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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
Main Authors: Li, Yi-Fan, Jackson, Keshia L, Stern, Javier E, Rabeler, Brandon, Patel, Kaushik P
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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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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. 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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. 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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. 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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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