Heart rate-arterial blood pressure relationship in conscious rat before vs. after spinal cord transection
1 Departments of Biology, and Chemistry and Physics, Asbury College, Wilmore 40390-1198; 2 Department of Physiology, University of Kentucky College of Medicine, Lexington 40536-0298; 3 Center for Biomedical Engineering, Wenner-Gren Laboratory, University of Kentucky, Lexington 40506-0070; 4 Card...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2002-09, Vol.283 (3), p.748-R756 |
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container_title | American journal of physiology. Regulatory, integrative and comparative physiology |
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creator | Baldridge, Bobby R Burgess, Don E Zimmerman, Ethan E Carroll, Jonathan J Sprinkle, Aletia G Speakman, Richard O Li, Sheng-Gang Brown, David R Taylor, Robert F Dworkin, Susan Randall, David C |
description | 1 Departments of Biology, and Chemistry and Physics,
Asbury College, Wilmore 40390-1198; 2 Department of
Physiology, University of Kentucky College of Medicine, Lexington
40536-0298; 3 Center for Biomedical Engineering,
Wenner-Gren Laboratory, University of Kentucky, Lexington
40506-0070; 4 Cardinal Hill Rehabilitation Hospital,
Lexington, Kentucky 40504; and 5 Department of
Behavioral Science, Pennsylvania State University College of
Medicine, Hershey, Pennsylvania 17033
This experiment quantified the
initial disruption and subsequent adaptation of the blood pressure
(BP)-heart rate (HR) relationship after spinal cord transection (SCT).
BP and HR were recorded for 4 h via an implanted catheter in
neurally intact, unanesthetized rats. The animals were then
anesthetized, and their spinal cords were severed at
T 1 -T 2 ( n = 5) or
T 4 -T 5 ( n = 6) or sham
lesioned ( n = 4). BP was recorded for 4 h daily
over the ensuing 6 days. The neurally intact rat showed a positive
cross correlation, with HR leading BP at the peak by 1.8 ± 0.8 (SD) s. The cross correlation in unanesthetized rats ( n = 2) under neuromuscular blockade was also positive, with HR leading.
After SCT at T 1 -T 2 , the cross correlation
became negative, with BP leading HR, and did not change during the next
6 days. The cross correlation also became negative 1-3 days after
SCT at T 4 -T 5 , but in four rats by
day 6 and thereafter the cross correlation progressively
reverted to a positive value. We propose that the positive cross
correlation with HR leading BP in the intact rat results from an
open-loop control that depends on intact supraspinal input to
sympathetic preganglionic neurons in the spinal cord. After descending
sympathetic pathways were severed at
T 1 -T 2 , the intact vagal pathway to the
sinoatrial node dominated BP regulation via the baroreflex. We suggest
that reestablishment of the positive correlation after SCT at
T 4 -T 5 was attributable to the surviving
sympathetic outflow to the heart and upper vasculature reasserting some
effective function, perhaps in association with decreased spinal
sympathetic hyperreflexia. The HR-BP cross correlation may index
progression of sympathetic dysfunction in pathological processes.
sympathetic; parasympathetic; dysautonomia; cross correlation; baroreflex |
doi_str_mv | 10.1152/ajpregu.00003.2002 |
format | Article |
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Asbury College, Wilmore 40390-1198; 2 Department of
Physiology, University of Kentucky College of Medicine, Lexington
40536-0298; 3 Center for Biomedical Engineering,
Wenner-Gren Laboratory, University of Kentucky, Lexington
40506-0070; 4 Cardinal Hill Rehabilitation Hospital,
Lexington, Kentucky 40504; and 5 Department of
Behavioral Science, Pennsylvania State University College of
Medicine, Hershey, Pennsylvania 17033
This experiment quantified the
initial disruption and subsequent adaptation of the blood pressure
(BP)-heart rate (HR) relationship after spinal cord transection (SCT).
