Noble D, Varghese A, Kohl P, Noble P
University Laboratory of Physiology, University of Oxford, United Kingdom.
Can J Cardiol. 1998 Jan;14(1):123-34.
The guinea-pig ventricular cell model, originally developed by Noble et al in 1991, has been greatly extended to include accumulation and depletion of calcium in a diadic space between the sarcolemma and the sarcoplasmic reticulum where, according to contempory understanding, the majority of calcium-induced calcium release is triggered. The calcium in this space is also assumed to play the major role in calcium-induced inactivation of the calcium current. Delayed potassium current equations have been developed to include the rapid (IKr) and slow (IKs) components of the delayed rectifier current based on the data of of Heath and Terrar, along with data from Sanguinetti and Jurkiewicz. Length- and tension-dependent changes in mechanical and electrophysiological processes have been incorporated as described recently by Kohl et al. Drug receptor interactions have started to be developed, using the sodium channel as the first target. The new model has been tested against experimental data on action potential clamp, and on force-interval and duration-interval relations; it has been found to reliably reproduce experimental observations.
豚鼠心室细胞模型最初由诺布尔等人于1991年开发,现已得到极大扩展,纳入了肌膜与肌浆网之间二联体空间中钙的积累和消耗情况。根据当代的认识,在该空间中,大部分钙诱导的钙释放由此触发。此空间中的钙还被认为在钙电流的钙诱导失活中起主要作用。基于希思和泰拉的数据以及桑吉内蒂和尤尔凯维茨的数据,已开发出延迟钾电流方程,以纳入延迟整流电流的快速(IKr)和慢速(IKs)成分。如科尔等人最近所述,机械和电生理过程中长度和张力依赖性变化已被纳入。药物受体相互作用已开始以钠通道作为首个靶点进行研究。新模型已根据动作电位钳、力-间期和时程-间期关系的实验数据进行了测试;结果发现它能可靠地重现实验观察结果。