Wang Teng, Huang Cong-xin, Jiang Hong, Tang Qi-zhu, Yang Bo, Wang Xi, Li Geng-shan
Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Zhonghua Xin Xue Guan Bing Za Zhi. 2005 Sep;33(9):843-7.
To investigate the relationship between the changes of the L-type calcium current (I(Ca, L)) and the calcium-activated transient outward chloride current (I(Cl, Ca)), and the repolarization characteristic of action potential in phase 1 under isoprenaline (ISO) stimulation in atrium myocytes of rabbit.
Atrium myocytes were obtained by enzymatic dissociation from a section of atrial free wall. The membrane currents and action potential were recorded by the whole-cell patch-clamp technique.
After recording I(Ca, L), atrium myocytes were perfused with ISO (1 micromol/L) immediately. Five minutes later, a transient outward current (I(to)) was significantly induced, and the peak of I(to) was gradually increased while I(Ca, L) gradually decreased with increasing in clamp voltage. The I(to) was resistant to 4-AP (3 mmol/L) but sensitive to DIDS (150 micromol/L, Cl(-) channel blocker). This current was blocked by CdCl(2) (200 micromol/L, Ca(2+) channel blocker). The elicited rate of I(to) was 91.67% (P < 0.05). (2) The shape of AP was like an inverse triangle with no plateau in Phase 2 after ISO (1 micromol/L) perfusion. Moreover, compared to the parameters of control group, APD(50) and APD(90) were significantly shortened from (65.4 +/- 4.2) ms and (95.8 +/- 3.8) ms to (12.8 +/- 3.8) ms and (27.0 +/- 4.7) ms, and reduced to 80.46% and 71.87%, respectively (P < 0.01, n = 12). 4-AP (3 mmol/L) had on obvious effect on the shape of AP, however, the plateau of AP in phase 2 was recovered by DIDS (150 micromol/L) perfusion, APD(50) and APD(90) were (41.1 +/- 4.5) ms and (79.6 +/- 3.4) ms respectively. Compared to the parameters of control group, there were no significant differences (P > 0.05, n = 12). These results indicated that ionic transport were changed by ISO perfusion in atrium myocytes and I(to) played an important role in the phase 1 repolarization of AP.
Before ISO administration, we could only observe I(Ca, L) in atrium myocytes of rabbit. After isoproterenol intervention, certain intracellular ionic consistency and membrane ionic channels were changed. Calcium activated chloride channel and I(to2) revealed obvious predominance which shorten APD significantly. Action potential showed a triangle with no plateau, suggesting an electrical remodeling in atrium myocytes. The remodeling of ionic channel is related possibly with the opening of Ca(2+)-activated Cl(-) current, which maybe the electrophysiological base of reentrant atrial tachycardia.
研究异丙肾上腺素(ISO)刺激下兔心房肌细胞L型钙电流(I(Ca,L))变化与钙激活瞬时外向氯电流(I(Cl,Ca))及动作电位1期复极化特性的关系。
采用酶解法分离兔心房游离壁获取心房肌细胞,运用全细胞膜片钳技术记录膜电流和动作电位。
(1)记录I(Ca,L)后,立即用ISO(1 μmol/L)灌流心房肌细胞。5分钟后,诱导出明显的瞬时外向电流(I(to)),随着钳制电压升高,I(to)峰值逐渐增大,而I(Ca,L)逐渐减小。I(to)对4-AP(3 mmol/L)不敏感,但对DIDS(150 μmol/L,Cl(-)通道阻滞剂)敏感。该电流可被CdCl(2)(200 μmol/L,Ca(2+)通道阻滞剂)阻断。I(to)诱发率为91.67%(P < 0.05)。(2)灌流ISO(1 μmol/L)后,动作电位形态呈倒三角形,2期无平台期。与对照组参数相比,APD(50)和APD(90)显著缩短,从(65.4 ± 4.2) ms和(95.8 ± 3.8) ms分别缩短至(12.8 ± 3.8) ms和(27.0 ± 4.7) ms,分别降至80.46%和71.87%(P < 0.01,n = 12)。4-AP(3 mmol/L)对动作电位形态无明显影响,然而,用DIDS(150 μmol/L)灌流可使动作电位2期平台期恢复,APD(50)和APD(90)分别为(41.1 ± 4.5) ms和(79.6 ± 3.4) ms。与对照组参数相比,差异无统计学意义(P > 0.05,n = 12)。这些结果表明,ISO灌流改变了心房肌细胞的离子转运,I(to)在动作电位1期复极化中起重要作用。
ISO给药前,兔心房肌细胞仅能观察到I(Ca,L)。异丙肾上腺素干预后,细胞内特定离子浓度和膜离子通道发生改变。钙激活氯通道和I(to2)明显占优势,显著缩短APD。动作电位呈无平台期的三角形,提示心房肌细胞发生电重构。离子通道重构可能与Ca(2+)激活Cl(-)电流的开放有关,这可能是折返性房性心动过速的电生理基础。