Multipotent Neurotrophin Antagonist Targets Brain-Derived Neurotrophic Factor and Nerve Growth Factor
Brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) are members of the neurotrophin family that normally play a role in the development and maintenance of the nervous system. However, neurotrophin dysregulation has been implicated in several neurodegenerative diseases and psychiat...
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Veröffentlicht in: | The Journal of pharmacology and experimental therapeutics 2010-02, Vol.332 (2), p.446-454 |
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description | Brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) are members of the neurotrophin family that normally play a role in the development and maintenance of the nervous system. However, neurotrophin dysregulation has been implicated in several neurodegenerative diseases and psychiatric disorders including Alzheimer's disease, Parkinson's disease, neuropathic pain, depression, and substance abuse. Despite their central role in the nervous system, neurotrophins have proved to be an elusive pharmacological target. Here, we describe a novel multipotent neurotrophin antagonist, 3-[(5E)-4-oxo-5-[[5-(4-sulfamoylphenyl)-2-furyl]methylene]-2-thioxo-thiazolidin-3-yl]propanoic acid (Y1036). Y1036 binds BDNF (KD = 3.5 ± 0.3 μM) and NGF (KD = 3.0 ± 0.4 μM) preventing either BDNF or NGF from interacting with their obligate receptor(s). Y1036 prevents both BDNF- and NGF-mediated trk activation, downstream activation of the p44/42 mitogen-activated protein kinase pathway, and neurotrophin-mediated differentiation of dorsal-root ganglion sensory neurons. Identification of a BDNF- and NGF-specific antagonist is of considerable interest in the study and treatment of diseases where dysregulation of multiple neurotrophins has been implicated. |
doi_str_mv | 10.1124/jpet.109.159079 |
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However, neurotrophin dysregulation has been implicated in several neurodegenerative diseases and psychiatric disorders including Alzheimer's disease, Parkinson's disease, neuropathic pain, depression, and substance abuse. Despite their central role in the nervous system, neurotrophins have proved to be an elusive pharmacological target. Here, we describe a novel multipotent neurotrophin antagonist, 3-[(5E)-4-oxo-5-[[5-(4-sulfamoylphenyl)-2-furyl]methylene]-2-thioxo-thiazolidin-3-yl]propanoic acid (Y1036). Y1036 binds BDNF (KD = 3.5 ± 0.3 μM) and NGF (KD = 3.0 ± 0.4 μM) preventing either BDNF or NGF from interacting with their obligate receptor(s). Y1036 prevents both BDNF- and NGF-mediated trk activation, downstream activation of the p44/42 mitogen-activated protein kinase pathway, and neurotrophin-mediated differentiation of dorsal-root ganglion sensory neurons. Identification of a BDNF- and NGF-specific antagonist is of considerable interest in the study and treatment of diseases where dysregulation of multiple neurotrophins has been implicated.</description><identifier>ISSN: 0022-3565</identifier><identifier>EISSN: 1521-0103</identifier><identifier>DOI: 10.1124/jpet.109.159079</identifier><identifier>PMID: 19923440</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Brain-Derived Neurotrophic Factor - antagonists & inhibitors ; Brain-Derived Neurotrophic Factor - metabolism ; Computer Simulation ; Mice ; Models, Molecular ; Molecular Sequence Data ; Nerve Growth Factor - antagonists & inhibitors ; Nerve Growth Factor - metabolism ; NIH 3T3 Cells ; PC12 Cells ; Phosphorylation - drug effects ; Propionates - pharmacokinetics ; Propionates - pharmacology ; Protein Binding ; Rats ; Signal Transduction - drug effects ; Thiazolidines - pharmacokinetics ; Thiazolidines - pharmacology</subject><ispartof>The Journal of pharmacology and experimental therapeutics, 2010-02, Vol.332 (2), p.446-454</ispartof><rights>2010 American Society for Pharmacology and Experimental Therapeutics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-5ee1cfd58a6732309e188f877c92ea76d7dd372971b3ca9d09e9584ac5338a453</citedby><cites>FETCH-LOGICAL-c377t-5ee1cfd58a6732309e188f877c92ea76d7dd372971b3ca9d09e9584ac5338a453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19923440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eibl, J.K.