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Interaction between glutamate and GABA systems in the integration of sympathetic outflow by the paraventricular nucleus of the hypothalamus
1 Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska; 2 Division of Basic Biomedical Science, College of Medicine, University of South Dakota, Vermillion, South Dakota; and 3 Department of Psychiatry, University of Cincinnati, Cincinnati, Ohio S...
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Published in: | American journal of physiology. Heart and circulatory physiology 2006-12, Vol.291 (6), p.H2847-H2856 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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creator | Li, Yi-Fan Jackson, Keshia L Stern, Javier E Rabeler, Brandon Patel, Kaushik P |
description | 1 Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska; 2 Division of Basic Biomedical Science, College of Medicine, University of South Dakota, Vermillion, South Dakota; and 3 Department of Psychiatry, University of Cincinnati, Cincinnati, Ohio
Submitted 10 June 2005
; accepted in final form 20 June 2006
The paraventricular nucleus (PVN) of the hypothalamus is a central site known to modulate sympathetic outflow. Excitatory and inhibitory neurotransmitters within the PVN dictate final outflow. The goal of the present study was to examine the role of the interaction between the excitatory neurotransmitter glutamate and the inhibitory neurotransmitter GABA in the regulation of sympathetic activity. In -chloralose- and urethane-anesthetized rats, microinjection of glutamate and N -methyl- D -aspartate (NMDA; 50, 100, and 200 pmol) into the PVN produced dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate. These responses were blocked by the NMDA receptor antagonist DL -2-amino-5-phosphonovaleric acid (AP-5). Microinjection of bicuculline, a GABA A receptor antagonist, into the PVN (50, 100, and 200 pmol) also produced significant, dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate; AP-5 also blocked these responses. Using microdialysis and HPLC/electrochemical detection techniques, we observed that bicuculline infusion into the PVN increased glutamate release. Using an in vitro hypothalamic slice preparation, we found that bicuculline increased the frequency of glutamate-mediated excitatory postsynaptic currents in PVN-rostral ventrolateral medullary projecting neurons, supporting a GABA A -mediated tonic inhibition of this excitatory input into these neurons. Together, these data indicate that 1 ) glutamate, via NMDA receptors, excites the presympathetic neurons within the PVN and increases sympathetic outflow and 2 ) this glutamate excitatory input is tonically inhibited by a GABA A -mediated mechanism.
glutamate-GABA interaction; renal sympathetic nerve activity
Address for reprint requests and other correspondence: K. P. Patel, Dept. of Cell and Integrative Physiology, Univ. of Nebraska Medical Center, 985850 Nebraska Medical Center, Omaha, NE 68198-5850 (e-mail: kpatel{at}unmc.edu ) |
doi_str_mv | 10.1152/ajpheart.00625.2005 |
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Submitted 10 June 2005
; accepted in final form 20 June 2006
The paraventricular nucleus (PVN) of the hypothalamus is a central site known to modulate sympathetic outflow. Excitatory and inhibitory neurotransmitters within the PVN dictate final outflow. The goal of the present study was to examine the role of the interaction between the excitatory neurotransmitter glutamate and the inhibitory neurotransmitter GABA in the regulation of sympathetic activity. In -chloralose- and urethane-anesthetized rats, microinjection of glutamate and N -methyl- D -aspartate (NMDA; 50, 100, and 200 pmol) into the PVN produced dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate. These responses were blocked by the NMDA receptor antagonist DL -2-amino-5-phosphonovaleric acid (AP-5). Microinjection of bicuculline, a GABA A receptor antagonist, into the PVN (50, 100, and 200 pmol) also produced significant, dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate; AP-5 also blocked these responses. Using microdialysis and HPLC/electrochemical detection techniques, we observed that bicuculline infusion into the PVN increased glutamate release. Using an in vitro hypothalamic slice preparation, we found that bicuculline increased the frequency of glutamate-mediated excitatory postsynaptic currents in PVN-rostral ventrolateral medullary projecting neurons, supporting a GABA A -mediated tonic inhibition of this excitatory input into these neurons. Together, these data indicate that 1 ) glutamate, via NMDA receptors, excites the presympathetic neurons within the PVN and increases sympathetic outflow and 2 ) this glutamate excitatory input is tonically inhibited by a GABA A -mediated mechanism.
glutamate-GABA interaction; renal sympathetic nerve activity
Address for reprint requests and other correspondence: K. P. Patel, Dept. of Cell and Integrative Physiology, Univ. of Nebraska Medical Center, 985850 Nebraska Medical Center, Omaha, NE 68198-5850 (e-mail: kpatel{at}unmc.edu )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00625.2005</identifier><identifier>PMID: 16877560</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>2-Amino-5-phosphonovalerate - pharmacology ; Amino acids ; Animals ; Bicuculline - pharmacology ; Blood Pressure - drug effects ; Blood Pressure - physiology ; Brain ; Dose-Response Relationship, Drug ; Excitatory Amino Acid Agonists - pharmacology ; GABA Antagonists - pharmacology ; GABA-A Receptor Antagonists ; gamma-Aminobutyric Acid - drug effects ; gamma-Aminobutyric Acid - metabolism ; Glutamic Acid - physiology ; Heart Rate - drug effects ; Heart Rate - physiology ; Male ; N-Methylaspartate - pharmacology ; Neurons ; Neurotransmitters ; Paraventricular Hypothalamic Nucleus - drug effects ; Paraventricular Hypothalamic Nucleus - physiology ; Rats ; Rats, Wistar ; Receptors, GABA-A - drug effects ; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors ; Receptors, N-Methyl-D-Aspartate - drug effects ; Receptors, N-Methyl-D-Aspartate - physiology ; Rodents ; Sympathetic Nervous System - drug effects ; Sympathetic Nervous System - physiology</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2006-12, Vol.291 (6), p.H2847-H2856</ispartof><rights>Copyright American Physiological Society Dec 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-a8d7365207df1913d65e55f913930c78388cee7c975c5b2e7e8559a47a2d4d5a3</citedby><cites>FETCH-LOGICAL-c453t-a8d7365207df1913d65e55f913930c78388cee7c975c5b2e7e8559a47a2d4d5a3</cites></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/16877560$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Yi-Fan</creatorcontrib><creatorcontrib>Jackson, Keshia L</creatorcontrib><creatorcontrib>Stern, Javier E</creatorcontrib><creatorcontrib>Rabeler, Brandon</creatorcontrib><creatorcontrib>Patel, Kaushik P</creatorcontrib><title>Interaction between glutamate and GABA systems in the integration of sympathetic outflow by the paraventricular nucleus of the hypothalamus</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska; 2 Division of Basic Biomedical Science, College of Medicine, University of South Dakota, Vermillion, South Dakota; and 3 Department of Psychiatry, University of Cincinnati, Cincinnati, Ohio
Submitted 10 June 2005
; accepted in final form 20 June 2006
The paraventricular nucleus (PVN) of the hypothalamus is a central site known to modulate sympathetic outflow. Excitatory and inhibitory neurotransmitters within the PVN dictate final outflow. The goal of the present study was to examine the role of the interaction between the excitatory neurotransmitter glutamate and the inhibitory neurotransmitter GABA in the regulation of sympathetic activity. In -chloralose- and urethane-anesthetized rats, microinjection of glutamate and N -methyl- D -aspartate (NMDA; 50, 100, and 200 pmol) into the PVN produced dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate. These responses were blocked by the NMDA receptor antagonist DL -2-amino-5-phosphonovaleric acid (AP-5). Microinjection of bicuculline, a GABA A receptor antagonist, into the PVN (50, 100, and 200 pmol) also produced significant, dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate; AP-5 also blocked these responses. Using microdialysis and HPLC/electrochemical detection techniques, we observed that bicuculline infusion into the PVN increased glutamate release. Using an in vitro hypothalamic slice preparation, we found that bicuculline increased the frequency of glutamate-mediated excitatory postsynaptic currents in PVN-rostral ventrolateral medullary projecting neurons, supporting a GABA A -mediated tonic inhibition of this excitatory input into these neurons. Together, these data indicate that 1 ) glutamate, via NMDA receptors, excites the presympathetic neurons within the PVN and increases sympathetic outflow and 2 ) this glutamate excitatory input is tonically inhibited by a GABA A -mediated mechanism.
