Monitoring of Liver Oxygenation During Neuroleptanalgesia in the Dog

In an animal study (7 mongrel dogs) the effects of neuroleptanalgesia (NLA) and combinations of NLA with nitrous oxide (N2O) and isoflurane on the macro- and microcirculation of the liver were investigated. Measurements were made in three steps. After NLA alone the dogs were supplementarily ventilat...

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Veröffentlicht in:Journal of investigative surgery 1992, Vol.5 (4), p.315-326
Hauptverfasser: Spiegel, Hans-Ullrich, Tschuschke, Christian, Holzgreve, Alfred, Brown, Silas, Brölsch, Christoph E., Hauss, Jan
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container_end_page 326
container_issue 4
container_start_page 315
container_title Journal of investigative surgery
container_volume 5
creator Spiegel, Hans-Ullrich
Tschuschke, Christian
Holzgreve, Alfred
Brown, Silas
Brölsch, Christoph E.
Hauss, Jan
description In an animal study (7 mongrel dogs) the effects of neuroleptanalgesia (NLA) and combinations of NLA with nitrous oxide (N2O) and isoflurane on the macro- and microcirculation of the liver were investigated. Measurements were made in three steps. After NLA alone the dogs were supplementarily ventilated with nitrous oxide/oxygen at a ratio of 2 :1. During the last step, 1 MAC isoflurane was added to the inspired gas. From the portal vein, arterial and mixed-venous systems' hemodynamic parameters, blood gases, and acid-base balance were recorded. As a parameter of oxygenation the tissue PO2 of the liver was measured with a multiwire surface electrode. During NLA stable hemodynamic conditions and a balanced acid-base status were observed. The nitrous oxide combination resulted in an increase of the mean pulmonary artery pressure of 16%. The addition of isoflurane had a negative inotropic effect: The heart index decreased to 74% of the starting value and the total peripheral resistance (TPR) increased by 27%. The summarized PO2 histograms under NLA and NLA/N2O showed arithmetic mean values of 34.1 and 35.2 mm Hg, respectively. The addition of isoflurane resulted in a left shift and a decrease of the mean value to 28.6 mm Hg. This histogram corresponds exactly to the oxygen pressure distribution in the dog liver during piritramide basic anesthesia. It seems that NLA and the combination of NLA/N2O increase the liver perfusion with a higher portal-venous and tissue PO2. This effect can be explained only by a massive change of visceral circulation. It is canceled by the addition of isoflurane.
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Measurements were made in three steps. After NLA alone the dogs were supplementarily ventilated with nitrous oxide/oxygen at a ratio of 2 :1. During the last step, 1 MAC isoflurane was added to the inspired gas. From the portal vein, arterial and mixed-venous systems' hemodynamic parameters, blood gases, and acid-base balance were recorded. As a parameter of oxygenation the tissue PO2 of the liver was measured with a multiwire surface electrode. During NLA stable hemodynamic conditions and a balanced acid-base status were observed. The nitrous oxide combination resulted in an increase of the mean pulmonary artery pressure of 16%. The addition of isoflurane had a negative inotropic effect: The heart index decreased to 74% of the starting value and the total peripheral resistance (TPR) increased by 27%. The summarized PO2 histograms under NLA and NLA/N2O showed arithmetic mean values of 34.1 and 35.2 mm Hg, respectively. The addition of isoflurane resulted in a left shift and a decrease of the mean value to 28.6 mm Hg. This histogram corresponds exactly to the oxygen pressure distribution in the dog liver during piritramide basic anesthesia. It seems that NLA and the combination of NLA/N2O increase the liver perfusion with a higher portal-venous and tissue PO2. This effect can be explained only by a massive change of visceral circulation. 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The addition of isoflurane resulted in a left shift and a decrease of the mean value to 28.6 mm Hg. This histogram corresponds exactly to the oxygen pressure distribution in the dog liver during piritramide basic anesthesia. It seems that NLA and the combination of NLA/N2O increase the liver perfusion with a higher portal-venous and tissue PO2. This effect can be explained only by a massive change of visceral circulation. It is canceled by the addition of isoflurane.