</creatorcontrib><creatorcontrib>Chapelsky, S.A.</creatorcontrib><creatorcontrib>Ross, G.M.</creatorcontrib><title>Multipotent Neurotrophin Antagonist Targets Brain-Derived Neurotrophic Factor and Nerve Growth Factor</title><title>The Journal of pharmacology and experimental therapeutics</title><addtitle>J Pharmacol Exp Ther</addtitle><description>Brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) are members of the neurotrophin family that normally play a role in the development and maintenance of the nervous system. However, neurotrophin dysregulation has been implicated in several neurodegenerative diseases and psychiatric disorders including Alzheimer's disease, Parkinson's disease, neuropathic pain, depression, and substance abuse. Despite their central role in the nervous system, neurotrophins have proved to be an elusive pharmacological target. Here, we describe a novel multipotent neurotrophin antagonist, 3-[(5E)-4-oxo-5-[[5-(4-sulfamoylphenyl)-2-furyl]methylene]-2-thioxo-thiazolidin-3-yl]propanoic acid (Y1036). Y1036 binds BDNF (KD = 3.5 ± 0.3 μM) and NGF (KD = 3.0 ± 0.4 μM) preventing either BDNF or NGF from interacting with their obligate receptor(s). Y1036 prevents both BDNF- and NGF-mediated trk activation, downstream activation of the p44/42 mitogen-activated protein kinase pathway, and neurotrophin-mediated differentiation of dorsal-root ganglion sensory neurons. Identification of a BDNF- and NGF-specific antagonist is of considerable interest in the study and treatment of diseases where dysregulation of multiple neurotrophins has been implicated.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Brain-Derived Neurotrophic Factor - antagonists & inhibitors</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Computer Simulation</subject><subject>Mice</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>Nerve Growth Factor - antagonists & inhibitors</subject><subject>Nerve Growth Factor - metabolism</subject><subject>NIH 3T3 Cells</subject><subject>PC12 Cells</subject><subject>Phosphorylation - drug effects</subject><subject>Propionates - pharmacokinetics</subject><subject>Propionates - pharmacology</subject><subject>Protein Binding</subject><subject>Rats</subject><subject>Signal Transduction - drug effects</subject><subject>Thiazolidines - pharmacokinetics</subject><subject>Thiazolidines - pharmacology</subject><issn>0022-3565</issn><issn>1521-0103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1PGzEQhq2qiITAubdqT-1pgz_j9ZECASQ-LnC2jD3JOtqst7Y3Ef--G22kcuE0mtHzjkbPIPSD4DkhlF9uOshzgtWcCIWl-oamRFBSYoLZdzTFmNKSiYWYoLOUNhgTzhfsFE2IUpRxjqcInvom-y5kaHPxDH0MOYau9m1x1WazDq1PuXg1cQ05FX-i8W15A9HvwH2mbbE0NodYmPYwjzso7mLY5_o4P0cnK9MkuDjWGXpb3r5e35ePL3cP11ePpWVS5lIAELtyojILySjDCkhVrSopraJg5MJJ55ikSpJ3Zo1yA6BExY0VjFWGCzZDv8e9XQx_e0hZb32y0DSmhdAnLRmnnFCBB_JyJG0MKUVY6S76rYkfmmB9UKsPaodG6VHtkPh53N2_b8H9548uB-DXCNR-Xe99BN3VJm6NDU1Yf2jGqKb68IAZUiMIg4qdh6iT9dBacEPIZu2C__KKfw1alts</recordid><startdate>201002</startdate><enddate>201002</enddate><creator>Eibl, J.K.</creator><creator>Chapelsky, S.A.</creator><creator>Ross, G.M.</creator><general>Elsevier Inc</general><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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201002</creationdate><title>Multipotent Neurotrophin Antagonist Targets Brain-Derived Neurotrophic Factor and Nerve Growth Factor</title><author>Eibl, J.K. ; Chapelsky, S.A. ; Ross, G.