Farkas A S, Acsai K, Nagy N, Tóth A, Fülöp F, Seprényi G, Birinyi P, Nánási P P, Forster T, Csanády M, Papp J G, Varró A, Farkas A
Second Department of Internal Medicine and Cardiology Centre, University of Szeged, Szeged, Hungary.
Br J Pharmacol. 2008 May;154(1):93-104. doi: 10.1038/bjp.2008.83. Epub 2008 Mar 10.
The Na(+)/Ca(2+) exchanger (NCX) may play a key role in myocardial contractility. The operation of the NCX is affected by the action potential (AP) configuration and the intracellular Na(+) concentration. This study examined the effect of selective NCX inhibition by 0.1, 0.3 and 1.0 microM SEA0400 on the myocardial contractility in the setting of different AP configurations and different intracellular Na(+) concentrations in rabbit and rat hearts.
The concentration-dependent effects of SEA0400 on I(Na/Ca) were studied in rat and rabbit ventricular cardiomyocytes using a patch clamp technique. Starling curves were constructed for isolated, Langendorff-perfused rat and rabbit hearts. The cardiac sarcolemmal NCX protein densities of both species were compared by immunohistochemistry.
SEA0400 inhibited I(Na/Ca) with similar efficacy in the two species; there was no difference between the inhibitions of the forward or reverse mode of the NCX in either species. SEA0400 increased the systolic and the developed pressure in the rat heart in a concentration-dependent manner, for example, 1.0 microM SEA0400 increased the maximum systolic pressures by 12% relative to the control, whereas it failed to alter the contractility in the rabbit heart. No interspecies difference was found in the cardiac sarcolemmal NCX protein densities.
NCX inhibition exerted a positive inotropic effect in the rat heart, but it did not influence the contractility of the rabbit heart. This implies that the AP configuration and the intracellular Na(+) concentration may play an important role in the contractility response to NCX inhibition.
钠钙交换体(NCX)可能在心肌收缩性中起关键作用。NCX的运转受动作电位(AP)构型和细胞内钠浓度的影响。本研究检测了0.1、0.3和1.0微摩尔SEA0400选择性抑制NCX对兔和大鼠心脏在不同AP构型及不同细胞内钠浓度情况下心肌收缩性的影响。
采用膜片钳技术研究了SEA0400对大鼠和兔心室肌细胞中I(Na/Ca)的浓度依赖性效应。构建了离体的、Langendorff灌注的大鼠和兔心脏的斯塔林曲线。通过免疫组织化学比较了两种动物心脏肌膜NCX蛋白密度。
SEA0400对两种动物的I(Na/Ca)抑制效果相似;两种动物中NCX正向或反向模式的抑制之间无差异。SEA0400以浓度依赖性方式增加大鼠心脏的收缩压和舒张期压力,例如,1.0微摩尔SEA0400使最大收缩压相对于对照组增加12%,而对兔心脏的收缩性无影响。在心脏肌膜NCX蛋白密度方面未发现种间差异。
抑制NCX对大鼠心脏有正性变力作用,但对兔心脏的收缩性无影响。这表明AP构型和细胞内钠浓度可能在对NCX抑制的收缩性反应中起重要作用。