BP and HR were recorded for 4 h via an implanted catheter in
neurally intact, unanesthetized rats. The animals were then
anesthetized, and their spinal cords were severed at
T 1 -T 2 ( n = 5) or
T 4 -T 5 ( n = 6) or sham
lesioned ( n = 4). BP was recorded for 4 h daily
over the ensuing 6 days. The neurally intact rat showed a positive
cross correlation, with HR leading BP at the peak by 1.8 ± 0.8 (SD) s. The cross correlation in unanesthetized rats ( n = 2) under neuromuscular blockade was also positive, with HR leading.
After SCT at T 1 -T 2 , the cross correlation
became negative, with BP leading HR, and did not change during the next
6 days. The cross correlation also became negative 1-3 days after
SCT at T 4 -T 5 , but in four rats by
day 6 and thereafter the cross correlation progressively
reverted to a positive value. We propose that the positive cross
correlation with HR leading BP in the intact rat results from an
open-loop control that depends on intact supraspinal input to
sympathetic preganglionic neurons in the spinal cord. After descending
sympathetic pathways were severed at
T 1 -T 2 , the intact vagal pathway to the
sinoatrial node dominated BP regulation via the baroreflex. We suggest
that reestablishment of the positive correlation after SCT at
T 4 -T 5 was attributable to the surviving
sympathetic outflow to the heart and upper vasculature reasserting some
effective function, perhaps in association with decreased spinal
sympathetic hyperreflexia. The HR-BP cross correlation may index
progression of sympathetic dysfunction in pathological processes.
sympathetic; parasympathetic; dysautonomia; cross correlation; baroreflex</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00003.2002</identifier><identifier>PMID: 12185010</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Baroreflex - physiology ; Blood Pressure - physiology ; Consciousness ; Heart Rate - physiology ; Parasympathetic Nervous System - physiology ; Rats ; Rats, Sprague-Dawley ; Spinal Cord Injuries - physiopathology ; Sympathetic Nervous System - physiology</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2002-09, Vol.283 (3), p.748-R756</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-e5fa4b1194f85dd8fb8f95a3ac28c2d193b3d02f6762622a824ed072341a6f9e3</citedby><cites>FETCH-LOGICAL-c387t-e5fa4b1194f85dd8fb8f95a3ac28c2d193b3d02f6762622a824ed072341a6f9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12185010$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baldridge, Bobby R</creatorcontrib><creatorcontrib>Burgess, Don E</creatorcontrib><creatorcontrib>Zimmerman, Ethan E</creatorcontrib><creatorcontrib>Carroll, Jonathan J</creatorcontrib><creatorcontrib>Sprinkle, Aletia G</creatorcontrib><creatorcontrib>Speakman, Richard O</creatorcontrib><creatorcontrib>Li, Sheng-Gang</creatorcontrib><creatorcontrib>Brown, David R</creatorcontrib><creatorcontrib>Taylor, Robert F</creatorcontrib><creatorcontrib>Dworkin, Susan</creatorcontrib><creatorcontrib>Randall, David C</creatorcontrib><title>Heart rate-arterial blood pressure relationship in conscious rat before vs. after spinal cord transection</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>1 Departments of Biology, and Chemistry and Physics,
Asbury College, Wilmore 40390-1198; 2 Department of
Physiology, University of Kentucky College of Medicine, Lexington
40536-0298; 3 Center for Biomedical Engineering,
Wenner-Gren Laboratory, University of Kentucky, Lexington
40506-0070; 4 Cardinal Hill Rehabilitation Hospital,
Lexington, Kentucky 40504; and 5 Department of
Behavioral Science, Pennsylvania State University College of
Medicine, Hershey, Pennsylvania 17033
This experiment quantified the
initial disruption and subsequent adaptation of the blood pressure
(BP)-heart rate (HR) relationship after spinal cord transection (SCT).
BP and HR were recorded for 4 h via an implanted catheter in
neurally intact, unanesthetized rats. The animals were then
anesthetized, and their spinal cords were severed at
T 1 -T 2 ( n = 5) or
T 4 -T 5 ( n = 6) or sham
lesioned ( n = 4). BP was recorded for 4 h daily
over the ensuing 6 days. The neurally intact rat showed a positive
cross correlation, with HR leading BP at the peak by 1.8 ± 0.8 (SD) s. The cross correlation in unanesthetized rats ( n = 2) under neuromuscular blockade was also positive, with HR leading.
