Dun Wen, Ozgen Nazira, Hirose Masanori, Sosunov Eugene A, Anyukhovsky Evgeny P, Rosen Michael R, Boyden Penelope A
Department of Pharmacology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Heart Rhythm. 2007 Apr;4(4):499-507. doi: 10.1016/j.hrthm.2006.12.032. Epub 2006 Dec 28.
Pulmonary veins (PVs) and the coronary sinus (CS) play pivotal roles in triggering some episodes of atrial fibrillation. In isolated rabbit right or left atrial preparations, a 3-hour intermittent burst pacing protocol shortens action potential duration (APD) in CS and PV, but not in sinus node (SN) and left Bachmann bundle (BB) regions.
The purpose of this study was to use patch clamp techniques to study the rapidly inactivating (I(to)) and sustained (I(sus)) K(+) currents as well as Ca(2+) currents (I(Ca)) in cells dispersed from intermittent burst pacing and sham PV, BB, CS, and SN regions to determine whether changes in these currents contributed to APD shortening.
Real-time polymerase chain reaction was performed for transient outward K(+) and Ca(2+) channel subunit mRNAs to determine if intermittent burst pacing affected expression levels.
I(to) densities were unaffected by intermittent burst pacing in PV and Bachmann bundle cells. mRNA levels of K(V)4.3, K(V)4.2, K(V)1.4, and KChIP2 subunits of I(to) in both regions were stable. In CS cells, I(to) densities in intermittent burst pacing were greater than in sham (P <.05), but there were no parallel mRNA changes. I(Ca) density of PV cells was reduced from 14.27 +/- 2.08 pA/pF (at -5 mV) in sham to 7.52 +/- 1.65 pA/pF in intermittent burst pacing PV cells (P <.05) due to a significant shift in voltage dependence of activation. These results were seen in the absence of mRNA changes in alpha(1C) and alpha(1D) Ca(2+) channel subunits. In contrast, intermittent burst pacing had no effect on Ca(2+) current densities and kinetics of CS cells, but decreased alpha(1)C and alpha(1)D mRNA levels.
There is region-specific remodeling of I(to) and I(Ca) by intermittent burst pacing protocols in rabbit atrium. Increased I(to) in CS cells could account for the APD shortening observed with intermittent burst pacing, whereas an intermittent burst pacing-induced shift in voltage dependence of activation may contribute to APD shortening in PV cells.
肺静脉(PVs)和冠状窦(CS)在引发某些房颤发作中起关键作用。在离体兔右心房或左心房标本中,3小时的间歇性猝发起搏方案可缩短CS和PV中的动作电位时程(APD),但在窦房结(SN)和左房束(BB)区域则不然。
本研究旨在使用膜片钳技术研究从间歇性猝发起搏及假手术处理的PV、BB、CS和SN区域分离的细胞中的快速失活钾电流(I(to))、持续钾电流(I(sus))以及钙电流(I(Ca)),以确定这些电流的变化是否导致了APD缩短。
对瞬时外向钾通道和钙通道亚基mRNA进行实时聚合酶链反应,以确定间歇性猝发起搏是否影响其表达水平。
间歇性猝发起搏对PV和房束细胞中的I(to)密度无影响。两个区域中I(to)的K(V)4.3、K(V)4.2、K(V)1.4和KChIP2亚基的mRNA水平均稳定。在CS细胞中,间歇性猝发起搏时的I(to)密度大于假手术组(P <.05),但mRNA水平无相应变化。由于激活电压依赖性的显著改变,PV细胞的I(Ca)密度从假手术组的14.27±2.08 pA/pF(在-5 mV时)降至间歇性猝发起搏PV细胞中的7.52±1.65 pA/pF(P <.05)。在α(1C)和α(1D)钙通道亚基mRNA无变化的情况下观察到了这些结果。相反,间歇性猝发起搏对CS细胞的钙电流密度和动力学无影响,但降低了α(1C)和α(1D) mRNA水平。
兔心房中的间歇性猝发起搏方案对I(to)和I(Ca)存在区域特异性重塑。CS细胞中I(to)增加可解释间歇性猝发起搏时观察到的APD缩短,而间歇性猝发起搏引起的激活电压依赖性改变可能导致PV细胞的APD缩短。