A mathematical model of pacemaker activity recorded from mouse small intestine

被引:39
作者
Youm, JB
Kim, N
Han, J
Kim, E
Joo, H
Leem, CH
Goto, G
Noma, A
Earm, YE
机构
[1] Seoul Natl Univ, Coll Med, Dept Physiol, Seoul 110799, South Korea
[2] Seoul Natl Univ, Coll Med, Natl Res Lab Cellular Signalling, Seoul 110799, South Korea
[3] Inje Univ, Cardiovasc Inst 2020, Coll Med,Mitochondrial Signalling Lab, Dept Physiol & Biophys, Pusan 614735, South Korea
[4] Univ Ulsan, Coll Med, Dept Physiol, Seoul 138736, South Korea
[5] Kyoto Univ, Fac Med, Dept Physiol, Kyoto 6068501, Japan
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2006年 / 364卷 / 1842期
关键词
Cajal cell; pacemaker; small intestine; simulation;
D O I
10.1098/rsta.2006.1759
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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, inathematical 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.
引用
收藏
页码:1135 / 1154
页数:20
相关论文
共 41 条
[1]   Regulation of inositol lipid-specific phospholipase C delta by changes in Ca2+ ion concentrations [J].
Allen, V ;
Swigart, P ;
Cheung, R ;
Cockcroft, S ;
Katan, M .
BIOCHEMICAL JOURNAL, 1997, 327 :545-552
[2]   INOSITOL PHOSPHATES AND CELL SIGNALING [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1989, 341 (6239) :197-205
[3]  
BERRIDGE MJ, 1990, J BIOL CHEM, V265, P9583
[4]   DEPOLARIZATION OF GUINEA-PIG VISCERAL SMOOTH-MUSCLE CAUSES HYDROLYSIS OF INOSITOL PHOSPHOLIPIDS [J].
BEST, L ;
BOLTON, TB .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1986, 333 (01) :78-82
[5]   BELL-SHAPED CALCIUM-RESPONSE CURVES OF INS(1,4,5)P3-GATED AND CALCIUM-GATED CHANNELS FROM ENDOPLASMIC-RETICULUM OF CEREBELLUM [J].
BEZPROZVANNY, I ;
WATRAS, J ;
EHRLICH, BE .
NATURE, 1991, 351 (6329) :751-754
[6]  
BIDEN TJ, 1986, J BIOL CHEM, V261, P1931
[7]   Proteins of interstitial cells of Cajal and intestinal smooth muscle, colocalized with caveolin-1 [J].
Cho, WJ ;
Daniel, EE .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 288 (03) :G571-G585
[8]   Identification of rhythmically active cells in guinea-pig stomach [J].
Dickens, EJ ;
Hirst, GDS ;
Tomita, T .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 514 (02) :515-531
[9]   Vagal inhibition in the antral region of guinea pig stomach [J].
Dickens, EJ ;
Edwards, FR ;
Hirst, GDS .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 279 (02) :G388-G399
[10]   An electrical description of the generation of slow waves in the antrum of the guinea-pig [J].
Edwards, FR ;
Hirst, GDS .
JOURNAL OF PHYSIOLOGY-LONDON, 2005, 564 (01) :213-232