The Chronic Treatment With 5-HT2A Receptor Agonists Affects the Behavior and the BDNF System in Mice
Serotonin 5-HT 2A receptors and the brain-derived neurotrophic factor (BDNF) are involved in the pathophysiology and treatment of many psychiatric diseases. However, the interaction between 5-HT 2A and BDNF is still poorly understood. In the present paper, the effects of chronic treatment with mixed...
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creator | Tsybko, Anton S. Ilchibaeva, Tatiana V. Filimonova, Elena A. Eremin, Dmitry V. Popova, Nina K. Naumenko, Vladimir S. |
description | Serotonin 5-HT
2A
receptors and the brain-derived neurotrophic factor (BDNF) are involved in the pathophysiology and treatment of many psychiatric diseases. However, the interaction between 5-HT
2A
and BDNF is still poorly understood. In the present paper, the effects of chronic treatment with mixed 5-HT
2A/2C
receptor agonist DOI, highly selective 5-HT
2A
agonists TCB-2 and 25CN-NBOH on behavior and the BDNF system have been investigated. Chronic treatment of males of C57Bl/6 mice with DOI, TCB-2 and 25CN-NBOH (1 mg/kg, i.p., 14 days) resulted in desensitization of 5-HT
2A
receptors. Treatment with 25CN-NBOH significantly increased startle amplitude. At the same time all used drugs failed to affect anxiety, exploratory and stereotyped behavior as well as spatial memory and learning. TCB-2 and 25CN-NBOH increased the BDNF mRNA level. All 5-HT
2A
agonists increased the proBDNF level but failed to alter the mature BDNF protein level. TrkB and p75
NTR
mRNA levels were affected by all utilized agonists. All drugs decreased the total level as well as membrane TrkB protein one indicating downregulation of TrkB receptors. All agonists decreased the membrane p75
NTR
protein level. Thus, we have shown for the first time that the chronic activation of the 5-HT
2A
receptor with agonists has affected the BDNF system almost on all levels—transcription, proBDNF production, TrkB and p75
NTR
receptors’ level. The obtained data suggested possible suppression in BDNF-TrkB signaling under chronic treatment with 5-HT
2A
agonists. |
doi_str_mv | 10.1007/s11064-020-03153-5 |
format | Article |
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2A
receptors and the brain-derived neurotrophic factor (BDNF) are involved in the pathophysiology and treatment of many psychiatric diseases. However, the interaction between 5-HT
2A
and BDNF is still poorly understood. In the present paper, the effects of chronic treatment with mixed 5-HT
2A/2C
receptor agonist DOI, highly selective 5-HT
2A
agonists TCB-2 and 25CN-NBOH on behavior and the BDNF system have been investigated. Chronic treatment of males of C57Bl/6 mice with DOI, TCB-2 and 25CN-NBOH (1 mg/kg, i.p., 14 days) resulted in desensitization of 5-HT
2A
receptors. Treatment with 25CN-NBOH significantly increased startle amplitude. At the same time all used drugs failed to affect anxiety, exploratory and stereotyped behavior as well as spatial memory and learning. TCB-2 and 25CN-NBOH increased the BDNF mRNA level. All 5-HT
2A
agonists increased the proBDNF level but failed to alter the mature BDNF protein level. TrkB and p75
NTR
mRNA levels were affected by all utilized agonists. All drugs decreased the total level as well as membrane TrkB protein one indicating downregulation of TrkB receptors. All agonists decreased the membrane p75
NTR
protein level. Thus, we have shown for the first time that the chronic activation of the 5-HT
2A
receptor with agonists has affected the BDNF system almost on all levels—transcription, proBDNF production, TrkB and p75
NTR
receptors’ level. The obtained data suggested possible suppression in BDNF-TrkB signaling under chronic treatment with 5-HT
2A
agonists.</description><identifier>ISSN: 0364-3190</identifier><identifier>EISSN: 1573-6903</identifier><identifier>DOI: 10.1007/s11064-020-03153-5</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Agonists ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Brain-derived neurotrophic factor ; Cell Biology ; Desensitization ; Drugs ; Exploratory behavior ; Medical treatment ; Membrane proteins ; Membranes ; Memory tasks ; Mental disorders ; Neurochemistry ; Neurology ; Neurosciences ; Original Paper ; Proteins ; Receptors ; Serotonin ; Serotonin S2 receptors ; Spatial analysis ; Spatial discrimination learning ; Spatial memory ; Stereotyped behavior ; Transcription ; TrkB receptors</subject><ispartof>Neurochemical research, 2020-12, Vol.45 (12), p.3059-3075</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-8cf944e38d2fd2deb21a4c0600b16e59f2f8723377bf339b3b7beb55d96a91383</citedby><cites>FETCH-LOGICAL-c352t-8cf944e38d2fd2deb21a4c0600b16e59f2f8723377bf339b3b7beb55d96a91383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11064-020-03153-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11064-020-03153-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Tsybko, Anton S.