Skip to main content
Log in

Muscle models: What is gained and what is lost by varying model complexity

  • Published:
Biological Cybernetics Aims and scope Submit manuscript

Abstract

Three structurally different types of models have evolved over the years to describe muscle-joint systems. The first, based on an input-output analysis of a given task, results in a simple second-order differential equation description that is adequate over a certain movement operating range. The second, based on the classic structural model of Hill (1938), results in a higher-order nonlinear model described by ordinary differntial equations. The third, based on an analysis of the biophysical contractile mechanism, results in a complex partial differential equation description. The advantages and disadvantages of each type of model are considered, based on the criteria of identifying the simplest model that can adequately simulate any fundamental type of human movement without modifying model parameters for different tasks. It is shown that an eighth-order Hill-based antagonistic muscle-joint model is able to satisfy these criteria for a given joint if each of the four basic mechanically-significant non-linearities of the system are included in the model. This same model structure has been used successfully for eight different muscle-joint systems, ranging in size from knee flexion-extension to eye rotation — the only difference between the models is in the parameter values. Second-order models are shown to be task-specific special cases of the input-output behavior of the eighth-order model, while the more complex biophysical models are hypothesized to have insignificant advantages and many disadvantages over the Hill-based model during normal human movement.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  • Agarwal GC, Gottlieb GL (1977) Compliance of the human ankle joint. J Biomed Eng 99:166–170

    Google Scholar 

  • Agarwal GC, Gottlieb GL (1985) Mathematical medeling and simulation of the postural control loop, Part III. CRC Crit Rev Bioeng 12:49–91

    Google Scholar 

  • Agarwal GC, German BM, Stark L (1970) Studies in postural control systems. Part I. Torque disturbance input. Part II. Tendon jerk input. IEEE Trans SCC 6:116–212, 122–126

    Google Scholar 

  • Bach TM, Chapman AE, Calvert TW (1983) Mechanical resonance of the human body during voluntary oscillations about the ankle joint. J Biomech 16:83–90

    Google Scholar 

  • Berthoz A, Metral S (1975) Behavior of a muscular group subjected to a sinusoidal and trapezoidal variation in force. J Appl Physiol 29:378–384

    Google Scholar 

  • Buchtal F, Schmalbruch H (1970) Contraction times and fiber types in intact human muscle. Acta Physiol Scand 79:435–452

    Google Scholar 

  • Cook JD, Stark L (1968) The human eye movement mechanism: experiments, modelling and model testing. Arch Ophthalmol 79:428–436

    Google Scholar 

  • Clark ME, Stark L (1974) Control of human eye movements. I. Modelling the extraocular muscle. Math Biosci 20:213–238

    Google Scholar 

  • Close RL (1972) Dynamic properties of mammalian skeletal muscle. Physiol Rev 52:129–197

    Google Scholar 

  • Crago PE, Houk JC, Hasan Z (1976) Regulatory actions of human stretch reflex. J Neurophysiol 39:925–935

    Google Scholar 

  • Dijk JHM van (1978) Simulation of human arm movemenents controlled by peripheral feedback. Biol Cybern 29:175–186

    Google Scholar 

  • Glantz SA (1974) A constitutive equation for the passive properties of muscle. J Biomech 7:137–145

    Google Scholar 

  • Gottlieb GL, Agarwal GC (1973) Modulation of postural reflexes by voluntary movement. 1. Modulation of the active limb. J Neurol Neurosurg Psychiatry 36:529–539

    Google Scholar 

  • Hannaford B, Nam MH, Ladshminarayanan V, Stark L (1984) Electromyographic evidence of neurological controller signals with viscous load. J Motor Behav 16:255–274

    Google Scholar 

  • Hatze H (1978) A general myocybernetic control model of skeletal muscle. Biol Cybern 28:143–157

    Google Scholar 

  • Hatze H (1981) Myocybernetic control models of skeletal muscle. Univ S Africa

  • Hill AV (1938) The heat of shortening and the dynamic constants of muscle. Proc R Soc London Ser B 126:136–195

    Google Scholar 

  • Hill TL (1975) Theoretical formalism for the sliding filament model of contraction of striated muscle, part II. Prog Biophys Mol Biol 29:105–159

    Google Scholar 

  • Hof AL, Van den Berg JW (1981) EMG to force processing: I. An electrical analogue of the Hill muscle model. J Biomech 14:747–758

    Google Scholar 

  • Hof AL, Van den Berg JW (1983) Calf muscle moment, work and efficiency in level waling; role of series elasticity. J Biomech 16:523–537

    Google Scholar 

  • Houk JC (1963) A mathematical model of the stretch reflex in human muscle systems. M.S. thesis, M.I.T., Cambridge

  • Huxley AF (1957) Muscle structure and theories of contraction. Prog Biophys Biophys Chem 7:257–318

