Sevoflurane exposure has minimal effect on cognitive function and does not alter microglial activation in adult monkeys
•An 8-hour exposure to sevoflurane did not cause an increase in neuroinflammation as measured by [18F]-FEPPA in aged monkeys.•Extended exposure to sevoflurane had minimal impact on the performance of aged monkeys trained on cognitive test battery.•Extended exposure to sevoflurane in aged adult anima...
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Veröffentlicht in: | Neurotoxicology (Park Forest South) 2019-03, Vol.71, p.159-167 |
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creator | Walters, Jennifer L. Zhang, Xuan Talpos, John C. Fogle, Charles M. Li, Mi Chelonis, John J. Paule, Merle G. |
description | •An 8-hour exposure to sevoflurane did not cause an increase in neuroinflammation as measured by [18F]-FEPPA in aged monkeys.•Extended exposure to sevoflurane had minimal impact on the performance of aged monkeys trained on cognitive test battery.•Extended exposure to sevoflurane in aged adult animals appears to be less neurotoxic then in young animals.
Postoperative Cognitive Dysfunction (POCD) is a complication that has been observed in a subset of adult and elderly individuals after general anesthesia and surgery. Although the pathogenesis of POCD is largely unknown, a growing body of preclinical research suggests that POCD may be caused by general anesthesia. A significant amount of research has examined the effects of general anesthesia on neurocognitive function in rodents, yet no studies have assessed the adverse effects of general anesthesia on brain function in adult nonhuman primates. Thus, this study sought to determine the effects of an extended exposure to sevoflurane anesthesia on cognitive function and neural inflammation in adult rhesus macaques. Five adult rhesus macaques (16–17 years of age) were exposed to sevoflurane anesthesia for 8 h and, and micro-positron emission tomography (PET)/computed tomography (CT) imaging and a battery of operant tasks were used to assess the effects of anesthesia exposure on 18F-labeled fluoroethoxybenzyl-N-(4-phenoxypyridin-3-yl) acetamide ([18F]-FEPPA) uptake, a biomarker of microglia activation, and aspects of complex cognitive function. Exposure to sevoflurane anesthesia for 8 h did not increase [18F]-FEPPA uptake in the adult monkey brain. Sevoflurane anesthesia significantly decreased accuracy (mean difference = 22.79) on a learning acquisition task 6 days after exposure [t(3) = 6.92, p = 0.006], but this effect did not persist when measured 1 week and 2 weeks after additional exposures. Further, sevoflurane anesthesia had no impact on performance in 4 additional cognitive tasks. These data suggest that exposure to anesthesia alone may not be sufficient to cause persistent POCD in adult populations. |
doi_str_mv | 10.1016/j.neuro.2018.12.008 |
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Postoperative Cognitive Dysfunction (POCD) is a complication that has been observed in a subset of adult and elderly individuals after general anesthesia and surgery. Although the pathogenesis of POCD is largely unknown, a growing body of preclinical research suggests that POCD may be caused by general anesthesia. A significant amount of research has examined the effects of general anesthesia on neurocognitive function in rodents, yet no studies have assessed the adverse effects of general anesthesia on brain function in adult nonhuman primates. Thus, this study sought to determine the effects of an extended exposure to sevoflurane anesthesia on cognitive function and neural inflammation in adult rhesus macaques. Five adult rhesus macaques (16–17 years of age) were exposed to sevoflurane anesthesia for 8 h and, and micro-positron emission tomography (PET)/computed tomography (CT) imaging and a battery of operant tasks were used to assess the effects of anesthesia exposure on 18F-labeled fluoroethoxybenzyl-N-(4-phenoxypyridin-3-yl) acetamide ([18F]-FEPPA) uptake, a biomarker of microglia activation, and aspects of complex cognitive function. Exposure to sevoflurane anesthesia for 8 h did not increase [18F]-FEPPA uptake in the adult monkey brain. Sevoflurane anesthesia significantly decreased accuracy (mean difference = 22.79) on a learning acquisition task 6 days after exposure [t(3) = 6.92, p = 0.006], but this effect did not persist when measured 1 week and 2 weeks after additional exposures. Further, sevoflurane anesthesia had no impact on performance in 4 additional cognitive tasks. These data suggest that exposure to anesthesia alone may not be sufficient to cause persistent POCD in adult populations.