Renal sensory and sympathetic nerves reinnervate the kidney in a similar time-dependent fashion after renal denervation in rats
Efferent renal sympathetic nerves reinnervate the kidney after renal denervation in animals and humans. Therefore, the long-term reduction in arterial pressure following renal denervation in drug-resistant hypertensive patients has been attributed to lack of afferent renal sensory reinnervation. How...
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creator | Mulder, Jan Hökfelt, Tomas Knuepfer, Mark M Kopp, Ulla C |
description | Efferent renal sympathetic nerves reinnervate the kidney after renal denervation in animals and humans. Therefore, the long-term reduction in arterial pressure following renal denervation in drug-resistant hypertensive patients has been attributed to lack of afferent renal sensory reinnervation. However, afferent sensory reinnervation of any organ, including the kidney, is an understudied question. Therefore, we analyzed the time course of sympathetic and sensory reinnervation at multiple time points (1, 4, and 5 days and 1, 2, 3, 4, 6, 9, and 12 wk) after renal denervation in normal Sprague-Dawley rats. Sympathetic and sensory innervation in the innervated and contralateral denervated kidney was determined as optical density (ImageJ) of the sympathetic and sensory nerves identified by immunohistochemistry using antibodies against markers for sympathetic nerves [neuropeptide Y (NPY) and tyrosine hydroxylase (TH)] and sensory nerves [substance P and calcitonin gene-related peptide (CGRP)]. In denervated kidneys, the optical density of NPY-immunoreactive (ir) fibers in the renal cortex and substance P-ir fibers in the pelvic wall was 6, 39, and 100% and 8, 47, and 100%, respectively, of that in the contralateral innervated kidney at 4 days, 4 wk, and 12 wk after denervation. Linear regression analysis of the optical density of the ratio of the denervated/innervated kidney versus time yielded similar intercept and slope values for NPY-ir, TH-ir, substance P-ir, and CGRP-ir fibers (all R(2) > 0.76). In conclusion, in normotensive rats, reinnervation of the renal sensory nerves occurs over the same time course as reinnervation of the renal sympathetic nerves, both being complete at 9 to 12 wk following renal denervation. |
doi_str_mv | 10.1152/ajpregu.00599.2012 |
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Therefore, the long-term reduction in arterial pressure following renal denervation in drug-resistant hypertensive patients has been attributed to lack of afferent renal sensory reinnervation. However, afferent sensory reinnervation of any organ, including the kidney, is an understudied question. Therefore, we analyzed the time course of sympathetic and sensory reinnervation at multiple time points (1, 4, and 5 days and 1, 2, 3, 4, 6, 9, and 12 wk) after renal denervation in normal Sprague-Dawley rats. Sympathetic and sensory innervation in the innervated and contralateral denervated kidney was determined as optical density (ImageJ) of the sympathetic and sensory nerves identified by immunohistochemistry using antibodies against markers for sympathetic nerves [neuropeptide Y (NPY) and tyrosine hydroxylase (TH)] and sensory nerves [substance P and calcitonin gene-related peptide (CGRP)]. In denervated kidneys, the optical density of NPY-immunoreactive (ir) fibers in the renal cortex and substance P-ir fibers in the pelvic wall was 6, 39, and 100% and 8, 47, and 100%, respectively, of that in the contralateral innervated kidney at 4 days, 4 wk, and 12 wk after denervation. Linear regression analysis of the optical density of the ratio of the denervated/innervated kidney versus time yielded similar intercept and slope values for NPY-ir, TH-ir, substance P-ir, and CGRP-ir fibers (all R(2) > 0.76). In conclusion, in normotensive rats, reinnervation of the renal sensory nerves occurs over the same time course as reinnervation of the renal sympathetic nerves, both being complete at 9 to 12 wk following renal denervation.