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-5ee1cfd58a6732309e188f877c92ea76d7dd372971b3ca9d09e9584ac5338a453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Brain-Derived Neurotrophic Factor - antagonists & inhibitors</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Computer Simulation</topic><topic>Mice</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>Nerve Growth Factor - antagonists & inhibitors</topic><topic>Nerve Growth Factor - metabolism</topic><topic>NIH 3T3 Cells</topic><topic>PC12 Cells</topic><topic>Phosphorylation - drug effects</topic><topic>Propionates - pharmacokinetics</topic><topic>Propionates - pharmacology</topic><topic>Protein Binding</topic><topic>Rats</topic><topic>Signal Transduction - drug effects</topic><topic>Thiazolidines - pharmacokinetics</topic><topic>Thiazolidines - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eibl, J.K.</creatorcontrib><creatorcontrib>Chapelsky, S.A.</creatorcontrib><creatorcontrib>Ross, G.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>MEDLINE - Academic</collection><jtitle>The Journal of pharmacology and experimental therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eibl, J.K.</au><au>Chapelsky, S.A.</au><au>Ross, G.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multipotent Neurotrophin Antagonist Targets Brain-Derived Neurotrophic Factor and Nerve Growth Factor</atitle><jtitle>The Journal of pharmacology and experimental therapeutics</jtitle><addtitle>J Pharmacol Exp Ther</addtitle><date>2010-02</date><risdate>2010</risdate><volume>332</volume><issue>2</issue><spage>446</spage><epage>454</epage><pages>446-454</pages><issn>0022-3565</issn><eissn>1521-0103</eissn><abstract>Brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) are members of the neurotrophin family that normally play a role in the development and maintenance of the nervous system. However, neurotrophin dysregulation has been implicated in several neurodegenerative diseases and psychiatric disorders including Alzheimer's disease, Parkinson's disease, neuropathic pain, depression, and substance abuse. Despite their central role in the nervous system, neurotrophins have proved to be an elusive pharmacological target. Here, we describe a novel multipotent neurotrophin antagonist, 3-[(5E)-4-oxo-5-[[5-(4-sulfamoylphenyl)-2-furyl]methylene]-2-thioxo-thiazolidin-3-yl]propanoic acid (Y1036). Y1036 binds BDNF (KD = 3.5 ± 0.3 μM) and NGF (KD = 3.0 ± 0.4 μM) preventing either BDNF or NGF from interacting with their obligate receptor(s). Y1036 prevents both BDNF- and NGF-mediated trk activation, downstream activation of the p44/42 mitogen-activated protein kinase pathway, and neurotrophin-mediated differentiation of dorsal-root ganglion sensory neurons. Identification of a BDNF- and NGF-specific antagonist is of considerable interest in the study and treatment of diseases where dysregulation of multiple neurotrophins has been implicated.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19923440</pmid><doi>10.1124/jpet.109.159079</doi><tpages>9</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Brain-Derived Neurotrophic Factor - antagonists & inhibitors Brain-Derived Neurotrophic Factor - metabolism Computer Simulation Mice Models, Molecular Molecular Sequence Data Nerve Growth Factor - antagonists & inhibitors Nerve Growth Factor - metabolism NIH 3T3 Cells PC12 Cells Phosphorylation - drug effects Propionates - pharmacokinetics Propionates - pharmacology Protein Binding Rats Signal Transduction - drug effects Thiazolidines - pharmacokinetics Thiazolidines - pharmacology |
title | Multipotent Neurotrophin Antagonist Targets Brain-Derived Neurotrophic Factor and Nerve Growth Factor |
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