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目的:研究胞外不同Ca2+浓度对豚鼠心室肌细胞钠钙交换电流(Na+Ca2+exchangecurent,INaCa)的影响和阿米洛利(amiloride)对该电流的作用。方法:建立缺血再灌时胞内Na+超载的细胞模型,用膜片钳全细胞技术,记录INaCa的电流电压关系曲线。结果:阿米洛利10-5,3×10-5和10-4mol·L-1,在+50mV时,对INaCa的抑制率分别是154%,226%和409%;在-80mV时抑制率分别是56%,146%和232%。结论:胞内Na+超载确可引起Na+Ca2+交换系统激活;阿米洛利对豚鼠心室肌细胞INaCa有抑制作用,且对INaCa外向成分的抑制作用大于对内向成分的抑制作用。
Objective: To study the effect of extracellular Ca2 + concentration on sodium-calcium exchange current (Na + Ca2 + exchangecurent, INaCa) in guinea pig ventricular myocytes and the effect of amiloride on this current. Methods: To establish a cell model of intracellular Na + overload during ischemia / reperfusion, and record the current-voltage curve of INa-Ca using patch-clamp whole cell technique. Results: The inhibitory rates of amiloride at 10-5, 3 × 10-5 and 10-4 mol·L-1 at +50 mV were 154%, 226% and 409, respectively %; At -80mV inhibition rates were 5.6%, 14.6% and 23.2%. CONCLUSION: Intracellular Na + overload can indeed activate Na +Ca2 + exchange system. Amiloride can inhibit the INaCa in guinea pig ventricular myocytes, and inhibit the INaCa extrinsic component more than the inwardinhibitory component.