Effects of halothane, enflurane, and isoflurane on measurements of Ca(2+) by calcium electrode and aequorin luminescence

• Published in: Analytical biochemistry 2000-08, Vol.284 (1), p.60-64
• Main Authors: Housmans, P R, Wanek, L A
• Format: Article
• Language: English
• Subjects: Aequorin - metabolism; Anesthetics, Inhalation - pharmacology; Calcium - metabolism; Chelating Agents - pharmacology; Dose-Response Relationship, Drug; Egtazic Acid - pharmacology; Electrochemistry; Electrodes; Enflurane - pharmacology; Halothane - pharmacology; Isoflurane - pharmacology; Luminescent Measurements; Time Factors
• ISSN: 0003-2697
• DOI: 10.1006/abio.2000.4688

We assessed the possible effects of the volatile halogenated anesthetics halothane, enflurane, and isoflurane on Ca(2+) electrode measurements and on the Ca(2+) sensitivity of the bioluminescent protein aequorin. In Ca(2+)-EGTA buffers of different pCa values (7. 870, 6.726, 6.033, 4.974, 4.038, and 2.995) and in serial Ca(2+) dilutions (10(-4), 10(-3), and 10(-2) M), halothane, enflurane, and isoflurane each caused a concentration-dependent and reversible increase in the absolute value of the negative electrode potential. Isoflurane and enflurane had larger effects than halothane. Neither of these anesthetics changed aequorin luminescence at any pCa tested in the range 2-8. There was no potentiation or inactivation of aequorin luminescence over a period of up to 2 h. These results suggest that (1) halothane, enflurane, and isoflurane interfere with Ca(2+) electrode measurements, most likely by changing the physicochemical properties of the membrane; (2) these anesthetics do not inactivate or otherwise modify the characteristics of the reaction of Ca(2+) with aequorin; and (3) these anesthetics do not change the apparent affinity of EGTA for Ca(2+).