Monitoring of anaesthesia in neurophysiological experiments
Cortical activity can be substantially changed by the type of anaesthetic used, and by its dose level. For easy monitoring of depth of anaesthesia we describe the changes in electroencephalogram and electrocardiogram accompanying changes in depth of anaesthesia in the cat. Anaesthesia was induced by...
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Veröffentlicht in: | Neuroreport 1999-03, Vol.10 (4), p.781-787 |
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creator | Kral, A Tillein, J Hartmann, R Klinke, R |
description | Cortical activity can be substantially changed by the type of anaesthetic used, and by its dose level. For easy monitoring of depth of anaesthesia we describe the changes in electroencephalogram and electrocardiogram accompanying changes in depth of anaesthesia in the cat. Anaesthesia was induced by the volatile anaesthetic isoflurane. The high-frequency components (around 30 Hz) in the electroencephalogram disappear in deep anaesthesia. The electrocardiogram also shows substantial changes in contamination due to muscle fasciculations with anaesthesia level. Fasciculations appear as noise in the electrocardiogram. The amplitude of the electrical muscle activity contaminating the ECG can be easily used for the maintainance of a constant level of anaesthesia during a neurophysiological experiment. |
doi_str_mv | 10.1097/00001756-199903170-00022 |
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For easy monitoring of depth of anaesthesia we describe the changes in electroencephalogram and electrocardiogram accompanying changes in depth of anaesthesia in the cat. Anaesthesia was induced by the volatile anaesthetic isoflurane. The high-frequency components (around 30 Hz) in the electroencephalogram disappear in deep anaesthesia. The electrocardiogram also shows substantial changes in contamination due to muscle fasciculations with anaesthesia level. Fasciculations appear as noise in the electrocardiogram. The amplitude of the electrical muscle activity contaminating the ECG can be easily used for the maintainance of a constant level of anaesthesia during a neurophysiological experiment.</description><identifier>ISSN: 0959-4965</identifier><identifier>EISSN: 1473-558X</identifier><identifier>DOI: 10.1097/00001756-199903170-00022</identifier><identifier>PMID: 10208548</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins, Inc</publisher><subject>Anesthesia ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Cats ; Electrocardiography - drug effects ; Electroencephalography - drug effects ; Electrophysiology ; General anesthesia. Technics. Complications. Neuromuscular blocking. Premedication. Surgical preparation. Sedation ; Medical sciences ; Muscle Relaxation - drug effects ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - physiology ; Neuromuscular Nondepolarizing Agents - pharmacology ; Neurophysiology - methods ; Pancuronium - pharmacology ; Vestibulocochlear Nerve - drug effects ; Vestibulocochlear Nerve - physiology</subject><ispartof>Neuroreport, 1999-03, Vol.10 (4), p.781-787</ispartof><rights>1999 Lippincott Williams & Wilkins, Inc.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4162-6df08b6b03e9d98de540bea96ad5abc2edd888a393e51bcf653e2626d81a98883</citedby><cites>FETCH-LOGICAL-c4162-6df08b6b03e9d98de540bea96ad5abc2edd888a393e51bcf653e2626d81a98883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1760765$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10208548$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kral, A</creatorcontrib><creatorcontrib>Tillein, J</creatorcontrib><creatorcontrib>Hartmann, R</creatorcontrib><creatorcontrib>Klinke, R</creatorcontrib><title>Monitoring of anaesthesia in neurophysiological experiments</title><title>Neuroreport</title><addtitle>Neuroreport</addtitle><description>Cortical activity can be substantially changed by the type of anaesthetic used, and by its dose level. For easy monitoring of depth of anaesthesia we describe the changes in electroencephalogram and electrocardiogram accompanying changes in depth of anaesthesia in the cat. Anaesthesia was induced by the volatile anaesthetic isoflurane. The high-frequency components (around 30 Hz) in the electroencephalogram disappear in deep anaesthesia. The electrocardiogram also shows substantial changes in contamination due to muscle fasciculations with anaesthesia level. Fasciculations appear as noise in the electrocardiogram. The amplitude of the electrical muscle activity contaminating the ECG can be easily used for the maintainance of a constant level of anaesthesia during a neurophysiological experiment.