- Open Access
Development of a mathematical model for predicting electrically elicited quadriceps femoris muscle forces during isovelocity knee joint motion
Journal of NeuroEngineering and Rehabilitation volume 5, Article number: 33 (2008)
Direct electrical activation of skeletal muscles of patients with upper motor neuron lesions can restore functional movements, such as standing or walking. Because responses to electrical stimulation are highly nonlinear and time varying, accurate control of muscles to produce functional movements is very difficult. Accurate and predictive mathematical models can facilitate the design of stimulation patterns and control strategies that will produce the desired force and motion. In the present study, we build upon our previous isometric model to capture the effects of constant angular velocity on the forces produced during electrically elicited concentric contractions of healthy human quadriceps femoris muscle. Modelling the isovelocity condition is important because it will enable us to understand how our model behaves under the relatively simple condition of constant velocity and will enable us to better understand the interactions of muscle length, limb velocity, and stimulation pattern on the force produced by the muscle.
An additional term was introduced into our previous isometric model to predict the force responses during constant velocity limb motion. Ten healthy subjects were recruited for the study. Using a KinCom dynamometer, isometric and isovelocity force data were collected from the human quadriceps femoris muscle in response to a wide range of stimulation frequencies and patterns. % error, linear regression trend lines, and paired t-tests were used to test how well the model predicted the experimental forces. In addition, sensitivity analysis was performed using Fourier Amplitude Sensitivity Test to obtain a measure of the sensitivity of our model's output to changes in model parameters.
Percentage RMS errors between modelled and experimental forces determined for each subject at each stimulation pattern and velocity showed that the errors were in general less than 20%. The coefficients of determination between the measured and predicted forces show that the model accounted for ~86% and ~85% of the variances in the measured force-time integrals and peak forces, respectively.
The range of predictive abilities of the isovelocity model in response to changes in muscle length, velocity, and stimulation frequency for each individual make it ideal for dynamic applications like FES cycling.
Functional Electrical Stimulation (FES) is the coordinated electrical excitation of paralyzed or weak muscles in patients with upper motor neuron lesions to produce functional movements such as sit-to-stand or walking . Traditionally, during FES, skeletal muscles are activated with constant-frequency trains (CFTs), where the pulses within each train are separated by regular interpulse intervals (IPIs; Fig. 1). However, studies have shown that varying the stimulation frequency within a train markedly affects the force production from the muscle . In addition, a recent study showed that varying the stimulation frequency and pattern across trains improved the muscles ability to produce 50° knee extension repetitively as compared to the performance elicited by CFTs . Interestingly, Garland and Griffin  also showed that motor units are activated with varying patterns during volitional contraction. Hence, the stimulation patterns for optimizing force production during FES are probably complex. One way to assist the search for the optimal pattern is to use mathematical models that can predict forces accurately to a range of physiological conditions and stimulation patterns. In addition, mathematical models used in conjunction with closed loop control would enable FES systems to deliver patterns customized for each person to perform a particular task while continuously adapting the stimulation protocols to the actual needs of the patient.
Phenomenological Hill-type [5–10], Huxley-type cross-bridge[11, 12], or analytical approaches [13, 14] have been developed to explore different aspects of muscle contraction under both isometric and non-isometric conditions. However, each of these models either: (a) could not predict the force or motion response to a range of stimulation frequencies and patterns, (b) have a large number of free parameters that make the model identification process difficult, (c) were not tested for intact human muscles, and (d) were evaluated only under isometric conditions.
Previously, our laboratory developed isometric models for rat gastrocnemius and soleus muscles that addressed the first two shortcomings outlined above. We then extended and modified these models for human quadriceps muscles under isometric fatigue and non-fatigue conditions [15–19]. Recently, comparisons of different isometric force models to fit and predict isometric forces in response to range of stimulation trains showed that our isometric model performed better than the linear models and had similar performance when compared to Bobet-Stein's model [20, 21]. Hence, for the present study, we build upon our isometric models to capture the effects of constant angular velocity (isovelocity) of the lower limb on the forces produced in response to electrical stimulation of the quadriceps femoris muscle. Modeling the isovelocity condition is important because it enables us to understand how our model behaves under the relatively simple condition of constant velocity before trying to model the more complicated non-isometric conditions, where limb velocities change as function of time. More importantly, the current model would enable us to better understand the interactions of muscle length, limb velocity, and stimulation pattern on the force produced by the muscle. This would, in turn, enable us to design stimulation patterns for FES. Hence the purposes of this study are to derive the equations to model the effect of velocity and stimulation on the muscle force under isovelocity conditions and determine if the model can capture the variations in force as a function of velocity when the muscle is activated with a range of stimulation frequencies, patterns, muscle lengths, and number of pulses.
The isovelocity model is based on the Hill-type isometric force model developed by our laboratory [5, 16, 17, 22]. This isometric model is used because it is the only model that can predict forces in response to a wide range of stimulation frequencies and because the parameters in the model have a physiological basis, which make it less phenomenological than other Hill-type models. Our model divides the contractile responses of the muscle are decomposed into two distinct physiological steps: activation dynamics and the force dynamics. In addition, we developed the equations of motion for the lower limb moving at constant velocities.
A number of complicated steps are involved between motor nerve activation by electrical stimulation and the force production by the muscle, such as release and uptake of calcium by the sarcoplasmic reticulum, binding of calcium to troponin, and the attachment of myosin filaments with actin . However, Ding and colleagues [16, 17, 22] found that it was sufficient to model this activation dynamics through a unitless factor, C N , to describe the rate-limiting step before the myofilaments mechanically slide across each other and generate force. The differential equation describing this dynamics is:
and whose analytical solution satisfying the initial conditions is
R i = 1 for i = 1
R i = 1 + (R0 - 1)exp[-(t i - ti-1)/τ c ] for i > 1.
