Krishnamurthy Gaurav, Ennis Daniel B, Itoh Akinobu, Bothe Wolfgang, Swanson Julia C, Karlsson Matts, Kuhl Ellen, Miller D Craig, Ingels Neil B
Department of Cardiothoracic Surgery, Stanford University, Stanford, California, USA.
Am J Physiol Heart Circ Physiol. 2008 Sep;295(3):H1141-H1149. doi: 10.1152/ajpheart.00284.2008. Epub 2008 Jul 11.
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 approximately 0), as the minimum stress reference state. Leaflet displacements were simulated during IVR using measured left ventricular and atrial pressures. The leaflet shear modulus (G(circ-rad)) and elastic moduli in both the commisure-commisure (E(circ)) and radial (E(rad)) 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: G(circ-rad) = 121 +/- 22 N/mm2, E(circ) = 43 +/- 18 N/mm2, and E(rad) = 11 +/- 3 N/mm2 (E(circ) > 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.
我们测量了瓣叶位移,并首次使用逆向有限元分析来定义体内二尖瓣(MV)瓣叶的材料特性。在17只绵羊中,将16个微型不透射线标记物缝在二尖瓣环上,16个缝在前叶二尖瓣上,每个乳头肌尖端缝1个。在三个完整心动周期内,从双平面视频荧光标记图像(60帧/秒)中获取四维坐标。以前负荷末期(IVR,此时瓣膜两侧压力差约为0)的标记坐标作为最小应力参考状态,建立前叶二尖瓣的有限元模型。使用测得的左心室和心房压力模拟IVR期间的瓣叶位移。使用可行方向法获得瓣叶剪切模量(G(circ-rad))以及瓣叶连合-连合方向(E(circ))和径向(E(rad))的弹性模量,以尽量减少模拟位移与测量位移之间的差异。组均值(±标准差)(17只动物,每只动物3次心跳,即51个心动周期)如下:G(circ-rad)=121±22N/mm2,E(circ)=43±18N/mm2,E(rad)=11±3N/mm2(E(circ)>E(rad),P<0.01)。这些值远高于先前体外研究报道的值,可能是由于瓣叶内被激活的神经控制收缩组织在切除组织中不活跃。这不仅对我们理解跳动心脏中的二尖瓣生理学具有重要意义,而且为开发更耐用的组织工程生物瓣膜提供了额外信息。