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Responses of mono- and bi-articular muscles to load perturbations of the human arm

Summary

We studied the behavior of muscles acting synergistically in elbow flexion in response to load perturbations. The perturbations were applied either proximally or distally to the elbow joint and consisted of single pulses or steps of torque and of pseudorandom sequences of torque pulses. They produced changes in angular position and torque at both the shoulder and elbow joints. The electromyographic (EMG) responses evoked in biceps, brachio-radialis and brachialis muscles were different when elbow and shoulder motion was in the same direction and when the two angular motions were oppositely directed. For example, elbow extension resulted both when a downward force perturbation was applied to the forearm as well as when a posteriorly directed force applied to the upper arm was released. Elbow flexors were activated at a short latency only in the former case and not in the latter. The modulation of EMG activity in elbow flexors evoked by the perturbations was related to the global motion of the limb, including the angular motions at both the shoulder and elbow joints. The time course of the EMG responses in biceps, which acts on both joints, differed from that of brachio-radialis and brachialis muscles, which act only at the elbow. The results are discussed in the context of the possible mechanisms responsible for the muscle responses to the perturbations.

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Reference

  • Abbs JH, Graco VL (1984) Control of complex motor gestures: orofacial muscle responses to load perturbations of lip during speech. J Neurophysiol 51: 705–723

    Google Scholar 

  • Baker J, Goldberg J, Herrmann G, Peterson B (1984) Optimal response planes and canal convergence in secondary neurons in vestibular nuclei of alert cats. Brain Res 294: 133–137

    Google Scholar 

  • Baker J, Goldberg J, Peterson B (1985) Spatial and temporal responses of the vestibulocollic reflex in decerebrate cats. J Neurophysiol 54: 735–756

    Google Scholar 

  • Cheney PD, Fetz EE (1984) Corticomotoneuronal cells contribute to long-latency stretch reflexes in the rhesus monkey. J Physiol (Lond) 349: 249–272, 1984

    Google Scholar 

  • Cole KJ, Gracco VL, Abbs JH (1984) Autogenic and nonautogenic sensorimotor actions in the control of multiarticulate hand movements. Exp Brain Res 56: 582–585

    Google Scholar 

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

    CAS  PubMed  Google Scholar 

  • Davies WDT (1970) System Identification for Self-adaptive Control. Wiley, London

    Google Scholar 

  • Dufresne JR, Soechting JF, Terzuolo CA (1978) Electromyographic response to pseudo-random torque disturbances of human forearm position. Neuroscience 3: 1213–1226

    Google Scholar 

  • Dufresne JR, Soechting JF, Terzuolo CA (1979) Reflex motor output to torque pulses in man: identification of short- and long-latency loops with individual feedback parameters. Neuroscience 4: 1493–1500

    Google Scholar 

  • Eccles JC, Eccles RM, Lundberg A (1957) The convergence of monosynaptic excitatory afferents onto many different species of alpha motoneurones. J Physiol (Lond) 137: 22–50

    Google Scholar 

  • Eccles RM, Lundberg A (1958) Integrative pattern of Ia synaptic actions on motoneurones of hip and knee muscles. J Physiol (Lond) 144: 271–298

    Google Scholar 

  • Eklund G, Hagbarth KE, Hagglund JV, Wallin EV (1982) The “late” reflex responses to muscle stretch: the resonance hypothesis versus the “long loop” hypothesis. J Physiol (Lond) 326: 79–90

    Google Scholar 

  • Evarts EV, Tanji J (1974) Gating of motor cortex reflexes by prior instruction. Brain Res 71: 479–494

    Google Scholar 

  • Fick R (1911) Anatomie und Mechanik der Gelenke, Vol. 3. Gustav Fischer, Jena

    Google Scholar 

  • Pritz N (1981) Ia-Synergismus an der vorderen Extremität der Katze. Ph.D. Thesis, Doktorarbeit Universität München

  • Ghez C, Shinoda Y (1978) Spinal mechanisms of the functional stretch reflex. Exp Brain Res 33: 55–68

    Google Scholar 

  • Gottlieb GL, Agarwal GC (1979) Response to sudden torques about ankle in man: myotatic reflex. J Neurophysiol 42: 91–106

    Google Scholar 

  • Hammond PH (1956) The influence of prior instruction to the subject on an apparently involuntary neuromuscular response. J Physiol (Lond) 132: 17–18

    Google Scholar 

  • Hollerbach JM, Flash T (1982) Dynamic interactions between limb segments during planar arm movement. Biol Cybern 44: 67–77

    CAS  PubMed  Google Scholar 

  • Jaeger RJ, Gottlieb GL, Agarwal GC (1982) Myoelectric responses at flexors and extensors of human wrist to step torque perturbations. J Neurophysiol 48: 388–401

    Google Scholar 

  • Lacquaniti F, Soechting JF (1982) Coordination of arm and wrist motion during a reaching task. J Neurosci 2: 399–408

    Google Scholar 

  • Lacquaniti F, Soechting JF (1984) Behavior of the stretch reflex in a multi-jointed limb. Brain Res 311: 161–166

    Google Scholar 

  • Lacquaniti F, Soechting JF (1986) EMG responses to load perturbations of the upper limb: effect of dynamic coupling between shoulder and elbow motion. Exp Brain Res 61: 482–496

    Google Scholar 

  • Marsden CD, Merton PA, Morton HB (1976) Stretch reflex and servo action in a variety of human muscles. J Physiol (London) 259: 531–560

    Google Scholar 

  • Matthews PBC (1984) Evidence from the use of vibration that the human long-latency stretch reflex depends upon spindle secondary afferents. J Physiol (London) 348: 383–415

    Google Scholar 

  • O'Leary DP, Honrubia V (1975) On-line identification of sensory systems using pseudorandom binary noise inputs. Biophys J 15: 505–532

    Google Scholar 

  • Robinson DA (1982) The use of matrices in analyzing the threedimensional behavior of the vestibulo-ocular reflex. Biol Cybern 46: 53–66

    Google Scholar 

  • Soechting JF (1984) Effect of target size on spatial and temporal characteristics of a pointing movement in man. Exp Brain Res 54: 121–132

    CAS  PubMed  Google Scholar 

  • Soechting JF, Dufresne JR, Lacquaniti F (1981) Time-varying properties of myotatic response in man during some simple motor tasks. J Neurophysiol 46: 1226–1243

    Google Scholar 

  • Soechting JF, Lacquaniti F (1981) Invariant characteristics of a pointing movement in man. J Neurosci 1: 710–720

    CAS  PubMed  Google Scholar 

  • Suzuki I, Timerick SJB, Wilson VJ (1985) Body position with respect to the head or body position in space is coded by lumbar interneurons. J Neurophysiol 54: 123–133

    Google Scholar 

  • Tatton WG, Forner SD, Gerstein GL, Chambers WW, Liu CN (1975) The effect of postcentral cortical lesions on motor reponses to sudden upper limb displacement in monkeys. Brain Res 96: 108–113

    Google Scholar 

  • Wiesendanger M, Miles TS (1982) Ascending pathway of lowthreshold afferents to the cerebral cortex and its possible role in motor control. Physiol Rev 62: 1234–1269

    Google Scholar 

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Lacquaniti, F., Soechting, J.F. Responses of mono- and bi-articular muscles to load perturbations of the human arm. Exp Brain Res 65, 135–144 (1986). https://doi.org/10.1007/BF00243836

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  • DOI: https://doi.org/10.1007/BF00243836

Key words

  • Load perturbations
  • Multijointed limb
  • Feedback control