Advertisement
Research Article| Volume 27, ISSUE 4, P513-524, April 1976

“Satellite potentials” and the duration of motor unit potentials in normal, neuropathic and myopathic muscles

      This paper is only available as a PDF. To read, Please Download here.

      Abstract

      Time-locked activity in the EMG was studied in normal, neuropathic and myopathic muscles, using the averaging technique. Normal and neuropathic muscles seemed in most cases not to differ with regard to the frequency nor the quality of “satellite signals”, i.e. small and short potentials joining the main component of the MUP with a constant interval, up to 26 ms in duration. In normal muscles 10% of the MUPs and in neuropathic muscles 12% had a satellite, which, when studied, showed no signs of blocking. However, in 2 patients with an apparent old spinal affection both an increased number and an increased latency of satellite signals were found. In the different myopathies studied 45% of the MUPs recorded consecutively were preceded or followed by an often increased number of tiny satellites. Sometimes the satellites joining the myopathic MUP formed a long (up to 60 ms) “tail” after the triggering component. On the basis of our results we conclude that in myopathies the total duration of MUPs is in certain cases pathologically increased rather than decreased.
      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Journal of the Neurological Sciences
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Buchthal F.
        An Introduction to Electromyography.
        in: Gyldendal, København1957: 1-43
        • Cöers C.
        • Telerman-Toppet N.
        • Gerard J.-M.
        Terminal innervation ratio in neuromuscular disease, Part 2 (Disorders of lower motor neuron, peripheral nerve, and muscle).
        Arch. Neurol. (Chic.). 1973; 29: 215-222
        • Desmedt J.
        • Borenstein S.
        Collateral innervation of muscle fibres by motor axons of dystrophic motor units.
        Nature (Lond.). 1973; 246: 500-501
        • Esslen E.
        Electromyographic findings on two types of misdirection of regenerating axons.
        Electroenceph. clin. Neurophysiol. 1960; 12: 738-741
        • Fullerton P.
        • Gilliatt R.
        Axon reflexes in human motor nerves.
        J. Neurol. Neurosurg. Psychiat. 1965; 28: 1-11
        • Gardner-Medwin D.
        Studies of the carrier state in the Duchenne type of muscular dystrophy, Part 2 (Quantitative electromyography as a method of carrier detection).
        J. Neurol. Neurosurg. Psychiat. 1968; 31: 124-134
        • Hudgson P.
        • Mastaglia F.L.
        Ultrastructural studies of diseased muscle.
        in: Walton J.N. Disorders of Voluntary Muscle. 3rd edition. Churchill, Edinburgh, London1974: 360-416
        • Kudina L.P.
        • Person P.S.
        “Split” motor unit potentials of the human muscle.
        Sechenov. physiol. J. U.S.S.R. 1971; 57 (in russian): 38-44
        • Lang H.
        • Tuomola H.
        Averaging and automatic analysis of EMG signals — Applications of a new method.
        Scand. J. Rehab. Med. 1974; : 33-36
        • Lang H.
        • Tuomola H.
        The time parameters of motor unit potentials recorded with multielectrodes and the summation technique.
        Electromyography. 1975; 15: 87-99
        • Lang H.
        • Vaahtoranta K.
        The baseline, the time characteristics and the slow afterwaves of the motor unit potential.
        Electroenceph. clin. Neurophysiol. 1973; 35: 387-394
        • Nissen-Petersen H.
        • Buchthal F.
        A delay line to record random action potentials.
        Electroenceph. clin. Neurophysiol. 1969; 26: 100-106
        • Norris F.H.
        Synchronous fasciculation in motor neuron disease.
        Arch. Neurol. (Chic.). 1965; 13: 495-500
        • Roth C.
        Décharge couplée réflexe d'axone moteur.
        Electromyography. 1971; 11: 459-465
        • Siward T.G.
        • Basmajian J.V.
        • Janda U.
        Effects of ischaemia of trained motor units.
        Amer. J. Phys. Med. 1968; 47: 64-71
        • Stålberg E.
        Propagation velocity in human muscle fibres in situ.
        Acta physiol. scand. 1966; 70: 112
        • Stålberg E.
        • Ekstedt J.
        Single fibre EMG and microphysiology of the motor unit in normal and diseased human muscle.
        in: New Developments in EMG and Clinical Neurophysiology. Vol. 1. S. Karger, Basel1973: 89-112
        • Stålberg E.
        • Trontelj J.V.
        Demonstration of axon reflexes in human motor nerve fibres.
        J. Neurol. Neurosurg. Psychiat. 1970; 33: 571-579
        • Stålberg E.
        • Trontelj J.V.
        • Janko M.
        Single fibre EMG findings in muscular dystrophy.
        in: Hausmanova-Petrusewicz I. Jedrzejowska H. Structure and Function of Normal and Diseased Muscle and Peripheral Nerve. Polish Medical Publishers, Warsaw1974: 185-190
        • Takahashi K.
        The coupling discharge in neurogenic muscular atrophy.
        Arch. Neurol. (Chic.). 1966; 14: 617-623