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Blockade of 5-Ht3 receptors in the septal area increases Fos expression in selected brain areas
Abstract Serotonin is widely distributed throughout the brain and is involved in a multiplicity of visceral, cognitive and behavioral responses. It has been previously shown that injections of different doses of ondansetron, a 5-HT3 receptor antagonist, into the medial septum/vertical limb of the di...
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Published in: | Autonomic neuroscience 2014-04, Vol.181, p.55-68 |
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description | Abstract Serotonin is widely distributed throughout the brain and is involved in a multiplicity of visceral, cognitive and behavioral responses. It has been previously shown that injections of different doses of ondansetron, a 5-HT3 receptor antagonist, into the medial septum/vertical limb of the diagonal band complex (MS/vDB) induce a hypertensive response in rats. On the other hand, administration of m-CPBG, a 5-HT3 agonist, into the MS/vDB inhibits the increase of blood pressure during restraint stress. However, it is unclear which neuronal circuitry is involved in these responses. The present study investigated Fos immunoreactive nuclei (Fos-IR) in different brain areas following the blockade of 5-HT3 receptors located in the MS/vDB in sham and in sinoaortic denervated (SAD) rats. Ondansetron injection into the MS/vDB increases Fos-IR in different brain areas including the limbic system (central amygdala and ventral part of the bed nucleus of the stria terminalis), hypothalamus (medial parvocellular parts of the paraventricular nucleus, anterodorsal preoptic area, dorsomedial hypothalamic nucleus), mesencephalon (ventrolateral periaqueductal gray region) and rhombencephalon (lateral parabrachial nucleus) in sham rats. Barodenervation results in higher Fos expression at the parvocellular and magnocellular part of the paraventricular nucleus, the lateral parabrachial nucleus, the central nucleus of amygdala, the locus coeruleus, the medial part of the nucleus of the solitary tract, the rostral ventrolateral medulla and the caudal ventrolateral medulla following 5-HT3 receptor blockade in the MS/vDB. Based on the present results and previous data showing a hypertensive response to ondansetron injected into the MS/vDB, it is reasonable to suggest that 5-HT3 receptors in the MS/vDB exert an inhibitory drive that may oscillate as a functional regulatory part of the complex central neuronal network participating in the control of blood pressure. |
doi_str_mv | 10.1016/j.autneu.2014.01.003 |
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It has been previously shown that injections of different doses of ondansetron, a 5-HT3 receptor antagonist, into the medial septum/vertical limb of the diagonal band complex (MS/vDB) induce a hypertensive response in rats. On the other hand, administration of m-CPBG, a 5-HT3 agonist, into the MS/vDB inhibits the increase of blood pressure during restraint stress. However, it is unclear which neuronal circuitry is involved in these responses. The present study investigated Fos immunoreactive nuclei (Fos-IR) in different brain areas following the blockade of 5-HT3 receptors located in the MS/vDB in sham and in sinoaortic denervated (SAD) rats. Ondansetron injection into the MS/vDB increases Fos-IR in different brain areas including the limbic system (central amygdala and ventral part of the bed nucleus of the stria terminalis), hypothalamus (medial parvocellular parts of the paraventricular nucleus, anterodorsal preoptic area, dorsomedial hypothalamic nucleus), mesencephalon (ventrolateral periaqueductal gray region) and rhombencephalon (lateral parabrachial nucleus) in sham rats. Barodenervation results in higher Fos expression at the parvocellular and magnocellular part of the paraventricular nucleus, the lateral parabrachial nucleus, the central nucleus of amygdala, the locus coeruleus, the medial part of the nucleus of the solitary tract, the rostral ventrolateral medulla and the caudal ventrolateral medulla following 5-HT3 receptor blockade in the MS/vDB. Based on the present results and previous data showing a hypertensive response to ondansetron injected into the MS/vDB, it is reasonable to suggest that 5-HT3 receptors in the MS/vDB exert an inhibitory drive that may oscillate as a functional regulatory part of the complex central neuronal network participating in the control of blood pressure.