Wakayama Yuji, Miura Masahito, Stuyvers Bruno D, Boyden Penelope A, ter Keurs Henk E D J
First Department of Internal Medicine, Tohoku University School of Medicine, Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Circ Res. 2005 Jun 24;96(12):1266-73. doi: 10.1161/01.RES.0000172544.56818.54. Epub 2005 Jun 2.
Ca2+ waves underlying triggered propagated contractions (TPCs) are initiated in damaged regions in cardiac muscle and cause arrhythmias. We studied Ca2+ waves underlying TPCs in rat cardiac trabeculae under experimental conditions that simulate the functional nonuniformity caused by local mechanical or ischemic local damage of myocardium. A mechanical discontinuity along the trabeculae was created by exposing the preparation to a small jet of solution with a composition that reduces excitation-contraction coupling (ECC) in myocytes within that segment. The jet solution contained either caffeine (5 mmol/L), 2,3-butanedione monoxime (BDM; 20 mmol/L), or low Ca2+ concentration ([Ca2+]; 0.2 mmol/L). Force was measured with a silicon strain gauge and sarcomere length with laser diffraction techniques in 15 trabeculae. Simultaneously, [Ca2+]i was measured locally using epifluorescence of Fura-2. The jet of solution was applied perpendicularly to a small muscle region (200 to 300 microm) at constant flow. When the jet contained caffeine, BDM, or low [Ca2+], during the stimulated twitch, muscle-twitch force decreased and the sarcomeres in the exposed segment were stretched by shortening normal regions outside the jet. Typical protocols for TPC induction (7.5 s-2.5 Hz stimulus trains at 23 degrees C; [Ca2+]o=2.0 mmol/L) reproducibly generated Ca2+ waves that arose from the border between shortening and stretched regions. Such Ca2+ waves started during force-relaxation of the last stimulated twitch of the train and propagated (0.2 to 2.8 mm/sec) into segments both inside and outside of the jet. Arrhythmias, in the form of nondriven rhythmic activity, were induced when the amplitude of the Ca2+-wave was increased by raising [Ca2+]o. Arrhythmias disappeared rapidly when uniformity of ECC throughout the muscle was restored by turning the jet off. These results show, for the first time, that nonuniform ECC can cause Ca2+ waves underlying TPCs and suggest that Ca2+ dissociated from myofilaments plays an important role in the initiation of Ca2+ waves.
引发性传播收缩(TPCs)背后的Ca2+波在心肌受损区域起始,并导致心律失常。我们在模拟由局部机械性或缺血性心肌局部损伤引起的功能不均匀性的实验条件下,研究了大鼠心脏小梁中TPCs背后的Ca2+波。通过将标本暴露于一股小的溶液射流来在小梁上制造机械性不连续,该溶液的成分会降低该节段内心肌细胞的兴奋-收缩偶联(ECC)。射流溶液含有咖啡因(5 mmol/L)、2,3-丁二酮单肟(BDM;20 mmol/L)或低Ca2+浓度([Ca2+];0.2 mmol/L)。用硅应变仪测量15个小梁的力,并用激光衍射技术测量肌节长度。同时,使用Fura-2的落射荧光局部测量[Ca2+]i。以恒定流速将溶液射流垂直施加于一个小的肌肉区域(200至300微米)。当射流含有咖啡因、BDM或低[Ca2+]时,在刺激的单收缩期间,肌肉单收缩力下降,且暴露节段中的肌节通过缩短射流外的正常区域而被拉伸。用于诱导TPCs的典型方案(在23℃下7.5秒-2.5赫兹刺激串;[Ca2+]o = 2.0 mmol/L)可重复性地产生从缩短区域和拉伸区域之间的边界处起始的Ca2+波。这种Ca2+波在刺激串的最后一次刺激单收缩的力松弛期间开始,并向射流内外的节段传播(0.2至2.8毫米/秒)。当通过提高[Ca2+]o增加Ca2+波的幅度时,会诱发以非驱动性节律活动形式出现的心律失常。当关闭射流恢复整个肌肉ECC的均匀性时,心律失常迅速消失。这些结果首次表明,不均匀的ECC可导致TPCs背后的Ca2+波,并提示从肌丝解离的Ca2+在Ca2+波的起始中起重要作用。