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Hyperpolarization-activated cyclic nucleotide-gated channel gene: the most possible therapeutic applications in the field of cardiac biological pacemakers.

机译:超极化激活的环状核苷酸门控通道基因:心脏生物学起搏器领域中最可能的治疗应用。

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摘要

The implantation of electronic devices has become the preferred treatment for symptomatic bradyarrhythmias. However, there are many shortcomings in electronic pacemakers. More recently, the data has suggested that application of hyperpolarization-activated cyclic nucleotide-gated (HCN) channel gene may hold great promise in development of biological pacemaker. The evidence for the hypotheses included that: (1) The expression of four HCN genes varies somewhat among cardiac tissue. And also, the main difference between pacemaker cells and common cardiomyocytes depends upon which HCN genes are fully expressed; (2) the animals lacking HCN channels show a pronounced cardiac phenotype, which is due to dysfunction of the sinus node; (3) it is suggested that primary defects in HCN channels might underlie certain cardiac arrhythmias in several families with hereditary sinus node dysfunction; (4) recently, several studies demonstrated that overexpression of HCN gene in myocytes via gene delivery or implantation of stem cells with overexpression of I(f) successfully induced automaticity of a biological pacemaker in arrhythmic animal models.
机译:电子设备的植入已成为有症状的心律失常的首选治疗方法。但是,电子起搏器存在许多缺点。最近,数据表明超极化激活的环状核苷酸门控(HCN)通道基因的应用可能在生物起搏器的发展中具有广阔的前景。假设的证据包括:(1)四个HCN基因的表达在心脏组织中有所不同。而且,起搏器细胞和普通心肌细胞之间的主要区别取决于哪些HCN基因被充分表达; (2)缺乏HCN通道的动物表现出明显的心脏表型,这是由于窦房结功能障碍所致; (3)有人认为,HCN通道的主要缺陷可能是遗传性窦房结功能不全的几个家庭中某些心律不齐的原因; (4)最近,一些研究表明,通过基因传递或干细胞的植入以及I(f)的过表达,HCN基因在心肌细胞中的过表达成功地诱导了心律失常动物模型中生物起搏器的自动化。

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