Activation of afferent renal nerves modulates RVLM-projecting PVN neurons
Renal denervation for the treatment of hypertension has proven to be successful; however, the underlying mechanism/s are not entirely clear. To determine if preautonomic neurons in the paraventricular nucleus (PVN) respond to afferent renal nerve (ARN) stimulation, extracellular single-unit recordin...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2015-05, Vol.308 (9), p.H1103-H1111 |
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description | Renal denervation for the treatment of hypertension has proven to be successful; however, the underlying mechanism/s are not entirely clear. To determine if preautonomic neurons in the paraventricular nucleus (PVN) respond to afferent renal nerve (ARN) stimulation, extracellular single-unit recording was used to investigate the contribution of the rostral ventrolateral medulla (RVLM)-projecting PVN (PVN-RVLM) neurons to the response elicited during stimulation of ARN. In 109 spontaneously active neurons recorded in the PVN of anesthetized rats, 25 units were antidromically activated from the RVLM. Among these PVN-RVLM neurons, 84% (21/25) were activated by ARN stimulation. The baseline discharge rate was significantly higher in these neurons than those PVN-RVLM neurons not activated by ARN stimulation (16%, 4/25). The responsiveness of these neurons to baroreflex activation induced by phenylephrine and activation of cardiac sympathetic afferent reflex (CSAR) was also examined. Almost all of the PVN neurons that responded to ARN stimulation were sensitive to baroreflex (95%) and CSAR (100%). The discharge characteristics for nonevoked neurons (not activated by RVLM antidromic stimulation) showed that 23% of these PVN neurons responded to ARN stimulation. All the PVN neurons that responded to ARN stimulation were activated by N-methyl-D-aspartate, and these responses were attenuated by the glutamate receptor blocker AP5. These experiments demonstrated that sensory information originating in the kidney is integrated at the level of preautonomic neurons within the PVN, providing a novel mechanistic insight for use of renal denervation in the modulation of sympathetic outflow in disease states such as hypertension and heart failure. |
doi_str_mv | 10.1152/ajpheart.00862.2014 |
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To determine if preautonomic neurons in the paraventricular nucleus (PVN) respond to afferent renal nerve (ARN) stimulation, extracellular single-unit recording was used to investigate the contribution of the rostral ventrolateral medulla (RVLM)-projecting PVN (PVN-RVLM) neurons to the response elicited during stimulation of ARN. In 109 spontaneously active neurons recorded in the PVN of anesthetized rats, 25 units were antidromically activated from the RVLM. Among these PVN-RVLM neurons, 84% (21/25) were activated by ARN stimulation. The baseline discharge rate was significantly higher in these neurons than those PVN-RVLM neurons not activated by ARN stimulation (16%, 4/25). The responsiveness of these neurons to baroreflex activation induced by phenylephrine and activation of cardiac sympathetic afferent reflex (CSAR) was also examined. Almost all of the PVN neurons that responded to ARN stimulation were sensitive to baroreflex (95%) and CSAR (100%). The discharge characteristics for nonevoked neurons (not activated by RVLM antidromic stimulation) showed that 23% of these PVN neurons responded to ARN stimulation. All the PVN neurons that responded to ARN stimulation were activated by N-methyl-D-aspartate, and these responses were attenuated by the glutamate receptor blocker AP5. These experiments demonstrated that sensory information originating in the kidney is integrated at the level of preautonomic neurons within the PVN, providing a novel mechanistic insight for use of renal denervation in the modulation of sympathetic outflow in disease states such as hypertension and heart failure.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00862.2014</identifier><identifier>PMID: 25637549</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Action Potentials ; Animals ; Arterial Pressure ; Baroreflex ; Cardiovascular Neurohormonal Regulation ; Electric Stimulation ; Experiments ; Glutamic Acid - metabolism ; Heart - innervation ; Heart failure ; Hypertension ; Kidney - innervation ; Kidneys ; Male ; Medulla Oblongata - drug effects ; Medulla Oblongata - metabolism ; Medulla Oblongata - physiology ; Neural Pathways - metabolism ; Neural Pathways - physiology ; Neurons ; Neurons, Afferent - drug effects ; Neurons, Afferent - physiology ; Neurotransmitter Agents - pharmacology ; Paraventricular Hypothalamic Nucleus - drug effects ; Paraventricular Hypothalamic Nucleus - metabolism ; Paraventricular Hypothalamic Nucleus - physiology ; Physiology ; Rats, Sprague-Dawley ; Sympathetic Nervous System - drug effects ; Sympathetic Nervous System - metabolism ; Sympathetic Nervous System - physiology ; Time Factors</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2015-05, Vol.308 (9), p.H1103-H1111</ispartof><rights>Copyright © 2015 the American Physiological Society.