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Gene expression of stretch-activated channels and mechanoelectric feedback in the heart.

机译:心脏中拉伸激活通道和机电反馈的基因表达。

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摘要

1. Mechanoelectric feedback (MEF) in the heart is the process by which mechanical forces on the myocardium can change its electrical properties. Mechanoelectric feedback has been demonstrated in many animal models, ranging from isolated cells, through isolated hearts to whole animals. In humans, MEF has been demonstrated directly in both the atria and the ventricles. It seems likely that MEF provides either the trigger or the substrate for some types of clinically important arrhythmias. 2. Mechanoelectric feedback may arise because of the presence of stretch-sensitive (or mechano-sensitive) ion channels in the cell membrane of the cardiac myocytes. Two types have been demonstrated: (i) a non-specific cation channel (stretch-activated channel (SAC); conductance of approximately 25 pS); and (ii) a potassium channel with a conductance of approximately 100 pS. The gene coding for the SAC has not yet been identified. The gene for the potassium channel is likely to be TREK, a member of the tandem pore potassium channel gene family. We have recorded stretch-sensitive potassium channels in rat isolated myocytes that have the properties of TREK channels expressed in heterologous systems. 3. It has been shown that TREK mRNA is expressed heterogeneously in the rat ventricular wall, with 17-fold more expression in endocardial compared with epicardial cells. This difference is reflected in the TREK currents recorded from endocardial and epicardial cells using whole-cell patch-clamp techniques, although the difference in current density was less pronounced (approximately threefold). Consistent with this, we show here that when the ventricle is stretched by inflation of an intraventricular balloon in a Langendorff perfused rat isolated heart, action potential shortening was more pronounced in the endocardium (30% shortening at 40 mmHg) compared with that in the epicardium (10% shortening at the same pressure). 4. Computer models of the mechanics of the (pig) heart show pronounced spatial variations in strain in themyocardium with large transmural differences (in the left ventricle in particular) and also large differences between the base and apex of the ventricle. 5. The importance of MEF and the non-homogeneous gene expression and strain distribution for arrhythmias is discussed.
机译:1.心脏中的机械电反馈(MEF)是心肌上的机械力可以改变其电特性的过程。机电电反馈已在许多动物模型中得到证实,从分离的细胞到心脏的分离,再到整个动物,都可以实现。在人类中,MEF已直接在心房和心室中得到证实。 MEF可能为某些类型的临床上重要的心律失常提供了触发因素或底物。 2.由于心肌细胞的细胞膜中存在拉伸敏感(或机械敏感)离子通道,因此可能会产生机电反馈。已经证明了两种类型:(i)非特异性阳离子通道(拉伸激活通道(SAC);电导率约为25 pS);以及(ii)钾通道,电导约为100 pS。尚未发现编码SAC的基因。钾通道的基因可能是TREK,它是串联孔钾通道基因家族的成员。我们已经在大鼠分离的心肌细胞中记录了舒张敏感性钾通道,该通道具有异源系统表达的TREK通道的特性。 3.已经显示,TREK mRNA在大鼠心室壁中异质表达,与心外膜细胞相比,心内膜中的表达高17倍。这种差异反映在使用全细胞膜片钳技术从心内膜和心外膜细胞记录的TREK电流中,尽管电流密度的差异不太明显(大约三倍)。与此相符的是,我们在这里表明,当在Langendorff灌注的大鼠离体心脏中通过心室球囊的充气使心室伸展时,与心外膜相比,心内膜的动作电位缩短更为明显(在40 mmHg时缩短30%)。 (在相同压力下缩短10%)。 4.(猪)心脏力学的计算机模型显示,它们在心肌中的应变具有明显的空间变化,具有较大的跨壁差异(尤其是在左心室中),并且在心室的基部和根尖之间也存在较大差异。 5.讨论了MEF的重要性以及心律不齐的非均一基因表达和菌株分布。

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