In vivo electrochemical evidence for simultaneous 5‐HT and histamine release in the rat substantia nigra pars reticulata following medial forebrain bundle stimulation
J. Neurochem. (2011) 118, 749–759. Exploring the mechanisms of serotonin [5‐hydroxytryptamine (5‐HT)] in the brain requires an in vivo method that combines fast temporal resolution with chemical selectivity. Fast‐scan cyclic voltammetry is a technique with sufficient temporal and chemical resolution...
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description | J. Neurochem. (2011) 118, 749–759.
Exploring the mechanisms of serotonin [5‐hydroxytryptamine (5‐HT)] in the brain requires an in vivo method that combines fast temporal resolution with chemical selectivity. Fast‐scan cyclic voltammetry is a technique with sufficient temporal and chemical resolution for probing dynamic 5‐HT neurotransmission events; however, traditionally it has not been possible to probe in vivo 5‐HT mechanisms. Recently, we optimized fast‐scan cyclic voltammetry for measuring 5‐HT release and uptake in vivo in the substantia nigra pars reticulata (SNR) with electrical stimulation of the dorsal raphe nucleus (DRN) in the rat brain. Here, we address technical challenges associated with rat DRN surgery by electrically stimulating 5‐HT projections in the medial forebrain bundle (MFB), a more accessible anatomical location. MFB stimulation elicits 5‐HT in the SNR; furthermore, we find simultaneous release of an additional species. We use electrochemical and pharmacological methods and describe physiological, anatomical and independent chemical analyses to identify this species as histamine. We also show pharmacologically that increasing the lifetime of extracellular histamine significantly decreases 5‐HT release, most likely because of increased activation of histamine H‐3 receptors that inhibit 5‐HT release. Despite this, under physiological conditions, we find by kinetic comparisons of DRN and MFB stimulations that the simultaneous release of histamine does not interfere with the quantitative 5‐HT concentration profile. We therefore present a novel and robust electrical stimulation of the MFB that is technically less challenging than DRN stimulation to study 5‐HT and histamine release in the SNR. |
doi_str_mv | 10.1111/j.1471-4159.2011.07352.x |
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Exploring the mechanisms of serotonin [5‐hydroxytryptamine (5‐HT)] in the brain requires an in vivo method that combines fast temporal resolution with chemical selectivity. Fast‐scan cyclic voltammetry is a technique with sufficient temporal and chemical resolution for probing dynamic 5‐HT neurotransmission events; however, traditionally it has not been possible to probe in vivo 5‐HT mechanisms. Recently, we optimized fast‐scan cyclic voltammetry for measuring 5‐HT release and uptake in vivo in the substantia nigra pars reticulata (SNR) with electrical stimulation of the dorsal raphe nucleus (DRN) in the rat brain. Here, we address technical challenges associated with rat DRN surgery by electrically stimulating 5‐HT projections in the medial forebrain bundle (MFB), a more accessible anatomical location. MFB stimulation elicits 5‐HT in the SNR; furthermore, we find simultaneous release of an additional species. We use electrochemical and pharmacological methods and describe physiological, anatomical and independent chemical analyses to identify this species as histamine. We also show pharmacologically that increasing the lifetime of extracellular histamine significantly decreases 5‐HT release, most likely because of increased activation of histamine H‐3 receptors that inhibit 5‐HT release. Despite this, under physiological conditions, we find by kinetic comparisons of DRN and MFB stimulations that the simultaneous release of histamine does not interfere with the quantitative 5‐HT concentration profile. We therefore present a novel and robust electrical stimulation of the MFB that is technically less challenging than DRN stimulation to study 5‐HT and histamine release in the SNR.