Buljubasic N, Rusch N J, Marijic J, Kampine J P, Bosnjak Z J
Department of Anesthesiology, Medical College of Wisconsin, Milwaukee 53226.
Anesthesiology. 1992 Jun;76(6):990-8. doi: 10.1097/00000542-199206000-00020.
The effects of halothane (0.75% and 1.5%) and isoflurane (2.6%) on macroscopic Ca2+ and K+ channel currents (ICa and IK, respectively) were investigated in voltage-clamped vascular muscle cells from the canine coronary artery. Single coronary arterial cells were dialyzed with K+ glutamate solution and superfused with Tyrode's solution for measurement of IK (n = 45). Stepwise depolarization from a holding potential of -60 mV to beyond -30 mV elicited an outward, slowly inactivating IK that had a macroscopic slope conductance of 18 nS. IK was reduced 75% by 10 mM 4-aminopyridine, a K+ channel antagonist. Compared to 4-aminopyridine, halothane at 0.75% and 1.5% reduced peak IK amplitude only by 14 +/- 2% and 36 +/- 3%, respectively. At approximately equianesthetic concentrations, 2.6% isoflurane suppressed IK less than did 1.5% halothane, reducing peak amplitude by 15 +/- 3%. In other sets of experiments, cells were dialyzed with 120 Cs(+)-glutamate solution and superfused with 10 mM BaCl2 or CaCl2 solutions to isolate ICa (n = 39) pharmacologically. Under these conditions, progressive depolarizing steps from -60 mV elicited a small inward current, which was potentiated 3.4-fold by equimolar substitution of Ba2+ for Ca2+ in the external solution and was blocked by 1 microM nifedipine. This inward current, which resembled L-type ICa, was blocked 37 +/- 4% and 70 +/- 4% in the presence of 0.75% and 1.5% halothane, respectively. Isoflurane (2.6%) also decreased ICa by 55 +/- 5%. It appears that while halothane and isoflurane suppress both IK and ICa, these anesthetics preferentially reduce ICa.(ABSTRACT TRUNCATED AT 250 WORDS)
在犬冠状动脉的电压钳制血管平滑肌细胞中,研究了氟烷(0.75%和1.5%)和异氟烷(2.6%)对宏观钙通道电流(ICa)和钾通道电流(IK)的影响。单个冠状动脉细胞用谷氨酸钾溶液透析,并用台氏液灌流以测量IK(n = 45)。从-60 mV的钳制电位逐步去极化至-30 mV以上,引发了一种外向、缓慢失活的IK,其宏观斜率电导为18 nS。10 mM 4-氨基吡啶(一种钾通道拮抗剂)使IK降低了75%。与4-氨基吡啶相比,0.75%和1.5%的氟烷分别仅使IK峰值幅度降低了14±2%和36±3%。在大约等效麻醉浓度下,2.6%的异氟烷对IK的抑制作用小于1.5%的氟烷,使峰值幅度降低了15±3%。在其他几组实验中,细胞用120 Cs(+)-谷氨酸溶液透析,并用10 mM BaCl2或CaCl2溶液灌流以药理学方式分离ICa(n = 39)。在这些条件下,从-60 mV进行逐步去极化步骤引发了一个小的内向电流,在外部溶液中用等摩尔的Ba2+替代Ca2+可使该电流增强3.4倍,并被1 microM硝苯地平阻断。这种内向电流类似于L型ICa,在存在0.75%和1.5%氟烷时分别被阻断37±4%和70±4%。2.6%的异氟烷也使ICa降低了55±5%。似乎虽然氟烷和异氟烷都抑制IK和ICa,但这些麻醉剂优先降低ICa。(摘要截断于250字)