In Eqns. (1) and (2), t (ms) is the time since the beginning of the stimulation train, t i (ms) is the time of the i th stimulation pulse since the beginning of the stimulation train, n is the number of stimulation pulses before time t in the train, and τ c (ms) is the time constant controlling the transient shape of C N . R i (unitless) is the scaling term that accounts for the difference in the degree of activation by each pulse relative to the first pulse in the train . The enhancement of R i is characterized by R0 (unitless) and its dynamics is characterized by τ c (ms). R i decays with interpulse interval t i -ti-1. Hence, R i = 1 for a pulse that occurs at a long time after the preceding pulse, and R i approaches R0 for the smallest interpulse interval tested, 5 ms.
When calcium binds to troponin, the inhibitory effect of tropomyosin is removed and results in the exposure of binding sites on actin. The crossbridges attach to actin and pull the actin filaments toward the center of the myosin filaments. The macroscopic result of this process is the shortening of the muscle and the generation of force. Force generation is modeled by a Hill-type representation of the skeletal muscle as shown in Fig. 1. Here the skeletal muscle is modeled as a spring (with stiffness k S ), a damper (with a damping coefficient b), and a motor (with velocity V). The series spring represents the tendonous portion and the series elastic component of the muscle , the damper represents the viscous resistance of the contractile and connective tissue , and the motor represents the contractile component or the sliding of actin and myosin filaments of muscle fibers . The series spring is assumed linear and the force exerted by the spring is given by
>F = k s x,
where k S is the spring constant or stiffness and x is the displacement of the spring under the force F.
The damper is also assumed linear and is given by
where b is the damping coefficient, y is the distance moved by the right hand side of the damper in Fig. 1, and is the relative velocity of the damper.
The contractile velocity V of the motor is given by
where z is the net displacement and the negative sign accounts for the fact that the motor is shortening. All shortening contractions are taken as negative in this study. The motor, which represents the contractile element, is driven by the strongly bound cross bridges [19, 27]. As there is a sigmoidal force-pCa relationship , Ding and coworkers  modeled the relationship between V and C N by a simple Michaelis-Menten term, C N /(K M + C N ). Hence, V is now given by
where B is the constant of proportionality and K M mathematically represents the sensitivity of strongly bound cross-bridges to Ca2+-troponin complex .
Differentiating Eqn. (3) with respect to time and using Eqn. (4) to eliminate and Eqn. (6) to eliminate gives
The term b/k s represents the time constant over which the force decays. Ding and colleagues [15, 22] expect the friction between actin and myosin to be higher during cross-bridge cycling due to binding between the fibers, so they set , where τ1 is the value of the time constant in the absence of bound cross-bridges and τ2 is the additional frictional component due to the cross-bridge binding. Using this for b/k s and replacing k s B with a new constant A, gives
As it is experimentally difficult to measure z and its derivative with respect to time, z is viewed as a function of the knee flexion angle θ. Thus, z is written as z = g(θ).
Differentiating k s z with respect to time gives
where = dθ/dt, is the angular velocity of the limb. Substituting Eqn. (9) into Eqn. (8) gives
When = 0, the above equation reduces to the isometric form explored in previous studies [16, 17, 22]. By assuming only A to be a function of the knee flexion angle θ, and by fixing other parameter at their 40° knee flexion angle values, the isometric form of the model is able to capture changes in force with muscle length. A was found to vary in a parabolic manner and was modeled as
A(θ) = a(40 - θ)2 + b(40 - θ) + A40,
where A40 is the value of A at 40° of knee flexion, and a and b are constants that need to be identified for each subject . Hence, A captures the effect of muscle length on the force due to stimulation and the model is able to predict the force response to a wide variety of stimulation frequencies.
It is necessary to identify the functional form of G(θ) to model the variation of force with velocity. As seen from Eqn. (9), G(θ) is dependent on an unknown function g(θ) and k S . Previous studies [29, 30] have used exponential functions to model the nonlinear relationship between knee flexion angle and joint stiffness torque. Hence, we assumed G(θ) to be of the form
G(θ) = V1θ exp(-V2θ),
where V1 and V2 are constants to be identified for each subject. In addition, Heckman and colleagues  and de Haan  showed that in cat and rat medial gastrocnemius muscle, the force-velocity relation was affected by stimulation frequency. Hence, to account for the coupling between force, velocity, and activation in our modeling we multiplied G(θ) by the Michaelis-Menten term C N /(K M + C N ). Considering the above assumption and the functional form of A(θ), Eqn. 10 can be written as
Eqns. (2) and (13) represent the complete set of equations for this study. In addition, the following constraints were imposed during estimation of model parameters and prediction of experimental forces for isovelocity movements: (1) θ ≥ 0, (2) A(θ) ≥ 0, and (3) F ≥ 0. The first constraint comes from the fact that we consider the motion of the leg between 90° to 0° of knee flexion. The second and third constraints were imposed to ensure that the force during stimulation is never negative. Eqns. (2) and (13) model the forces due to stimulation of the muscle and are governed by ten parameters: R0, τ c , a, b, A40, τ1, τ2, K M , V1, and V2 (see Table 1).
It is important to understand the practical meaning of F in Eqn. (13). The model must be fitted to experimental force data to evaluate the parameters (see SectionB.5). The experimental force is measured in a Kin-Com machine by placing a force transducer above the ankle joint (see Equipment and experimental setup section). When the quadriceps femoris muscle is stimulated, it exerts a force on the patellar ligament, which then transfers the quadriceps force onto the tibia in a complicated manner . Hence, the quadriceps muscle exerts a force, F, on the transducer placed above the ankle joint. This force F is a function of patellar tendon force and the distance from the center of the force transducer to the center of knee rotation. Hence, the F in Eqn. (13) is now the force above the ankle joint exerted by the quadriceps in response to stimulations through the knee joint. From here on, we define this force (F) as the force due to the stimulation, as we have done previously [15, 18], so that the parameters incorporate the kinematic transfer of force from the muscle to the transducer.
Equations of motion
Fig. 2B shows a schematic representation of the leg when the tibia is moving at a constant angular velocity, with the stimulations being applied to the quadriceps femoris muscle. The instantaneous moment dynamic equation about the center of knee rotation when the tibia is moving at constant angular velocity is:
F EXT L - T STIM + mg cosθ·l + H = 0,
where F EXT is the resistance the Kin-Com exerts above the ankle joint to move the tibia with a constant angular velocity and is the measured force from the Kin-Com,T STIM is the torque at the knee joint due to stimulation of the quadriceps femoris muscle, mg is the weight of the tibia and foot, H is the resistance moment to knee extension due to visco-elasticity of the musculotendon complex of the knee joint, θ is the knee flexion angle, l is the distance between knee center of rotation and center of mass of the leg below the knee, and L is the length of the lever arm from the center of the force transducer above the ankle joint to the center of knee rotation. The right hand side of Eqn. (14) is zero because there is no angular acceleration during the isovelocity phase of the contraction. Because the experimental force is measured with a force transducer placed just above the ankle joint we can write
T STIM = F·L,
where F and L are as defined before. Substituting Eqn. (15) into Eqn. (14) and rearranging we get
To model the resistance to knee extension, H, due to visco-elasticity of the musculotendon complex of the knee joint, it is necessary to consider stiffness and damping factors, which are functions of knee flexion angle and angular velocity, respectively [13, 34]. These functions are complicated and nonlinear [29, 34, 35]. Preliminary passive force measurements on healthy subjects, where the knee was extended at a constant velocity, showed that H/L = R cos(θ) well represented the measured data. R was found to be independent of θ or for healthy subjects, which may not be the case of spinal cord injured and stroke patients, where other passive factors like spasticity play an important rule. The above form of H/L simplifies equation 16 to
Replacing by M in Eqn. (17) we obtain,
F EXT = F - M cosθ.
Thus, to obtain muscle force due to stimulation, F, it is necessary to add M cosθ to F EXT , the force measured by the Kin-Com force transducer. This was done during data analysis (see Experimental procedure for model development section for details), so that experimental forces can be compared to model predictions.
Ten healthy subjects (5 women and 5 men with a BMI ≤ 32) ranging in age 18 to 35 years were recruited for this study (see Fig. 3). Data collected from three subjects were used to develop the form of the model. Data from these three subjects and three additional subjects that were not used for model development, were used to validate the model (Fig. 3). In an effort to simplify the model, linear correlations between different model parameters determined for the six subjects tested. However, because these relationships were inconclusive, we tested four additional subjects (Fig. 3). Before testing, each subject signed an informed consent form approved by the University of Delaware Human Subject Review Board. All the subjects recruited for the study were acclimatized to electrical stimulation as they have previously participated in studies that involved electrical stimulation.
Equipment and experimental setup
Subjects were seated on a computer controlled (KinCom III 500-11, Chattecx Corporation, Chattanooga, TN) dynamometer with their hips flexed to ~75° . The dynamometer axis was aligned with the knee joint axis and the force transducer pad was positioned anteriorly against the tibia, 4 cm proximal to the lateral malleolus. Two 7.62 cm × 12.7 cm self-adhesive electrodes were used to stimulate the muscle. With the knee positioned at 90°, the anode was placed proximally over the motor point of the rectus femoris portion of the quadriceps femoris muscle. The cathode was placed distally over the vastus medialis motor point with the knee in 15° of flexion to compensate for skin movement during knee extension . The trunk, pelvis, and thigh of the leg being tested were each stabilized with inelastic straps. A Grass S8800 stimulator with an SIU8T stimulus isolation unit (Grass Instruments, West Warwick, RI) was used for stimulation. The stimulator was driven by a personal computer using customized LabView (National Instruments, Austin, TX) software. Force and motion data from the transducer were sampled at 200 Hz using an analog-to-digital board. The data were then analyzed using a custom program written in LabView.
Using a KinCom dynamometer, isometric and isovelocity force data were collected from the human quadriceps femoris muscle in response to electrical stimulation. Each subjects performed a maximum voluntary isometric contraction (MVIC) of the quadriceps femoris muscle with the knee positioned at 90° of flexion. The burst-superimposition technique was used to ensure that a true maximal contraction was being performed . Next, with the knee at 90° flexion the stimulation amplitude was set to activate ~20% of the muscle MVIC using a 300 ms-long 100-Hz stimulation train. Once the amplitude was set, it was held constant for the remainder of the session. The pulse duration was fixed at 600 μs throughout this study. To ensure consistency in the force responses to stimulation, we first potentiated the muscle using 14-Hz, 770 ms long trains before delivering the parameterizing and testing trains (see the section below for details of the parameterizing and testing trains).
