Campbell Kenneth B, Chandra Murali, Kirkpatrick Robert D, Slinker Bryan K, Hunter William C
Department of Veterinary and Comparative Anatomy, Washington State University, Pullman, WA 99163, USA.
Am J Physiol Heart Circ Physiol. 2004 Apr;286(4):H1535-45. doi: 10.1152/ajpheart.01029.2003.
To describe the dynamics of constantly activated cardiac muscle, we propose that length affects force via both recruitment and distortion of myosin cross bridges. This hypothesis was quantitatively tested for descriptive and explanative validity. Skinned cardiac muscle fibers from animals expressing primarily alpha-myosin heavy chain (MHC) (mouse, rat) or beta-MHC (rabbit, ferret) were activated with solutions from pCa 6.1 to 4.3. Activated fibers were subjected to small-amplitude length perturbations [deltaL(t)] rich in frequency content between 0.1 and 40 Hz. In descriptive validation tests, the model was fit to the ensuing force response [deltaF(t)] in the time domain. In fits to 118 records, the model successfully accounted for most of the measured variation in deltaF(t) (R(2) range, 0.997-0.736; median, 0.981). When some residual variations in deltaF(t) were not accounted for by the model (as at low activation), there was very little coherence (<0.5) between these residual force variations and the applied deltaL(t) input function, indicating that something other than deltaL(t) was causing the measured variation in deltaF(t). With one exception, model parameters were estimated with standard errors on the order of 1% or less. Thus parameters of the recruitment component of the model could be uniquely separated from parameters of the distortion component of the model and parameters estimated from any given fiber could be considered unique to that fiber. In explanative validation tests, we found that recruitment and distortion parameters were positively correlated with independent assessments of the physiological entity they were assumed to represent. The recruitment distortion model was judged to be valid from both descriptive and explanative perspectives and is, therefore, a useful construct for describing and explaining dynamic force-length relationships in constantly activated cardiac muscle.
为了描述持续激活的心肌动力学,我们提出长度通过肌球蛋白横桥的募集和变形来影响力。对这一假设进行了定量测试,以验证其描述和解释的有效性。用从pCa 6.1到4.3的溶液激活主要表达α-肌球蛋白重链(MHC)(小鼠、大鼠)或β-MHC(兔子、雪貂)的动物的去皮肤心肌纤维。对激活的纤维施加频率范围在0.1至40 Hz之间、富含频率成分的小幅度长度扰动[δL(t)]。在描述性验证测试中,该模型在时域中拟合随后的力响应[δF(t)]。在对118条记录的拟合中,该模型成功解释了δF(t)中大部分测量到的变化(R²范围为0.997 - 0.736;中位数为0.981)。当模型无法解释δF(t)中的一些残余变化时(如在低激活状态下),这些残余力变化与施加的δL(t)输入函数之间的相干性非常低(<0.5),这表明除了δL(t)之外,还有其他因素导致了测量到的δF(t)变化。除了一个例外,模型参数的估计标准误差在1%或更低的量级。因此,模型募集成分的参数可以与模型变形成分的参数唯一区分开来,并且从任何给定纤维估计的参数可以被认为是该纤维特有的。在解释性验证测试中,我们发现募集和变形参数与它们被假定代表的生理实体的独立评估呈正相关。从描述性和解释性角度来看,募集 - 变形模型都被认为是有效的,因此,它是描述和解释持续激活的心肌中动态力 - 长度关系的一个有用结构。