Effects of Isoflurane on Cardiovascular System and Sympathovagal Balance in New Zealand White Rabbits

SUMMARYWe investigated the effects of isoflurane on the rabbit cardiovascular system at several end-tidal concentrations. Furthermore, because isoflurane has been reported to produce tachycardia while reducing sympathetic nervous activity and baroreflex function, we evaluated whether the chronotropi...

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Veröffentlicht in:Journal of cardiovascular pharmacology 1996-10, Vol.28 (4), p.513-518
Hauptverfasser: Marano, Giuseppe, Grigioni, Mauro, Tiburzi, Florindo, Vergari, Alessandro, Zanghi, Filippo
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container_end_page 518
container_issue 4
container_start_page 513
container_title Journal of cardiovascular pharmacology
container_volume 28
creator Marano, Giuseppe
Grigioni, Mauro
Tiburzi, Florindo
Vergari, Alessandro
Zanghi, Filippo
description SUMMARYWe investigated the effects of isoflurane on the rabbit cardiovascular system at several end-tidal concentrations. Furthermore, because isoflurane has been reported to produce tachycardia while reducing sympathetic nervous activity and baroreflex function, we evaluated whether the chronotropic effects of isoflurane could be due to a vagal withdrawal. ECG, mean arterial pressure (MAP), and heart rate (HR) were obtained in rabbits the conscious, unsedated state and during isoflurane anesthesia by telemetric device. Measurements of pH, oxygen, carbon dioxide, plasma catecholamines, baroreflex sensitivity, and spectral analysis of HR variability were made in nonanesthetized and anesthetized animals. Isoflurane caused an increase in HR at 0.5, 1, and 1.5 minimum alveolar concentration (MAC) and a decrease in systolic and diastolic blood pressure (SBP, DBP) and MAP at 1 and 1.5 MAC. Biochemical analysis showed that isoflurane-mediated cardiovascular effects were not accompanied by any significant changes in plasma norepinephrine (NE) and epinephrine (Epi) levels. Neither were any significant differences in plasma catecholamine levels noted between anesthetized and awake animals. The analysis of spectral components of HR variability and baroreflex function indicated that isoflurane induced a marked reduction in the low- and high-frequency spectral power of HR variability and in baroreflex sensitivity. Tachycardia under isoflurane was suppressed dose dependently by the administration of clonidine or atenolol and was not influenced by bilateral vagotomy. Collectively, our results indicate that cardiovascular effects induced by isoflurane in smaller animals such as rabbits are similar to those observed in humans and other animal species. We showed that isoflurane-induced tachycardia is mainly the result of a vagal withdrawal rather than a baroreflex response, even though a marginal role of baroreflex in heart response to higher concentrations of isoflurane cannot be excluded.
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Furthermore, because isoflurane has been reported to produce tachycardia while reducing sympathetic nervous activity and baroreflex function, we evaluated whether the chronotropic effects of isoflurane could be due to a vagal withdrawal. ECG, mean arterial pressure (MAP), and heart rate (HR) were obtained in rabbits the conscious, unsedated state and during isoflurane anesthesia by telemetric device. Measurements of pH, oxygen, carbon dioxide, plasma catecholamines, baroreflex sensitivity, and spectral analysis of HR variability were made in nonanesthetized and anesthetized animals. Isoflurane caused an increase in HR at 0.5, 1, and 1.5 minimum alveolar concentration (MAC) and a decrease in systolic and diastolic blood pressure (SBP, DBP) and MAP at 1 and 1.5 MAC. Biochemical analysis showed that isoflurane-mediated cardiovascular effects were not accompanied by any significant changes in plasma norepinephrine (NE) and epinephrine (Epi) levels. Neither were any significant differences in plasma catecholamine levels noted between anesthetized and awake animals. The analysis of spectral components of HR variability and baroreflex function indicated that isoflurane induced a marked reduction in the low- and high-frequency spectral power of HR variability and in baroreflex sensitivity. Tachycardia under isoflurane was suppressed dose dependently by the administration of clonidine or atenolol and was not influenced by bilateral vagotomy. Collectively, our results indicate that cardiovascular effects induced by isoflurane in smaller animals such as rabbits are similar to those observed in humans and other animal species. 