</description><identifier>ISSN: 1566-0702</identifier><identifier>EISSN: 1872-7484</identifier><identifier>DOI: 10.1016/j.autneu.2014.01.003</identifier><identifier>PMID: 24507935</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>5-HT3 receptor ; Advanced Basic Science ; Animals ; Autonomic Denervation ; Barodenervation ; Baroreflex - drug effects ; Baroreflex - physiology ; Blood Pressure - drug effects ; Blood Pressure - physiology ; Brain - drug effects ; Brain - metabolism ; Brain - physiopathology ; c-Fos ; Cell Count ; Cell Nucleus - drug effects ; Cell Nucleus - metabolism ; Heart Rate - drug effects ; Heart Rate - physiology ; Male ; Medical Education ; Ondansetron ; Ondansetron - pharmacology ; Pressoreceptors - physiopathology ; Proto-Oncogene Proteins c-fos - metabolism ; Rats ; Rats, Wistar ; Receptors, Serotonin, 5-HT3 - metabolism ; Septal area ; Septum of Brain - drug effects ; Septum of Brain - metabolism ; Serotonin 5-HT3 Receptor Antagonists - pharmacology</subject><ispartof>Autonomic neuroscience, 2014-04, Vol.181, p.55-68</ispartof><rights>Elsevier B.V.</rights><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-f7789f87b5c5d31dcc4ac54dbbba112b2159ac8798b2ceb6672a8047722fed8e3</citedby><cites>FETCH-LOGICAL-c365t-f7789f87b5c5d31dcc4ac54dbbba112b2159ac8798b2ceb6672a8047722fed8e3</cites><orcidid>0000-0002-2569-4630</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24507935$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Urzedo-Rodrigues, Lilia S</creatorcontrib><creatorcontrib>Ferreira, Hilda S</creatorcontrib><creatorcontrib>Santana, Rejane Conceição</creatorcontrib><creatorcontrib>Luz, Carla Patrícia</creatorcontrib><creatorcontrib>Perrone, Camila F</creatorcontrib><creatorcontrib>Fregoneze, Josmara B</creatorcontrib><title>Blockade of 5-Ht3 receptors in the septal area increases Fos expression in selected brain areas</title><title>Autonomic neuroscience</title><addtitle>Auton Neurosci</addtitle><description>Abstract Serotonin is widely distributed throughout the brain and is involved in a multiplicity of visceral, cognitive and behavioral responses. It has been previously shown that injections of different doses of ondansetron, a 5-HT3 receptor antagonist, into the medial septum/vertical limb of the diagonal band complex (MS/vDB) induce a hypertensive response in rats. On the other hand, administration of m-CPBG, a 5-HT3 agonist, into the MS/vDB inhibits the increase of blood pressure during restraint stress. However, it is unclear which neuronal circuitry is involved in these responses. The present study investigated Fos immunoreactive nuclei (Fos-IR) in different brain areas following the blockade of 5-HT3 receptors located in the MS/vDB in sham and in sinoaortic denervated (SAD) rats. Ondansetron injection into the MS/vDB increases Fos-IR in different brain areas including the limbic system (central amygdala and ventral part of the bed nucleus of the stria terminalis), hypothalamus (medial parvocellular parts of the paraventricular nucleus, anterodorsal preoptic area, dorsomedial hypothalamic nucleus), mesencephalon (ventrolateral periaqueductal gray region) and rhombencephalon (lateral parabrachial nucleus) in sham rats. Barodenervation results in higher Fos expression at the parvocellular and magnocellular part of the paraventricular nucleus, the lateral parabrachial nucleus, the central nucleus of amygdala, the locus coeruleus, the medial part of the nucleus of the solitary tract, the rostral ventrolateral medulla and the caudal ventrolateral medulla following 5-HT3 receptor blockade in the MS/vDB. Based on the present results and previous data showing a hypertensive response to ondansetron injected into the MS/vDB, it is reasonable to suggest that 5-HT3 receptors in the MS/vDB exert an inhibitory drive that may oscillate as a functional regulatory part of the complex central neuronal network participating in the control of blood pressure.