Temperature-independent inhibition of L-type calcium currents by halothane and sevoflurane in human atrial cardiomyocytes

Rocco Hüneke, Daniela Zitzelsberger, Jens Fassl, Eberhard Jüngling, Stefan Brose, Wolfgang Buhre, Rolf Rossaint, Andreas Lückhoff

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

Background: Cardiac L-type calcium currents (ICa,L) are affected by volatile anesthetics, possibly contributing to their side effects. Actions of anesthetics on ion channels are usually studied in vitro at room temperature. However, the solubility of anesthetic gases as well as ICa,L are markedly sensitive to the study temperature. Therefore, temperature-dependent effects of halothane and sevoflurane on cardiac ICa,L were analyzed. Methods: ICa,L were studied at 21°C and 36°C with the patch clamp technique in isolated human atrial cardiomyocytes. Concentrations of anesthetics brought into solution by gassing at both temperatures were determined with gas chromatography. Results: The aqueous concentrations of halothane and sevoflurane were linearly related to their concentration in the gas phase (1 to 3 minimum alveolar concentration [MAC]). At 21°C, the slope of this relation was 0.52 and 0.12 mM/vol % for halothane and sevoflurane, respectively, and decreased at 36°C to 0.29 and 0.09 mM/vol %, respectively. ICa,L displayed significantly higher current amplitudes at 36°C than at 21°C and significantly accelerated time-dependent inactivation. Halothane (1-2 MAC) and sevoflurane (1-3 MAC) evoked stronger inhibitions of ICa,L at 21°C than at 36°C. In spite of different temperature-dependent current amplitudes, the fractional (percent) inhibition of ICa,L showed the same linear relationship to the concentrations of halothane and sevoflurane in the bath medium at both temperatures, as revealed from present and previous experiments. Conclusions: Inhibition of I Ca,L by halothane and sevoflurane is determined by the aqueous concentration of the anesthetics, independently of the temperature. Increased solubility may explain the stronger effects of the anesthetics at lower temperatures.

Original languageEnglish
Pages (from-to)409-416
Number of pages8
JournalAnesthesiology
Volume101
Issue number2
DOIs
StatePublished - Aug 1 2004
Externally publishedYes

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