Kano T, Nishi K
Am J Physiol. 1986 Aug;251(2 Pt 2):H324-30. doi: 10.1152/ajpheart.1986.251.2.H324.
Effects of changing external pH on delayed afterdepolarization (DAD) induced by a train of electrical stimuli in the rabbit ventricular papillary muscle fibers were examined using a conventional microelectrode technique in vitro. Preparations were superfused with Tyrode solution containing norepinephrine (3 X 10(-6) M), and the external pH was decreased. After a train of driven action potentials, DAD was induced at pH 7.0 in the presence of norepinephrine. The amplitude of the DAD induced by norepinephrine at pH 7.0 increased as the stimulus cycle length was shortened and as the number of applied stimuli increased. The increase in the amplitude of DAD resulted in yielding one or multiple nondriven action potentials. DAD, thus initiated, was completely suppressed by a further decrease of external pH to 6.7-6.0. Lidocaine and adriamycin depressed the amplitude of DAD, but verapamil did not. The results imply that only slight lowering of the external pH induced by ischemic conditions or by other means would provoke DAD which, in turn, would result in triggered activity in situ.
采用传统的体外微电极技术,研究了改变细胞外pH值对家兔心室乳头肌纤维串刺激诱发的延迟后去极化(DAD)的影响。用含去甲肾上腺素(3×10⁻⁶M)的台氏液灌流标本,并降低细胞外pH值。在去甲肾上腺素存在的情况下,当细胞外pH值为7.0时,一串驱动动作电位后可诱发DAD。去甲肾上腺素在pH 7.0时诱发的DAD幅度随着刺激周期长度的缩短和刺激次数的增加而增大。DAD幅度的增加导致产生一个或多个非驱动动作电位。如此引发的DAD可通过将细胞外pH值进一步降至6.7 - 6.0而完全被抑制。利多卡因和阿霉素可降低DAD的幅度,但维拉帕米则不能。结果表明,缺血状态或其他因素引起的细胞外pH值轻微降低即可诱发DAD,进而导致原位触发活动。