</description><subject>5-HT3 receptor</subject><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>Autonomic Denervation</subject><subject>Barodenervation</subject><subject>Baroreflex - drug effects</subject><subject>Baroreflex - physiology</subject><subject>Blood Pressure - drug effects</subject><subject>Blood Pressure - physiology</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain - physiopathology</subject><subject>c-Fos</subject><subject>Cell Count</subject><subject>Cell Nucleus - drug effects</subject><subject>Cell Nucleus - metabolism</subject><subject>Heart Rate - drug effects</subject><subject>Heart Rate - physiology</subject><subject>Male</subject><subject>Medical Education</subject><subject>Ondansetron</subject><subject>Ondansetron - pharmacology</subject><subject>Pressoreceptors - physiopathology</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Serotonin, 5-HT3 - metabolism</subject><subject>Septal area</subject><subject>Septum of Brain - drug effects</subject><subject>Septum of Brain - metabolism</subject><subject>Serotonin 5-HT3 Receptor Antagonists - pharmacology</subject><issn>1566-0702</issn><issn>1872-7484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNks1u1TAQhSMEoqXwBgh5ySZh7MQ_2SBBRSlSpS5o15ZjT4Rvc-OLJ0Ht2-PoFhZs6Go81jcz0jmnqt5yaDhw9WHXuHWZcW0E8K4B3gC0z6pTbrSodWe65-UtlapBgzipXhHtAMBAr15WJ6KToPtWnlb285T8nQvI0shkfbm0LKPHw5IysTiz5QcyKq2bmMvoypcvhZDYRSKG94eMRDHNG0s4oV8wsCG70m48va5ejG4ifPNYz6rbiy8355f11fXXb-efrmrfKrnUo9amH40epJeh5cH7znnZhWEYHOdiEFz2zhvdm0F4HJTSwhnotBZixGCwPaveH_cecvq5Ii12H8njNLkZ00qWS6601MroJ6DA26KgFgXtjqjPiSjjaA857l1-sBzs5oLd2aMLdnPBArfFhTL27vHCOuwx_B36I3sBPh4BLJL8ipgt-YizxxCL-osNKf7vwr8L_BTn6N10hw9Iu7TmuchtuSVhwX7fkrAFgXclBCBN-xvCBq7s</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Urzedo-Rodrigues, Lilia S</creator><creator>Ferreira, Hilda S</creator><creator>Santana, Rejane Conceição</creator><creator>Luz, Carla Patrícia</creator><creator>Perrone, Camila F</creator><creator>Fregoneze, Josmara B</creator><general>Elsevier B.V</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><scope>7TK</scope><orcidid>https://orcid.org/0000-0002-2569-4630</orcidid></search><sort><creationdate>201404</creationdate><title>Blockade of 5-Ht3 receptors in the septal area increases Fos expression in selected brain areas</title><author>Urzedo-Rodrigues, Lilia S ; Ferreira, Hilda S ; Santana, Rejane Conceição ; Luz, Carla Patrícia ; Perrone, Camila F ; Fregoneze, Josmara B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-f7789f87b5c5d31dcc4ac54dbbba112b2159ac8798b2ceb6672a8047722fed8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>5-HT3 receptor</topic><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Autonomic Denervation</topic><topic>Barodenervation</topic><topic>Baroreflex - drug effects</topic><topic>Baroreflex - physiology</topic><topic>Blood Pressure - drug effects</topic><topic>Blood Pressure - physiology</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain - physiopathology</topic><topic>c-Fos</topic><topic>Cell Count</topic><topic>Cell Nucleus - drug effects</topic><topic>Cell Nucleus - metabolism</topic><topic>Heart Rate - drug effects</topic><topic>Heart Rate - physiology</topic><topic>Male</topic><topic>Medical Education</topic><topic>Ondansetron</topic><topic>Ondansetron - pharmacology</topic><topic>Pressoreceptors - physiopathology</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Serotonin, 5-HT3 - metabolism</topic><topic>Septal area</topic><topic>Septum of Brain - drug effects</topic><topic>Septum of Brain - metabolism</topic><topic>Serotonin 5-HT3 Receptor Antagonists - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Urzedo-Rodrigues, Lilia S</creatorcontrib><creatorcontrib>Ferreira, Hilda