</description><identifier>ISSN: 0161-813X</identifier><identifier>EISSN: 1872-9711</identifier><identifier>DOI: 10.1016/j.neuro.2018.12.008</identifier><identifier>PMID: 30605762</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Activation ; Adult monkey ; Anesthesia ; Anesthetics, Inhalation - toxicity ; Animals ; Biomarkers ; Brain ; Brain - drug effects ; Brain - metabolism ; Brain - pathology ; Cognition ; Cognitive ability ; Cognitive tasks ; Computed tomography ; Conditioning, Operant - drug effects ; Encephalitis - chemically induced ; Exposure ; Female ; Fluorine isotopes ; Geriatrics ; Learning - drug effects ; Macaca mulatta ; Male ; Microglia ; Microglia - drug effects ; Microglia - metabolism ; microPET imaging ; Monkeys ; Neural inflammation ; Neuroimaging ; Older people ; Operant conditioning ; Pathogenesis ; Positron emission ; Positron emission tomography ; Primates ; Rodents ; Sevoflurane ; Sevoflurane - toxicity ; Surgery ; Tomography</subject><ispartof>Neurotoxicology (Park Forest South), 2019-03, Vol.71, p.159-167</ispartof><rights>2018</rights><rights>Copyright © 2018. Published by Elsevier B.V.</rights><rights>Copyright Elsevier BV Mar 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-f397cb617ad946715792247d9d17f2f80edbddc351ab642ef16d12a01c8c7bca3</citedby><cites>FETCH-LOGICAL-c387t-f397cb617ad946715792247d9d17f2f80edbddc351ab642ef16d12a01c8c7bca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuro.2018.12.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30605762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Walters, Jennifer L.</creatorcontrib><creatorcontrib>Zhang, Xuan</creatorcontrib><creatorcontrib>Talpos, John C.</creatorcontrib><creatorcontrib>Fogle, Charles M.</creatorcontrib><creatorcontrib>Li, Mi</creatorcontrib><creatorcontrib>Chelonis, John J.</creatorcontrib><creatorcontrib>Paule, Merle G.</creatorcontrib><title>Sevoflurane exposure has minimal effect on cognitive function and does not alter microglial activation in adult monkeys</title><title>Neurotoxicology (Park Forest South)</title><addtitle>Neurotoxicology</addtitle><description>•An 8-hour exposure to sevoflurane did not cause an increase in neuroinflammation as measured by [18F]-FEPPA in aged monkeys.•Extended exposure to sevoflurane had minimal impact on the performance of aged monkeys trained on cognitive test battery.•Extended exposure to sevoflurane in aged adult animals appears to be less neurotoxic then in young animals.
Postoperative Cognitive Dysfunction (POCD) is a complication that has been observed in a subset of adult and elderly individuals after general anesthesia and surgery. Although the pathogenesis of POCD is largely unknown, a growing body of preclinical research suggests that POCD may be caused by general anesthesia. A significant amount of research has examined the effects of general anesthesia on neurocognitive function in rodents, yet no studies have assessed the adverse effects of general anesthesia on brain function in adult nonhuman primates. Thus, this study sought to determine the effects of an extended exposure to sevoflurane anesthesia on cognitive function and neural inflammation in adult rhesus macaques. Five adult rhesus macaques (16–17 years of age) were exposed to sevoflurane anesthesia for 8 h and, and micro-positron emission tomography (PET)/computed tomography (CT) imaging and a battery of operant tasks were used to assess the effects of anesthesia exposure on 18F-labeled fluoroethoxybenzyl-N-(4-phenoxypyridin-3-yl) acetamide ([18F]-FEPPA) uptake, a biomarker of microglia activation, and aspects of complex cognitive function. Exposure to sevoflurane anesthesia for 8 h did not increase [18F]-FEPPA uptake in the adult monkey brain. Sevoflurane anesthesia significantly decreased accuracy (mean difference = 22.79) on a learning acquisition task 6 days after exposure [t(3) = 6.92, p = 0.006], but this effect did not persist when measured 1 week and 2 weeks after additional exposures. Further, sevoflurane anesthesia had no impact on performance in 4 additional cognitive tasks. These data suggest that exposure to anesthesia alone may not be sufficient to cause persistent POCD in adult populations.