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首页> 外文期刊>The Journal of Physiology >Requirement of neuronal- and cardiac-type sodium channels for murine sinoatrial node pacemaking.
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Requirement of neuronal- and cardiac-type sodium channels for murine sinoatrial node pacemaking.

机译:鼠窦房结起搏需要神经元和心脏型钠通道。

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摘要

The majority of Na+ channels in the heart are composed of the tetrodotoxin (TTX)-resistant (KD, 2-6 microm) Nav1.5 isoform; however, recently it has been shown that TTX-sensitive (KD, 1-10 nm) neuronal Na+ channel isoforms (Nav1.1, Nav1.3 and Nav1.6) are also present and functionally important in the myocytes of the ventricles and the sinoatrial (SA) node. In the present study, in mouse SA node pacemaker cells, we investigated Na+ currents under physiological conditions and the expression of cardiac and neuronal Na+ channel isoforms. We identified two distinct Na+ current components, TTX resistant and TTX sensitive. At 37 degrees C, TTX-resistant iNa and TTX-sensitive iNa started to activate at approximately -70 and approximately -60 mV, and peaked at -30 and -10 mV, with a current density of 22 +/- 3 and 18 +/- 1 pA pF(-1), respectively. TTX-sensitive iNa inactivated at more positive potentials as compared to TTX-resistant iNa. Using action potential clamp, TTX-sensitive iNa was observed to activate late during the pacemaker potential. Using immunocytochemistry and confocal microscopy, different distributions of the TTX-resistant cardiac isoform, Nav1.5, and the TTX-sensitive neuronal isoform, Nav1.1, were observed: Nav1.5 was absent from the centre of the SA node, but present in the periphery of the SA node, whereas Nav1.1 was present throughout the SA node. Nanomolar concentrations (10 or 100 nm) of TTX, which block TTX-sensitive iNa, slowed pacemaking in both intact SA node preparations and isolated SA node cells without a significant effect on SA node conduction. In contrast, micromolar concentrations (1-30 microm) of TTX, which block TTX-resistant iNa as well as TTX-sensitive iNa, slowed both pacemaking and SA node conduction. It is concluded that two Na+ channel isoforms are important for the functioning of the SA node: neuronal (putative Nav1.1) and cardiac Nav1.5 isoforms are involved in pacemaking, although the cardiac Nav1.5 isoform alone is involved in the propagation of the action potential from the SA node to the surrounding atrial muscle.
机译:心脏中的大多数Na +通道均由抗河豚毒素(TTX)(KD,2-6微米)Nav1.5亚型组成。然而,最近显示,在心室和脑室的心肌细胞中还存在TTX敏感(KD,1-10 nm)神经元Na +通道亚型(Nav1.1,Nav1.3和Nav1.6),并且在功能上很重要。窦房(SA)节点。在本研究中,在小鼠SA节点起搏器细胞中,我们研究了生理条件下的Na +电流以及心脏和神经元Na +通道亚型的表达。我们确定了两个不同的Na +电流成分:TTX抗性和TTX敏感。在37摄氏度时,耐TTX的iNa和对TTX敏感的iNa在大约-70和-60 mV处开始激活,并在-30和-10 mV处达到峰值,电流密度为22 +/- 3和18 +分别为1 pA pF(-1)。与抗TTX的iNa相比,对TTX敏感的iNa的失活程度更高。使用动作电位钳,观察到TTX敏感的iNa在起搏器电位的后期激活。使用免疫细胞化学和共聚焦显微镜,观察到TTX耐药性心脏亚型Nav1.5和TTX敏感神经元亚型Nav1.1的分布不同:SA节点中心不存在Nav1.5,但存在在SA节点的外围,而Nav1.1在整个SA节点中都存在。阻断TTX敏感性iNa的TTX的纳摩尔浓度(10或100 nm),减慢了完整SA节点准备和分离的SA节点细胞的起搏速度,而对SA节点传导没有显着影响。相反,TTX的微摩尔浓度(1-30微米)会阻断耐TTX的iNa以及对TTX敏感的iNa,从而减慢起搏和SA结传导。结论是,两个Na +通道同工型对SA节点的功能很重要:神经元(可能的Nav1.1)和心脏Nav1.5的同工型参与起搏,尽管仅心脏Nav1.5的同工型参与了心脏的传播。从SA结到周围心房肌的动作电位。

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