Experimental procedure for model development
First, three subjects were recruited to participate in two testing sessions. A 48-hour rest period separated the two sessions. During the first session, testing was performed isometrically at angles of 15°, 40°, 65°, and 90°. The order of testing for the four angles was randomly determined and five minutes of rest was provided between each angle. Five minutes following the isometric testing, subjects were tested at one of the four isovelocity speeds of -25°/s, -75°/s, -125°/s, or -200°/s (all shortening velocities are assigned negative values in this study). During the second session, subjects were tested at the remaining three velocities. The order of testing the three velocities was randomly determined and five minutes of rest was provided between each velocity.
For the isometric testing, two one-second long trains were used to stimulate the muscle. Each train had an initial interpulse interval (IPI) of 5 ms and the remaining IPIs were either 20 or 80 ms (Fig. 1). These two variable-frequency trains (VFTs) were referred to as VFT20 and VFT80, respectively. Previous study by Ding and colleagues  showed that our model had the best predictive ability for human quadriceps femoris muscle if the model's parameter values were identified using force responses to these two trains. Within the stimulation protocol, first the VFT80 train followed the VFT20 train and then these trains were delivered in reverse order. Only one train was delivered every 10 s to minimize muscle fatigue. For the isovelocity study, 16 different trains were used: six constant-frequency trains (CFTs) referred to as CFT10, CFT20, CFT30, CFT50, CFT70, and CFT100; six VFTs referred to as VFT20, VFT30, VFT50, VFT70, VFT80, and VFT100; and four doublet frequency trains (DFTs) with 5 ms doublets throughout the train referred to as DFT30, DFT50, DFT70, and DFT100 (Fig. 1). The maximum number of pulses in each train was limited to 50, except for VFT20, which had a maximum of 51 pulses.
During isovelocity testing the KinCom was set to the Isokinetic mode, where the subjects remained passive and the KinCom arm moved the leg at predetermined speeds. The leg motion was initiated at 110° of knee flexion and stimulation began when the leg reached 90° of knee flexion and was terminated at 15° of knee flexion, unless all the pulses were already delivered. The KinCom arm moved the leg to 0° of knee flexion and then returned the leg back to 110° of knee flexion at a constant velocity of 25°/s. A 10 s rest time was provided before delivering the next train. Software, custom written in LabView, was used to determine the timing of each of the pulses delivered to each subject. In addition, force data were collected while passively moving the leg at constant velocity of -25°/s, -75°/s, -125°/s, and -200°/s from 110° to 0° of knee flexion to determine the value of M. The absolute value of M cosθ was then added to the measured force data, F EXT , to obtain the stimulation muscle-joint force, F (Eqn. 18) throughout the study.
Parameter identification for model development: Based on our model derivation, the term G(θ) explicitly modeled the effect of velocity on the force produced by the muscle. In turn, G(θ) is characterized by the parameters V1 and V2. Hence, all the isometric parameters a, b, A40, τ1, τ2, and K M were assumed to be constant for isovelocity conditions and only parameters V1 and V2 were identified under isovelocity conditions. Under isometric conditions the angular velocity, , is zero hence Eqn. (13) reduces to
Ding and colleagues [16, 17] have shown that a fixed value of 20 ms for τ c and 2 for R0 are sufficient for human quadriceps muscles under non-fatigue condition. Based on the results of our previous study the values A40, τ1, τ2, and, K M  are identified first at 40° of knee flexion by fitting Eqns. (1) and (12) to the forces produced by stimulating the muscle with a combination of VFT20 and VFT80 trains (Fig. 4). These parameter values were then kept fixed and the values of a and b were identified at knee flexion angles of 15°, 65°, and 90° by fitting the measured force response to the VFT20-VFT80 train combination. The values of a and b were obtained by first determining the value of A from fitting the VFT20-VFT80 force responses at angles of 15°, 65°, and 90°  and then fitting the values of A at the above four angles to the parabolic equation given by a(40 - θ)2 + b(40 - θ) + A40. Fitting of measured and modeled data was carried out using a derivate based optimization technique in MATLAB.
Under isovelocity conditions, first the value of M was obtained by fitting the function M cosθ to the passive knee extension force data from 90° to 15° of knee flexion at each of the four velocities. The absolute value of M cosθ was then added to the measured force data, F EXT , to obtain the stimulation muscle-joint force, F (Eqn. 18). The model (Eqns. 1 and 13) was then fitted to the forces elicited by the VFT20-VFT80 train combination at -25°/s, -75°/s, -125°/s, and -200°/s to obtain the values of V1 and V2 at each of four velocities. This was done to determine the best velocity to identify the values of V1 and V2. For all the data collected, the two occurrences of each of the stimulation trains were averaged to reduce the effects of physiological variability on the muscle's response to each train.
Results for model development
From Fig. 5 we see that -200°/s is the only velocity that the model both fits the VFT20-VFT80 force data at its own velocity well (i.e., -200°/s, Fig. 5p), and predicts the VFT20-VFT80 force data at each of the other three velocities very well (Figs. 5m, 5n, 5o). Similar results are observed for the other two subjects. Hence, for the model development and validation stages, the VFT20-VFT80 train combination at -200°/s is used to identify the values of V1 and V2. In addition, because the values of M at different velocities are generally within ten percent of each other, the value of M at -200°/s is used to correct all isovelocity measured data (See Table 2).
Validation of the model
The model was validated by determining its ability to predict forces in response to wide range stimulation frequencies and patterns at velocities of -25°/s, -75°/s, -125°/s, and -200°/s. Data were collected from three additional subjects. The same protocol used for the first three subjects recruited for the model development phase was tested and the data for the six subjects were pooled (Fig. 3).
