Serotonin increases the excitability of the hypothalamic paraventricular nucleus magnocellular neurons
Recent evidence that 5‐hydroxytryptamine (5‐HT or serotonin) enhances the release and the gene expression of vasopressin and oxytocin in the hypothalamic paraventricular nucleus (PVN) suggests that 5‐HT can excite the PVN magnocellular neurons. The objective of this study was to examine the underlyi...
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description | Recent evidence that 5‐hydroxytryptamine (5‐HT or serotonin) enhances the release and the gene expression of vasopressin and oxytocin in the hypothalamic paraventricular nucleus (PVN) suggests that 5‐HT can excite the PVN magnocellular neurons. The objective of this study was to examine the underlying mechanisms for such excitatory action in the electrophysiologically identified hypothalamic PVN magnocellular neurons in rats using whole‐cell patch‐clamp. We found that 5‐HT weakly depolarizes 33.3% of PVN magnocellular neurons in the presence of tetrodotoxin. A minuscule inward current was produced by 5‐HT in 48% of the cells, which was attenuated when the 5‐HT4 antagonist GR113808 or the 5‐HT7 antagonist SB269970 was added. In addition, 5‐HT reduced the frequency of miniature inhibitory postsynaptic currents in a dose‐dependent manner. This inhibition was mimicked by the 5‐HT1B agonist CP93129, and reversed in the presence of 5‐HT1B antagonists cyanopindolol and SB224289. Besides, 5‐HT induced a biphasic effect on the frequency of miniature excitatory postsynaptic currents, comprising a transient inhibition and a delayed concentration‐dependent excitation (onset latency ∼ 5 min). The facilitation was mimicked by the 5‐HT2A/2C agonist DOI and abolished in the presence of the 5‐HT2C antagonist RS102221. Our findings reveal that 5‐HT directly increases the excitability of the PVN magnocellular neurons via multiple receptor subtypes and mechanisms. This may help understanding the regulation of 5‐HT‐induced hormone release and feeding behavior in the PVN. |
doi_str_mv | 10.1111/j.1460-9568.2007.05547.x |
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N. ; Chow, Billy K. C. ; Yung, Wing-Ho</creator><creatorcontrib>Ho, Sara S. N. ; Chow, Billy K. C. ; Yung, Wing-Ho</creatorcontrib><description>Recent evidence that 5‐hydroxytryptamine (5‐HT or serotonin) enhances the release and the gene expression of vasopressin and oxytocin in the hypothalamic paraventricular nucleus (PVN) suggests that 5‐HT can excite the PVN magnocellular neurons. The objective of this study was to examine the underlying mechanisms for such excitatory action in the electrophysiologically identified hypothalamic PVN magnocellular neurons in rats using whole‐cell patch‐clamp. We found that 5‐HT weakly depolarizes 33.3% of PVN magnocellular neurons in the presence of tetrodotoxin. A minuscule inward current was produced by 5‐HT in 48% of the cells, which was attenuated when the 5‐HT4 antagonist GR113808 or the 5‐HT7 antagonist SB269970 was added. In addition, 5‐HT reduced the frequency of miniature inhibitory postsynaptic currents in a dose‐dependent manner. This inhibition was mimicked by the 5‐HT1B agonist CP93129, and reversed in the presence of 5‐HT1B antagonists cyanopindolol and SB224289. Besides, 5‐HT induced a biphasic effect on the frequency of miniature excitatory postsynaptic currents, comprising a transient inhibition and a delayed concentration‐dependent excitation (onset latency ∼ 5 min). The facilitation was mimicked by the 5‐HT2A/2C agonist DOI and abolished in the presence of the 5‐HT2C antagonist RS102221. Our findings reveal that 5‐HT directly increases the excitability of the PVN magnocellular neurons via multiple receptor subtypes and mechanisms. 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N.</creatorcontrib><creatorcontrib>Chow, Billy K. C.</creatorcontrib><creatorcontrib>Yung, Wing-Ho</creatorcontrib><title>Serotonin increases the excitability of the hypothalamic paraventricular nucleus magnocellular neurons</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Recent evidence that 5‐hydroxytryptamine (5‐HT or serotonin) enhances the release and the gene expression of vasopressin and oxytocin in the hypothalamic paraventricular nucleus (PVN) suggests that 5‐HT can excite the PVN magnocellular neurons. The objective of this study was to examine the underlying mechanisms for such excitatory action in the electrophysiologically identified hypothalamic PVN magnocellular neurons in rats using whole‐cell patch‐clamp. We found that 