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Influence of intravenously administered lidocaine on cerebral blood flow in a baboon model standardized under controlled general anaesthesia using single-photon emission tomography and technetium-99m hexamethylpropylene amine oxime
Authors:I C Dormehl  M D W Lipp  N Hugo  M Daublaender  J A Picard
Institution:(1) AEC Institute for Life Sciences, University of Pretoria, P.O. Box 2034, 0001 Pretoria, South Africa;(2) Klinik für Anästhesiologie, Johannes Gutenberg Universität, Postfach 3960, D-6500 Mainz, Germany;(3) Stadtkrankenhaus Landau, Abteilung für Mund-, Kiefer- und Gesichtschirurgie, D-6740 Landau, Germany;(4) H.A. Grové Research Centre, Soutpansberg Road, 0002 Pretoria, South Africa
Abstract:The baboon under general anaesthesia as a model to assess drug-induced cerebral blood flow changes (Delta CBF) using single-photon emission tomography (SPET) offers great in vivo possibilities but has to comply with demands on control of anaesthesia-related influencing factors, such as P aCO2 changes. The model sought in this study and described here allows control of P aCO2, in the baboon under thiopentone anaesthesia by ventilation, and was evaluated for the functional dependence of Delta CBF vs Delta P aCO2, using SPET technetium-99m hexamethylpropylene amine oxime (HMPAO) and the split-dose method together with controlled ventilation. During the experiment the model was validated for normal reactivity to P aCO2 changes, and subsequently applied to investigate the mechanisms (still uncertain) of CBF increase known to follow administration of the local anaesthetic lidocaine. Six baboons received 6 mg/kg lidocaine intravenously. CBF was measured between two consecutive SPET acquisitions (split-dose method) respectively relating to HM-PAO distributions in the brain before and after the injection of lidocaine. Meanwhile the animals were maintained at constant respiratory rate and volume. The results indicate that the correlation between Delta CBF and the ensuing fall in PaCO2 deviated from the baseline pattern from the model and confirmed a cerebrovascular contribution to the lidocaine-induced CBF increase. This agreed well with mean and systolic blood pressure changes and heart rate. Correspondence to: I.C. Dormehl
Keywords:Ventilated anaesthetised baboon model  Technetium-99m hexamethylpropylene amine oxime single-photon emission tomography  Drug-induced cerebral blood flow changes  Lidocaine
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