Institute of Biomedical and Life Sciences, West Medical Building, University of Glasgow, Glasgow G12 8QQ, UK.
J Physiol. 2010 Dec 1;588(Pt 23):4731-42. doi: 10.1113/jphysiol.2010.193375. Epub 2010 Oct 4.
Spontaneous Ca²(+) waves in cardiac muscle cells are thought to arise from the sequential firing of local Ca²(+) sparks via a fire-diffuse-fire mechanism. This study compares the ability of the ryanodine receptor (RyR) blocker ruthenium red (RuR) to inhibit these two types of Ca²(+) release in permeabilised rabbit ventricular cardiomyocytes. Perfusing with 600 nm Ca²(+) (50 μm EGTA) caused regular spontaneous Ca²(+) waves that were imaged with the fluorescence from Fluo-5F using a laser-scanning confocal microscope. Addition of 4 μm RuR caused complete inhibition of Ca²(+) waves in 50% of cardiomyocytes by 2 min and in 100% by 4 min. Separate experiments used 350 μm EGTA (600 nm Ca²(+)) to limit Ca²(+) diffusion but allow the underlying Ca(2+) sparks to be imaged. The time course of RuR-induced inhibition did not match that of waves. After 2 min of RuR, none of the characteristics of the Ca²(+) sparks were altered, and after 4 min Ca²(+) spark frequency was reduced ∼40%; no sparks could be detected after 10 min. Measurements of Ca(2+) within the SR lumen using Fluo-5N showed an increase in intra-SR Ca²(+) during the initial 2-4 min of perfusion with RuR in both wave and spark conditions. Computational modelling suggests that the sensitivity of Ca²(+) waves to RuR block depends on the number of RyRs per cluster. Therefore inhibition of Ca²(+) waves without affecting Ca²(+) sparks may be explained by block of small, non-spark producing clusters of RyRs that are important to the process of Ca²(+) wave propagation.
心肌细胞中的自发 Ca²⁺波被认为是通过“火扩散火”机制,由局部 Ca²⁺火花的顺序点火引起的。本研究比较了兰尼碱受体(RyR)阻断剂钌红(RuR)抑制通透化兔心室心肌细胞中这两种类型 Ca²⁺释放的能力。用含有 50 μm EGTA 的 600 nm Ca²⁺(600 nm Ca²⁺)灌流引起了有规律的自发 Ca²⁺波,并用激光扫描共聚焦显微镜通过 Fluo-5F 的荧光来成像。加入 4 μm RuR 在 2 分钟内使 50%的心肌细胞中 Ca²⁺波完全抑制,在 4 分钟内使 100%的心肌细胞中 Ca²⁺波完全抑制。单独的实验用 350 μm EGTA(600 nm Ca²⁺)限制 Ca²⁺扩散,但允许成像基础的 Ca²⁺火花。RuR 诱导的抑制的时间进程与波的时间进程不匹配。在 RuR 孵育 2 分钟后,Ca²⁺火花的所有特征均未改变,并且在 4 分钟后 Ca²⁺火花频率降低了约 40%;在 10 分钟后无法检测到火花。用 Fluo-5N 测量 SR 腔室内的 Ca²⁺显示,在 RuR 灌注的最初 2-4 分钟内,在波和火花条件下,SR 腔内的 Ca²⁺增加。计算模型表明,Ca²⁺波对 RuR 阻断的敏感性取决于每个簇中的 RyR 数量。因此,不影响 Ca²⁺火花而抑制 Ca²⁺波可能是由于阻断了对 Ca²⁺波传播过程很重要的小的、不产生火花的 RyR 簇。