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Inhibitory effect of aprindine on Na+/Ca2+ exchange current in guinea-pig cardiac ventricular myocytes

机译:阿普林定对豚鼠心室肌​​细胞Na + / Ca2 +交换电流的抑制作用

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摘要

class="enumerated" style="list-style-type:decimal">Using the whole-cell voltage clamp technique, the effect of aprindine on Na+/Ca2+ exchange current (INCX) was examined in guinea-pig single cardiac ventricular myocytes and CCL39 fibroblasts expressing a dog cardiac Na+/Ca2+ exchanger (NCX1).INCX was recorded by ramp pulses from the holding potential of −60 mV with the external solution containing 140 mM Na+ and 1 mM Ca2+, and the pipette solution containing 20 mM Na+, 20 mM BAPTA and 13 mM Ca2+ (433 nM free Ca2+).External application of aprindine suppressed INCX in a concentration-dependent manner. The IC50 values of outward (measured at 50 mV) and inward (measured at −100 mV) INCX components were 48.8 and 51.8 μM with Hill coefficients of 1.3 and 1, respectively.Intracellular application of trypsin via the pipette solution did not change the blocking effect of aprindine, suggesting that aprindine does not affect the exchanger from the cytoplasmic side.Aprindine inhibited INCX of a mutant NCX1 with a deletion of amino acids 247 – 671 in the large intracellular domain between the transmembrane segments 5 and 6 in a similar manner to that of the wild-type, suggesting that the site of aprindine inhibition is not in the large intracellular domain of NCX1.A kinetic study indicated that aprindine was cooperatively competitive with KB-R7943, another inhibitor of NCX and that aprindine was a competitive inhibitor with respect to external Ca2+.We conclude that aprindine may modestly inhibit INCX in a therapeutic range of concentrations (around 2.5∼6.9 μM) possibly at an external or intra-membranous site of the exchanger.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 使用全细胞电压钳技术,检查了豚鼠单心室心肌细胞中阿普林定对Na + / Ca 2 + 交换电流(INCX)的影响表达犬心脏Na + / Ca 2 + 交换子(NCX1)的CCL39成纤维细胞。 INCX由-的保持电位通过斜坡脉冲记录60 mV,外部溶液中含有140 mM Na + 和1 mM Ca 2 + ,移液器中含有20 mM Na + ,20 mM BAPTA和13 mM Ca 2 + (433 nM游离Ca 2 + )。 外用阿普林定以浓度依赖性方式抑制INCX 。向外(在50 componentsmV处测量)和向内(在-100 mV处测量)INCX组分的IC50值分别为48.8和51.8μM,希尔系数分别为1.3和1。 通过胰蛋白酶在细胞内应用胰蛋白酶移液器溶液未改变阿普林定的阻断作用,表明阿普林定不会从细胞质侧影响交换子。 阿普林定抑制突变型NCX1的INCX,并在大范围内删除了247 – 671位氨基酸。跨膜区段5和6之间的细胞内结构域与野生型相似,表明阿普林定抑制位点不在NCX1的大细胞内结构域。 动力学研究表明aprindine与NCX的另一种抑制剂KB-R7943具有协同竞争性,并且aprindine在外部Ca 2 + 方面是竞争性抑制剂。 我们得出结论,aprindine可能适度抑制INCX在治疗浓度范围内d 2.5〜6.9μM),可能在交换器的外部或膜内位置。

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