5‐HT weakly depolarizes 33.3% of PVN magnocellular neurons in the presence of tetrodotoxin. A minuscule inward current was produced by 5‐HT in 48% of the cells, which was attenuated when the 5‐HT4 antagonist GR113808 or the 5‐HT7 antagonist SB269970 was added. In addition, 5‐HT reduced the frequency of miniature inhibitory postsynaptic currents in a dose‐dependent manner. This inhibition was mimicked by the 5‐HT1B agonist CP93129, and reversed in the presence of 5‐HT1B antagonists cyanopindolol and SB224289. Besides, 5‐HT induced a biphasic effect on the frequency of miniature excitatory postsynaptic currents, comprising a transient inhibition and a delayed concentration‐dependent excitation (onset latency ∼ 5 min). The facilitation was mimicked by the 5‐HT2A/2C agonist DOI and abolished in the presence of the 5‐HT2C antagonist RS102221. Our findings reveal that 5‐HT directly increases the excitability of the PVN magnocellular neurons via multiple receptor subtypes and mechanisms. This may help understanding the regulation of 5‐HT‐induced hormone release and feeding behavior in the PVN.</description><subject>5-HT1B receptor</subject><subject>5-HT2C receptor</subject><subject>Action Potentials - drug effects</subject><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>Dose-Response Relationship, Drug</subject><subject>Excitatory Postsynaptic Potentials - drug effects</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>GABA Antagonists - pharmacology</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Hypothalamo-Hypophyseal System - secretion</subject><subject>Inhibitory Postsynaptic Potentials - drug effects</subject><subject>Inhibitory Postsynaptic Potentials - physiology</subject><subject>Male</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Neurons - secretion</subject><subject>Organ Culture Techniques</subject><subject>Paraventricular Hypothalamic Nucleus - drug effects</subject><subject>Paraventricular Hypothalamic Nucleus - metabolism</subject><subject>Paraventricular Hypothalamic Nucleus - secretion</subject><subject>patch-clamp</subject><subject>Patch-Clamp Techniques</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reaction Time - drug effects</subject><subject>Reaction Time - physiology</subject><subject>Receptors, Serotonin - drug effects</subject><subject>Receptors, Serotonin - metabolism</subject><subject>Serotonin - metabolism</subject><subject>Serotonin - pharmacology</subject><subject>Serotonin Antagonists - pharmacology</subject><subject>Serotonin Receptor Agonists - pharmacology</subject><subject>Sodium Channel Blockers - pharmacology</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synaptic Transmission - physiology</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtv1DAUhS0EokPhL6Cs2CX4ET-yYIGqMgVVg8pDdGfdODeMhzwGOykz_56kGZUl9cbW9fmOrXMISRjN2LTe7jKWK5oWUpmMU6ozKmWus8MTsnq4eEpWtJAiNUzdnpEXMe4opUbl8jk5Y1oqZphYkforhn7oO98lvnMBIWJMhi0meHB-gNI3fjgmfX0_2x73_bCFBlrvkj0EuMNuCN6NDYSkG12DY0xa-Nn1DptmmeIY-i6-JM9qaCK-Ou3n5PuHy28XV-n15_XHi_fXqZOU69TwUnODOXDKXFVXAJw5w4sCak1VrhyUrKiEQi0YFyXmlDtpQNTKqJKZSpyTN4vvPvS_R4yDbX2cPwMd9mO0kwvVRvD_CjmVXAlKJ6FZhC70MQas7T74FsLRMmrnMuzOzpnbOXM7l2Hvy7CHCX19emMsW6z-gaf0J8G7RfDHN3h8tLG9_LSZTxOfLryPAx4eeAi_rNJCS_tjs7ZifaO_bG6VXYu_MXyp3A</recordid><startdate>200705</startdate><enddate>200705</enddate><creator>Ho, Sara S. N.</creator><creator>Chow, Billy K. C.</creator><creator>Yung, Wing-Ho</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>200705</creationdate><title>Serotonin increases the excitability of the hypothalamic paraventricular nucleus magnocellular neurons</title><author>Ho, Sara S. N. ; Chow, Billy K. C. ; Yung, Wing-Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5027-82b728e4a201cdfdaa21c8299af70646cab19d36e73123be402c58a3f686b18d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>5-HT1B receptor</topic><topic>5-HT2C receptor</topic><topic>Action Potentials - drug effects</topic><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Dose-Response Relationship, Drug</topic><topic>Excitatory Postsynaptic Potentials - drug effects</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>GABA Antagonists - pharmacology</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Hypothalamo-Hypophyseal System - secretion</topic><topic>Inhibitory Postsynaptic Potentials - drug effects</topic><topic>Inhibitory Postsynaptic Potentials - physiology</topic><topic>Male</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Neurons - secretion</topic><topic>Organ Culture Techniques</topic><topic>Paraventricular