%0 Journal Article %1 yang-clarkb %A Yang, Jin %A Jr., John W. Clark %A Bryan, Robert M. %A Robertson, Claudia S. %D 2003 %J Med Eng Phys %K arteries muscle %N 8 %P 711 - 717 %R 10.1016/S1350-4533(03)00101-2 %T The myogenic response in isolated rat cerebrovascular arteries: vessel model %U http://www.sciencedirect.com/science/article/pii/S1350453303001012 %V 25 %X We develop an integrated model of isolated rat arterial resistance vessel (RV), which can simulate its major property of myogenic response. The vascular smooth muscle cell is an important component of the wall of this vessel, and serves as a vasomotor organ providing the active tension generation that underlies the myogenic response of the wall to stretch. In the previous study, we focused on the development of a smooth muscle cell model that can mimic the strain-sensing and force-generating features of the myogenic mechanism. In the current model, we embed this cell model in a larger vessel wall configuration, and couple the time course of cellular contractile activation to macroscopic changes in vessel diameter. The integrated model is used to mimic published pressure-vessel diameter data obtained from isolated RVs that are mounted in a hydraulic test apparatus. The model provides biophysically based insights into the myogenic mechanism as it responds to changes in transmural pressure, in the presence and absence of Ca2+ blockers applied to the bathing fluid. It mimics measured data very well and provides a model that is able to link events at subcellular level to macroscopic changes in vessel diameter. The model initiates a mechanistic approach to investigate myogenic response, which has not been taken previously by any other models.

@article{yang-clarkb, abstract = {We develop an integrated model of isolated rat arterial resistance vessel (RV), which can simulate its major property of myogenic response. The vascular smooth muscle cell is an important component of the wall of this vessel, and serves as a vasomotor organ providing the active tension generation that underlies the myogenic response of the wall to stretch. In the previous study, we focused on the development of a smooth muscle cell model that can mimic the strain-sensing and force-generating features of the myogenic mechanism. In the current model, we embed this cell model in a larger vessel wall configuration, and couple the time course of cellular contractile activation to macroscopic changes in vessel diameter. The integrated model is used to mimic published pressure-vessel diameter data obtained from isolated RVs that are mounted in a hydraulic test apparatus. The model provides biophysically based insights into the myogenic mechanism as it responds to changes in transmural pressure, in the presence and absence of Ca2+ blockers applied to the bathing fluid. It mimics measured data very well and provides a model that is able to link events at subcellular level to macroscopic changes in vessel diameter. The model initiates a mechanistic approach to investigate myogenic response, which has not been taken previously by any other models.}, added-at = {2013-01-07T13:49:24.000+0100}, author = {Yang, Jin and Jr., John W. Clark and Bryan, Robert M. and Robertson, Claudia S.}, biburl = {https://www.bibsonomy.org/bibtex/255fee103227edd2c1e81fe33db4287de/jehiorns}, doi = {10.1016/S1350-4533(03)00101-2}, interhash = {1b1455cc05320603432209f10895d4d5}, intrahash = {55fee103227edd2c1e81fe33db4287de}, issn = {1350-4533}, journal = {Med Eng Phys}, keywords = {arteries muscle}, note = {<ce:title>Cerebrovascular Modelling</ce:title>}, number = 8, pages = {711 - 717}, timestamp = {2013-01-07T15:43:39.000+0100}, title = {The myogenic response in isolated rat cerebrovascular arteries: vessel model}, url = {http://www.sciencedirect.com/science/article/pii/S1350453303001012}, volume = 25, year = 2003 }