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Cajal间质细胞中起搏器电位随机行为的建模。

Modeling of stochastic behavior of pacemaker potential in interstitial cells of Cajal.

作者信息

Youm Jae Boum, Leem Chae Hun, Lee Sung Ryul, Song In-Sung, Kim Hyoung Kyu, Heo Hye Jin, Kim Byung Joo, Kim Nari, Han Jin

机构信息

Department of Physiology, College of Medicine, Cardiovascular and Metabolic Disease Center, Inje University, Busan, South Korea.

Department of Physiology University of Ulsan College of Medicine, Seoul, South Korea.

出版信息

Prog Biophys Mol Biol. 2014 Sep;116(1):56-69. doi: 10.1016/j.pbiomolbio.2014.09.002. Epub 2014 Sep 17.

Abstract

It is widely accepted that interstitial cells of Cajal (ICCs) generate pacemaker potentials to propagate slow waves along the whole gastrointestinal tract. Previously, we constructed a biophysically based model of ICCs in mouse small intestine to explain the pacemaker mechanism. Our previous model, however, could not explain non-uniformity of pacemaker potentials and random occurrence of unitary potentials, thus we updated our model. The inositol 1,4,5-trisphosphate (IP3)-mediated Ca(2+) mobilization is a key event to drive the cycle of pacemaker activity and was updated to reproduce its stochastic behavior. The stochasticity was embodied by simulating random opening and closing of individual IP3-mediated Ca(2+) channel. The updated model reproduces the stochastic features of pacemaker potentials in ICCs. Reproduced pacemaker potentials are not uniform in duration and interval. The resting and peak potentials are -75.5 ± 1.1 mV and -0.8 ± 0.5 mV, respectively (n = 55). Frequency of pacemaker potential is 14.3 ± 0.4 min(-1) (n = 10). Width at half-maximal amplitude of pacemaker potential is 902 ± 6 ms (n = 55). There are random events of unitary potential-like depolarization. Finally, we compared our updated model with a recently published model to speculate which ion channel is the best candidate to drive pacemaker depolarization. In conclusion, our updated mathematical model could now reproduce stochastic features of pacemaker activity in ICCs.

摘要

人们普遍认为, Cajal间质细胞(ICCs)产生起搏电位,以沿整个胃肠道传播慢波。此前,我们构建了一个基于生物物理学的小鼠小肠ICC模型来解释起搏机制。然而,我们之前的模型无法解释起搏电位的不均匀性和单一电位的随机出现,因此我们对模型进行了更新。肌醇1,4,5-三磷酸(IP3)介导的Ca(2+)动员是驱动起搏活动周期的关键事件,并进行了更新以重现其随机行为。随机性通过模拟单个IP3介导的Ca(2+)通道的随机开放和关闭来体现。更新后的模型重现了ICC中起搏电位的随机特征。重现的起搏电位在持续时间和间隔上并不均匀。静息电位和峰值电位分别为-75.5±1.1 mV和-0.8±0.5 mV(n = 55)。起搏电位的频率为14.3±0.4 min(-1)(n = 10)。起搏电位半最大振幅处的宽度为902±6 ms(n = 55)。存在类似单一电位去极化的随机事件。最后,我们将更新后的模型与最近发表的模型进行比较,以推测哪个离子通道是驱动起搏去极化的最佳候选者。总之,我们更新后的数学模型现在可以重现ICC中起搏活动的随机特征。

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