| Literature DB >> 28168652 |
P Mason McClatchey1,2,3, Fan Wu4, I Mark Olfert5, Christopher G Ellis6, Daniel Goldman6, Jane E B Reusch2,4, Jefferson C Frisbee7.
Abstract
Metabolic syndrome (MS) in obese Zucker rats (OZR) is associated with impaired skeletal muscle performance and blunted hyperemia. Studies suggest that reduced O2 diffusion capacity is required to explain compromised muscle performance and that heterogeneous microvascular perfusion distribution is critical. We modeled tissue oxygenation during muscle contraction in control and OZR skeletal muscle using physiologically realistic relationships. Using a network model of Krogh cylinders with increasing perfusion asymmetry and increased plasma skimming, we predict increased perfusion heterogeneity and decreased muscle oxygenation in OZR, with partial recovery following therapy. Notably, increasing O2 delivery had less impact on VO2 than equivalent decreases in O2 delivery, providing a mechanism for previous empirical work associating perfusion heterogeneity and impaired O2 extraction. We demonstrate that increased skeletal muscle perfusion asymmetry is a defining characteristic of MS and must be considered to effectively model and understand blood-tissue O2 exchange in this model of human disease.Entities:
Keywords: Blood flow control; Microcirculation; Oxygenation; Rodent models of obesity; Simulation
Mesh:
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Year: 2017 PMID: 28168652 PMCID: PMC5893163 DOI: 10.1007/s12265-017-9732-6
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 4.132