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从小鼠小肠记录的起搏器活动的数学模型。

A mathematical model of pacemaker activity recorded from mouse small intestine.

作者信息

Youm Jae Boum, Kim Nari, Han Jin, Kim Euiyong, Joo Hyun, Leem Chae Hun, Goto Gazunori, Noma Akinori, Earm Yung E

机构信息

Mitochondrial Signaling Laboratory, Department of Physiology and Biophysics, College of Medicine, 2020 Cardiovascular Institute, Inje University Busan 614-735, South Korea.

出版信息

Philos Trans A Math Phys Eng Sci. 2006 May 15;364(1842):1135-54. doi: 10.1098/rsta.2006.1759.

Abstract

The pacemaker activity of interstitial cells of Cajal (ICCs) has been known to initiate the propagation of slow waves along the whole gastrointestinal tract through spontaneous and repetitive generation of action potentials. We studied the mechanism of the pacemaker activity of ICCs in the mouse small intestine and tested it using a mathematical model. The model includes ion channels, exchanger, pumps and intracellular machinery for Ca2+ regulation. The model also incorporates inositol 1,4,5-triphosphate (IP3) production and IP3-mediated Ca2+ release activities. Most of the parameters were obtained from the literature and were modified to fit the experimental results of ICCs from mouse small intestine. We were then able to compose a mathematical model that simulates the pacemaker activity of ICCs. The model generates pacemaker potentials regularly and repetitively as long as the simulation continues. The frequency was set at 20 min(-1) and the duration at 50% repolarization was 639 ms. The resting and overshoot potentials were -78 and +1.2 mV, respectively. The reconstructed pacemaker potentials closely matched those obtained from animal experiments. The model supports the idea that cyclic changes in [Ca2+]i and [IP3] play key roles in the generation of ICC pacemaker activity in the mouse small intestine.

摘要

已知 Cajal 间质细胞(ICCs)的起搏活动通过自发且重复地产生动作电位,启动慢波沿整个胃肠道的传播。我们研究了小鼠小肠中 ICCs 起搏活动的机制,并使用数学模型进行了测试。该模型包括离子通道、离子交换体、泵以及用于 Ca2+调节的细胞内机制。模型还纳入了肌醇 1,4,5 - 三磷酸(IP3)的产生和 IP3 介导的 Ca2+释放活动。大多数参数取自文献,并进行了修改以符合从小鼠小肠 ICCs 获得的实验结果。然后,我们能够构建一个模拟 ICCs 起搏活动的数学模型。只要模拟持续进行,该模型就会定期且重复地产生起搏电位。频率设定为 20 min(-1),复极化 50%时的持续时间为 639 ms。静息电位和超射电位分别为 -78 mV 和 +1.2 mV。重建的起搏电位与从动物实验获得的电位紧密匹配。该模型支持这样一种观点,即细胞内 Ca2+浓度([Ca2+]i)和 IP3 的周期性变化在小鼠小肠 ICCs 起搏活动的产生中起关键作用。

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