</creatorcontrib><creatorcontrib>Ilchibaeva, Tatiana V.</creatorcontrib><creatorcontrib>Filimonova, Elena A.</creatorcontrib><creatorcontrib>Eremin, Dmitry V.</creatorcontrib><creatorcontrib>Popova, Nina K.</creatorcontrib><creatorcontrib>Naumenko, Vladimir S.</creatorcontrib><title>The Chronic Treatment With 5-HT2A Receptor Agonists Affects the Behavior and the BDNF System in Mice</title><title>Neurochemical research</title><addtitle>Neurochem Res</addtitle><description>Serotonin 5-HT
2A
receptors and the brain-derived neurotrophic factor (BDNF) are involved in the pathophysiology and treatment of many psychiatric diseases. However, the interaction between 5-HT
2A
and BDNF is still poorly understood. In the present paper, the effects of chronic treatment with mixed 5-HT
2A/2C
receptor agonist DOI, highly selective 5-HT
2A
agonists TCB-2 and 25CN-NBOH on behavior and the BDNF system have been investigated. Chronic treatment of males of C57Bl/6 mice with DOI, TCB-2 and 25CN-NBOH (1 mg/kg, i.p., 14 days) resulted in desensitization of 5-HT
2A
receptors. Treatment with 25CN-NBOH significantly increased startle amplitude. At the same time all used drugs failed to affect anxiety, exploratory and stereotyped behavior as well as spatial memory and learning. TCB-2 and 25CN-NBOH increased the BDNF mRNA level. All 5-HT
2A
agonists increased the proBDNF level but failed to alter the mature BDNF protein level. TrkB and p75
NTR
mRNA levels were affected by all utilized agonists. All drugs decreased the total level as well as membrane TrkB protein one indicating downregulation of TrkB receptors. All agonists decreased the membrane p75
NTR
protein level. Thus, we have shown for the first time that the chronic activation of the 5-HT
2A
receptor with agonists has affected the BDNF system almost on all levels—transcription, proBDNF production, TrkB and p75
NTR
receptors’ level. The obtained data suggested possible suppression in BDNF-TrkB signaling under chronic treatment with 5-HT
2A
agonists.</description><subject>Agonists</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain-derived neurotrophic factor</subject><subject>Cell Biology</subject><subject>Desensitization</subject><subject>Drugs</subject><subject>Exploratory behavior</subject><subject>Medical treatment</subject><subject>Membrane proteins</subject><subject>Membranes</subject><subject>Memory tasks</subject><subject>Mental disorders</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Original Paper</subject><subject>Proteins</subject><subject>Receptors</subject><subject>Serotonin</subject><subject>Serotonin S2 receptors</subject><subject>Spatial analysis</subject><subject>Spatial discrimination learning</subject><subject>Spatial memory</subject><subject>Stereotyped behavior</subject><subject>Transcription</subject><subject>TrkB receptors</subject><issn>0364-3190</issn><issn>1573-6903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE1LAzEQhoMoWD_-gKeAFy-rk8xmP461foIfoBWPYTc7abe0uzVJBf-90RUED54GZp7nZXgZOxJwKgDyMy8EZGkCEhJAoTBRW2wkVI5JVgJusxFgPKMoYZfteb8AiJoUI9ZM58Qnc9d3reFTR1VYURf4axvmXCU3UznmT2RoHXrHx7NI-eD52FoycYbontO8em_jteqaYXHxcMWfP3ygFW87ft8aOmA7tlp6OvyZ--zl6nI6uUnuHq9vJ-O7xKCSISmMLdOUsGikbWRDtRRVaiADqEVGqrTSFrlEzPPaIpY11nlNtVJNmVWlwAL32cmQu3b924Z80KvWG1ouq476jdcyVamAtCwgosd_0EW_cV38LlI5SpXFvEjJgTKu996R1WvXrir3oQXor-L1ULyOxevv4rWKEg6Sj3A3I_cb_Y_1CSfFgzA</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Tsybko, Anton S.</creator><creator>Ilchibaeva, Tatiana V.</creator><creator>Filimonova, Elena A.</creator><creator>Eremin, Dmitry V.</creator><creator>Popova, Nina K.</creator><creator>Naumenko, Vladimir S.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20201201</creationdate><title>The Chronic Treatment With 5-HT2A Receptor Agonists Affects the Behavior and the BDNF System in Mice</title><author>Tsybko, Anton S. ; Ilchibaeva, Tatiana V. ; Filimonova, Elena A. ; Eremin, Dmitry V. ; Popova, Nina K. ; Naumenko, Vladimir S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-8cf944e38d2fd2deb21a4c0600b16e59f2f8723377bf339b3b7beb55d96a91383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Agonists</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain-derived neurotrophic factor</topic><topic>Cell Biology</topic><topic>Desensitization</topic><topic>Drugs</topic><topic>Exploratory behavior</topic><topic>Medical treatment</topic><topic>Membrane proteins</topic><topic>Membranes</topic><topic>Memory tasks</topic><topic>Mental disorders</topic><topic>Neurochemistry</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Original Paper</topic><topic>Proteins</topic><topic>Receptors</topic><topic>Serotonin</topic><topic>Serotonin S2 receptors</topic><topic>Spatial analysis</topic><topic>Spatial discrimination learning</topic><topic>Spatial memory</topic><topic>Stereotyped behavior</topic><topic>Transcription</topic><topic>TrkB receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsybko, Anton S.</creatorcontrib><creatorcontrib>Ilchibaeva, Tatiana V.</creatorcontrib><creatorcontrib>Filimonova, Elena A.</creatorcontrib><creatorcontrib>Eremin, Dmitry V.</creatorcontrib><creatorcontrib>Popova, Nina K.</creatorcontrib><creatorcontrib>Naumenko, Vladimir S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</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>Technology Research Database</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>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Neurochemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsybko, Anton S.</au><au>Ilchibaeva, Tatiana V.</au><au>Filimonova, Elena A.</au><au>Eremin, Dmitry V.</au><au>Popova, Nina K.</au><au>Naumenko, Vladimir S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Chronic Treatment With 5-HT2A Receptor Agonists Affects the Behavior and the BDNF System in Mice</atitle><jtitle>Neurochemical research</jtitle><stitle>Neurochem Res</stitle><date>2020-12-01</date><risdate>2020</risdate><volume>45</volume><issue>12</issue><spage>3059</spage><epage>3075</epage><pages>3059-3075</pages><issn>0364-3190</issn><eissn>1573-6903</eissn><abstract>Serotonin 5-HT
2A
receptors and the brain-derived neurotrophic factor (BDNF) are involved in the pathophysiology and treatment of many psychiatric diseases. However, the interaction between 5-HT
2A
and BDNF is still poorly understood. In the present paper, the effects of chronic treatment with mixed 5-HT
2A/2C
receptor agonist DOI, highly selective 5-HT
2A
agonists TCB-2 and 25CN-NBOH on behavior and the BDNF system have been investigated. Chronic treatment of males of C57Bl/6 mice with DOI, TCB-2 and 25CN-NBOH (1 mg/kg, i.p., 14 days) resulted in desensitization of 5-HT
2A
receptors. Treatment with 25CN-NBOH significantly increased startle amplitude. At the same time all used drugs failed to affect anxiety, exploratory and stereotyped behavior as well as spatial memory and learning. TCB-2 and 25CN-NBOH increased the BDNF mRNA level. All 5-HT
2A
agonists increased the proBDNF level but failed to alter the mature BDNF protein level. TrkB and p75
NTR
mRNA levels were affected by all utilized agonists. All drugs decreased the total level as well as membrane TrkB protein one indicating downregulation of TrkB receptors. All agonists decreased the membrane p75
NTR
protein level. Thus, we have shown for the first time that the chronic activation of the 5-HT
2A
receptor with agonists has affected the BDNF system almost on all levels—transcription, proBDNF production, TrkB and p75
NTR
receptors’ level. The obtained data suggested possible suppression in BDNF-TrkB signaling under chronic treatment with 5-HT
2A
agonists.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s11064-020-03153-5</doi><tpages>17</tpages></addata></record> |
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subjects | Agonists Biochemistry Biomedical and Life Sciences Biomedicine Brain-derived neurotrophic factor Cell Biology Desensitization Drugs Exploratory behavior Medical treatment Membrane proteins Membranes Memory tasks Mental disorders Neurochemistry Neurology Neurosciences Original Paper Proteins Receptors Serotonin Serotonin S2 receptors Spatial analysis Spatial discrimination learning Spatial memory Stereotyped behavior Transcription TrkB receptors |
title | The Chronic Treatment With 5-HT2A Receptor Agonists Affects the Behavior and the BDNF System in Mice |
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