Literature DB >> 11145474

The effects of anesthetics on cortical spreading depression elicitation and c-fos expression in rats.

Y Kitahara1, K Taga, H Abe, K Shimoji.   

Abstract

The effects of anesthetics on the generation of cortical spreading depression (CSD) were investigated. Volatile anesthetics halothane, isoflurane, sevoflurane (0.5, 1.0, and 2.0 MAC), and the intravenous anesthetic pentobarbital were studied. Cortical spreading depression was induced by 3M-KCl applied to a surface of brain cortex for 30 minutes. Direct current (DC) potential was recorded, and the number, amplitude, and duration of CSDs were observed. With increasing concentrations of each volatile anesthetic, there was a dose-related reduction in CSD frequency but not in CSD amplitude. At 2.0 MAC of sevoflurane the suppression of CSD was less than with the other volatile anesthetics. In addition, the influence of anesthetics on expression of c-fos mRNA was investigated. Additional animals anesthetized by isoflurane or sevoflurane were studied. Five CSDs were elicited by electric stimulation (0.5 mV, 1 second) in each animal. In situ hybridization with 35S-labeled oligonucleotides was used to evaluate the level of c-fos mRNA. The expression of c-fos was observed in the hemisphere in which CSD was elicited, but there was no difference in expression of c-fos among the groups. We conclude that volatile anesthetics can induce suppression of CSD elicitation in a dose dependent manner, but that at high concentrations sevoflurane is significantly less effective than other volatile agents. Pentobarbital has the least effect on KCl-induced CSD. These data suggest that the choice of anesthetics can impact the results of studies examining membrane depolarization and the ionic changes initiated by CSD.

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Year:  2001        PMID: 11145474     DOI: 10.1097/00008506-200101000-00005

Source DB:  PubMed          Journal:  J Neurosurg Anesthesiol        ISSN: 0898-4921            Impact factor:   3.956


  16 in total

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2.  Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.

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Journal:  J Neurosci       Date:  2011-04-13       Impact factor: 6.167

3.  Unilateral cortical spreading depression affects sleep need and induces molecular and electrophysiological signs of synaptic potentiation in vivo.

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Journal:  Cereb Cortex       Date:  2010-03-26       Impact factor: 5.357

Review 4.  Pharmacological targeting of spreading depression in migraine.

Authors:  Katharina Eikermann-Haerter; Anil Can; Cenk Ayata
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5.  Systematic review of the pharmacological agents that have been tested against spreading depolarizations.

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Journal:  J Cereb Blood Flow Metab       Date:  2018-04-20       Impact factor: 6.200

6.  Delayed secondary phase of peri-infarct depolarizations after focal cerebral ischemia: relation to infarct growth and neuroprotection.

Authors:  Jed A Hartings; Michael L Rolli; X-C May Lu; Frank C Tortella
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7.  Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.

Authors:  Katharina Eikermann-Haerter; Ergin Dileköz; Chiho Kudo; Sean I Savitz; Christian Waeber; Michael J Baum; Michel D Ferrari; Arn M J M van den Maagdenberg; Michael A Moskowitz; Cenk Ayata
Journal:  J Clin Invest       Date:  2008-12-22       Impact factor: 14.808

8.  N-methyl-D-aspartate induces cortical hyperemia through cortical spreading depression-dependent and -independent mechanisms in rats.

Authors:  Laura Lenti; Ferenc Domoki; Tamás Gáspár; James A Snipes; Ferenc Bari; David W Busija
Journal:  Microcirculation       Date:  2009-10       Impact factor: 2.628

9.  The impact of anesthetics and hyperoxia on cortical spreading depression.

Authors:  Chiho Kudo; Ala Nozari; Michael A Moskowitz; Cenk Ayata
Journal:  Exp Neurol       Date:  2008-04-11       Impact factor: 5.330

10.  Peri-infarct depolarizations during focal ischemia in the awake Spontaneously Hypertensive Rat. Minimizing anesthesia confounds in experimental stroke.

Authors:  K Kudo; L Zhao; T S Nowak
Journal:  Neuroscience       Date:  2016-03-26       Impact factor: 3.590

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