Fig. 5. The effects of sevoflurane (SEV) on the angiotensin II–elicited increase in intracellular Ca2+concentration ([Ca2+]i) in rat aortic smooth muscle. The endothelium-denuded rat aortic strips were treated with the fura-2 solution and were then exposed to 0 (control), 3.4, 5.1, or 8.5% sevoflurane for 15 min. The amount of fluorescence in the presence of angiotensin II (10−7m) was measured using a fluorometer. [Ca2+]iwas indicated as F340:F380 and was expressed as a percentage of the 30 mm KCl–elicited increase in [Ca2+]i(n = 7–9; control).

Fig. 5. The effects of sevoflurane (SEV) on the angiotensin II–elicited increase in intracellular Ca2+concentration ([Ca2+]i) in rat aortic smooth muscle. The endothelium-denuded rat aortic strips were treated with the fura-2 solution and were then exposed to 0 (control), 3.4, 5.1, or 8.5% sevoflurane for 15 min. The amount of fluorescence in the presence of angiotensin II (10−7m) was measured using a fluorometer. [Ca2+]iwas indicated as F340:F380 and was expressed as a percentage of the 30 mm KCl–elicited increase in [Ca2+]i(n = 7–9; control).

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