</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00599.2012</identifier><identifier>PMID: 23408032</identifier><identifier>CODEN: AJPRDO</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Calcitonin Gene-Related Peptide - metabolism ; Cardiovascular and Renal Integration ; Denervation ; Image Processing, Computer-Assisted ; Immunoglobulins ; Immunohistochemistry ; Intubation ; Kidney - innervation ; Kidney Pelvis - innervation ; Kidney Pelvis - physiology ; Kidneys ; Male ; Nerve Regeneration - physiology ; Neural Control ; Neuropeptide Y - metabolism ; Physiology ; Rats ; Rats, Sprague-Dawley ; Regression Analysis ; Rodents ; Sensory Receptor Cells - physiology ; Substance P - metabolism ; Sympathectomy ; Sympathetic Nervous System - physiology ; Tyrosine 3-Monooxygenase - metabolism</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2013-04, Vol.304 (8), p.R675-R682</ispartof><rights>Copyright American Physiological Society Apr 15, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c534t-4ce01eecce7f41a2695795855670f7dcd2060845c5d770943aae55d656973be73</citedby><cites>FETCH-LOGICAL-c534t-4ce01eecce7f41a2695795855670f7dcd2060845c5d770943aae55d656973be73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,550,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23408032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:126549108$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Mulder, Jan</creatorcontrib><creatorcontrib>Hökfelt, Tomas</creatorcontrib><creatorcontrib>Knuepfer, Mark M</creatorcontrib><creatorcontrib>Kopp, Ulla C</creatorcontrib><title>Renal sensory and sympathetic nerves reinnervate the kidney in a similar time-dependent fashion after renal denervation in rats</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>Efferent renal sympathetic nerves reinnervate the kidney after renal denervation in animals and humans. Therefore, the long-term reduction in arterial pressure following renal denervation in drug-resistant hypertensive patients has been attributed to lack of afferent renal sensory reinnervation. However, afferent sensory reinnervation of any organ, including the kidney, is an understudied question. Therefore, we analyzed the time course of sympathetic and sensory reinnervation at multiple time points (1, 4, and 5 days and 1, 2, 3, 4, 6, 9, and 12 wk) after renal denervation in normal Sprague-Dawley rats. Sympathetic and sensory innervation in the innervated and contralateral denervated kidney was determined as optical density (ImageJ) of the sympathetic and sensory nerves identified by immunohistochemistry using antibodies against markers for sympathetic nerves [neuropeptide Y (NPY) and tyrosine hydroxylase (TH)] and sensory nerves [substance P and calcitonin gene-related peptide (CGRP)]. In denervated kidneys, the optical density of NPY-immunoreactive (ir) fibers in the renal cortex and substance P-ir fibers in the pelvic wall was 6, 39, and 100% and 8, 47, and 100%, respectively, of that in the contralateral innervated kidney at 4 days, 4 wk, and 12 wk after denervation. Linear regression analysis of the optical density of the ratio of the denervated/innervated kidney versus time yielded similar intercept and slope values for NPY-ir, TH-ir, substance P-ir, and CGRP-ir fibers (all R(2) > 0.76). In conclusion, in normotensive rats, reinnervation of the renal sensory nerves occurs over the same time course as reinnervation of the renal sympathetic nerves, both being complete at 9 to 12 wk following renal denervation.</description><subject>Animals</subject><subject>Calcitonin Gene-Related Peptide - metabolism</subject><subject>Cardiovascular and Renal Integration</subject><subject>Denervation</subject><subject>Image Processing, Computer-Assisted</subject><subject>Immunoglobulins</subject><subject>Immunohistochemistry</subject><subject>Intubation</subject><subject>Kidney - innervation</subject><subject>Kidney Pelvis - innervation</subject><subject>Kidney Pelvis - physiology</subject><subject>Kidneys</subject><subject>Male</subject><subject>Nerve Regeneration - physiology</subject><subject>Neural Control</subject><subject>Neuropeptide Y - metabolism</subject><subject>Physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regression Analysis</subject><subject>Rodents</subject><subject>Sensory Receptor Cells - physiology</subject><subject>Substance P - metabolism</subject><subject>Sympathectomy</subject><subject>Sympathetic Nervous System - physiology</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNpdkkuLFDEUhYMoTjv6B1xIwI2bavOuykaQwRcMCKLrkEluTaenKlUmqZFe-ddNTbeD4yqXnO-e3BsOQi8p2VIq2Vu7nxNcL1tCpNZbRih7hDZVYA0VmjxGG8IVbxSl-gw9y3lPCBFc8KfojHFBOsLZBv3-BtEOOEPMUzpgGz3Oh3G2ZQclOBwh3ULGCUJcS1sAVwXfBB_hgEPEFucwhsEmXMIIjYcZoodYcG_zLkwV6AukarC-UoU7k_W-9iZb8nP0pLdDhhen8xz9-Pjh-8Xn5vLrpy8X7y8bJ7kojXBAKIBz0PaCWqa0bLXspFQt6VvvPCOKdEI66duWaMGtBSm9kkq3_Apafo6ao2_-BfNyZeYURpsOZrLBnK5uagVGciqorvy7I1-VEbyrKyU7PGh7qMSwM9fTreGK1clINXhzMkjTzwVyMWPIDobBRpiWbChnHWOKdryir_9D99OS6ocdKcGl7mSl2JFyaco5QX8_DCVmzYM55cHc5cGseahNr_5d477lbwD4H2H3thw</recordid><startdate>20130415</startdate><enddate>20130415</enddate><creator>Mulder, Jan</creator><creator>Hökfelt, Tomas</creator><creator>Knuepfer, Mark M</creator><creator>Kopp, Ulla C</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><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20130415</creationdate><title>Renal