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Furthermore, because isoflurane has been reported to produce tachycardia while reducing sympathetic nervous activity and baroreflex function, we evaluated whether the chronotropic effects of isoflurane could be due to a vagal withdrawal. ECG, mean arterial pressure (MAP), and heart rate (HR) were obtained in rabbits the conscious, unsedated state and during isoflurane anesthesia by telemetric device. Measurements of pH, oxygen, carbon dioxide, plasma catecholamines, baroreflex sensitivity, and spectral analysis of HR variability were made in nonanesthetized and anesthetized animals. Isoflurane caused an increase in HR at 0.5, 1, and 1.5 minimum alveolar concentration (MAC) and a decrease in systolic and diastolic blood pressure (SBP, DBP) and MAP at 1 and 1.5 MAC. Biochemical analysis showed that isoflurane-mediated cardiovascular effects were not accompanied by any significant changes in plasma norepinephrine (NE) and epinephrine (Epi) levels. Neither were any significant differences in plasma catecholamine levels noted between anesthetized and awake animals. The analysis of spectral components of HR variability and baroreflex function indicated that isoflurane induced a marked reduction in the low- and high-frequency spectral power of HR variability and in baroreflex sensitivity. Tachycardia under isoflurane was suppressed dose dependently by the administration of clonidine or atenolol and was not influenced by bilateral vagotomy. Collectively, our results indicate that cardiovascular effects induced by isoflurane in smaller animals such as rabbits are similar to those observed in humans and other animal species. 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Neuromuscular blocking agents</subject><subject>Animals</subject><subject>Atenolol - pharmacology</subject><subject>Baroreflex - drug effects</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiovascular Physiological Phenomena</subject><subject>Cardiovascular System - drug effects</subject><subject>Clonidine - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epinephrine - blood</subject><subject>Heart Rate - drug effects</subject><subject>Isoflurane - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Norepinephrine - blood</subject><subject>Pharmacology. Drug treatments</subject><subject>Rabbits</subject><subject>Sympathetic Nervous System - drug effects</subject><subject>Tachycardia - chemically induced</subject><subject>Tachycardia - physiopathology</subject><subject>Vagotomy</subject><subject>Vagus Nerve - drug effects</subject><issn>0160-2446</issn><issn>1533-4023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kV1PwyAUhonRzDn9CSZceFuF8lG41GXqkkUTP2LiTUPpwVW7doHWZf9e5ubu5OLA4X1fcvKAEKbkkhKdXZG4BOM8oVpLuumSTZEHaEgFYwknKTtEQ0IlSVLO5TE6CeGTEMpFJgdooJSmKhNDBBPnwHYBtw5PQ-vq3psGcNvgsfFl1X6bYPvaePy8Dh0ssGnKeFwsTTeP2oep8Y2pTWMBVw1-gBV-h01f4rd51QF-MkVRdeEUHTlTBzjb7SP0ejt5Gd8ns8e76fh6llgRh0-MUMQ5TqBQUvKsAM2UK4VMMxCCWMaE1lxZCZJLroTQhcxAO5A6LbW1jo2Q2r5rfRuCB5cvfbUwfp1Tkm_A5X_g8j243ysZo-fb6LIvFlDugztSUb_Y6ZGIqV3EZKuwt7E0VSzj0ca3tlVbd-DDV92vwOfzSKWb5_99G_sBAPGE8Q</recordid><startdate>199610</startdate><enddate>199610</enddate><creator>Marano, Giuseppe</creator><creator>Grigioni, Mauro</creator><creator>Tiburzi, Florindo</creator><creator>Vergari, Alessandro</creator><creator>Zanghi, Filippo</creator><general>Lippincott-Raven Publishers</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199610</creationdate><title>Effects of Isoflurane on Cardiovascular System and Sympathovagal Balance in New Zealand White Rabbits</title><author>Marano, Giuseppe ; Grigioni, Mauro ; Tiburzi, Florindo ; Vergari, Alessandro ; Zanghi, Filippo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5006-a580ff40eb86647be938fd5627e550c3359948c6e64648559b67e9fe692d9ccf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Anesthetics, Inhalation - pharmacology</topic><topic>Anesthetics. Neuromuscular blocking agents</topic><topic>Animals</topic><topic>Atenolol - pharmacology</topic><topic>Baroreflex - drug effects</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiovascular Physiological Phenomena</topic><topic>Cardiovascular System - drug effects</topic><topic>Clonidine - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epinephrine - blood</topic><topic>Heart Rate - drug effects</topic><topic>Isoflurane - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Norepinephrine - blood</topic><topic>Pharmacology. Drug treatments</topic><topic>Rabbits</topic><topic>Sympathetic Nervous System - drug effects</topic><topic>Tachycardia - chemically induced</topic><topic>Tachycardia - physiopathology</topic><topic>Vagotomy</topic><topic>Vagus Nerve - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marano, Giuseppe</creatorcontrib><creatorcontrib>Grigioni, Mauro</creatorcontrib><creatorcontrib>Tiburzi, Florindo</creatorcontrib><creatorcontrib>Vergari, Alessandro</creatorcontrib><creatorcontrib>Zanghi, Filippo</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of cardiovascular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marano, Giuseppe</au><au>Grigioni, Mauro</au><au>Tiburzi, Florindo</au><au>Vergari, Alessandro</au><au>Zanghi, Filippo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Isoflurane on Cardiovascular System and Sympathovagal Balance in New Zealand White Rabbits</atitle><jtitle>Journal of cardiovascular pharmacology</jtitle><addtitle>J Cardiovasc Pharmacol</addtitle><date>1996-10</date><risdate>1996</risdate><volume>28</volume><issue>4</issue><spage>513</spage><epage>518</epage><pages>513-518</pages><issn>0160-2446</issn><eissn>1533-4023</eissn><coden>JCPCDT</coden><abstract>SUMMARYWe investigated the effects of isoflurane on the rabbit cardiovascular system at several end-tidal concentrations. Furthermore, because isoflurane has been reported to produce tachycardia while reducing sympathetic nervous activity and baroreflex function, we evaluated whether the chronotropic effects of isoflurane could be due to a vagal withdrawal. ECG, mean arterial pressure (MAP), and heart rate (HR) were obtained in rabbits the conscious, unsedated state and during isoflurane anesthesia by telemetric device. Measurements of pH, oxygen, carbon dioxide, plasma catecholamines, baroreflex sensitivity, and spectral analysis of HR variability were made in nonanesthetized and anesthetized animals. Isoflurane caused an increase in HR at 0.5, 1, and 1.5 minimum alveolar concentration (MAC) and a decrease in systolic and diastolic blood pressure (SBP, DBP) and MAP at 1 and 1.5 MAC. Biochemical analysis showed that isoflurane-mediated cardiovascular effects were not accompanied by any significant changes in plasma norepinephrine (NE) and epinephrine (Epi) levels. Neither were any significant differences in plasma catecholamine levels noted between anesthetized and awake animals. The analysis of spectral components of HR variability and baroreflex function indicated that isoflurane induced a marked reduction in the low- and high-frequency spectral power of HR variability and in baroreflex sensitivity. Tachycardia under isoflurane was suppressed dose dependently by the administration of clonidine or atenolol and was not influenced by bilateral vagotomy. Collectively, our results indicate that cardiovascular effects induced by isoflurane in smaller animals such as rabbits are similar to those observed in humans and other animal species. We showed that isoflurane-induced tachycardia is mainly the result of a vagal withdrawal rather than a baroreflex response, even though a marginal role of baroreflex in heart response to higher concentrations of isoflurane cannot be excluded.</abstract><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>8891875</pmid><doi>10.1097/00005344-199610000-00006</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Journals@Ovid LWW Legacy Archive; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete
subjects Anesthetics, Inhalation - pharmacology
Anesthetics. Neuromuscular blocking agents
Animals
Atenolol - pharmacology
Baroreflex - drug effects
Biological and medical sciences
Blood Pressure - drug effects
Cardiovascular Physiological Phenomena
Cardiovascular System - drug effects
Clonidine - pharmacology
Dose-Response Relationship, Drug
Epinephrine - blood
Heart Rate - drug effects
Isoflurane - pharmacology
Male
Medical sciences
Neuropharmacology
Norepinephrine - blood
Pharmacology. Drug treatments
Rabbits
Sympathetic Nervous System - drug effects
Tachycardia - chemically induced
Tachycardia - physiopathology
Vagotomy
Vagus Nerve - drug effects
title Effects of Isoflurane on Cardiovascular System and Sympathovagal Balance in New Zealand White Rabbits
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