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*Department of Anesthesiology and Intensive Care, Karolinska Hospital and Institute, Stockholm, Sweden;
Department of Anesthesia, St. Bartholomews Hospital;
Department of Anesthesia, Kings College School of Medicine and Dentistry, University of London, London, United Kingdom; and
§The Nobel Institute for Neurophysiology, Karolinska Institute, Stockholm, Sweden
Address correspondence and reprint requests to Henning Joensen, MD, Department of Anesthesiology and Intensive Care, Odense University Hospital, DK-5000 Odense C, Denmark. Address e-mail to henning.joensen{at}dadlnet.dk
Whether volatile anesthetics have an effect on the peripheral chemoreceptors is controversial, possibly because of differences in end-tidal CO2 concentrations. We studied the effect of isoflurane on the hypoxic chemosensitivity of carotid body chemoreceptors at three different PaCO2 levels before and during the administration of 1.0% isoflurane (0.5 minimum alveolar anesthetic concentration) in six normothermic New Zealand white rabbits anesthetized with thiopental. The response of the chemoreceptors was fitted to the equation: Frequency (Hz) = a + b x PaCO2 + c x (1/PaO2) + Dx (1/PaO2)2. Mean values for the coefficients a, b, c and d for the control state were -4.5, 0.13, 771, and 6332, respectively. This relationship was not changed by addition of isoflurane at 1.0% end-tidal concentration (P = 0.40, analysis of variance). We conclude that isoflurane at 1.0% end-tidal concentration does not depress the hypoxic response of rabbit carotid body chemoreceptors during either hypo-, normo-, or hypercapnia.
Implications: By measuring single-fiber chemoreceptor activity in anesthetized rabbits, we showed that isoflurane at 1.0% end-tidal concentration does not depress the hypoxic chemosensitivity of peripheral chemoreceptors during either hypo-, normo-, or hypercapnia in this species.
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