</description><subject>Activation</subject><subject>Adult monkey</subject><subject>Anesthesia</subject><subject>Anesthetics, Inhalation - toxicity</subject><subject>Animals</subject><subject>Biomarkers</subject><subject>Brain</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Cognition</subject><subject>Cognitive ability</subject><subject>Cognitive tasks</subject><subject>Computed tomography</subject><subject>Conditioning, Operant - drug effects</subject><subject>Encephalitis - chemically induced</subject><subject>Exposure</subject><subject>Female</subject><subject>Fluorine isotopes</subject><subject>Geriatrics</subject><subject>Learning - drug effects</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>Microglia</subject><subject>Microglia - drug effects</subject><subject>Microglia - metabolism</subject><subject>microPET imaging</subject><subject>Monkeys</subject><subject>Neural inflammation</subject><subject>Neuroimaging</subject><subject>Older people</subject><subject>Operant conditioning</subject><subject>Pathogenesis</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Primates</subject><subject>Rodents</subject><subject>Sevoflurane</subject><subject>Sevoflurane - toxicity</subject><subject>Surgery</subject><subject>Tomography</subject><issn>0161-813X</issn><issn>1872-9711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EokvhEyAhS1y4JHicbOwcOKCKf1IlDoDEzXLscfGStRc7Wei3Z9otHDhwGmv0e-OZ9xh7CqIFAcPLXZtwLbmVAnQLshVC32Mb0Eo2owK4zzZEQaOh-3rGHtW6EwK2ahgfsrNODIKecsN-fsJjDvNabEKOvw65rgX5N1v5Pqa4tzPHENAtPCfu8lWKSzwiD2tyS6SWTZ77jJWnvHA7L1hI50q-miNJLUFHewtGYv06L3yf03e8ro_Zg2Dnik_u6jn78vbN54v3zeXHdx8uXl82rtNqaUI3KjcNoKwf-0HR_qOUvfKjBxVk0AL95L3rtmCnoZcYYPAgrQCnnZqc7c7Zi9PcQ8k_VqyL2cfqcJ7p3rxWI2HoxTj2HRD6_B90l9eSaDsjpZBKa72VRHUniq6stWAwh0I-lWsDwtzkYnbmNhdzk4sBaSgXUj27m71Oe_R_NX-CIODVCUAy4xixmOoiJoc-FrLf-Bz_-8FvRAWhyQ</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Walters, Jennifer L.</creator><creator>Zhang, Xuan</creator><creator>Talpos, John C.</creator><creator>Fogle, Charles M.</creator><creator>Li, Mi</creator><creator>Chelonis, John J.</creator><creator>Paule, Merle G.</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>201903</creationdate><title>Sevoflurane exposure has minimal effect on cognitive function and does not alter microglial activation in adult monkeys</title><author>Walters, Jennifer L. ; Zhang, Xuan ; Talpos, John C. ; Fogle, Charles M. ; Li, Mi ; Chelonis, John J. ; Paule, Merle G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-f397cb617ad946715792247d9d17f2f80edbddc351ab642ef16d12a01c8c7bca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Activation</topic><topic>Adult monkey</topic><topic>Anesthesia</topic><topic>Anesthetics, Inhalation - toxicity</topic><topic>Animals</topic><topic>Biomarkers</topic><topic>Brain</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Cognition</topic><topic>Cognitive ability</topic><topic>Cognitive tasks</topic><topic>Computed tomography</topic><topic>Conditioning, Operant - drug effects</topic><topic>Encephalitis - chemically induced</topic><topic>Exposure</topic><topic>Female</topic><topic>Fluorine isotopes</topic><topic>Geriatrics</topic><topic>Learning - drug effects</topic><topic>Macaca mulatta</topic><topic>Male</topic><topic>Microglia</topic><topic>Microglia - drug effects</topic><topic>Microglia - metabolism</topic><topic>microPET imaging</topic><topic>Monkeys</topic><topic>Neural inflammation</topic><topic>Neuroimaging</topic><topic>Older people</topic><topic>Operant conditioning</topic><topic>Pathogenesis</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Primates</topic><topic>Rodents</topic><topic>Sevoflurane</topic><topic>Sevoflurane - toxicity</topic><topic>Surgery</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Walters, Jennifer L.