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Regional distribution of hyperpolarization-activated current (If) and hyperpolarization-activated cyclic nucleotide-gated channel mRNA expression in ventricular cells from control and hypertrophied rat hearts

机译:对照和肥大大鼠心脏的心室细胞中超极化激活电流(If)和超极化激活环核苷酸门控通道mRNA表达的区域分布

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摘要

Hyperpolarization-activated inward current (If) and changes in the messenger RNA (mRNA) expression levels of hyperpolarization-activated cyclic nucleotide-gated channel (HCN)2 and HCN4 encoding If channels of the rat heart were studied in control and hypertrophied myocytes isolated from three ventricular regions: the septum (S), the left ventricular free wall (LV) and the right ventricular free wall (RV). Electrophysiological experiments were conducted by ruptured and perforated-patch clamp techniques and quantification of mRNA levels was carried out by quantitative reverse transcriptase polymerase chain reaction. The occurrence, density and maximal specific conductance of If were found to be significantly higher in hypertrophied ventricular myocytes isolated from S and LV than in those isolated from RV or sham-operated rats. Half-maximal activation potential, the slope of the activation curve and the threshold for activation were similar in ventricular myocytes from sham and aortic stenosed rats in the three regions studied. Isoproterenol 1 micromol l-1 increased current size by shifting current activation to more positive potentials in both sham and hypertrophied myocytes. When we studied the mRNA levels of If channel isoforms present in the ventricle, we found a significant increase of HCN2 and HCN4 mRNA levels in hypertrophied myocytes from S and LV but not in RV. We conclude that the occurrence, density and conductance of If is higher in hypertrophied than in control ventricular myocytes, S being the region where all these changes were most evident. These findings are associated with a higher expression of HCN2 and HCN4 mRNA levels in the two regions that developed hypertrophy.
机译:超极化激活的内向电流(If)和超极化激活的环状核苷酸门控通道(HCN)2和HCN4编码的信使RNA(mRNA)表达水平的变化如果研究了大鼠心脏的对照和肥大性心肌细胞三个心室区域:隔垫(S),左心室游离壁(LV)和右心室游离壁(RV)。通过破裂和穿孔膜钳技术进行电生理实验,并通过定量逆转录酶聚合酶链反应进行mRNA水平的定量。发现在分离自S和LV的肥厚型心室肌细胞中,If的发生,密度和最大比电导显着高于分离自RV或假手术大鼠的肥大心室肌细胞。在所研究的三个区域中,假手术和主动脉狭窄大鼠的心室肌细胞的半最大激活电位,激活曲线的斜率和激活阈值相似。异丙肾上腺素1微摩尔l-1通过将电流激活转移至假和肥大型心肌细胞中更多的正电位来增加电流大小。当我们研究心室中If通道亚型的mRNA水平时,我们发现来自S和LV的肥大性心肌细胞中HCN2和HCN4 mRNA水平显着增加,而RV中则没有。我们得出结论,肥厚性细胞中If的发生,密度和电导率高于对照室性心肌细胞,S是所有这些变化最明显的区域。这些发现与在肥大的两个区域中HCN2和HCN4 mRNA水平的更高表达有关。

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