</rights><rights>Copyright American Physiological Society May 1, 2015</rights><rights>Copyright © 2015 the American Physiological Society 2015 American Physiological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-7ee77d259ba11dbb941ea5b6f1760c7704050e48e2ac80d8eb57fbd87b554b2f3</citedby><cites>FETCH-LOGICAL-c499t-7ee77d259ba11dbb941ea5b6f1760c7704050e48e2ac80d8eb57fbd87b554b2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3038,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25637549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Bo</creatorcontrib><creatorcontrib>Zheng, Hong</creatorcontrib><creatorcontrib>Liu, Xuefei</creatorcontrib><creatorcontrib>Patel, Kaushik P</creatorcontrib><title>Activation of afferent renal nerves modulates RVLM-projecting PVN neurons</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Renal denervation for the treatment of hypertension has proven to be successful; however, the underlying mechanism/s are not entirely clear. To determine if preautonomic neurons in the paraventricular nucleus (PVN) respond to afferent renal nerve (ARN) stimulation, extracellular single-unit recording was used to investigate the contribution of the rostral ventrolateral medulla (RVLM)-projecting PVN (PVN-RVLM) neurons to the response elicited during stimulation of ARN. In 109 spontaneously active neurons recorded in the PVN of anesthetized rats, 25 units were antidromically activated from the RVLM. Among these PVN-RVLM neurons, 84% (21/25) were activated by ARN stimulation. The baseline discharge rate was significantly higher in these neurons than those PVN-RVLM neurons not activated by ARN stimulation (16%, 4/25). The responsiveness of these neurons to baroreflex activation induced by phenylephrine and activation of cardiac sympathetic afferent reflex (CSAR) was also examined. Almost all of the PVN neurons that responded to ARN stimulation were sensitive to baroreflex (95%) and CSAR (100%). The discharge characteristics for nonevoked neurons (not activated by RVLM antidromic stimulation) showed that 23% of these PVN neurons responded to ARN stimulation. All the PVN neurons that responded to ARN stimulation were activated by N-methyl-D-aspartate, and these responses were attenuated by the glutamate receptor blocker AP5. These experiments demonstrated that sensory information originating in the kidney is integrated at the level of preautonomic neurons within the PVN, providing a novel mechanistic insight for use of renal denervation in the modulation of sympathetic outflow in disease states such as hypertension and heart failure.</description><subject>Action Potentials</subject><subject>Animals</subject><subject>Arterial Pressure</subject><subject>Baroreflex</subject><subject>Cardiovascular Neurohormonal Regulation</subject><subject>Electric Stimulation</subject><subject>Experiments</subject><subject>Glutamic Acid - metabolism</subject><subject>Heart - innervation</subject><subject>Heart failure</subject><subject>Hypertension</subject><subject>Kidney - innervation</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medulla Oblongata - drug effects</subject><subject>Medulla Oblongata - metabolism</subject><subject>Medulla Oblongata - physiology</subject><subject>Neural Pathways - metabolism</subject><subject>Neural Pathways - physiology</subject><subject>Neurons</subject><subject>Neurons, Afferent - drug effects</subject><subject>Neurons, Afferent - physiology</subject><subject>Neurotransmitter Agents - pharmacology</subject><subject>Paraventricular Hypothalamic Nucleus - drug effects</subject><subject>Paraventricular Hypothalamic Nucleus - metabolism</subject><subject>Paraventricular Hypothalamic Nucleus - physiology</subject><subject>Physiology</subject><subject>Rats, Sprague-Dawley</subject><subject>Sympathetic Nervous System - drug effects</subject><subject>Sympathetic Nervous System - metabolism</subject><subject>Sympathetic Nervous System - physiology</subject><subject>Time Factors</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkVtLxDAQhYMoul5-gSAFX3zpmkuTtC-CLN5gvSDqa0ja6W6XtqlJu-C_N-uuor5kAvOdw8wchI4JHhPC6bledHPQrh9jnAo6ppgkW2gUOjQmnGXbaISZYLEgjO-hfe8XGGMuBdtFe5QLJnmSjdDdZd5XS91Xto1sGemyBAdtH4VH11ELbgk-amwx1LoPv-e36X3cObuAIGtn0dPbQ4AGZ1t_iHZKXXs42tQD9Hp99TK5jaePN3eTy2mcJ1nWxxJAyoLyzGhCCmOyhIDmRpRECpxLiRPMMSQpUJ2nuEjBcFmaIpWG88TQkh2gi7VvN5gGijxM63StOlc12n0oqyv1t9NWczWzS5VwTgjlweBsY-Ds-wC-V03lc6hr3YIdvCJCyjTNBJUBPf2HLuzgwmVWVEoyhgMaKLamcme9d1D-DEOwWkWlvqNSX1GpVVRBdfJ7jx_NdzbsE2xPkok</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Xu, Bo</creator><creator>Zheng, Hong</creator><creator>Liu, Xuefei</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150501</creationdate><title>Activation of afferent renal nerves modulates RVLM-projecting