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首页> 外文期刊>Journal of cardiovascular electrophysiology >pH-Regulated Na(+) influx into the mammalian ventricular myocyte: the relative role of Na(+)-H(+) exchange and Na(+)-HCO Co-transport.
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pH-Regulated Na(+) influx into the mammalian ventricular myocyte: the relative role of Na(+)-H(+) exchange and Na(+)-HCO Co-transport.

机译:pH调节的Na(+)流入哺乳动物的心室肌细胞:Na(+)-H(+)交换和Na(+)-HCO协同转运的相对作用。

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摘要

In the heart, intracellular Na(+) concentration (Na(+) (i)) is a controller of intracellular Ca(2+) signaling, and hence of key aspects of cell contractility and rhythm. Na(+) (i) will be influenced by variation in Na(+) influx. In the present work, we consider one source of Na(+) influx, sarcolemmal acid extrusion. Acid extrusion is accomplished by sarcolemmal H(+) and HCO(3) (-) transporters that import Na(+) ions while exporting H(+) or importing HCO(3) (-). The capacity of this system to import Na(+) is enormous, up to four times the maximum capacity of the Na(+)-K(+) ATPase to extrude Na(+) ions from the cell. In this review we consider the role of Na(+)-H(+) exchange (NHE) and Na(+)-HCO(3) (-)co-transport (NBC) in mediating Na(+) influx into cardiac myocytes. We consider, in particular, the role of NBC, as so little is known about Na(+) influx through this transporter. We show that both proteins mediate significant Na(+) influx and that although, in the ventricular myocyte, NBC-mediated Na(+) influx is less than through NHE, the proportions may be altered under a variety of conditions, including exposure to catecholamines, membrane depolarization, and interference with activity of the enzyme, carbonic anhydrase.
机译:在心脏中,细胞内Na(+)浓度(Na(+)(i))是细胞内Ca(2+)信号传导的控制器,因此是细胞收缩性和节律的关键方面。 Na(+)(i)将受到Na(+)流入量变化的影响。在目前的工作中,我们考虑到Na(+)涌入的一种来源,肌膜酸挤压。酸挤压是通过肌膜H(+)和HCO(3)(-)转运蛋白完成的,该转运蛋白在导入H(+)或导入HCO(3)(-)的同时导入Na(+)离子。该系统导入Na(+)的能力是巨大的,最多是Na(+)-K(+)ATPase从细胞中挤出Na(+)离子的最大能力的四倍。在这篇综述中,我们考虑了Na(+)-H(+)交换(NHE)和Na(+)-HCO(3)(-)共转运(NBC)在介导Na(+)流入心肌细胞中的作用。我们特别考虑NBC的作用,因为关于Na(+)通过该转运蛋白的流入知之甚少。我们显示这两种蛋白质都介导大量的Na(+)流入,尽管在心室肌细胞中,NBC介导的Na(+)流入少于通过NHE,但在各种条件下,包括暴露于儿茶酚胺的情况下,其比例可能会改变,膜去极化和干扰酶碳酸酐酶的活性。

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