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局部麻醉药与钙拮抗剂在豚鼠心肌中的功能相互作用:2. 布比卡因和硝苯地平的电生理研究。

Functional interaction between local anaesthetics and calcium antagonists in guineapig myocardium: 2. Electrophysiological studies with bupivacaine and nifedipine.

作者信息

Wulf H, Gödicke J, Herzig S

机构信息

Department of Anaesthesiology and Intensive Care Medicine, Hospital of the Christian-Albrechts University, Kiel, Germany.

出版信息

Br J Anaesth. 1994 Sep;73(3):364-70. doi: 10.1093/bja/73.3.364.

DOI:10.1093/bja/73.3.364
PMID:7946865
Abstract

The negative inotropic effect of local anaesthetics is potentiated by several calcium antagonists in guineapig myocardium [1]. Therefore, we studied which effects on cardiac ionic currents could be responsible for this interaction. Concentration-response curves for bupivacaine were studied in isolated guineapig atria and papillary muscles (slow action potentials). Effects on action potentials were assessed in the absence (n = 7 atria, n = 8 papillary muscles) or presence of nifedipine (8 x 10(-8) mol litre-1 in n = 8 atria, 10(-8) mol litre-1 in n = 8 papillary muscles). The effect on the Ca2+ current was assessed directly using the patch-clamp technique in guineapig ventricular myocytes. Bupivacaine reduced contractile force and upstroke velocity of atrial action potentials. Only the negative inotropic effect was potentiated in the presence of nifedipine. Force and upstroke velocity of slow action potentials were diminished by bupivacaine. Both variables were affected at significantly smaller concentrations of bupivacaine when given in combination with nifedipine. The Ca2+ current was reduced significantly by bupivacaine 5 x 10(-5) mol litre-1 (mean -18 (SD 7)%, n = 9). Its effect was accentuated in the presence of nifedipine 10(-9) mol litre-1 (-47 (4)%, n = 7). Bupivacaine 3 x 10(-4) mol litre-1 given alone exerted a comparable effect (-53 (4)%, n = 4). Variables indicative of Ca2+ channel function (contractile force, upstroke of slow but not normal action potentials, Ca2+ inward current) revealed potentiation of the effects of bupivacaine by nifedipine.

摘要

在豚鼠心肌中,几种钙拮抗剂可增强局部麻醉药的负性肌力作用[1]。因此,我们研究了对心脏离子电流的哪些影响可能是这种相互作用的原因。在分离的豚鼠心房和乳头肌(慢动作电位)中研究了布比卡因的浓度-反应曲线。在不存在(n = 7个心房,n = 8个乳头肌)或存在硝苯地平(心房中8×10⁻⁸摩尔/升,n = 8;乳头肌中10⁻⁸摩尔/升,n = 8)的情况下评估对动作电位的影响。使用膜片钳技术在豚鼠心室肌细胞中直接评估对Ca²⁺电流的影响。布比卡因降低了心房动作电位的收缩力和上升速度。仅在存在硝苯地平的情况下负性肌力作用增强。布比卡因降低了慢动作电位的力和上升速度。当与硝苯地平联合使用时,在显著更低的布比卡因浓度下这两个变量就受到影响。5×10⁻⁵摩尔/升的布比卡因使Ca²⁺电流显著降低(平均-18(标准差7)%,n = 9)。在10⁻⁹摩尔/升的硝苯地平存在时其作用增强(-47(4)%,n = 7)。单独给予3×10⁻⁴摩尔/升的布比卡因产生类似的作用(-53(4)%,n = 4)。指示Ca²⁺通道功能的变量(收缩力、慢动作电位而非正常动作电位的上升、Ca²⁺内向电流)显示硝苯地平增强了布比卡因的作用。

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