Erschienen in:
01.12.2010 | Reports of Original Investigations
Sevoflurane does not alter norepinephrine-induced intracellular Ca2+ changes in the diabetic rat aorta
verfasst von:
Keisuke Fujii, MD, Koji Ogawa, MD, Yasuyuki Tokinaga, MD, Hiroshi Iranami, MD, Yoshio Hatano, MD
Erschienen in:
Canadian Journal of Anesthesia/Journal canadien d'anesthésie
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Ausgabe 12/2010
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Abstract
Purpose
The effect of volatile anesthetics on the mechanism(s) of vascular contraction in diabetes mellitus (DM) has not been fully understood. The current study was designed to determine the effects of sevoflurane on the norepinephrine (NE)-induced changes in contractile state and intracellular Ca2+ concentrations ([Ca2+]i) in the spontaneously developing type 2 DM rat.
Methods
The effects of sevoflurane on NE (10−6M)-induced vasoconstriction and increase in [Ca2+]i in the aortas from Otsuka Long-Evans Tokushima Fatty (OLETF) rats, a type 2 DM model, and from age-matched control Long-Evans Tokushima Otsuka (LETO) rats were investigated using an isometric force transducer and fluorometer with fura-2 as an indicator of [Ca2+]i.
Results
Norepinephrine-induced increases in tension and [Ca2+]i in OLETF rats were 54.8%, 95% confidence interval (CI) 36.9-72.6% and 58.8%, 95% CI 51.5-66.1%, respectively, and in LETO rats they were 46.4%, 95% CI 39.0-53.7% and 53.8%, 95% CI 46.9-60.7%, respectively, when expressed as the percentage relative to that induced by KCl 30 mM. In LETO rats, sevoflurane at a concentration of 3.4% inhibited the vascular contraction (9.4%, 95% CI 6.3-12.6%; P < 0.001) and the increase in [Ca2+]i (33.3%, 95% CI 27.4-39.2%; P = 0.002). In OLETF rats, however, sevoflurane failed to affect either the NE-induced contraction (43.6%, 95% CI 28.3-58.9%; P = 0.68) or the elevation in [Ca2+]i (60.5%, 95% CI 56.3-64.8%; P = 0.93).
Conclusion
Sevoflurane at clinically relevant concentrations inhibited the NE-induced increase in [Ca2+]i in the aortic smooth muscle from normal rats but not in that from type 2 DM rats. Thus, a Ca2+- signalling pathway resistant to sevoflurane appears to exist in the type 2 DM rat aorta.