Microcirculatory network structures and models
- PMID: 11144675
- DOI: 10.1114/1.1308495
Microcirculatory network structures and models
Abstract
Terminal vascular beds exhibit a high degree of heterogeneity. Pertinent parameters are nonlinearly related, and their distributions are not independent. The classical "typical vessel" approach using averaged values for different vessel classes may not lead to a correct understanding of physiology and pathophysiology of terminal vascular beds. Such problems can be avoided by studying microcirculatory functions at the network level using a combination of experiments and theoretical models. In this approach, distributions and relationships of pertinent parameters are measured in vivo, leading to the development of comprehensive databases. Such databases can be analyzed and complemented by suitable mathematical models, permitting estimation of parameters that are difficult to measure, and critical assessment of quantitative theories and hypotheses for microvascular function. This collaborative process between experimentally and theoretically oriented investigators may be facilitated in the future by the development of web-based repositories of experimental data and theoretical models.
Similar articles
-
Modeling structural adaptation of microcirculation.Microcirculation. 2008 Nov;15(8):753-64. doi: 10.1080/10739680802229076. Microcirculation. 2008. PMID: 18802843 Free PMC article. Review.
-
Structural adaptation of microvascular networks: functional roles of adaptive responses.Am J Physiol Heart Circ Physiol. 2001 Sep;281(3):H1015-25. doi: 10.1152/ajpheart.2001.281.3.H1015. Am J Physiol Heart Circ Physiol. 2001. PMID: 11514266
-
Simulation of microcirculatory hemodynamics: estimation of boundary condition using particle swarm optimization.Biomed Mater Eng. 2014;24(6):2341-7. doi: 10.3233/BME-141047. Biomed Mater Eng. 2014. PMID: 25226934
-
The role of wall shear stress in microvascular network adaptation.Adv Exp Med Biol. 1992;316:31-9. doi: 10.1007/978-1-4615-3404-4_4. Adv Exp Med Biol. 1992. PMID: 1288092
-
Why networks?Int J Microcirc Clin Exp. 1992 May;11(2):123-32. Int J Microcirc Clin Exp. 1992. PMID: 1612826 Review.
Cited by
-
Oxygen transport in the microcirculation and its regulation.Microcirculation. 2013 Feb;20(2):117-37. doi: 10.1111/micc.12017. Microcirculation. 2013. PMID: 23025284 Free PMC article. Review.
-
Microvascular repair: post-angiogenesis vascular dynamics.Microcirculation. 2012 Nov;19(8):676-95. doi: 10.1111/j.1549-8719.2012.00207.x. Microcirculation. 2012. PMID: 22734666 Free PMC article. Review.
-
Blood cell interactions and segregation in flow.Ann Biomed Eng. 2008 Apr;36(4):534-44. doi: 10.1007/s10439-007-9429-0. Epub 2008 Jan 11. Ann Biomed Eng. 2008. PMID: 18188702 Free PMC article. Review.
-
Deformability of Red Blood Cells and Correlation with ATP Content during Storage as Leukocyte-Depleted Whole Blood.Transfus Med Hemother. 2012 Aug;39(4):277-282. doi: 10.1159/000339809. Epub 2012 Jul 2. Transfus Med Hemother. 2012. PMID: 22969698 Free PMC article.
-
Deformability limits of Plasmodium falciparum-infected red blood cells.Cell Microbiol. 2009 Sep;11(9):1340-53. doi: 10.1111/j.1462-5822.2009.01334.x. Epub 2009 Apr 30. Cell Microbiol. 2009. PMID: 19438513 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources