Defining electrical communication in skeletal muscle resistance arteries: a computational approach

被引:89
作者
Diep, HK
Vigmond, EJ
Segal, SS
Welsh, DG
机构
[1] Univ Calgary, Fac Med, Dept Elect & Comp Engn, Calgary, AB T2N 4N1, Canada
[2] Yale Univ, John B Pierce Lab, New Haven, CT USA
[3] Yale Univ, Dept Cellular & Mol Physiol, New Haven, CT USA
[4] Univ Calgary, Smooth Muscle Res Grp, Calgary, AB, Canada
[5] Univ Calgary, Dept Physiol & Biophys, Calgary, AB, Canada
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2005年 / 568卷 / 01期
关键词
D O I
10.1113/jphysiol.2005.090233
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Vascular cells communicate electrically to coordinate their activity and control tissue blood flow. To foster a quantitative understanding of this fundamental process, we developed a computational model that was structured to mimic a skeletal muscle resistance artery. Each endothelial cell and smooth muscle cell in our virtual artery was treated as the electrical equivalent of a capacitor coupled in parallel with a non-linear resistor representing ionic conductance; intercellular gap junctions were represented by ohmic resistors. Simulations revealed that the vessel wall is not a syncytium, in which electrical stimuli spread equally to all constitutive cells. Indeed, electrical signals spread in a differential manner among and between endothelial cells and smooth muscle cells according to the initial stimulus. The predictions of our model agree with physiological data from the feed artery of the hamster retractor muscle. Cell orientation and coupling resistance were the principal factors that enable electrical signals to spread differentially along and between the two cell types. Our computational observations also illustrated how gap junctional coupling enables the vessel wall to filter and transform transient electrical events into sustained voltage responses. Functionally, differential electrical communication would permit discrete regions of smooth muscle activity to locally regulate blood flow and the endotheliurn to coordinate regional changes in tissue perfusion.
引用
收藏
页码:267 / 281
页数:15
相关论文
共 34 条
[1]   Resolution of smooth muscle and endothelial pathways for conduction along hamster cheek pouch arterioles [J].
Bartlett, IS ;
Segal, SS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (02) :H604-H612
[2]  
Crane GJ, 2001, MICROCIRCULATION, V8, P33
[3]   Impaired conduction of vasodilation along arterioles in connexin40-deficient mice [J].
de Wit, C ;
Roos, F ;
Bolz, SS ;
Kirchhoff, S ;
Krüger, O ;
Willecke, K ;
Pohl, U .
CIRCULATION RESEARCH, 2000, 86 (06) :649-655
[4]  
Emerson GG, 2000, CIRC RES, V87, P474
[5]   Conduction of hyperpolarization along hamster feed arteries: augmentation by acetylcholine [J].
Emerson, GG ;
Neild, TO ;
Segal, SS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (01) :H102-H109
[6]   Endothelial cell pathway for conduction of hyperpolarization and vasodilation along hamster feed artery [J].
Emerson, GG ;
Segal, SS .
CIRCULATION RESEARCH, 2000, 86 (01) :94-100
[7]   Morphology favors an endothelial cell pathway for longitudinal conduction within arterioles [J].
Haas, TL ;
Duling, BR .
MICROVASCULAR RESEARCH, 1997, 53 (02) :113-120
[8]   Voltage dependence of the coupling of Ca2+ sparks to BKCa channels in urinary bladder smooth muscle [J].
Herrera, GM ;
Heppner, TJ ;
Nelson, MT .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (03) :C481-C490
[9]   ANALYSIS OF EXCITATORY JUNCTIONAL POTENTIALS RECORDED FROM ARTERIOLES [J].
HIRST, GDS ;
NEILD, TO .
JOURNAL OF PHYSIOLOGY-LONDON, 1978, 280 (JUL) :87-104
[10]   Enzymatic isolation and characterization of single vascular smooth muscle cells from cremasteric arterioles [J].
Jackson, WF ;
Huebner, JM ;
Rusch, NJ .
MICROCIRCULATION-LONDON, 1997, 4 (01) :35-50