Data analysis for model validation
% error, linear regression trend lines, and paired t-tests were used to test how well the model predicted the experimental forces. Mean % errors between the model and experimental forces normalized to the experimental peak force and measured at each 5 ms time interval were calculated for each subject. The experimentally measured and model's predicted force-time integrals and peak forces were averaged across six subjects at each velocity and at each stimulation pattern. Paired t-tests were used to compare the average measured and predicted data. The paired t-test comparisons were considered significant if p = 0.05. Linear regression trend lines were used to determine how well the model predicted the force-time integrals (area under the force-time plots) and the peak forces for each train tested at each velocity for all the six subjects. The slope of the trend line was set to one and the intercept was set to zero. A perfectly accurate model would have a coefficient of determination, R2, of one.
Because a model with fewer parameters has better predictive abilities and is desired by designers of the FES systems , we have tried to limit the number of free parameters for model. We therefore determined the linear correlations between parameters V1 and V2 and each of the other model parameters for the six subjects tested, i.e., V1-vs-a, V1-vs-b, V1-vs-A40, V1-vs-K M , V1-vs-τ1, V1-vs-τ2, V2-vs-a, V2-vs-b, V2-vs-A40, V2-vs-K M , V2-vs-τ1, and V2-vs-τ2. However, because these relationships were inconclusive, we tested four more subjects (see Fig. 3). Each of the four subjects participated in one testing session. The procedure for testing them was similar to that described above, except that these four subjects were tested only with VFT20 and VFT80 trains under isometric conditions of 15°, 40°, 65°, and 90° of knee flexion and at the isovelocity speed of -200°/s. The values of each of the parameters (a, b, A40, τ1, τ2, K M , V1, and V2) were then obtained as described above. For each of the above relationships we fitted the data with a linear trend-line and calculated the R2 values for all the 10 subjects tested. R2 values for the relationships of parameters V1 and V2 with the other model parameters showed that only parameters b and τ2 had a high correlation to V2 with R2 values of 0.62 and 0.81 (p = 0.00035), respectively (see Table 3). Because the correlation between V2 and τ2 was greater than the correlation between V2and b, we adopted the relationship between V2 and τ2 that was given by
V2 = 0.0002 * τ2 + 0.0048.
The above empirical relationship between V2 and τ2 was then incorporated in the model and the force responses to the VFT20-VFT80 train combination at -200°/s were fit again to calculate the new value of V1 for the six subjects used to validate the model.
Sensitivity analysis was performed using Fourier Amplitude Sensitivity Test (FAST) to obtain a measure of the sensitivity of our model's output to changes in model parameters. The FAST method was used to estimate the expected value and variance of the output, and the contribution of individual inputs to the variance of the output . The ratio of the contribution of each input to the total output variance is referred to as the first order sensitivity index and can be used to rank the inputs . For the current sensitivity analysis, the output of the model was the force-time integral (area under the force-time curve) in response to a 50-pulse, 33-Hz stimulation train at each of the four velocities tested and under isometric conditions at 90° of knee flexion. Parameters τ c and R0 were kept fixed at 20-ms and 2, respectively, and equation 20 was used to calculate the value of V2. Values of the other seven parameters were varied within the following ranges: a (-0.003 to -0.0005), b (-0.22 to -0.02), A40 (1.5 to 8.7), τ1 (26 to 76), τ2 (58 to 280), K M (0.15 to 0.66), and V1 (0.0007 to 0.0028). The range of values for the above seven parameters were determined based on the parameter values of 10 subjects in the current study. SIMLAB  software was used to carry out the sensitivity analysis. A total of 623 sample sets were generated using Monte Carlo methods. Each sample set consisted of the different values of the eight model parameters. FAST first order sensitivity index was calculated for each parameter. The higher the value of the sensitivity index of a parameter, the greater is the sensitivity of the model output (force-time integral) to changes in that model parameter.
Sensitivity analysis showed that under isometric conditions at 90° of knee flexion, parameters a, b, A40, and τ2 accounted for ~85% of the total variation of the force-time integral (Fig. 6). Also, parameter V1 had no effect on the output under the isometric condition. This result is not surprising as parameter V1 accounts for the effects velocity. At faster speeds the output variance is dominated by parameters A40 and τ2 (Fig. 6). For example, at a shortening speed of 200°/s parameters A40 and τ2 account for ~25% and ~56% of the output variance, respectively. In addition, with increase in shortening velocity from 0°/s to 200°/s, the percentage of the output variance accounted by parameter τ2 increased from 18.74% at 0°/s to 55.94% at 200°/s (Fig. 6). This is because parameter τ2 is related to parameter V2 through equation 20 and with increasing shortening velocities the effects of parameter V2 on the output of the model increases. At all the five speed conditions tested, the contributions of parameters τ1, K M , and V1 to the output variance was small (Fig. 6).
Predicted and experimental force data in response to simulation from a typical subject are shown in Fig 7. The model was first parameterized under isometric and isovelocity conditions to identify the model parameters (Fig. 7a and 7b). Then, the model predicted the force response to wide range of stimulation patterns and inter-pulse intervals at the four velocities tested (Fig. 7c–k). Percentage RMS errors between modeled and experimental forces determined for each subject at each stimulation pattern and velocity showed that the errors were in general less than 20% (Table 4).
At -75°/s, -125°/s, and -200°/s there were no significant differences between the measured and predicted peak forces for each of the IPIs and patterns tested (Figs. 8c, 8e, and 8g). In contrast, at -25°/s the model underestimated the peak forces at IPIs of 30 and 50 ms for both the CFTs and VFTs and at IPIs of 50 and 70 ms for the DFTs (Fig. 8a). For the force-time integrals, at -25°/s there were no significant differences between the measured and predicted force-time integrals for any of the IPIs and patterns tested. In contrast, at -75°/s and -125°/s the model overestimated the force-time integrals for several IPIs of the CFTs, VFTs, and DFTs (see Figs. 8d and 8f). At -200°/s, however, the model underestimated the force-time integrals for CFT10 and CFT30 (Fig. 8h).