</description><subject>animal model (dog)</subject><subject>Animals</subject><subject>Atropine - administration &amp; dosage</subject><subject>Blood Gas Analysis</subject><subject>Blood Pressure - drug effects</subject><subject>Catheterization, Swan-Ganz</subject><subject>Dogs</subject><subject>Droperidol - administration &amp; dosage</subject><subject>Fentanyl - administration &amp; dosage</subject><subject>Hemodynamics - drug effects</subject><subject>Hydrogen-Ion Concentration</subject><subject>isoflurane</subject><subject>Isoflurane - pharmacology</subject><subject>Liver - blood supply</subject><subject>Liver - metabolism</subject><subject>Liver - surgery</subject><subject>liver oxygenation</subject><subject>Microcirculation - drug effects</subject><subject>Monitoring, Physiologic</subject><subject>Neuroleptanalgesia</subject><subject>nitrous oxide</subject><subject>Nitrous Oxide - pharmacology</subject><subject>Oxygen Consumption</subject><subject>Pancuronium - administration &amp; 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dosage</topic><topic>Fentanyl - administration &amp; dosage</topic><topic>Hemodynamics - drug effects</topic><topic>Hydrogen-Ion Concentration</topic><topic>isoflurane</topic><topic>Isoflurane - pharmacology</topic><topic>Liver - blood supply</topic><topic>Liver - metabolism</topic><topic>Liver - surgery</topic><topic>liver oxygenation</topic><topic>Microcirculation - drug effects</topic><topic>Monitoring, Physiologic</topic><topic>Neuroleptanalgesia</topic><topic>nitrous oxide</topic><topic>Nitrous Oxide - pharmacology</topic><topic>Oxygen Consumption</topic><topic>Pancuronium - administration &amp; dosage</topic><topic>Pirinitramide - administration &amp; dosage</topic><topic>Vascular Resistance - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spiegel, Hans-Ullrich</creatorcontrib><creatorcontrib>Tschuschke, Christian</creatorcontrib><creatorcontrib>Holzgreve, Alfred</creatorcontrib><creatorcontrib>Brown, Silas</creatorcontrib><creatorcontrib>Brölsch, Christoph E.</creatorcontrib><creatorcontrib>Hauss, Jan</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>Journal of investigative surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spiegel, Hans-Ullrich</au><au>Tschuschke, Christian</au><au>Holzgreve, Alfred</au><au>Brown, Silas</au><au>Brölsch, Christoph E.</au><au>Hauss, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monitoring of Liver Oxygenation During Neuroleptanalgesia in the Dog</atitle><jtitle>Journal of investigative surgery</jtitle><addtitle>J Invest Surg</addtitle><date>1992</date><risdate>1992</risdate><volume>5</volume><issue>4</issue><spage>315</spage><epage>326</epage><pages>315-326</pages><issn>0894-1939</issn><eissn>1521-0553</eissn><abstract>In an animal study (7 mongrel dogs) the effects of neuroleptanalgesia (NLA) and combinations of NLA with nitrous oxide (N2O) and isoflurane on the macro- and microcirculation of the liver were investigated. Measurements were made in three steps. After NLA alone the dogs were supplementarily ventilated with nitrous oxide/oxygen at a ratio of 2 :1. During the last step, 1 MAC isoflurane was added to the inspired gas. From the portal vein, arterial and mixed-venous systems' hemodynamic parameters, blood gases, and acid-base balance were recorded. As a parameter of oxygenation the tissue PO2 of the liver was measured with a multiwire surface electrode. During NLA stable hemodynamic conditions and a balanced acid-base status were observed. The nitrous oxide combination resulted in an increase of the mean pulmonary artery pressure of 16%. The addition of isoflurane had a negative inotropic effect: The heart index decreased to 74% of the starting value and the total peripheral resistance (TPR) increased by 27%. The summarized PO2 histograms under NLA and NLA/N2O showed arithmetic mean values of 34.1 and 35.2 mm Hg, respectively. The addition of isoflurane resulted in a left shift and a decrease of the mean value to 28.6 mm Hg. This histogram corresponds exactly to the oxygen pressure distribution in the dog liver during piritramide basic anesthesia. It seems that NLA and the combination of NLA/N2O increase the liver perfusion with a higher portal-venous and tissue PO2. This effect can be explained only by a massive change of visceral circulation. It is canceled by the addition of isoflurane.</abstract><cop>United States</cop><pub>Informa UK Ltd</pub><pmid>1472485</pmid><doi>10.3109/08941939209012449</doi><tpages>12</tpages></addata></record>
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ispartof Journal of investigative surgery, 1992, Vol.5 (4), p.315-326
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language eng
recordid cdi_pubmed_primary_1472485
source Taylor & Francis:Master (3349 titles); MEDLINE
subjects animal model (dog)
Animals
Atropine - administration & dosage
Blood Gas Analysis
Blood Pressure - drug effects
Catheterization, Swan-Ganz
Dogs
Droperidol - administration & dosage
Fentanyl - administration & dosage
Hemodynamics - drug effects
Hydrogen-Ion Concentration
isoflurane
Isoflurane - pharmacology
Liver - blood supply
Liver - metabolism
Liver - surgery
liver oxygenation
Microcirculation - drug effects
Monitoring, Physiologic
Neuroleptanalgesia
nitrous oxide
Nitrous Oxide - pharmacology
Oxygen Consumption
Pancuronium - administration & dosage
Pirinitramide - administration & dosage
Vascular Resistance - drug effects
title Monitoring of Liver Oxygenation During Neuroleptanalgesia in the Dog
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