Differential Effects of Anaesthesia on the phMRI Response to Acute Ketamine Challenge
Duncan J. Hodkinson, Carmen de Groote, Shane McKie, J. F. William Deakin, Steve R. Williams
Journal of Advances in Medicine and Medical Research · pp. 373–385 · Published 12 May 2012
10.9734/BJMMR/2012/1412Abstract
Aims: Pharmacological-challenge magnetic resonance imaging (phMRI) is powerful new tool enabling researchers to map the central effects of neuroactive drugs in vivo. To employ this technique pre-clinically, head movements and the stress of restraint are usually reduced by maintaining animals under general anaesthesia. However, interactions between the drug of interest and the anaesthetic employed may potentially confound data interpretation. NMDA receptor (NMDAR) antagonists used widely to mimic schizophrenia have recently been shown to interact with the anaesthetic halothane. It may be the case that neural and cerebrovascular responses to NMDAR antagonists are dependent on the types of anaesthetic used. Methodology: We compared the phMRI response to NMDAR antagonist ketamine in rats maintained under α-chloralose to those under isoflurane anaesthesia. A randomized placebo/vehicle controlled design was used in each of the anaesthetic groups. Results: Changes in the anaesthetic agent resulted in two very different profiles of activity. In the case of α-chloralose, positive activations in cortical and sub-cortical structures reflected a response which was similar to patterns seen in healthy human volunteers and metabolic maps of conscious rats. However, the use of isoflurane completely reversed such effects, causing widespread deactivations in the cortex and hippocampus. Conclusion: This study provides initial evidence for a drug-anesthetic interaction between ketamine and isoflurane that is very different from responses to α-chloralose-ketamine
Cited by 49
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Kealy J, Commins S, Lowry JP. · Neuropharmacology · 2017
Tomimatsu Y, Cash D, Suzuki M · Neuroscience · 2016
Paasonen J, Salo RA, Shatillo A · Eur Neuropsychopharmacol · 2016
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