Affiliation:
1. School of Mathematics & Statistics, University of Sydney, Sydney, NSW 2006, Australia
2. Department of Medical Pharmacology & Physiology, University of Missouri, Columbia, MO 65212, USA
Abstract
Lymphatic valves operate in a fluid-dynamically viscous environment that has little in common with that of cardiac valves, and accordingly have a different, axially lengthened, shape. A previously developed 3D fluid/structure interaction model of a lymphatic valve was extended to allow the simulation of stages of valve closure after the leaflets come together. This required that the numerical leaflet be prevented from passing into space occupied by the similar other leaflet. The resulting large deflections of the leaflet and lesser deflections of the rest of the valve were mapped as functions of the transvalvular pressure. In a second new development, the model was reconstructed to allow the vessel wall to have different material properties on either side of where the valve leaflet inserts into the wall. As part of this, a new pre-processing scheme was devised which allows easier construction of models with modified valve dimensions, and techniques for successfully interfacing the CAD software to the FE software are described. A two-fold change in wall properties either side of the leaflet made relatively little difference to valve operation apart from affecting the degree of sinus distension during valve closure. However, the numerically permitted strains were modest (<14%), and did not allow examination of the large-scale highly nonlinear elastic properties exhibited by real lymphatic vessels. A small series of murine popliteal, mesenteric, and inguinal-axillary lymphatic vessel segments containing a valve were experimentally investigated ex vivo. The pressure–diameter curves measured just upstream and just downstream of the valve were parameterised by computing the difference in tubular distensibility at three values of transmural pressure. In the popliteal and mesenteric segments, it was found that the distensibility was usually greater just downstream, i.e., in the sinus region, than upstream, at low and intermediate transmural pressure. However, there was wide variation in the extent of difference, and possible reasons for this are discussed.
Funder
National Institutes of Health
Subject
General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology
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