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.2011.07352.x</identifier><identifier>PMID: 21682723</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Biological and medical sciences ; Brain ; Central nervous system ; Central neurotransmission. Neuromudulation. Pathways and receptors ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Dimaprit - analogs & derivatives ; Dimaprit - pharmacology ; dorsal raphe nucleus ; Electric Stimulation - methods ; Electrical stimuli ; Electrochemistry - methods ; fast‐scan cyclic voltammetry ; Fundamental and applied biological sciences. Psychology ; Histamine ; Histamine - metabolism ; Histamine - pharmacology ; Histamine Agonists - pharmacology ; Histamine H3 Antagonists - pharmacology ; histamine N‐methyltransferase ; Kinetics ; Linear Models ; Male ; Medial forebrain bundle ; Medial Forebrain Bundle - physiology ; Medical sciences ; Neural Pathways - physiology ; Neurochemistry ; Neurology ; Neurotransmission ; Piperidines - pharmacology ; Probes ; Raphe Nuclei - physiology ; Rats ; Rats, Sprague-Dawley ; Rodents ; Serotonin ; Serotonin - metabolism ; Serotonin - pharmacology ; SKF 91488 ; Substantia Nigra - metabolism ; substantia nigra pars reticulata ; Surgery ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of neurochemistry, 2011-09, Vol.118 (5), p.749-759</ispartof><rights>2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry</rights><rights>2015 INIST-CNRS</rights><rights>2011 The Authors. Journal of Neurochemistry © 2011 International Society for Neurochemistry.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6282-b5afb129cb0d0620ffa6f95ba276d8d3505d038f0872da11f4f1d63a876c691e3</citedby><cites>FETCH-LOGICAL-c6282-b5afb129cb0d0620ffa6f95ba276d8d3505d038f0872da11f4f1d63a876c691e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.2011.07352.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.2011.07352.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27923,27924,45573,45574,46408,46832</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24511808$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21682723$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hashemi, Parastoo</creatorcontrib><creatorcontrib>Dankoski, Elyse C.</creatorcontrib><creatorcontrib>Wood, Kevin M.</creatorcontrib><creatorcontrib>Ambrose, Rebecca Ellen</creatorcontrib><creatorcontrib>Wightman, Robert Mark</creatorcontrib><title>In vivo electrochemical evidence for simultaneous 5‐HT and histamine release in the rat substantia nigra pars reticulata following medial forebrain bundle stimulation</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>J. Neurochem. (2011) 118, 749–759.
Exploring the mechanisms of serotonin [5‐hydroxytryptamine (5‐HT)] in the brain requires an in vivo method that combines fast temporal resolution with chemical selectivity. Fast‐scan cyclic voltammetry is a technique with sufficient temporal and chemical resolution for probing dynamic 5‐HT neurotransmission events; however, traditionally it has not been possible to probe in vivo 5‐HT mechanisms. Recently, we optimized fast‐scan cyclic voltammetry for measuring 5‐HT release and uptake in vivo in the substantia nigra pars reticulata (SNR) with electrical stimulation of the dorsal raphe nucleus (DRN) in the rat brain. Here, we address technical challenges associated with rat DRN surgery by electrically stimulating 5‐HT projections in the medial forebrain bundle (MFB), a more accessible anatomical location. MFB stimulation elicits 5‐HT in the SNR; furthermore, we find simultaneous release of an additional species. We use electrochemical and pharmacological methods and describe physiological, anatomical and independent chemical analyses to identify this species as histamine. We also show pharmacologically that increasing the lifetime of extracellular histamine significantly decreases 5‐HT release, most likely because of increased activation of histamine H‐3 receptors that inhibit 5‐HT release. Despite this, under physiological conditions, we find by kinetic comparisons of DRN and MFB stimulations that the simultaneous release of histamine does not interfere with the quantitative 5‐HT concentration profile. We therefore present a novel and robust electrical stimulation of the MFB that is technically less challenging than DRN stimulation to study 5‐HT and histamine release in the SNR.