glutamate-GABA interaction; renal sympathetic nerve activity
Address for reprint requests and other correspondence: K. P. Patel, Dept. of Cell and Integrative Physiology, Univ. of Nebraska Medical Center, 985850 Nebraska Medical Center, Omaha, NE 68198-5850 (e-mail: kpatel{at}unmc.edu )</description><subject>2-Amino-5-phosphonovalerate - pharmacology</subject><subject>Amino acids</subject><subject>Animals</subject><subject>Bicuculline - pharmacology</subject><subject>Blood Pressure - drug effects</subject><subject>Blood Pressure - physiology</subject><subject>Brain</subject><subject>Dose-Response Relationship, Drug</subject><subject>Excitatory Amino Acid Agonists - pharmacology</subject><subject>GABA Antagonists - pharmacology</subject><subject>GABA-A Receptor Antagonists</subject><subject>gamma-Aminobutyric Acid - drug effects</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>Glutamic Acid - physiology</subject><subject>Heart Rate - drug effects</subject><subject>Heart Rate - physiology</subject><subject>Male</subject><subject>N-Methylaspartate - pharmacology</subject><subject>Neurons</subject><subject>Neurotransmitters</subject><subject>Paraventricular Hypothalamic Nucleus - drug effects</subject><subject>Paraventricular Hypothalamic Nucleus - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, GABA-A - drug effects</subject><subject>Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors</subject><subject>Receptors, N-Methyl-D-Aspartate - drug effects</subject><subject>Receptors, N-Methyl-D-Aspartate - physiology</subject><subject>Rodents</subject><subject>Sympathetic Nervous System - drug effects</subject><subject>Sympathetic Nervous System - physiology</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkctu1DAUhiMEokPhCZBQxIJdpr7EdiJWQ9WbVIlNWVse52SSkRMHXzrkGXjpei4UhIRYHcv_9x3Z-rPsPUZLjBm5UNupA-XCEiFO2JIgxF5ki5SQAjNav8wWiHJacEzZWfbG-y1KhOD0dXaGeSUE42iR_bwbAzilQ2_HfA1hBzDmGxODGlSAXI1NfrP6ssr97AMMPu_HPHSQRoCNUwfLtikdJpXuQ69zG0Nr7C5fzwdyUk49whhcr6NRLh-jNhD93trH3TzZ0CmjhujfZq9aZTy8O83z7Nv11cPlbXH_9ebucnVf6JLRUKiqEZQzgkTT4hrThjNgrE2nmiItKlpVGkDoWjDN1gQEVIzVqhSKNGXDFD3PPh33Ts5-j-CDHHqvwRg1go1e8gpTyrD4L4hrLkpKqgR-_Avc2ujG9AlJSM14SUiZIHqEtLPeO2jl5PpBuVliJPeNyl-NykOjct9osj6cVsf1AM1v51RhAj4fga7fdLvegZy62ffW2M0sr6MxD_AjPK8mNZZc3pKqFHJq2mRf_Nt-fs8fFn0CZBTHIA</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Li, Yi-Fan</creator><creator>Jackson, Keshia L</creator><creator>Stern, Javier E</creator><creator>Rabeler, Brandon</creator><creator>Patel, Kaushik P</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20061201</creationdate><title>Interaction between glutamate and GABA systems in the integration of sympathetic outflow by the paraventricular nucleus of the hypothalamus</title><author>Li, Yi-Fan ; Jackson, Keshia L ; Stern, Javier E ; Rabeler, Brandon ; Patel, Kaushik P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-a8d7365207df1913d65e55f913930c78388cee7c975c5b2e7e8559a47a2d4d5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>2-Amino-5-phosphonovalerate - pharmacology</topic><topic>Amino acids</topic><topic>Animals</topic><topic>Bicuculline - pharmacology</topic><topic>Blood Pressure - drug effects</topic><topic>Blood Pressure - physiology</topic><topic>Brain</topic><topic>Dose-Response Relationship, Drug</topic><topic>Excitatory Amino Acid Agonists - pharmacology</topic><topic>GABA Antagonists - pharmacology</topic><topic>GABA-A Receptor Antagonists</topic><topic>gamma-Aminobutyric Acid - drug effects</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>Glutamic Acid - physiology</topic><topic>Heart Rate - drug effects</topic><topic>Heart Rate - physiology</topic><topic>Male</topic><topic>N-Methylaspartate - pharmacology</topic><topic>Neurons</topic><topic>Neurotransmitters</topic><topic>Paraventricular Hypothalamic Nucleus - drug effects</topic><topic>Paraventricular Hypothalamic Nucleus - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, GABA-A - drug effects</topic><topic>Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors</topic><topic>Receptors, N-Methyl-D-Aspartate - drug effects</topic><topic>Receptors, N-Methyl-D-Aspartate - physiology</topic><topic>Rodents</topic><topic>Sympathetic Nervous System - drug effects</topic><topic>Sympathetic Nervous System - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Yi-Fan</creatorcontrib><creatorcontrib>Jackson, Keshia L</creatorcontrib><creatorcontrib>Stern, Javier E</creatorcontrib><creatorcontrib>Rabeler, Brandon</creatorcontrib><creatorcontrib>Patel, Kaushik P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Yi-Fan</au><au>Jackson, Keshia L</au><au>Stern, Javier E</au><au>Rabeler, Brandon</au><au>Patel, Kaushik P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction between glutamate and GABA systems in the integration of sympathetic outflow by the paraventricular nucleus of the hypothalamus</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>291</volume><issue>6</issue><spage>H2847</spage><epage>H2856</epage><pages>H2847-H2856</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>1 Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska; 2 Division of Basic Biomedical Science, College of Medicine, University of South Dakota, Vermillion, South Dakota; and 3 Department of Psychiatry, University of Cincinnati, Cincinnati, Ohio
Submitted 10 June 2005
; accepted in final form 20 June 2006
The paraventricular nucleus (PVN) of the hypothalamus is a central site known to modulate sympathetic outflow. Excitatory and inhibitory neurotransmitters within the PVN dictate final outflow. The goal of the present study was to examine the role of the interaction between the excitatory neurotransmitter glutamate and the inhibitory neurotransmitter GABA in the regulation of sympathetic activity. In -chloralose- and urethane-anesthetized rats, microinjection of glutamate and N -methyl- D -aspartate (NMDA; 50, 100, and 200 pmol) into the PVN produced dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate. These responses were blocked by the NMDA receptor antagonist DL -2-amino-5-phosphonovaleric acid (AP-5). Microinjection of bicuculline, a GABA A receptor antagonist, into the PVN (50, 100, and 200 pmol) also produced significant, dose-dependent increases in renal sympathetic nerve activity, blood pressure, and heart rate; AP-5 also blocked these responses. Using microdialysis and HPLC/electrochemical detection techniques, we observed that bicuculline infusion into the PVN increased glutamate release. Using an in vitro hypothalamic slice preparation, we found that bicuculline increased the frequency of glutamate-mediated excitatory postsynaptic currents in PVN-rostral ventrolateral medullary projecting neurons, supporting a GABA A -mediated tonic inhibition of this excitatory input into these neurons. Together, these data indicate that 1 ) glutamate, via NMDA receptors, excites the presympathetic neurons within the PVN and increases sympathetic outflow and 2 ) this glutamate excitatory input is tonically inhibited by a GABA A -mediated mechanism.
glutamate-GABA interaction; renal sympathetic nerve activity
Address for reprint requests and other correspondence: K. P. Patel, Dept. of Cell and Integrative Physiology, Univ. of Nebraska Medical Center, 985850 Nebraska Medical Center, Omaha, NE 68198-5850 (e-mail: kpatel{at}unmc.edu )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>16877560</pmid><doi>10.1152/ajpheart.00625.2005</doi></addata></record> |
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subjects | 2-Amino-5-phosphonovalerate - pharmacology Amino acids Animals Bicuculline - pharmacology Blood Pressure - drug effects Blood Pressure - physiology Brain Dose-Response Relationship, Drug Excitatory Amino Acid Agonists - pharmacology GABA Antagonists - pharmacology GABA-A Receptor Antagonists gamma-Aminobutyric Acid - drug effects gamma-Aminobutyric Acid - metabolism Glutamic Acid - physiology Heart Rate - drug effects Heart Rate - physiology Male N-Methylaspartate - pharmacology Neurons Neurotransmitters Paraventricular Hypothalamic Nucleus - drug effects Paraventricular Hypothalamic Nucleus - physiology Rats Rats, Wistar Receptors, GABA-A - drug effects Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors Receptors, N-Methyl-D-Aspartate - drug effects Receptors, N-Methyl-D-Aspartate - physiology Rodents Sympathetic Nervous System - drug effects Sympathetic Nervous System - physiology |
title | Interaction between glutamate and GABA systems in the integration of sympathetic outflow by the paraventricular nucleus of the hypothalamus |
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