After SCT at T 1 -T 2 , the cross correlation
became negative, with BP leading HR, and did not change during the next
6 days. The cross correlation also became negative 1-3 days after
SCT at T 4 -T 5 , but in four rats by
day 6 and thereafter the cross correlation progressively
reverted to a positive value. We propose that the positive cross
correlation with HR leading BP in the intact rat results from an
open-loop control that depends on intact supraspinal input to
sympathetic preganglionic neurons in the spinal cord. After descending
sympathetic pathways were severed at
T 1 -T 2 , the intact vagal pathway to the
sinoatrial node dominated BP regulation via the baroreflex. We suggest
that reestablishment of the positive correlation after SCT at
T 4 -T 5 was attributable to the surviving
sympathetic outflow to the heart and upper vasculature reasserting some
effective function, perhaps in association with decreased spinal
sympathetic hyperreflexia. The HR-BP cross correlation may index
progression of sympathetic dysfunction in pathological processes.
sympathetic; parasympathetic; dysautonomia; cross correlation; baroreflex</description><subject>Animals</subject><subject>Baroreflex - physiology</subject><subject>Blood Pressure - physiology</subject><subject>Consciousness</subject><subject>Heart Rate - physiology</subject><subject>Parasympathetic Nervous System - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Spinal Cord Injuries - physiopathology</subject><subject>Sympathetic Nervous System - physiology</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1qGzEUhUVoSRy3L5BF0Cq7mepnfjTLYpK6EAiUdC000pWtII-m0kwSv33l2iaraqML93wfl4PQDSUlpTX7pl7GCJu5JPnxkhHCLtAiL1hBq458QgvCG140lHZX6DqllxyreMUv0RVlVNSEkgVya1BxwlFNUOQBolMe9z4Eg7M8pTkCjuDV5MKQtm7EbsA6j9qFOR0w3IMNOfSaSqxsFuA0uiFLdIgGT1ENCfSB_oI-W-UTfD39S_T74f55tS4en378XH1_LDQX7VRAbVXV55srK2pjhO2F7WrFlWZCM0M73nNDmG3ahjWMKcEqMKRlvKKqsR3wJbo7escY_syQJrlzSYP3aoB8s2wZoZw3XQ6yY1DHkFIEK8fodiruJSXyULA8FSz_FSwPBWfo9mSf-x2YD-TUaA50x8DWbbZvLoIct_vkgg-bvXyYvX-G9-lsZoJLLn-1lZCjsZkt_s-ej_lg-F-ALZ-D</recordid><startdate>20020901</startdate><enddate>20020901</enddate><creator>Baldridge, Bobby R</creator><creator>Burgess, Don E</creator><creator>Zimmerman, Ethan E</creator><creator>Carroll, Jonathan J</creator><creator>Sprinkle, Aletia G</creator><creator>Speakman, Richard O</creator><creator>Li, Sheng-Gang</creator><creator>Brown, David R</creator><creator>Taylor, Robert F</creator><creator>Dworkin, Susan</creator><creator>Randall, David C</creator><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>7X8</scope></search><sort><creationdate>20020901</creationdate><title>Heart rate-arterial blood pressure relationship in conscious rat before vs. after spinal cord transection</title><author>Baldridge, Bobby R ; Burgess, Don E ; Zimmerman, Ethan E ; Carroll, Jonathan J ; Sprinkle, Aletia G ; Speakman, Richard O ; Li, Sheng-Gang ; Brown, David R ; Taylor, Robert F ; Dworkin, Susan ; Randall, David C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-e5fa4b1194f85dd8fb8f95a3ac28c2d193b3d02f6762622a824ed072341a6f9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Baroreflex - physiology</topic><topic>Blood Pressure - physiology</topic><topic>Consciousness</topic><topic>Heart Rate - physiology</topic><topic>Parasympathetic Nervous System - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Spinal Cord Injuries - physiopathology</topic><topic>Sympathetic Nervous System - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baldridge, Bobby R</creatorcontrib><creatorcontrib>Burgess, Don E</creatorcontrib><creatorcontrib>Zimmerman, Ethan E</creatorcontrib><creatorcontrib>Carroll, Jonathan J</creatorcontrib><creatorcontrib>Sprinkle, Aletia G</creatorcontrib><creatorcontrib>Speakman, Richard O</creatorcontrib><creatorcontrib>Li, Sheng-Gang</creatorcontrib><creatorcontrib>Brown, David