</creatorcontrib><creatorcontrib>Zhang, Xuan</creatorcontrib><creatorcontrib>Talpos, John C.</creatorcontrib><creatorcontrib>Fogle, Charles M.</creatorcontrib><creatorcontrib>Li, Mi</creatorcontrib><creatorcontrib>Chelonis, John J.</creatorcontrib><creatorcontrib>Paule, Merle G.</creatorcontrib><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Neurotoxicology (Park Forest South)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Walters, Jennifer L.</au><au>Zhang, Xuan</au><au>Talpos, John C.</au><au>Fogle, Charles M.</au><au>Li, Mi</au><au>Chelonis, John J.</au><au>Paule, Merle G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sevoflurane exposure has minimal effect on cognitive function and does not alter microglial activation in adult monkeys</atitle><jtitle>Neurotoxicology (Park Forest South)</jtitle><addtitle>Neurotoxicology</addtitle><date>2019-03</date><risdate>2019</risdate><volume>71</volume><spage>159</spage><epage>167</epage><pages>159-167</pages><issn>0161-813X</issn><eissn>1872-9711</eissn><abstract>•An 8-hour exposure to sevoflurane did not cause an increase in neuroinflammation as measured by [18F]-FEPPA in aged monkeys.•Extended exposure to sevoflurane had minimal impact on the performance of aged monkeys trained on cognitive test battery.•Extended exposure to sevoflurane in aged adult animals appears to be less neurotoxic then in young animals.
Postoperative Cognitive Dysfunction (POCD) is a complication that has been observed in a subset of adult and elderly individuals after general anesthesia and surgery. Although the pathogenesis of POCD is largely unknown, a growing body of preclinical research suggests that POCD may be caused by general anesthesia. A significant amount of research has examined the effects of general anesthesia on neurocognitive function in rodents, yet no studies have assessed the adverse effects of general anesthesia on brain function in adult nonhuman primates. Thus, this study sought to determine the effects of an extended exposure to sevoflurane anesthesia on cognitive function and neural inflammation in adult rhesus macaques. Five adult rhesus macaques (16–17 years of age) were exposed to sevoflurane anesthesia for 8 h and, and micro-positron emission tomography (PET)/computed tomography (CT) imaging and a battery of operant tasks were used to assess the effects of anesthesia exposure on 18F-labeled fluoroethoxybenzyl-N-(4-phenoxypyridin-3-yl) acetamide ([18F]-FEPPA) uptake, a biomarker of microglia activation, and aspects of complex cognitive function. Exposure to sevoflurane anesthesia for 8 h did not increase [18F]-FEPPA uptake in the adult monkey brain. Sevoflurane anesthesia significantly decreased accuracy (mean difference = 22.79) on a learning acquisition task 6 days after exposure [t(3) = 6.92, p = 0.006], but this effect did not persist when measured 1 week and 2 weeks after additional exposures. Further, sevoflurane anesthesia had no impact on performance in 4 additional cognitive tasks. These data suggest that exposure to anesthesia alone may not be sufficient to cause persistent POCD in adult populations.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30605762</pmid><doi>10.1016/j.neuro.2018.12.008</doi><tpages>9</tpages></addata></record> |
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subjects | Activation Adult monkey Anesthesia Anesthetics, Inhalation - toxicity Animals Biomarkers Brain Brain - drug effects Brain - metabolism Brain - pathology Cognition Cognitive ability Cognitive tasks Computed tomography Conditioning, Operant - drug effects Encephalitis - chemically induced Exposure Female Fluorine isotopes Geriatrics Learning - drug effects Macaca mulatta Male Microglia Microglia - drug effects Microglia - metabolism microPET imaging Monkeys Neural inflammation Neuroimaging Older people Operant conditioning Pathogenesis Positron emission Positron emission tomography Primates Rodents Sevoflurane Sevoflurane - toxicity Surgery Tomography |
title | Sevoflurane exposure has minimal effect on cognitive function and does not alter microglial activation in adult monkeys |
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