    Google Scholar 

  • Gottlieb GL, Agarwal GC (1978) Dependence of human ankle compliance on joint angle. J Biomech 11:177–181

    Google Scholar 

  • Joyce GC, Rack PMH (1969) Isotonic lengthening and shortening movements of cat soleus muscle. J Physiol 204:475–491

    Google Scholar 

  • Joyce GC, Rack PMH (1974) The effects of load and tremor at the normal human elbow joint. J Physiol 240:375–396

    Google Scholar 

  • Joyce GC, Rack PMH, Westbury DR (1969) The mechanical properties of cat soleus muscle during controlled lengthening and shortening movements. J Physiol 204:461–474

    Google Scholar 

  • Komi PV (1973) Measurement of the force-velocity relationship in human muscle under concentric and eccentric contractions. Biomech III, Med Sport 8:224–229

    Google Scholar 

  • Lacquaniti F, Licata F, Soechting JF (1982) The mechanical behavior of the human forearm in response to transient perturbations. Biol Cybern44:33–46

    Google Scholar 

  • Pedotti A, Krishnan VV, Stark L (1978) Optimization of muscle force sequencing in human locomotion. Math Biosci 38:57–76

    Google Scholar 

  • Perrine JJ, Edgerton VR (1978) Muscle force-velocity and powervelocity relationships under isokinetic loading. Med Sci Sports Exerc 10:159–166

    Google Scholar 

  • Sapega AA, Nicholas JA, Sokolow D, Saraniti A (1982) The nature of the torque “overshoot” in Cybex isokinetic dynanometry. Med Sci Sports Exerc 14:368–375

    Google Scholar 

  • Stark L (1968) Neurological control systems. Plenum Press, New York

    Google Scholar 

  • Stein RB, Lee RG (1981) Tremor and clonus. In: Kandel ER (ed) Handbook of physiology, vol II. Am Physiol Soc, pp 325–344

  • Thorstensson AG, Larsson L, Tesch P, Karlsson J (1976) Muscle strengthe and fiber composition in athletes and sedentary men. Med Sci Sports Exerc 9:26–30

    Google Scholar 

  • Viviani P, Soetching JF, Terzuolo CA (1976) Influence of mechanical properties on the relation between EMG activity and torque. J Physiol (Paris) 72:45–58

    Google Scholar 

  • Wadman WJ, van der Gon D, Geuze RH, Derkson R (1980) Muscle activation patterns for fast goal-directed arm movements. J Human Movem Stud 6:19–37

    Google Scholar 

  • Wilkie DR (1950) Relation between force and velocity in human muscle. J Physiol 110:249–280

    Google Scholar 

  • Winters JM (1985) Generalized analysis and design of antagonistic muscle models: effect of nonlinear properties on the control of human movement. Ph. D. thesis, Univ Calif, Berkeley

  • Winters JM (1986) Muscle as an actuator for intelligent robots. 2nd World Conference on Robotics Research, Scottsdale, Arizona, MS 86-760: 1–18

  • Winters JM, Bagley AM (1986) Biomechanical modelling of muscle-joint systems: why it is useful. Eng Med Biol. In press

  • Winters JM, Nam MH, Stark L (1984) Modeling dynamical interaction between fast and slow movement: fast saccadic eye movement behavior in the presence of the slower VOR. Math Biosci 68:159–187

    Google Scholar 

  • Winters JM, Stark L (1985a) Analysis of fundamental human movement patterns through the use of in-depth antagonistic muscle models. IEEE Trans BME 32:826–839

    Google Scholar 

  • Winters JM, Stark L (1985b) Simulation of fundamental movements. II. Co-contraction. Proc IEEE Eng Med Biol 7:45–50

    Google Scholar 

  • Wood JE, Mann RW (1981) A sliding-filament cross-bridge ensemble model of muscle contraction for mechanical transients. Math Biosci 57:211–263

    Google Scholar 

  • Yates JWE, Kamon E (1983) A comparison of peak and constant angle torque-velocity curves for fast and slow-twitch populations. Eur J Appl Physiol 51:67–74

    Google Scholar 

  • Zahalak GI (1981) A distribution-moment approximation for kinetic theories of muscular contraction. Math Biosci 55:89–114

    Google Scholar 

  • Zahalak GI, Heyman SJ (1979) A quantitative evaluation of the frequency-response characteristics of active human skeletal muscle in vivo. J Biomech 11:28–37

    Google Scholar 

  • Zangemeister WH, Lehman S, Stark L (1981) Simulation of head movement trajectories: model and fit to main sequence. Biol Cybern 41:19–32

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Winters, J.M., Stark, L. Muscle models: What is gained and what is lost by varying model complexity. Biol. Cybern. 55, 403–420 (1987). https://doi.org/10.1007/BF00318375

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00318375

Keywords

Navigation