Zile M R, Cowles M K, Buckley J M, Richardson K, Cowles B A, Baicu C F, Cooper G I V, Gharpuray V
Department of Medicine, Gazes Cardiac Research Institute, Medical University of South Carolina, Charleston, SC 29401, USA.
Am J Physiol. 1998 Jun;274(6 Pt 2):H2188-202. doi: 10.1152/ajpheart.1998.274.6.h2188.
Diastolic dysfunction is an important cause of congestive heart failure; however, the basic mechanisms causing diastolic congestive heart failure are not fully understood, especially the role of the cardiac muscle cell, or cardiocyte, in this process. Before the role of the cardiocyte in this pathophysiology can be defined, methods for measuring cardiocyte constitutive properties must be developed and validated. Thus this study was designed to evaluate a new method to characterize cardiocyte constitutive properties, the gel stretch method. Cardiocytes were isolated enzymatically from normal feline hearts and embedded in a 2% agarose gel containing HEPES-Krebs buffer and laminin. This gel was cast in a shape that allowed it to be placed in a stretching device. The ends of the gel were held between a movable roller and fixed plates that acted as mandibles. Distance between the right and left mandibles was increased using a stepper motor system. The force applied to the gel was measured by a force transducer. The resultant cardiocyte strain was determined by imaging the cells with a microscope, capturing the images with a CCD camera, and measuring cardiocyte and sarcomere length changes. Cardiocyte stress was characterized with a finite-element method. These measurements of cardiocyte stress and strain were used to determine cardiocyte stiffness. Two variables affecting cardiocyte stiffness were measured, the passive elastic spring and viscous damping. The passive spring was assessed by increasing the force on the gel at 1 g/min, modeling the resultant stress vs. strain relationship as an exponential [sigma = A/k(ekepsilon - 1)]. In normal cardiocytes, A = 23.0 kN/m2 and k = 16. Viscous damping was assessed by examining the loop area between the stress vs. strain relationship during 1 g/min increases and decreases in force. Normal cardiocytes had a finite loop area = 1.39 kN/m2, indicating the presence of viscous damping. Thus the gel stretch method provided accurate measurements of cardiocyte constitutive properties. These measurements have allowed the first quantitative assessment of passive elastic spring properties and viscous damping in normal mammalian cardiocytes.
舒张功能障碍是充血性心力衰竭的一个重要原因;然而,导致舒张性充血性心力衰竭的基本机制尚未完全明确,尤其是心肌细胞(即心肌)在此过程中的作用。在明确心肌细胞在这种病理生理过程中的作用之前,必须开发并验证测量心肌细胞固有特性的方法。因此,本研究旨在评估一种表征心肌细胞固有特性的新方法——凝胶拉伸法。通过酶解法从正常猫心脏中分离出心肌细胞,并将其包埋在含有HEPES - Krebs缓冲液和层粘连蛋白的2%琼脂糖凝胶中。将该凝胶制成特定形状,以便能够放置在拉伸装置中。凝胶的两端夹在一个可移动的滚轮和充当钳口的固定板之间。使用步进电机系统增加左右钳口之间的距离。通过力传感器测量施加在凝胶上的力。通过用显微镜对细胞成像、用CCD相机捕捉图像并测量心肌细胞和肌节长度变化来确定产生的心肌细胞应变。用有限元方法表征心肌细胞应力。这些心肌细胞应力和应变的测量用于确定心肌细胞硬度。测量了影响心肌细胞硬度的两个变量,即被动弹性弹簧和粘性阻尼。通过以1 g/min的速度增加凝胶上的力来评估被动弹簧,将所得应力与应变关系建模为指数关系[σ = A/k(ekε - 1)]。在正常心肌细胞中,A = 23.0 kN/m2,k = 16。通过检查在1 g/min的力增加和减少过程中应力与应变关系之间的回线面积来评估粘性阻尼。正常心肌细胞的有限回线面积为1.39 kN/m2,表明存在粘性阻尼。因此,凝胶拉伸法提供了对心肌细胞固有特性的准确测量。这些测量首次对正常哺乳动物心肌细胞的被动弹性弹簧特性和粘性阻尼进行了定量评估。