The myogenic response in isolated rat cerebrovascular arteries: a smooth muscle cell model
Catherine
Lloyd
Auckland Bioengineering Institute, The University of Auckland
Model Status
This model does not run in OpenCell or COR due to missing parameter values.
Model Structure
ABSTRACT: Previous models of the cerebrovascular smooth muscle cell have not addressed the interaction between the electrical, chemical, and mechanical components of cell function during the development of active tension. These models are primarily electrical, biochemical or mechanical in their orientation, and do not permit a full exploration of how the smooth muscle responds to electrical or mechanical forcing. To address this issue, we have developed a new model that consists of two major components: electrochemical and chemomechanical subsystem models of the smooth muscle cell. Included in the electrochemical model are models of the electrophysiological behavior of the cell membrane, fluid compartments, Ca2+ release and uptake by the sarcoplasmic reticulum (SR), and cytosolic Ca2+ buffering, particularly by calmodulin (CM). With this subsystem model, we can study the mechanics of the production of intracellular Ca2+ transient in response to membrane voltage clamp pulses. The chemomechanical model includes models of: (a) the chemical kinetics of myosin phosphorylation, and the formation of phosphorylated (cycling) myosin cross-bridges with actin, as well as attached (non-cycling) latch-type cross-bridges; and (b) a model of force generation and mechanical coupling to the contractile filaments and their attachments to protein structures and the skeletal framework of the cell. The two subsystem models are tested independently and compared with data. Likewise, the complete (combined) cell model responses to voltage pulse stimulation under isometric and isotonic conditions are calculated and compared with measured single cell length-force and force-velocity data obtained from literature. This integrated cell model provides biophysically based explanations of electrical, chemical, and mechanical phenomena in cerebrovascular smooth muscle, and has considerable utility as an adjunct to laboratory research and experimental design.
The original paper reference is cited below:
The myogenic response in isolated rat cerebrovascular arteries: smooth muscle cell model, Jin Yang, John W. Clark Jr., Robert M. Bryan, and Claudia Robertson, 2003, Medical Engineering and Physics, 25, 691-709. PubMed ID: 12900184
cell diagram
Schematic diagrams of: A) the electrochemical model; B) the multi-state kinetic model of CaCM dependent myosin phosphorylation and cross-bridge formation; and C) functional block diagram of the whole integrated smooth muscle cell model.
signal transduction
rat
myogenesis
calcium dynamics
electrophysiology
cerebral arteries
Smooth Muscle Cell
smooth muscle
11709436
2003-09-09
Catherine Lloyd
Jr.
John
Clark
W
Jin
Yang
2003-10
Catherine
Lloyd
May
c.lloyd@auckland.ac.nz
This is the CellML description of Yang et al's 2003 model of the myogenic response in a smooth muscle cell.
The myogenic response in isolated rat cerebrovascular arteries: smooth muscle cell model
25
691
709
Yang et al's 2003 model of the myogenic response in a smooth muscle cell.
Smooth Muscle Cell
Rat
The University of Auckland, Auckland Bioengineering Institute
Claudia
Robertson
Medical Engineering and Physics
keyword
Robert
Bryan
M
The University of Auckland
Auckland Bioengineering Institute