sensory and sympathetic nerves reinnervate the kidney in a similar time-dependent fashion after renal denervation in rats</title><author>Mulder, Jan ; Hökfelt, Tomas ; Knuepfer, Mark M ; Kopp, Ulla C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-4ce01eecce7f41a2695795855670f7dcd2060845c5d770943aae55d656973be73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Calcitonin Gene-Related Peptide - metabolism</topic><topic>Cardiovascular and Renal Integration</topic><topic>Denervation</topic><topic>Image Processing, Computer-Assisted</topic><topic>Immunoglobulins</topic><topic>Immunohistochemistry</topic><topic>Intubation</topic><topic>Kidney - innervation</topic><topic>Kidney Pelvis - innervation</topic><topic>Kidney Pelvis - physiology</topic><topic>Kidneys</topic><topic>Male</topic><topic>Nerve Regeneration - physiology</topic><topic>Neural Control</topic><topic>Neuropeptide Y - metabolism</topic><topic>Physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regression Analysis</topic><topic>Rodents</topic><topic>Sensory Receptor Cells - physiology</topic><topic>Substance P - metabolism</topic><topic>Sympathectomy</topic><topic>Sympathetic Nervous System - physiology</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mulder, Jan</creatorcontrib><creatorcontrib>Hökfelt, Tomas</creatorcontrib><creatorcontrib>Knuepfer, Mark M</creatorcontrib><creatorcontrib>Kopp, Ulla C</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><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mulder, Jan</au><au>Hökfelt, Tomas</au><au>Knuepfer, Mark M</au><au>Kopp, Ulla C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Renal sensory and sympathetic nerves reinnervate the kidney in a similar time-dependent fashion after renal denervation in rats</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2013-04-15</date><risdate>2013</risdate><volume>304</volume><issue>8</issue><spage>R675</spage><epage>R682</epage><pages>R675-R682</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><coden>AJPRDO</coden><abstract>Efferent renal sympathetic nerves reinnervate the kidney after renal denervation in animals and humans. Therefore, the long-term reduction in arterial pressure following renal denervation in drug-resistant hypertensive patients has been attributed to lack of afferent renal sensory reinnervation. However, afferent sensory reinnervation of any organ, including the kidney, is an understudied question. Therefore, we analyzed the time course of sympathetic and sensory reinnervation at multiple time points (1, 4, and 5 days and 1, 2, 3, 4, 6, 9, and 12 wk) after renal denervation in normal Sprague-Dawley rats. Sympathetic and sensory innervation in the innervated and contralateral denervated kidney was determined as optical density (ImageJ) of the sympathetic and sensory nerves identified by immunohistochemistry using antibodies against markers for sympathetic nerves [neuropeptide Y (NPY) and tyrosine hydroxylase (TH)] and sensory nerves [substance P and calcitonin gene-related peptide (CGRP)]. In denervated kidneys, the optical density of NPY-immunoreactive (ir) fibers in the renal cortex and substance P-ir fibers in the pelvic wall was 6, 39, and 100% and 8, 47, and 100%, respectively, of that in the contralateral innervated kidney at 4 days, 4 wk, and 12 wk after denervation. Linear regression analysis of the optical density of the ratio of the denervated/innervated kidney versus time yielded similar intercept and slope values for NPY-ir, TH-ir, substance P-ir, and CGRP-ir fibers (all R(2) > 0.76). In conclusion, in normotensive rats, reinnervation of the renal sensory nerves occurs over the same time course as reinnervation of the renal sympathetic nerves, both being complete at 9 to 12 wk following renal denervation.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>23408032</pmid><doi>10.1152/ajpregu.00599.2012</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Calcitonin Gene-Related Peptide - metabolism Cardiovascular and Renal Integration Denervation Image Processing, Computer-Assisted Immunoglobulins Immunohistochemistry Intubation Kidney - innervation Kidney Pelvis - innervation Kidney Pelvis - physiology Kidneys Male Nerve Regeneration - physiology Neural Control Neuropeptide Y - metabolism Physiology Rats Rats, Sprague-Dawley Regression Analysis Rodents Sensory Receptor Cells - physiology Substance P - metabolism Sympathectomy Sympathetic Nervous System - physiology Tyrosine 3-Monooxygenase - metabolism |
title | Renal sensory and sympathetic nerves reinnervate the kidney in a similar time-dependent fashion after renal denervation in rats |
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