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SLC8A1基因编码的功能和结构描述

2022.8.22
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zhaoqisun

致力于为分析测试行业奉献终身

在心肌细胞中,Ca(2+)浓度在收缩时的高水平和舒张时的低水平之间交替收缩过程中ca(2+)浓度的增加主要是由于细胞内储存的ca(2+)释放所致。然而,一些Ca(2+)也通过肌膜(质膜)进入细胞在松弛过程中,ca(2+)被隔离在细胞内的储存中。为了防止细胞内存储物超载,必须从细胞中挤出穿过肌膜的Ca(2+)Na+-Ca(2+)交换剂是Ca(2+)在弛豫过程中从细胞中挤出的主要机制在心脏中,交换器可能在洋地黄作用中起关键作用。心肌细胞兴奋后,交换器是使心肌细胞恢复静息状态的主要机制。

In cardiac myocytes, Ca(2+) concentrations alternate between high levels during contraction and low levels during relaxation. The increase in Ca(2+) concentration during contraction is primarily due to release of Ca(2+) from intracellular stores. However, some Ca(2+) also enters the cell through the sarcolemma (plasma membrane). During relaxation, Ca(2+) is sequestered within the intracellular stores. To prevent overloading of intracellular stores, the Ca(2+) that entered across the sarcolemma must be extruded from the cell. The Na(+)-Ca(2+) exchanger is the primary mechanism by which the Ca(2+) is extruded from the cell during relaxation. In the heart, the exchanger may play a key role in digitalis action. The exchanger is the dominant mechanism in returning the cardiac myocyte to its resting state following excitation.

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