Hypothalamic Nucleus - drug effects</topic><topic>Paraventricular Hypothalamic Nucleus - metabolism</topic><topic>Paraventricular Hypothalamic Nucleus - secretion</topic><topic>patch-clamp</topic><topic>Patch-Clamp Techniques</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reaction Time - drug effects</topic><topic>Reaction Time - physiology</topic><topic>Receptors, Serotonin - drug effects</topic><topic>Receptors, Serotonin - metabolism</topic><topic>Serotonin - metabolism</topic><topic>Serotonin - pharmacology</topic><topic>Serotonin Antagonists - pharmacology</topic><topic>Serotonin Receptor Agonists - pharmacology</topic><topic>Sodium Channel Blockers - pharmacology</topic><topic>Synaptic Transmission - drug effects</topic><topic>Synaptic Transmission - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ho, Sara S. N.</creatorcontrib><creatorcontrib>Chow, Billy K. C.</creatorcontrib><creatorcontrib>Yung, Wing-Ho</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ho, Sara S. N.</au><au>Chow, Billy K. C.</au><au>Yung, Wing-Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serotonin increases the excitability of the hypothalamic paraventricular nucleus magnocellular neurons</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2007-05</date><risdate>2007</risdate><volume>25</volume><issue>10</issue><spage>2991</spage><epage>3000</epage><pages>2991-3000</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Recent evidence that 5‐hydroxytryptamine (5‐HT or serotonin) enhances the release and the gene expression of vasopressin and oxytocin in the hypothalamic paraventricular nucleus (PVN) suggests that 5‐HT can excite the PVN magnocellular neurons. The objective of this study was to examine the underlying mechanisms for such excitatory action in the electrophysiologically identified hypothalamic PVN magnocellular neurons in rats using whole‐cell patch‐clamp. We found that 5‐HT weakly depolarizes 33.3% of PVN magnocellular neurons in the presence of tetrodotoxin. A minuscule inward current was produced by 5‐HT in 48% of the cells, which was attenuated when the 5‐HT4 antagonist GR113808 or the 5‐HT7 antagonist SB269970 was added. In addition, 5‐HT reduced the frequency of miniature inhibitory postsynaptic currents in a dose‐dependent manner. This inhibition was mimicked by the 5‐HT1B agonist CP93129, and reversed in the presence of 5‐HT1B antagonists cyanopindolol and SB224289. Besides, 5‐HT induced a biphasic effect on the frequency of miniature excitatory postsynaptic currents, comprising a transient inhibition and a delayed concentration‐dependent excitation (onset latency ∼ 5 min). The facilitation was mimicked by the 5‐HT2A/2C agonist DOI and abolished in the presence of the 5‐HT2C antagonist RS102221. Our findings reveal that 5‐HT directly increases the excitability of the PVN magnocellular neurons via multiple receptor subtypes and mechanisms. This may help understanding the regulation of 5‐HT‐induced hormone release and feeding behavior in the PVN.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17561813</pmid><doi>10.1111/j.1460-9568.2007.05547.x</doi><tpages>10</tpages></addata></record> |
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subjects | 5-HT1B receptor 5-HT2C receptor Action Potentials - drug effects Action Potentials - physiology Animals Dose-Response Relationship, Drug Excitatory Postsynaptic Potentials - drug effects Excitatory Postsynaptic Potentials - physiology GABA Antagonists - pharmacology Hypothalamo-Hypophyseal System - drug effects Hypothalamo-Hypophyseal System - metabolism Hypothalamo-Hypophyseal System - secretion Inhibitory Postsynaptic Potentials - drug effects Inhibitory Postsynaptic Potentials - physiology Male Neurons - drug effects Neurons - metabolism Neurons - secretion Organ Culture Techniques Paraventricular Hypothalamic Nucleus - drug effects Paraventricular Hypothalamic Nucleus - metabolism Paraventricular Hypothalamic Nucleus - secretion patch-clamp Patch-Clamp Techniques rat Rats Rats, Sprague-Dawley Reaction Time - drug effects Reaction Time - physiology Receptors, Serotonin - drug effects Receptors, Serotonin - metabolism Serotonin - metabolism Serotonin - pharmacology Serotonin Antagonists - pharmacology Serotonin Receptor Agonists - pharmacology Sodium Channel Blockers - pharmacology Synaptic Transmission - drug effects Synaptic Transmission - physiology |
title | Serotonin increases the excitability of the hypothalamic paraventricular nucleus magnocellular neurons |
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