><topic>Transcription, Genetic - drug effects</topic><topic>Transcription, Genetic - physiology</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwaninger, M</creatorcontrib><creatorcontrib>Schöfl, C</creatorcontrib><creatorcontrib>Blume, R</creatorcontrib><creatorcontrib>Rössig, L</creatorcontrib><creatorcontrib>Knepel, W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwaninger, M</au><au>Schöfl, C</au><au>Blume, R</au><au>Rössig, L</au><au>Knepel, W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition by antidepressant drugs of cyclic AMP response element-binding protein/cyclic AMP response element-directed gene transcription</atitle><jtitle>Molecular pharmacology</jtitle><addtitle>Mol Pharmacol</addtitle><date>1995-06-01</date><risdate>1995</risdate><volume>47</volume><issue>6</issue><spage>1112</spage><epage>1118</epage><pages>1112-1118</pages><issn>0026-895X</issn><eissn>1521-0111</eissn><abstract>Clinical observations agree that antidepressant drugs are effective only after a lag phase of 1-3 weeks. This delay could
be explained at the molecular level by an action on gene transcription. Transcription of many genes is directed by the cAMP/Ca(2+)-responsive
element (CRE) and its cognate transcription factor CRE-binding protein (CREB). Membrane depolarization and cAMP induce the
phosphorylation of CREB at Ser-119 and thereby stimulate the transcriptional activity of CREB. The effect of antidepressant
drugs on CREB/CRE-directed gene transcription was investigated using transient transfections of reporter fusion genes in HIT
and PC-12 cells. Clomipramine, imipramine, fluoxetine, doxepin, desipramine, amitriptyline, maprotiline, mianserin, and trazodone
inhibited CRE-directed gene transcription that was stimulated by membrane depolarization, with IC50 values between 70 nM and
1.73 microM. Desipramine had no effect on transcription after stimulation by cAMP but blocked the synergistic effect of cAMP
and membrane depolarization to the level of stimulation by cAMP alone. Upon membrane depolarization, desipramine reduced the
phosphorylation of CREB at Ser-119 and also blocked the depolarization-induced increase in the intracellular free Ca2+ concentration
in HIT cells. Thus, by interfering with the depolarization-induced activation of the transcription factor CREB, antidepressant
drugs can inhibit CRE-directed gene transcription, which could underlie the pharmacological effects of these clinically important
drugs.</abstract><cop>United States</cop><pub>American Society for Pharmacology and Experimental Therapeutics</pub><pmid>7603449</pmid><tpages>7</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Antidepressive Agents - pharmacology Base Sequence Calcium - metabolism Cricetinae Cyclic AMP Response Element-Binding Protein - antagonists & inhibitors Cyclic AMP Response Element-Binding Protein - physiology Desipramine - pharmacology DNA Ion Transport - drug effects Molecular Sequence Data PC12 Cells Phosphorylation Rats Regulatory Sequences, Nucleic Acid - drug effects Transcription, Genetic - drug effects Transcription, Genetic - physiology Tumor Cells, Cultured |
title | Inhibition by antidepressant drugs of cyclic AMP response element-binding protein/cyclic AMP response element-directed gene transcription |
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