In general, the model predicted the IPI for each pattern that produced the maximum force-time integrals and the maximum peak forces (Fig 8). For example, at -25°/s the maximum force-time integral for both predicted and measured data occurred at an IPI of 50 ms for the CFT, 50 ms for the VFT, and 70 ms for the DFT. The coefficients of determination between the measured and predicted forces showed that the model accounted for ~86% and ~85% (average values for the four velocities tested) of the variances in the measured force-time integrals and peak forces, respectively (Fig. 9).
In this study we developed a mathematical model of healthy human quadriceps femoris muscle that predicted forces under isovelocity conditions. Our results showed that our model had the ability to predict the force responses of the quadriceps femoris muscle to a wide range of clinically relevant stimulation frequencies and patterns when the leg was moved at a variety of constant velocities. In the current model, by identifying the values of the parameters a, b, A40, τ1, τ2, and K M under isometric conditions, only the value of the parameter V1 needed to be identified at -200°/s for the model to capture the shortening and lengthening forces of the muscle over a wide range of constant velocities. All the above parameters were identified by fitting the force responses to only two trains, the VFT20-VFT80 train combination.
The term G(θ) (see Eqn. (12)) was motivated by the formulation that represents the muscle by a motor-damper-spring combination in series. Other than this new term, the current model used the same equations used for the isometric models that we developed previously [16–18]. In isometric contractions, the motor's rate of shortening is balanced by the damper and spring to produce muscle force. For shortening contractions, however, the shortening of the muscle reduces stretching of the damper and spring, resulting in lower muscle forces. Physiologically, because the cross-bridge recycling rate, which is modeled as the motor's rate of shortening, is finite, increased rates of shortening reduce the stretching of the muscle's viscous and elastic components, resulting in lower muscle forces. The exact form of the function G(θ) = V1θ exp(-V2θ) captures the above non-isometric effects and accounts for the influence of the knee joint kinematics on the force-velocity relationship. Interestingly, a correlation was found between the parameters V2 and τ2 (see Eqn. (20)). Wexler and colleagues  have shown that τ2 varied in muscles with different fiber type composition. Previous studies have shown that fiber type composition plays an important role in influencing the force-velocity relationship [43, 44]. The influence of fiber type on the force-velocity relationship in the current model was captured through the parameter V2, which was incorporated in the function G(θ) = V1θ exp(-V2θ); the relationships between model parameters and muscle type were supported by the τ2-V2 relationship.
Our model showed that knee joint angle where the stimulation was initiated affects the shape of the force velocity relationship, and consequently the zero force shortening velocity during shortening velocities (Fig. 10a and 10b). In addition, when the muscle was stimulated throughout the range of motion, our model captured the classical force-velocity behavior during shortening contractions, predicted that the peak forces produced during lengthening contractions are higher than isometric and shortening contractions, and showed that the peak forces initially rise with increases in lengthening velocity and then plateau with further increases (Fig 10c). More quantitatively, the model predicted that the peak force during lengthening contractions was 1.4 times the isomeric peak force (at optimal muscle length) in response to a stimulation frequency of 100 Hz (data were averaged for six subjects tested). This observation was consistent with previously published experimental data that showed that the force during the plateau portion of the eccentric contractions was 1.4 times the force during isometric contractions . Figure 10d shows the effect of limiting the maximum number of pulses to 50. The limitation on the number of pulses being delivered to the muscle affected the shape of the force-velocity curves during shortening and lengthening contractions, which was qualitatively consistent with the experimental data [45, 46]. Hence, factors like number of pulses, IPI, and muscle length when the stimulation is initiated, which are important factors in an FES application, affect the shape of the force-velocity curve and should be considered when developing models for a FES application.
During eccentric contractions, the muscle lengthens instead of shortening. Such contractions are characterized by higher forces than isometric and shortening contractions and are important parts of many functional activities, such as walking. Hill-type models that predict eccentric muscle forces use a separate set of equations to describe the behavior of the muscle during eccentric contractions . For the current model only one set of equations were necessary. The reason for the model's ability to predict lengthening contractions was due to the coupling between G(θ) and C N /(K M + C N ) (see Eqn. 13). G(θ) increases with lengthening velocity whereas C N /(K M + C N ) decreases. At a given stimulation frequency, the greater the lengthening velocity the fewer the number of pulses delivered and, hence, smaller the value of C N . The increase in G(θ) with lengthening velocity was, therefore, compensated by a decrease in C N /(K M + C N ) and helped to maintain the peak forces at almost a constant value with increasing velocities in the flat portion of the force-lengthening velocity curve (see Figs. 10c and 10d).
The current model development and verification were done for healthy human quadriceps femoris muscle under isovelocity conditions. Because of the various assumptions made in developing the current model, the model may not be valid when applied to other muscle groups, when muscles become fatigued, or to patient population. For example, the assumptions of having τ c at a fixed value of 20 ms or that parameter M is independent of joint velocity may not be valid for spinal cord injured or stroke patients. In addition, for these and other patient populations reflex activity needs to be considered when predicting the forces in response to electrical stimulation. Also, for the current model to be useful for an FES application like walking, the model needs to predict the angular velocity based on the load and stimulation pattern. Finally, the current modelling work only considered the effect of stimulation frequency and pattern. Future modelling work will also need to predict the effects of stimulation intensity on the forces produced by the muscle.
