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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004766naa a2200433 4500
001oai:DiVA.org:liu-50387
003SwePub
008091011s2008 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-503872 URI
024a https://doi.org/10.1152/ajpheart.00284.20082 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Krishnamurthy, G.u Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States, Department of Mechanical Engineering, Stanford University, Stanford, CA, United States4 aut
2451 0a Material properties of the ovine mitral valve anterior leaflet in vivo from inverse finite element analysis
264 1b American Physiological Society,c 2008
338 a print2 rdacarrier
520 a We measured leaflet displacements and used inverse finite-element analysis to define, for the first time, the material properties of mitral valve (MV) leaflets in vivo. Sixteen miniature radiopaque markers were sewn to the MV annulus, 16 to the anterior MV leaflet, and 1 on each papillary muscle tip in 17 sheep. Four-dimensional coordinates were obtained from biplane videofluoroscopic marker images (60 frames/s) during three complete cardiac cycles. A finite-element model of the anterior MV leaflet was developed using marker coordinates at the end of isovolumic relaxation (IVR, when the pressure difference across the valve is ~0), as the minimum stress reference state. Leaflet displacements were simulated during IVR using measured left ventricular and atrial pressures. The leaflet shear modulus (Gcirc-rad) and elastic moduli in both the commisure-commisure (Ecirc) and radial (Erad) directions were obtained using the method of feasible directions to minimize the difference between simulated and measured displacements. Group mean (±SD) values (17 animals, 3 heartbeats each, i.e., 51 cardiac cycles) were as follows: Gcirc-rad = 121 ± 22 N/mm2, Ecirc = 43 ± 18 N/mm2, and Erad = 11 ± 3 N/mm2 (Ecirc > E rad, P < 0.01). These values, much greater than those previously reported from in vitro studies, may result from activated neurally controlled contractile tissue within the leaflet that is inactive in excised tissues. This could have important implications, not only to our understanding of mitral valve physiology in the beating heart but for providing additional information to aid the development of more durable tissue-engineered bioprosthetic valves. Copyright © 2008 the American Physiological Society.
653 a Inverse finite-element analysis
653 a Mitral valve material properties
653 a Ovine model
653 a Radiopaque markers
653 a TECHNOLOGY
653 a TEKNIKVETENSKAP
700a Ennis, D.B.u Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States4 aut
700a Itoh, A.u Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States4 aut
700a Bothe, W.u Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States4 aut
700a Swanson, J.C.u Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States4 aut
700a Karlsson, Mattsu Linköpings universitet,Mekanisk värmeteori och strömningslära,Tekniska högskolan4 aut0 (Swepub:liu)matka16
700a Kuh, E.u Department of Mechanical Engineering, Stanford University, Stanford, CA, United States4 aut
700a Miller, D.C.u Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States4 aut
700a Ingels, Jr. N.B.u Ingels Jr., N.B., Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States, Laboratory of Cardiovascular Physiology and Biophysics, Research Institute, Palo Alto Medical Foundation, Palo Alto, CA, United States, Laboratory of Cardiovascular Physiology and Biophysics, Research Institute, Palo Alto Medical Foundation, 795 El Camino Real, Palo Alto, CA 94301-2302, United States4 aut
710a Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States, Department of Mechanical Engineering, Stanford University, Stanford, CA, United Statesb Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, United States4 org
773t American Journal of Physiology. Heart and Circulatory Physiologyd : American Physiological Societyg 295:3q 295:3x 0363-6135x 1522-1539
856u https://europepmc.org/articles/pmc2544494
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-50387
8564 8u https://doi.org/10.1152/ajpheart.00284.2008

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