PVN neurons</title><author>Xu, Bo ; Zheng, Hong ; Liu, Xuefei ; Patel, Kaushik P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-7ee77d259ba11dbb941ea5b6f1760c7704050e48e2ac80d8eb57fbd87b554b2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Action Potentials</topic><topic>Animals</topic><topic>Arterial Pressure</topic><topic>Baroreflex</topic><topic>Cardiovascular Neurohormonal Regulation</topic><topic>Electric Stimulation</topic><topic>Experiments</topic><topic>Glutamic Acid - metabolism</topic><topic>Heart - innervation</topic><topic>Heart failure</topic><topic>Hypertension</topic><topic>Kidney - innervation</topic><topic>Kidneys</topic><topic>Male</topic><topic>Medulla Oblongata - drug effects</topic><topic>Medulla Oblongata - metabolism</topic><topic>Medulla Oblongata - physiology</topic><topic>Neural Pathways - metabolism</topic><topic>Neural Pathways - physiology</topic><topic>Neurons</topic><topic>Neurons, Afferent - drug effects</topic><topic>Neurons, Afferent - physiology</topic><topic>Neurotransmitter Agents - pharmacology</topic><topic>Paraventricular Hypothalamic Nucleus - drug effects</topic><topic>Paraventricular Hypothalamic Nucleus - metabolism</topic><topic>Paraventricular Hypothalamic Nucleus - physiology</topic><topic>Physiology</topic><topic>Rats, Sprague-Dawley</topic><topic>Sympathetic Nervous System - drug effects</topic><topic>Sympathetic Nervous System - metabolism</topic><topic>Sympathetic Nervous System - physiology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Bo</creatorcontrib><creatorcontrib>Zheng, Hong</creatorcontrib><creatorcontrib>Liu, Xuefei</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Bo</au><au>Zheng, Hong</au><au>Liu, Xuefei</au><au>Patel, Kaushik P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activation of afferent renal nerves modulates RVLM-projecting PVN neurons</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>308</volume><issue>9</issue><spage>H1103</spage><epage>H1111</epage><pages>H1103-H1111</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Renal denervation for the treatment of hypertension has proven to be successful; however, the underlying mechanism/s are not entirely clear. To determine if preautonomic neurons in the paraventricular nucleus (PVN) respond to afferent renal nerve (ARN) stimulation, extracellular single-unit recording was used to investigate the contribution of the rostral ventrolateral medulla (RVLM)-projecting PVN (PVN-RVLM) neurons to the response elicited during stimulation of ARN. In 109 spontaneously active neurons recorded in the PVN of anesthetized rats, 25 units were antidromically activated from the RVLM. Among these PVN-RVLM neurons, 84% (21/25) were activated by ARN stimulation. The baseline discharge rate was significantly higher in these neurons than those PVN-RVLM neurons not activated by ARN stimulation (16%, 4/25). The responsiveness of these neurons to baroreflex activation induced by phenylephrine and activation of cardiac sympathetic afferent reflex (CSAR) was also examined. Almost all of the PVN neurons that responded to ARN stimulation were sensitive to baroreflex (95%) and CSAR (100%). The discharge characteristics for nonevoked neurons (not activated by RVLM antidromic stimulation) showed that 23% of these PVN neurons responded to ARN stimulation. All the PVN neurons that responded to ARN stimulation were activated by N-methyl-D-aspartate, and these responses were attenuated by the glutamate receptor blocker AP5. These experiments demonstrated that sensory information originating in the kidney is integrated at the level of preautonomic neurons within the PVN, providing a novel mechanistic insight for use of renal denervation in the modulation of sympathetic outflow in disease states such as hypertension and heart failure.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>25637549</pmid><doi>10.1152/ajpheart.00862.2014</doi><oa>free_for_read</oa></addata></record> |
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subjects | Action Potentials Animals Arterial Pressure Baroreflex Cardiovascular Neurohormonal Regulation Electric Stimulation Experiments Glutamic Acid - metabolism Heart - innervation Heart failure Hypertension Kidney - innervation Kidneys Male Medulla Oblongata - drug effects Medulla Oblongata - metabolism Medulla Oblongata - physiology Neural Pathways - metabolism Neural Pathways - physiology Neurons Neurons, Afferent - drug effects Neurons, Afferent - physiology Neurotransmitter Agents - pharmacology Paraventricular Hypothalamic Nucleus - drug effects Paraventricular Hypothalamic Nucleus - metabolism Paraventricular Hypothalamic Nucleus - physiology Physiology Rats, Sprague-Dawley Sympathetic Nervous System - drug effects Sympathetic Nervous System - metabolism Sympathetic Nervous System - physiology Time Factors |
title | Activation of afferent renal nerves modulates RVLM-projecting PVN neurons |
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