</description><subject>Anesthesia</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cats</subject><subject>Electrocardiography - drug effects</subject><subject>Electroencephalography - drug effects</subject><subject>Electrophysiology</subject><subject>General anesthesia. Technics. Complications. Neuromuscular blocking. Premedication. Surgical preparation. Sedation</subject><subject>Medical sciences</subject><subject>Muscle Relaxation - drug effects</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - physiology</subject><subject>Neuromuscular Nondepolarizing Agents - pharmacology</subject><subject>Neurophysiology - methods</subject><subject>Pancuronium - pharmacology</subject><subject>Vestibulocochlear Nerve - drug effects</subject><subject>Vestibulocochlear Nerve - physiology</subject><issn>0959-4965</issn><issn>1473-558X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkclOwzAQQC0EoqXwCygHxC1gJ_EmTqhik4q4gMTNcpJJa0jjYCcq_XtcUpYLwnOwZL8Ze94gFBF8RrDk5zgswimLiZQSp4TjOJwkyQ4ak4ynMaXieReNsaQyziSjI3Tg_UtAJCZiH40ITrCgmRiji3vbmM4608wjW0W60eC7BXijI9NEDfTOtou1N7a2c1PoOoL3FpxZQtP5Q7RX6drD0XafoKfrq8fpbTx7uLmbXs7iIiMsiVlZYZGzHKcgSylKoBnOQUumS6rzIoGyFELoVKZASV5UjKaQsISVgmgZbtIJOh3qts6-9eF_aml8AXWtG7C9V0yG4Jz8CxKeSC7FBhQDWDjrvYNKtaEn7daKYLUxrL4Mq2_D6tNwSD3evtHnSyh_JQ5KA3CyBbQPwiqnm8L4H44zzEOLE5QN2MrWHTj_WvcrcGoBuu4W6q8Bpx8c45Nc</recordid><startdate>19990317</startdate><enddate>19990317</enddate><creator>Kral, A</creator><creator>Tillein, J</creator><creator>Hartmann, R</creator><creator>Klinke, R</creator><general>Lippincott Williams & Wilkins, Inc</general><general>Lippincott Williams and Wilkins</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><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19990317</creationdate><title>Monitoring of anaesthesia in neurophysiological experiments</title><author>Kral, A ; Tillein, J ; Hartmann, R ; Klinke, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4162-6df08b6b03e9d98de540bea96ad5abc2edd888a393e51bcf653e2626d81a98883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Anesthesia</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cats</topic><topic>Electrocardiography - drug effects</topic><topic>Electroencephalography - drug effects</topic><topic>Electrophysiology</topic><topic>General anesthesia. Technics. Complications. Neuromuscular blocking. Premedication. Surgical preparation. Sedation</topic><topic>Medical sciences</topic><topic>Muscle Relaxation - drug effects</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - physiology</topic><topic>Neuromuscular Nondepolarizing Agents - pharmacology</topic><topic>Neurophysiology - methods</topic><topic>Pancuronium - pharmacology</topic><topic>Vestibulocochlear Nerve - drug effects</topic><topic>Vestibulocochlear Nerve - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kral, A</creatorcontrib><creatorcontrib>Tillein, J</creatorcontrib><creatorcontrib>Hartmann, R</creatorcontrib><creatorcontrib>Klinke, R</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><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroreport</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kral, A</au><au>Tillein, J</au><au>Hartmann, R</au><au>Klinke, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monitoring of anaesthesia in neurophysiological experiments</atitle><jtitle>Neuroreport</jtitle><addtitle>Neuroreport</addtitle><date>1999-03-17</date><risdate>1999</risdate><volume>10</volume><issue>4</issue><spage>781</spage><epage>787</epage><pages>781-787</pages><issn>0959-4965</issn><eissn>1473-558X</eissn><abstract>Cortical activity can be substantially changed by the type of anaesthetic used, and by its dose level. For easy monitoring of depth of anaesthesia we describe the changes in electroencephalogram and electrocardiogram accompanying changes in depth of anaesthesia in the cat. Anaesthesia was induced by the volatile anaesthetic isoflurane. The high-frequency components (around 30 Hz) in the electroencephalogram disappear in deep anaesthesia. The electrocardiogram also shows substantial changes in contamination due to muscle fasciculations with anaesthesia level. Fasciculations appear as noise in the electrocardiogram. The amplitude of the electrical muscle activity contaminating the ECG can be easily used for the maintainance of a constant level of anaesthesia during a neurophysiological experiment.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>10208548</pmid><doi>10.1097/00001756-199903170-00022</doi><tpages>7</tpages></addata></record> |
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subjects | Anesthesia Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Cats Electrocardiography - drug effects Electroencephalography - drug effects Electrophysiology General anesthesia. Technics. Complications. Neuromuscular blocking. Premedication. Surgical preparation. Sedation Medical sciences Muscle Relaxation - drug effects Muscle, Skeletal - drug effects Muscle, Skeletal - physiology Neuromuscular Nondepolarizing Agents - pharmacology Neurophysiology - methods Pancuronium - pharmacology Vestibulocochlear Nerve - drug effects Vestibulocochlear Nerve - physiology |
title | Monitoring of anaesthesia in neurophysiological experiments |
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