R</creatorcontrib><creatorcontrib>Taylor, Robert F</creatorcontrib><creatorcontrib>Dworkin, Susan</creatorcontrib><creatorcontrib>Randall, David 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>MEDLINE - Academic</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>Baldridge, Bobby R</au><au>Burgess, Don E</au><au>Zimmerman, Ethan E</au><au>Carroll, Jonathan J</au><au>Sprinkle, Aletia G</au><au>Speakman, Richard O</au><au>Li, Sheng-Gang</au><au>Brown, David R</au><au>Taylor, Robert F</au><au>Dworkin, Susan</au><au>Randall, David C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heart rate-arterial blood pressure relationship in conscious rat before vs. after spinal cord transection</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2002-09-01</date><risdate>2002</risdate><volume>283</volume><issue>3</issue><spage>748</spage><epage>R756</epage><pages>748-R756</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><abstract>1 Departments of Biology, and Chemistry and Physics,
Asbury College, Wilmore 40390-1198; 2 Department of
Physiology, University of Kentucky College of Medicine, Lexington
40536-0298; 3 Center for Biomedical Engineering,
Wenner-Gren Laboratory, University of Kentucky, Lexington
40506-0070; 4 Cardinal Hill Rehabilitation Hospital,
Lexington, Kentucky 40504; and 5 Department of
Behavioral Science, Pennsylvania State University College of
Medicine, Hershey, Pennsylvania 17033
This experiment quantified the
initial disruption and subsequent adaptation of the blood pressure
(BP)-heart rate (HR) relationship after spinal cord transection (SCT).
BP and HR were recorded for 4 h via an implanted catheter in
neurally intact, unanesthetized rats. The animals were then
anesthetized, and their spinal cords were severed at
T 1 -T 2 ( n = 5) or
T 4 -T 5 ( n = 6) or sham
lesioned ( n = 4). BP was recorded for 4 h daily
over the ensuing 6 days. The neurally intact rat showed a positive
cross correlation, with HR leading BP at the peak by 1.8 ± 0.8 (SD) s. The cross correlation in unanesthetized rats ( n = 2) under neuromuscular blockade was also positive, with HR leading.
After SCT at T 1 -T 2 , the cross correlation
became negative, with BP leading HR, and did not change during the next
6 days. The cross correlation also became negative 1-3 days after
SCT at T 4 -T 5 , but in four rats by
day 6 and thereafter the cross correlation progressively
reverted to a positive value. We propose that the positive cross
correlation with HR leading BP in the intact rat results from an
open-loop control that depends on intact supraspinal input to
sympathetic preganglionic neurons in the spinal cord. After descending
sympathetic pathways were severed at
T 1 -T 2 , the intact vagal pathway to the
sinoatrial node dominated BP regulation via the baroreflex. We suggest
that reestablishment of the positive correlation after SCT at
T 4 -T 5 was attributable to the surviving
sympathetic outflow to the heart and upper vasculature reasserting some
effective function, perhaps in association with decreased spinal
sympathetic hyperreflexia. The HR-BP cross correlation may index
progression of sympathetic dysfunction in pathological processes.
sympathetic; parasympathetic; dysautonomia; cross correlation; baroreflex</abstract><cop>United States</cop><pmid>12185010</pmid><doi>10.1152/ajpregu.00003.2002</doi></addata></record> |
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source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Baroreflex - physiology Blood Pressure - physiology Consciousness Heart Rate - physiology Parasympathetic Nervous System - physiology Rats Rats, Sprague-Dawley Spinal Cord Injuries - physiopathology Sympathetic Nervous System - physiology |
title | Heart rate-arterial blood pressure relationship in conscious rat before vs. after spinal cord transection |
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