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[兔心脏真正起搏点窦房结快速去极化中缓慢激活的电压依赖性钠电流贡献]

[Slow activated voltage-dependent sodium current contribution in fast depolarization in the rabbit heart true pacemaker sinoatrial node].

作者信息

Golovko V A

出版信息

Ross Fiziol Zh Im I M Sechenova. 2009 Apr;95(4):387-97.

Abstract

The functional role of INa in initiation and conduction of cardiac true pacemaker activity remains uncertain. Therefore the goal of this work was to study the effects of Na+ substitution of action potentials parameters of the sinoatrial area cells. Transmembrane action potentials were recorded with 15 to 40 MOmega glass microelectrodes filled with 2.5 M KCl. The final preparations was about 5 x 3 mm in size, contained a portion sinoatrial node and the adjacent fragment of tissue of the right branch of the sinoatrial ring bundle and crista terminalis. All strips were allowed to beat spontaneously. We have registered that Na+ replacement of 50% in external solution causes an almost two-fold monotonous decrease of dV/dtmax and overshoot values of primary (3.2 V/s, n = 15), latent pacemaker (17 V/s, n = 16) and "conducting"-like cells (130 V/s, n = 16, control, 35 C) as compared with the control. Finally (at 30 min exposure) action potential frequency is slowed dowb by 20-30%. True pacemaker cells decreased action potential amplitude from 65 to 9 mV for 20-30 min 50% Na solution exposure. It should be noted that the cells of the "conducting"-like type demonstrated the generation block of action potential 30% Na exposure. At the same time dV/dtmax monotonously decreased from 3.1 to 1.5 V/s (true pacemaker) 16 vs 7 V/s (latent) and from 130 to 1.8 v/s ("conducting"). In our opinion, these facts deserve particular attention because it has been reported earlier that tetrodotoxin (20 mcM) addition in to the control solution caused the decrease of dV/dt from 100 to 4 V/s in latent pacemaker, whereas action potential amplitude is decreased by only some mV and the rate of beating by 1.5 times. As for true pacemaker cells, the TTX does not influence them.

摘要

心肌真正起搏活动的起始和传导过程中,钠电流(INa)的功能作用仍不明确。因此,本研究的目的是探讨用钠离子替代物对窦房区域细胞动作电位参数的影响。使用填充有2.5M KCl的15至40兆欧玻璃微电极记录跨膜动作电位。最终制备的组织大小约为5×3毫米,包含一部分窦房结以及窦房环束右支和终嵴的相邻组织片段。所有组织条均允许自发搏动。我们记录到,与对照组相比,细胞外溶液中50%的钠离子被替代后,原初起搏细胞(3.2V/s,n = 15)、潜在起搏细胞(17V/s,n = 16)和“传导样”细胞(130V/s,n = 16,对照组,35℃)的dV/dtmax和超射值几乎呈两倍的单调下降。最后(暴露30分钟时),动作电位频率减慢20 - 30%。在50%钠离子溶液中暴露20 - 30分钟后,真正的起搏细胞动作电位幅度从65mV降至9mV。需要注意的是,“传导样”类型的细胞在30%钠离子暴露时表现出动作电位产生阻滞。同时,dV/dtmax单调下降,真正起搏细胞从3.1V/s降至1.5V/s,潜在起搏细胞从16V/s降至7V/s,“传导样”细胞从130V/s降至1.8V/s。我们认为,这些事实值得特别关注,因为此前有报道称,在对照溶液中加入河豚毒素(20μM)会使潜在起搏细胞的dV/dt从100V/s降至4V/s,而动作电位幅度仅降低几毫伏,搏动频率降低1.5倍。至于真正的起搏细胞,河豚毒素对其没有影响。

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