This study showed that the current model predicted the forces in response to a wide range of stimulation frequencies and constant velocities in able-bodied human quadriceps muscles. Our model did not assume an a priori force-velocity relationship. Rather, the relationship was a natural outcome of modeling the viscoelastic and contractile behavior of the muscle. The range of predictive abilities of the isovelocity model in response to changes in muscle length, velocity, and stimulation frequency for each individual make it ideal for dynamic applications like FES cycling . In FES cycling where an external motor maintains the speed of cycling constant, our model can be used to design stimulation patterns that can produce the targeted level of power output from the muscle.
Bajd T, Kralj A, Turk R, Benko H, Sega J: Use of functional electrical stimulation in the rehabilitation of patients with incomplete spinal cord injuries. J Biomed Eng 1989,11(2):96-102. 10.1016/0141-5425(89)90115-5
Binder-Macleod S, Kesar T: Catchlike property of skeletal muscle: recent findings and clinical implications. Muscle Nerve 2005,31(6):681-693. 10.1002/mus.20290
Kebaetse MB, Binder-Macleod SA: Strategies that improve human skeletal muscle performance during repetitive, non-isometric contractions. Pflugers Arch 2004,448(5):525-532. 10.1007/s00424-004-1279-0
Garland SJ, Griffin L: Motor unit double discharges: statistical anomaly or functional entity? Can J Appl Physiol 1999,24(2):113-130.
Ding J, Wexler AS, Binder-Macleod SA: A mathematical model that predicts the force-frequency relationship of human skeletal muscle. Muscle Nerve 2002,26(4):477-485. 10.1002/mus.10198
Brown IE, Cheng EJ, Loeb GE: Measured and modeled properties of mammalian skeletal muscle. II. The effects of stimulus frequency on force-length and force-velocity relationships. J Muscle Res Cell Motil 1999,20(7):627-643. 10.1023/A:1005585030764
Dorgan SJ, O'Malley MJ: A mathematical model for skeletal muscle activated by N-let pulse trains. IEEE Trans Rehabil Eng 1998,6(3):286-299. 10.1109/86.712226
Shue GH, Crago PE: Muscle-tendon model with length history-dependent activation-velocity coupling. Ann Biomed Eng 1998,26(3):369-380. 10.1114/1.93
Riener R, Quintern J, Schmidt G: Biomechanical model of the human knee evaluated by neuromuscular stimulation. J Biomech 1996,29(9):1157-1167. 10.1016/0021-9290(96)00012-7
Durfee WK, Palmer KI: Estimation of force-activation, force-length, and force-velocity properties in isolated, electrically stimulated muscle. IEEE Trans Biomed Eng 1994,41(3):205-216. 10.1109/10.284939
Stein RB, Bobet J, Oguztöreli MN, Fryer M: The kinetics relating calcium and force in skeletal muscle. Biophysical Journal 1988, 54: 705-716.
Zahalak GI, Ma SP: Muscle activation and contraction: constitutive relations based directly on cross-bridge kinetics. J Biomech Eng 1990,112(1):52-62. 10.1115/1.2891126
Ferrarin M, Pedotti A: The relationship between electrical stimulus and joint torque: a dynamic model. IEEE Trans Rehabil Eng 2000,8(3):342-352. 10.1109/86.867876
Bobet J, Stein RB: A simple model of force generation by skeletal muscle during dynamic isometric contractions. IEEE Trans Biomed Eng 1998,45(8):1010-1016. 10.1109/10.704869
Ding J, Binder-Macleod SA, Wexler AS: Two-step, predictive, isometric force model tested on data from human and rat muscles. J Appl Physiol 1998,85(6):2176-2189.
Ding J, Wexler AS, Binder-Macleod SA: Development of a mathematical model that predicts optimal muscle activation patterns by using brief trains. J Appl Physiol 2000,88(3):917-925.
Ding J, Wexler AS, Binder-Macleod SA: A predictive model of fatigue in human skeletal muscles. J Appl Physiol 2000,89(4):1322-1332.
Perumal R, Wexler AS, Ding J, Binder-Macleod SA: Modeling the length dependence of isometric force in human quadriceps muscles. J Biomech 2002,35(7):919-930. 10.1016/S0021-9290(02)00049-0
Wexler AS, Ding J, Binder-Macleod SA: A mathematical model that predicts skeletal muscle force. IEEE Trans Biomed Eng 1997,44(5):337-348. 10.1109/10.568909
Bobet J, Gossen ER, Stein RB: A comparison of models of force production during stimulated isometric ankle dorsiflexion in humans. IEEE Trans Neural Syst Rehabil Eng 2005,13(4):444-451. 10.1109/TNSRE.2005.858461
Frey Law LA, Shields RK: Mathematical models use varying parameter strategies to represent paralyzed muscle force properties: a sensitivity analysis. J Neuroengineering Rehabil 2005, 2: 12. 10.1186/1743-0003-2-12
Ding J: Mathematical models that predict muscle isometric forces and fatigue. In PhD Thesis. University of Delaware; 2001.
Rüegg JC: Calcium in muscle contraction. Springer-Verlag; 1992.
Duchateau J, Hainaut K: Nonlinear summation of contractions in striated muscle. I. Twitch potentiation in human muscle. J Muscle Res Cell Motil 1986,7(1):11-17. 10.1007/BF01756197
Hill AV: First and last experiments in muscle mechanics. Cambridge Univ. Press, Cambridge; 1970.
