Changes in discharge rate of fusimotor neurones provoked by fatiguing contractions of cat triceps surae muscles.

1. Changes in discharge rate of thirty‐one fusimotor neurones to triceps surae muscles during long‐lasting, fatiguing contractions of these muscles were studied in decerebrate cats. Discharges of fusimotor neurones were recorded from the nerve filaments. Muscle contractions were elicited by electrical stimulation of either the muscle nerves (twenty‐one neurones) or the corresponding ventral roots (ten neurones), until the muscle tension fell to about 30% of its initial value. 2. Early and late changes could be recognized in fusimotor discharge rate during long‐lasting muscle contraction. The early changes obviously not related to muscle fatigue, consisted of an initial increase at the onset of muscle contraction and a subsequent decrease to or below the resting discharge level. The late change in discharge rate, supposedly related to muscle fatigue, was an increase developing gradually towards the end of muscle contraction, ranging at its peak from 2 to 15 impulses/s (mean value 5.5 impulses/s, n = 31) and outlasting the contraction for 20‐320 s. 3. When the contracting muscle was made ischaemic the late increase in fusimotor discharge rate started earlier and was maintained until the arterial clamp was removed. After severing the muscle nerves distal to the site of stimulation no changes, a slight sustained increase, or else a decrease in fusimotor discharge rate occurred during electrical stimulation of either muscle nerves or ventral roots. At its cessation the spontaneous firing rate was reassumed immediately. Stimulation of the distal stumps of the severed nerves elicited no changes in fusimotor discharge rate. 4. It is proposed that the late increase in fusimotor discharge rate may appear due to autogenetic excitation of fusimotor neurones by discharge from group III and IV muscle afferent fibres provoked and/or enhanced by metabolic products liberated in muscle tissue during the fatiguing contraction. The fusimotor firing was estimated to remain elevated to a level twice that of the spontaneous activity on average for approximately 120 s after the muscle contraction. Its functional role in muscle fatigue is discussed.

[1]  W. Z. Rymer,et al.  Increased inhibitory effects on close synergists during muscle fatigue in the decerebrate cat , 1988, Brain Research.

[2]  H. Johansson,et al.  Effects of electrical and natural stimulation of skin afferents on the γ-spindle system of the triceps surae muscle , 1989, Neuroscience Research.

[3]  BY P. H. Ellaway,et al.  Recurrent inhibition of fusimotor neurones exhibiting background discharges in the decerebrate and the spinal cat , 1971, The Journal of physiology.

[4]  R L BENNETT,et al.  Electromyography of fatigue. , 1951, Archives of physical medicine and rehabilitation.

[5]  S. Mense,et al.  Effects of a carrageenan-induced myositis on the discharge properties of group III and IV muscle receptors in the cat. , 1988, Journal of neurophysiology.

[6]  P H Ellaway,et al.  Closely coupled excitation of γ‐motoneurones by group III muscle afferents with low mechanical threshold in the cat , 1982, The Journal of physiology.

[7]  R. Hutton,et al.  Dynamic and static stretch responses in muscle spindle receptors in fatigued muscle. , 1985, Medicine and science in sports and exercise.

[8]  R. Hutton,et al.  Stretch sensitivity of Golgi tendon organs in fatigued gastrocnemius muscle. , 1986, Medicine and science in sports and exercise.

[9]  S. Garner,et al.  Reduced voluntary electromyographic activity after fatiguing stimulation of human muscle. , 1988, The Journal of physiology.

[10]  H. Johansson,et al.  Actions on gamma‐motoneurones elicited by electrical stimulation of group II muscle afferent fibres in the hind limb of the cat. , 1983, The Journal of physiology.

[11]  S. Mense,et al.  Responses in muscle afferent fibres of slow conduction velocity to contractions and ischaemia in the cat. , 1983, The Journal of physiology.

[12]  S. Mense,et al.  Muscle receptors with group IV afferent fibres responding to application of bradykinin , 1975, Brain Research.

[13]  Ksenija Jovanovic´,et al.  Reflex effects on γ fusimotor neurones of chemically induced discharges in small-diameter muscle afferents in decerebrate cats , 1990, Brain Research.

[14]  R. Anastasijevic,et al.  Discharge rate and reflex responses of fusimotor neurons during muscle ischemia , 1987, Experimental Neurology.

[15]  T. Waldrop,et al.  Effect of ischemia on responses of group III and IV afferents to contraction. , 1984, Journal of applied physiology: respiratory, environmental and exercise physiology.

[16]  M. Kaufman,et al.  Effect of metabolic products of muscular contraction on discharge of group III and IV afferents. , 1988, Journal of applied physiology.

[17]  K. Hagbarth,et al.  Tonic vibration reflexes elicited during fatigue from maximal voluntary contractions in man. , 1990, The Journal of physiology.

[18]  R. Johansson,et al.  Reflex origin for the slowing of motoneurone firing rates in fatigue of human voluntary contractions. , 1986, The Journal of physiology.

[19]  B. Saltin,et al.  Lactate and potassium fluxes from human skeletal muscle during and after intense, dynamic, knee extensor exercise. , 1990, Acta physiologica Scandinavica.

[20]  C. Hunt,et al.  RELATION OF FUNCTION TO DIAMETER IN AFFERENT FIBERS OF MUSCLE NERVES , 1954, The Journal of general physiology.

[21]  H Johansson,et al.  Actions on gamma‐motoneurones elicited by electrical stimulation of group III muscle afferent fibres in the hind limb of the cat. , 1983, The Journal of physiology.

[22]  U. Proske,et al.  Can lactate-evoked cardiovascular responses be used to identify muscle ergoreceptors? , 1987, Brain Research.

[23]  M. Piercey,et al.  Discharge patterns of Renshaw cells evoked by volleys in ipsilateral cutaneous and high-threshold muscle afferents and their relationship to reflexes recorded in ventral roots. , 1974, Journal of neurophysiology.

[24]  T. Sears,et al.  Continuous conduction in demyelinated mammalian nerve fibres , 1976, Nature.

[25]  J. Longhurst,et al.  Sensitization of group III muscle afferents to static contraction by arachidonic acid. , 1990, Journal of applied physiology.

[26]  A. Lundberg,et al.  Supraspinal control of interneurones mediating spinal reflexes , 1959, The Journal of physiology.

[27]  P. Matthews,et al.  The discharge from muscle spindles as an indicator of γ‐efferent paralysis by procaine , 1958, The Journal of Physiology.