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钙敏感型 RyR 通道致敏后自发钙波过程中腔内钙离子的变化。

Changes in intra-luminal calcium during spontaneous calcium waves following sensitization of ryanodine receptor channels.

机构信息

Department of Molecular Biophysics and Physiology, Rush University Medical Center, Chicago, IL, USA.

出版信息

Channels (Austin). 2010 Mar-Apr;4(2):87-92. doi: 10.4161/chan.4.2.11019. Epub 2010 Mar 22.

Abstract

Cardiac contraction during systole is dependent on action potential-triggered Ca(2+) release from the sarcoplasmic reticulum (SR) through ryanodine receptor (RyR) channels. SR Ca(2+) release can also occur spontaneously during diastole, which causes a decrease in Ca(2+) content within the SR and contributes to arrhythmogenesis. Here, we use measurements of cytosolic Ca(2+) and intra-SR Ca(2+) (Ca(2+)) to examine how RyR sensitization alters spontaneous SR Ca(2+) release events in rabbit ventricular myocytes. RyR sensitization with caffeine (250 microM) increased the open probability of single RyR channels, increased the initial frequency and amplitude of local SR Ca(2+) release events (Ca(2+) sparks), and decreased the Ca(2+) level where Ca(2+) sparks terminated. In intact myocytes, caffeine applied during rest after steady-state electrical stimulation increased the frequency of spontaneous Ca(2+) waves and decreased the Ca(2+) level where waves terminated. These effects caused a marked loss of SR Ca(2+) content. Therefore, increasing RyR activity has complex effects on cardiac function. Increased RyR activity during systole is beneficial as it increases SR Ca(2+) release and contractile strength. However, increased RyR activity during diastole produces spontaneous, arrhythmogenic Ca(2+) release events that lower SR Ca(2+) content and subsequently decrease contractility.

摘要

心脏收缩期的收缩依赖于动作电位触发肌浆网(SR)中的 Ca2+通过兰尼碱受体(RyR)通道释放。SR 中的 Ca2+也可以在舒张期自发释放,这会导致 SR 中的 Ca2+含量降低,并有助于心律失常的发生。在这里,我们使用细胞浆 Ca2+和内 SR Ca2+([Ca2+](SR))的测量来研究 RyR 敏化如何改变兔心室肌细胞中自发的 SR Ca2+释放事件。用咖啡因(250μM)敏化 RyR 增加了单个 RyR 通道的开放概率,增加了局部 SR Ca2+释放事件(Ca2+火花)的初始频率和幅度,并降低了 Ca2+火花终止时的[Ca2+](SR)水平。在完整的心肌细胞中,在稳定的电刺激后静息期应用咖啡因增加了自发 Ca2+波的频率,并降低了 Ca2+波终止时的[Ca2+](SR)水平。这些作用导致 SR Ca2+含量明显丢失。因此,增加 RyR 活性对心脏功能有复杂的影响。收缩期 RyR 活性的增加是有益的,因为它增加了 SR Ca2+的释放和收缩力。然而,舒张期 RyR 活性的增加会产生自发的、心律失常的 Ca2+释放事件,从而降低 SR Ca2+含量,随后降低收缩力。

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