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Central nervous system</subject><subject>Central neurotransmission. Neuromudulation. Pathways and receptors</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dimaprit - analogs & derivatives</subject><subject>Dimaprit - pharmacology</subject><subject>dorsal raphe nucleus</subject><subject>Electric Stimulation - methods</subject><subject>Electrical stimuli</subject><subject>Electrochemistry - methods</subject><subject>fast‐scan cyclic voltammetry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Histamine</subject><subject>Histamine - metabolism</subject><subject>Histamine - pharmacology</subject><subject>Histamine Agonists - pharmacology</subject><subject>Histamine H3 Antagonists - pharmacology</subject><subject>histamine N‐methyltransferase</subject><subject>Kinetics</subject><subject>Linear Models</subject><subject>Male</subject><subject>Medial forebrain bundle</subject><subject>Medial Forebrain Bundle - physiology</subject><subject>Medical sciences</subject><subject>Neural Pathways - physiology</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neurotransmission</subject><subject>Piperidines - pharmacology</subject><subject>Probes</subject><subject>Raphe Nuclei - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Serotonin</subject><subject>Serotonin - metabolism</subject><subject>Serotonin - pharmacology</subject><subject>SKF 91488</subject><subject>Substantia Nigra - metabolism</subject><subject>substantia nigra pars reticulata</subject><subject>Surgery</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks2OFCEUhStG47Sjr2CIiXHVLVAFRS00MR3HGTPRzbgmtyiqmw4FLVA9MzsfYR7D5_JJpOy2_dkoGyD3u-ceyCkKRPCC5PVysyBVTeYVYc2CYkIWuC4ZXdzcK2bHwv1ihjGl8xJX9KR4FOMGY8IrTh4WJ5RwQWtazoqvFw7tzM4jbbVKwau1HowCi_TOdNopjXofUDTDaBM47ceI2Lcvd-dXCFyH1iYmGIzTKOR-iBoZh9I6XyGhOLa56pIB5MwqANpCiBlMRo0WEmRla_21cSs06M7kmXmUbgNkjXZ0ndUopmkwJOPd4-JBDzbqJ4f9tPh09vZqeT6__PjuYvnmcq44FXTeMuhbQhvV4g5zivseeN-wFmjNO9GVDLMOl6LHoqYdENJXPel4CaLmijdEl6fF673udmyzLaVdCmDlNpgBwq30YOSfFWfWcuV3siSMcc6ywIuDQPCfRx2THExU2tr998kG16TGTNB_kkKUJW54U2fy2V_kxo_B5X-YIMwFEThDYg-p4GMMuj-aJlhOsZEbOaVDTumQU2zkj9jIm9z69PdHHxt_5iQDzw8AxJyOPoBTJv7iKkayBZG5V3vu2lh9-98G5PsPy-lUfgeSjeMq</recordid><startdate>201109</startdate><enddate>201109</enddate><creator>Hashemi, Parastoo</creator><creator>Dankoski, Elyse C.</creator><creator>Wood, Kevin M.</creator><creator>Ambrose, Rebecca Ellen</creator><creator>Wightman, Robert Mark</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>IQODW</scope><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>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201109</creationdate><title>In vivo electrochemical evidence for simultaneous 5‐HT and histamine release in the rat substantia nigra pars reticulata following medial forebrain bundle stimulation</title><author>Hashemi, Parastoo ; Dankoski, Elyse C. ; Wood, Kevin M. ; Ambrose, Rebecca Ellen ; Wightman, Robert Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6282-b5afb129cb0d0620ffa6f95ba276d8d3505d038f0872da11f4f1d63a876c691e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain</topic><topic>Central nervous system</topic><topic>Central neurotransmission. Neuromudulation. Pathways and receptors</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dimaprit - analogs & derivatives</topic><topic>Dimaprit - pharmacology</topic><topic>dorsal raphe nucleus</topic><topic>Electric Stimulation - methods</topic><topic>Electrical stimuli</topic><topic>Electrochemistry - methods</topic><topic>fast‐scan cyclic voltammetry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Histamine</topic><topic>Histamine - metabolism</topic><topic>Histamine - pharmacology</topic><topic>Histamine Agonists - pharmacology</topic><topic>Histamine H3 Antagonists - pharmacology</topic><topic>histamine N‐methyltransferase</topic><topic>Kinetics</topic><topic>Linear Models</topic><topic>Male</topic><topic>Medial forebrain bundle</topic><topic>Medial Forebrain Bundle - physiology</topic><topic>Medical sciences</topic><topic>Neural Pathways - physiology</topic><topic>Neurochemistry</topic><topic>Neurology</topic><topic>Neurotransmission</topic><topic>Piperidines - pharmacology</topic><topic>Probes</topic><topic>Raphe Nuclei - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Serotonin</topic><topic>Serotonin - metabolism</topic><topic>Serotonin - pharmacology</topic><topic>SKF 91488</topic><topic>Substantia Nigra - metabolism</topic><topic>substantia nigra pars reticulata</topic><topic>Surgery</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashemi, Parastoo</creatorcontrib><creatorcontrib>Dankoski, Elyse C.