S</creatorcontrib><creatorcontrib>Santana, Rejane Conceição</creatorcontrib><creatorcontrib>Luz, Carla Patrícia</creatorcontrib><creatorcontrib>Perrone, Camila F</creatorcontrib><creatorcontrib>Fregoneze, Josmara B</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><collection>Neurosciences Abstracts</collection><jtitle>Autonomic neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Urzedo-Rodrigues, Lilia S</au><au>Ferreira, Hilda S</au><au>Santana, Rejane Conceição</au><au>Luz, Carla Patrícia</au><au>Perrone, Camila F</au><au>Fregoneze, Josmara B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blockade of 5-Ht3 receptors in the septal area increases Fos expression in selected brain areas</atitle><jtitle>Autonomic neuroscience</jtitle><addtitle>Auton Neurosci</addtitle><date>2014-04</date><risdate>2014</risdate><volume>181</volume><spage>55</spage><epage>68</epage><pages>55-68</pages><issn>1566-0702</issn><eissn>1872-7484</eissn><abstract>Abstract Serotonin is widely distributed throughout the brain and is involved in a multiplicity of visceral, cognitive and behavioral responses. It has been previously shown that injections of different doses of ondansetron, a 5-HT3 receptor antagonist, into the medial septum/vertical limb of the diagonal band complex (MS/vDB) induce a hypertensive response in rats. On the other hand, administration of m-CPBG, a 5-HT3 agonist, into the MS/vDB inhibits the increase of blood pressure during restraint stress. However, it is unclear which neuronal circuitry is involved in these responses. The present study investigated Fos immunoreactive nuclei (Fos-IR) in different brain areas following the blockade of 5-HT3 receptors located in the MS/vDB in sham and in sinoaortic denervated (SAD) rats. Ondansetron injection into the MS/vDB increases Fos-IR in different brain areas including the limbic system (central amygdala and ventral part of the bed nucleus of the stria terminalis), hypothalamus (medial parvocellular parts of the paraventricular nucleus, anterodorsal preoptic area, dorsomedial hypothalamic nucleus), mesencephalon (ventrolateral periaqueductal gray region) and rhombencephalon (lateral parabrachial nucleus) in sham rats. Barodenervation results in higher Fos expression at the parvocellular and magnocellular part of the paraventricular nucleus, the lateral parabrachial nucleus, the central nucleus of amygdala, the locus coeruleus, the medial part of the nucleus of the solitary tract, the rostral ventrolateral medulla and the caudal ventrolateral medulla following 5-HT3 receptor blockade in the MS/vDB. Based on the present results and previous data showing a hypertensive response to ondansetron injected into the MS/vDB, it is reasonable to suggest that 5-HT3 receptors in the MS/vDB exert an inhibitory drive that may oscillate as a functional regulatory part of the complex central neuronal network participating in the control of blood pressure.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24507935</pmid><doi>10.1016/j.autneu.2014.01.003</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-2569-4630</orcidid></addata></record> |
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subjects | 5-HT3 receptor Advanced Basic Science Animals Autonomic Denervation Barodenervation Baroreflex - drug effects Baroreflex - physiology Blood Pressure - drug effects Blood Pressure - physiology Brain - drug effects Brain - metabolism Brain - physiopathology c-Fos Cell Count Cell Nucleus - drug effects Cell Nucleus - metabolism Heart Rate - drug effects Heart Rate - physiology Male Medical Education Ondansetron Ondansetron - pharmacology Pressoreceptors - physiopathology Proto-Oncogene Proteins c-fos - metabolism Rats Rats, Wistar Receptors, Serotonin, 5-HT3 - metabolism Septal area Septum of Brain - drug effects Septum of Brain - metabolism Serotonin 5-HT3 Receptor Antagonists - pharmacology |
title | Blockade of 5-Ht3 receptors in the septal area increases Fos expression in selected brain areas |
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