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人类窦房结中的起搏电流(I(f))

Pacemaker current (I(f)) in the human sinoatrial node.

作者信息

Verkerk Arie O, Wilders Ronald, van Borren Marcel M G J, Peters Ron J G, Broekhuis Eli, Lam Kayan, Coronel Ruben, de Bakker Jacques M T, Tan Hanno L

机构信息

Heart Failure Research Center, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Eur Heart J. 2007 Oct;28(20):2472-8. doi: 10.1093/eurheartj/ehm339. Epub 2007 Sep 6.

Abstract

AIMS

Animal studies revealed that the hyperpolarization-activated pacemaker current, I(f), contributes to action potential (AP) generation in sinoatrial node (SAN) and significantly determines heart rate. I(f) is becoming a novel therapy target to modulate heart rate. Yet, no studies have demonstrated that I(f) is functionally present and contributes to pacemaking in human SAN. We aimed to study I(f) properties in human SAN.

METHODS AND RESULTS

In a patient undergoing SAN excision, we identified SAN using epicardial activation mapping. From here, we isolated myocytes and recorded APs and I(f) using patch-clamp techniques. Pacemaker cells generated spontaneous APs (cycle length 828 +/- 15 ms) following slow diastolic depolarization, maximal diastolic potential - 61.7 +/- 4.3 mV, and maximal AP upstroke velocity 4.6 +/- 1.2 V/s. They exhibited an hyperpolarization-activated inward current, blocked by external Cs(+) (2 mmol/L), characterizing it as I(f). Fully-activated conductance was 75.2 +/- 3.8 pS/pF, reversal potential - 22.1 +/- 2.4 mV, and half-maximal activation voltage and slope factor of steady-state activation - 96.9 +/- 2.7 and - 8.8 +/- 0.5 mV. Activation time constant ranged from approximately 350 ms (-130 mV) to approximately 1 s (-100 mV), deactivation time constant 156 +/- 45 ms (-40 mV). The role of I(f) in pacemaker activity was demonstrated by slowing of pacemaker cell diastolic depolarization and beating rate by Cs(+).

CONCLUSION

I(f) is functionally expressed in human SAN and probably contributes to pacemaking in human SAN.

摘要

目的

动物研究表明,超极化激活的起搏电流I(f)有助于窦房结(SAN)动作电位(AP)的产生,并显著决定心率。I(f)正成为调节心率的新治疗靶点。然而,尚无研究表明I(f)在人类SAN中具有功能活性并参与起搏活动。我们旨在研究人类SAN中I(f)的特性。

方法与结果

在一名接受SAN切除的患者中,我们通过心外膜激动标测识别出SAN。由此,我们分离出心肌细胞,并使用膜片钳技术记录AP和I(f)。起搏细胞在缓慢舒张期去极化后产生自发性AP(周期长度828±15毫秒),最大舒张电位为-61.7±4.3毫伏,最大AP上升速度为4.6±1.2伏/秒。它们表现出一种超极化激活的内向电流,可被细胞外Cs+(2毫摩尔/升)阻断,将其表征为I(f)。完全激活电导为75.2±3.8皮秒/皮法,反转电位为-22.1±2.4毫伏,稳态激活的半最大激活电压和斜率因子分别为-96.9±2.7和-8.8±0.5毫伏。激活时间常数范围约为350毫秒(-130毫伏)至约1秒(-100毫伏),失活时间常数为156±45毫秒(-40毫伏)。Cs+减慢起搏细胞舒张期去极化和搏动频率,证明了I(f)在起搏活动中的作用。

结论

I(f)在人类SAN中具有功能表达,可能参与人类SAN的起搏活动。

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