TY - JOUR
T1 - Neuroprotective effect of volatile anesthetic agents
T2 - Molecular mechanisms
AU - Matchett, Gerald A.
AU - Allard, Martin W.
AU - Martin, Robert D.
AU - Zhang, John H.
N1 - Neurol Res. 2009 Mar;31(2):128-34. doi: 10.1179/174313209X393546. Research Support, N.I.H., Extramural; Review
PY - 2009/3
Y1 - 2009/3
N2 - Introduction: Intra-operative cerebral ischemia can be catastrophic, and volatile anesthetic agents have been recognized for their potential neuroprotective properties since the 1960s. In this review, we examine the neuroprotective effects of five volatile anesthetic agents in current or recent clinical use: isoflurane, sevoflurane, desflurane, halothane and enflurane. Methods: A review of publications in the National Library of Medicine and National Institutes of Health database from 1970 to 2007 was conducted. Results: Volatile anesthetic agents have been shown to be neuroprotective in multiple animal works of ischemic brain injury. Short-term neuroprotection (<1 week post-ischemia) in experimental cerebral ischemia has been reported in multiple works, although long-term neuroprotection (≥ 1 week post-ischemia) remains controversial. Comparison works have not demonstrated superiority of one specific volatile agent over another in experimental models of brain injury. Relatively few human works have examined the protective effects of volatile anesthetic agents and conclusive evidence of a neuroprotective effect has yet to emerge from human works. Conclusion: Proposed mechanisms related to the neuroprotective effect of volatile anesthetic agents include activation of ATP-dependent potassium channels, up-regulation of nitric oxide synthase, reduction of excitotoxic stressors and cerebral metabolic rate, augmentation of peri- ischemic cerebral blood flow and up-regulation of antiapoptotic factors including MAP kinases.
AB - Introduction: Intra-operative cerebral ischemia can be catastrophic, and volatile anesthetic agents have been recognized for their potential neuroprotective properties since the 1960s. In this review, we examine the neuroprotective effects of five volatile anesthetic agents in current or recent clinical use: isoflurane, sevoflurane, desflurane, halothane and enflurane. Methods: A review of publications in the National Library of Medicine and National Institutes of Health database from 1970 to 2007 was conducted. Results: Volatile anesthetic agents have been shown to be neuroprotective in multiple animal works of ischemic brain injury. Short-term neuroprotection (<1 week post-ischemia) in experimental cerebral ischemia has been reported in multiple works, although long-term neuroprotection (≥ 1 week post-ischemia) remains controversial. Comparison works have not demonstrated superiority of one specific volatile agent over another in experimental models of brain injury. Relatively few human works have examined the protective effects of volatile anesthetic agents and conclusive evidence of a neuroprotective effect has yet to emerge from human works. Conclusion: Proposed mechanisms related to the neuroprotective effect of volatile anesthetic agents include activation of ATP-dependent potassium channels, up-regulation of nitric oxide synthase, reduction of excitotoxic stressors and cerebral metabolic rate, augmentation of peri- ischemic cerebral blood flow and up-regulation of antiapoptotic factors including MAP kinases.
KW - Cerebral ischemia
KW - Desflurane
KW - Enflurane
KW - Halothane
KW - Isoflurane
KW - Sevoflurane
KW - Neuroprotective Agents/administration & dosage
KW - Humans
KW - Regional Blood Flow/drug effects
KW - Anesthetics, Inhalation/administration & dosage
KW - Brain Ischemia/metabolism
KW - Databases, Factual/statistics & numerical data
KW - Animals
KW - Ion Channels/drug effects
KW - Disease Models, Animal
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UR - https://www.mendeley.com/catalogue/d7866490-8ed7-313d-960b-a2ee1b6a9bc9/
U2 - 10.1179/174313209X393546
DO - 10.1179/174313209X393546
M3 - Article
C2 - 19298752
SN - 0161-6412
VL - 31
SP - 128
EP - 134
JO - Neurological Research
JF - Neurological Research
IS - 2
ER -