</creatorcontrib><creatorcontrib>Wood, Kevin M.</creatorcontrib><creatorcontrib>Ambrose, Rebecca Ellen</creatorcontrib><creatorcontrib>Wightman, Robert Mark</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashemi, Parastoo</au><au>Dankoski, Elyse C.</au><au>Wood, Kevin M.</au><au>Ambrose, Rebecca Ellen</au><au>Wightman, Robert Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo electrochemical evidence for simultaneous 5‐HT and histamine release in the rat substantia nigra pars reticulata following medial forebrain bundle stimulation</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2011-09</date><risdate>2011</risdate><volume>118</volume><issue>5</issue><spage>749</spage><epage>759</epage><pages>749-759</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>J. Neurochem. (2011) 118, 749–759.
Exploring the mechanisms of serotonin [5‐hydroxytryptamine (5‐HT)] in the brain requires an in vivo method that combines fast temporal resolution with chemical selectivity. Fast‐scan cyclic voltammetry is a technique with sufficient temporal and chemical resolution for probing dynamic 5‐HT neurotransmission events; however, traditionally it has not been possible to probe in vivo 5‐HT mechanisms. Recently, we optimized fast‐scan cyclic voltammetry for measuring 5‐HT release and uptake in vivo in the substantia nigra pars reticulata (SNR) with electrical stimulation of the dorsal raphe nucleus (DRN) in the rat brain. Here, we address technical challenges associated with rat DRN surgery by electrically stimulating 5‐HT projections in the medial forebrain bundle (MFB), a more accessible anatomical location. MFB stimulation elicits 5‐HT in the SNR; furthermore, we find simultaneous release of an additional species. We use electrochemical and pharmacological methods and describe physiological, anatomical and independent chemical analyses to identify this species as histamine. We also show pharmacologically that increasing the lifetime of extracellular histamine significantly decreases 5‐HT release, most likely because of increased activation of histamine H‐3 receptors that inhibit 5‐HT release. Despite this, under physiological conditions, we find by kinetic comparisons of DRN and MFB stimulations that the simultaneous release of histamine does not interfere with the quantitative 5‐HT concentration profile. We therefore present a novel and robust electrical stimulation of the MFB that is technically less challenging than DRN stimulation to study 5‐HT and histamine release in the SNR.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21682723</pmid><doi>10.1111/j.1471-4159.2011.07352.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Brain Central nervous system Central neurotransmission. Neuromudulation. Pathways and receptors Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dimaprit - analogs & derivatives Dimaprit - pharmacology dorsal raphe nucleus Electric Stimulation - methods Electrical stimuli Electrochemistry - methods fast‐scan cyclic voltammetry Fundamental and applied biological sciences. Psychology Histamine Histamine - metabolism Histamine - pharmacology Histamine Agonists - pharmacology Histamine H3 Antagonists - pharmacology histamine N‐methyltransferase Kinetics Linear Models Male Medial forebrain bundle Medial Forebrain Bundle - physiology Medical sciences Neural Pathways - physiology Neurochemistry Neurology Neurotransmission Piperidines - pharmacology Probes Raphe Nuclei - physiology Rats Rats, Sprague-Dawley Rodents Serotonin Serotonin - metabolism Serotonin - pharmacology SKF 91488 Substantia Nigra - metabolism substantia nigra pars reticulata Surgery Vertebrates: nervous system and sense organs |
title | In vivo electrochemical evidence for simultaneous 5‐HT and histamine release in the rat substantia nigra pars reticulata following medial forebrain bundle stimulation |
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