Martin A, Martin L, Morton B: Theoretical and experimental behavior of muscle viscosity coefficient during maximal concentric actions. Eur J Appl Physiol Occup Physiol 1994,69(6):539-544. 10.1007/BF00239872
Aidley DJ: The Physiology of Excitable Cells. New York: Cambridge University Press; 1989.
Allen DG, Blinks JR: The interpretation of light signals from aequorin-injected skeletal and cardiac muscle cells: a new method of calibration. In: Detection and Measurement of Free Ca2+ in Cells. A.K. Amsterdam: Elsevier/North-Holland; 1979.
Mansour JM, Audu ML: The passive elastic moment at the knee and its influence on human gait. J Biomech 1986,19(5):369-373. 10.1016/0021-9290(86)90013-8
Riener R, Edrich T: Identification of passive elastic joint moments in the lower extremities. J Biomech 1999,32(5):539-544. 10.1016/S0021-9290(99)00009-3
Heckman CJ, Weytjens JL, Loeb GE: Effect of velocity and mechanical history on the forces of motor units in the cat medial gastrocnemius muscle. J Neurophysiol 1992,68(5):1503-1515.
de Haan A: The influence of stimulation frequency on force-velocity characteristics of in situ rat medial gastrocnemius muscle. Exp Physiol 1998,83(1):77-84.
Buff HU, Jones LC, Hungerford DS: Experimental determination of forces transmitted through the patello-femoral joint. J Biomech 1988,21(1):17-23. 10.1016/0021-9290(88)90187-X
Stein RB, Momose K, Bobet J: Biomechanics of human quadriceps muscles during electrical stimulation. J Biomech 1999,32(4):347-357. 10.1016/S0021-9290(98)00187-0
Riener R: Model-based development of neuroprosthesis for paraplegic patients. Philos Trans R Soc Lond B Biol Sci 1999,354(1385):877-894. 10.1098/rstb.1999.0440
Binder-Macleod SA, Lee SC, Baadte SA: Reduction of the fatigue-induced force decline in human skeletal muscle by optimized stimulation trains. Arch Phys Med Rehabil 1997,78(10):1129-1137. 10.1016/S0003-9993(97)90140-4
Lee SC, Binder-Macleod SA: Effects of activation frequency on dynamic performance of human fresh and fatigued muscles. J Appl Physiol 2000,88(6):2166-2175.
Snyder-Mackler L, De Luca PF, Williams PR, Eastlack ME, Bartolozzi AR 3rd: Reflex inhibition of the quadriceps femoris muscle after injury or reconstruction of the anterior cruciate ligament. J Bone Joint Surg Am 1994,76(4):555-560.
Abbas JJ, Riener R: Using Mathematical Models and Advanced Control Systems Techniques to Enhance Neuroprosthesis Function. Neuromodulation 2001, 4: 187-195. 10.1046/j.1525-1403.2001.00187.x
Cukier R, Fortuin C, Shuler K, Petschek A, Schailby J: Study of the sensitivity of the coupled reaction systems to uncertainties in rate coefficients: I. Theory. Journal of Chemical Physics 1973,59(8):3873-3878. 10.1063/1.1680571
Saltelli A, Chan K, Scott E: Sensitivity Analysis. John Wiley and Son, Ltd.: West Sussex, England; 2000.
SIMLAB: Simulation Environment for uncertainty and sensitivity analysis, developed by Joint Research Center of the European Commission. 2.2nd edition. 2004.
Phillips CA, Petrofsky JS: Velocity of contraction of skeletal muscle as a function of activation and fiber composition: a mathematical model. J Biomech 1980,13(7):549-558. 10.1016/0021-9290(80)90055-X
Baratta RV, Solomonow M, Best R, Zembo M, D'Ambrosia R: Architecture-based force-velocity models of load-moving skeletal muscles. Clin Biomech (Bristol, Avon) 1995,10(3):149-155. 10.1016/0268-0033(95)93705-X
Dudley GA, Harris RT, Duvoisin MR, Hather BM, Buchanan P: Effect of voluntary vs. artificial activation on the relationship of muscle torque to speed. J Appl Physiol 1990,69(6):2215-2221.
Harris RT, Dudley GA: Factors limiting force during slow, shortening actions of the quadriceps femoris muscle group in vivo. Acta Physiol Scand 1994,152(1):63-71. 10.1111/j.1748-1716.1994.tb09785.x
Hunt KJ, Stone B, Negard NO, Schauer T, Fraser MH, Cathcart AJ, Ferrario C, Ward SA, Grant S: Control strategies for integration of electric motor assist and functional electrical stimulation in paraplegic cycling: utility for exercise testing and mobile cycling. IEEE Trans Neural Syst Rehabil Eng 2004,12(1):89-101. 10.1109/TNSRE.2003.819955
The authors would like to thank Dr. Jun Ding for her helpful comments. This study was supported by the National Institutes of Health Grants HD 36797, HD38582, and NR010786.
The authors declare that they have no competing interests.
RP was involved with mathematical modeling, subject recruitment, data-collection, analysis, and manuscript preparation. SABM and ASW were involved in all aspects of the study, supervised the design and coordination of the study, and provided critical revisions of the manuscript. All authors read and approved of the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Perumal, R., Wexler, A.S. & Binder-Macleod, S.A. Development of a mathematical model for predicting electrically elicited quadriceps femoris muscle forces during isovelocity knee joint motion. J NeuroEngineering Rehabil 5, 33 (2008) doi:10.1186/1743-0003-5-33
- Knee Flexion
- Peak Force
- Stimulation Frequency
- Force Response
- Functional Electrical Stimulation