Excitability following antidromic activation in spinal motoneurones supplying red muscles

It is well known that red muscles may be distinguished from pale muscles by the slowness of their contraction (Fulton, 1926; Denny-Brown, 1929b). In addition, Denny-Brown (1929a) found that red muscle has a lower threshold for postural reflexes, including the stretch reflex, than fast pale muscle. A histological study of fibre diameter has also revealed that the average diameter of motor fibres to the slow red extensors is smaller than for those to the pale extensors, although there is a considerable overlap (Eccles & Sherrington, 1930). While these findings might suggest some specific differences in properties between motoneurones supplying red and pale muscles, no systematic approach has been made toward this problem until recently. By studying stretch reflexes in the state of post-tetanic potentiation it has recently been suggested that spinal motoneurones innervating extrafusal muscle fibres may be classified into two subgroups (Granit, Henatsch & Steg, 1956; Granit, Phillips, Skoglund & Steg, 1957). The tonic type is characterized by a long-lasting reflex discharge to sustained muscle stretch and may also be distinguished from the other, phasic, type of motoneurones by its slower frequency of discharge. Intracellular recording from spinal motoneurones has shown that the motoneurones of slow red muscles have after-hyperpolarization of greater duration than those of fast pale muscles (Eccles, Eccles & Lundberg, 1957 a). In the latter study it was postulated that the discharge frequency of motoneurones under continuous synaptic excitation is controlled by the duration of after-hyperpolarization. It appears that tonic motoneurones in general tend to activate red muscles. As would be expected from the diameter spectrum of motor fibres to the ankle extensors (Eccles & Sherrington, 1930), soleus motoneurones have generally shown a slower axonal conduction velocity than gastrocnemius motoneurones (Eccles et al. 1957 a). The observation that the phasic axonal spike is large and the tonic small when recorded in the same

[1]  J. Fulton Muscular Contraction and the Reflex Control of Movement , 1928, The Indian Medical Gazette.

[2]  C. Sherrington,et al.  Numbers and Contraction-Values of Individual Motor-Units Examined in some Muscles of the Limb , 1930 .

[3]  Electronic Integrator with Immediate Digital Output , 1958 .

[4]  J. Eccles,et al.  Durations of After-hyperpolarization of Motoneurones supplying Fast and Slow Muscles , 1957, Nature.

[5]  C. G. Phillips,et al.  Differentiation of tonic from phasic alpha ventral horn cells by stretch, pinna and crossed extensor reflexes. , 1957, Journal of neurophysiology.

[6]  C. Hunt,et al.  TEMPORAL FLUCTUATION IN EXCITABILITY OF SPINAL MOTONEURONS AND ITS INFLUENCE ON MONOSYNAPTIC REFLEX RESPONSE , 1955, The Journal of general physiology.

[7]  J. Eccles,et al.  The specific ionic conductances and the ionic movements across the motoneuronal membrane that produce the inhibitory post‐synaptic potential , 1955, The Journal of physiology.

[8]  David P. C. Lloyd,et al.  MONOSYNAPTIC REFLEX RESPONSES OF INDIVIDUAL MOTONEURONS , 1955, The Journal of general physiology.

[9]  D. P. Lloyd AFTER-CURRENTS, AFTER-POTENTIALS, EXCITABILITY, AND VENTRAL ROOT ELECTROTONUS IN SPINAL MOTONEURONS , 1951, The Journal of general physiology.

[10]  J. Eccles,et al.  The recording of potentials from motoneurones with an intracellular electrode , 1952, The Journal of physiology.

[11]  A. Hodgkin,et al.  THE IONIC BASIS OF ELECTRICAL ACTIVITY IN NERVE AND MUSCLE , 1951 .

[12]  R. Granit,et al.  The behaviour of tonic α and β motoneurones during stimulation of recurrent collaterals , 1957 .

[13]  K. Koketsu,et al.  Cholinergic and inhibitory synapses in a pathway from motor‐axon collaterals to motoneurones , 1954, The Journal of physiology.

[14]  D. Denny-Brown,et al.  On the Nature of Postural Reflexes , 1929 .

[15]  R. Granit,et al.  Tonic and phasic ventral horn cells differentiated by post-tetanic potentiation in cat extensors. , 1956, Acta physiologica Scandinavica.

[16]  C. Hunt,et al.  Properties of spinal interneurones , 1959, The Journal of physiology.

[17]  J. Eccles,et al.  The action potentials of the alpha motoneurones supplying fast and slow muscles , 1958, The Journal of physiology.

[18]  V. Brooks,et al.  Localization of stretch reflexes by recurrent inhibition. , 1958, Science.

[19]  J. Eccles,et al.  The electrical properties of the motoneurone membrane , 1955, The Journal of physiology.

[20]  D. Denny-Brown,et al.  The Histological Features of Striped Muscle in Relation to Its Functional Activity , 1929 .

[21]  P. Fatt,et al.  Membrane permeability change during inhibitory transmitter action in crustacean muscle , 1958, The Journal of physiology.

[22]  J. Eccles,et al.  After-potentials and excitability of spinal motoneurones following antidromic activation. , 1950, Journal of neurophysiology.

[23]  T. Araki,et al.  Response of single motoneurons to direct stimulation in toad's spinal cord. , 1955, Journal of neurophysiology.

[24]  J. Eccles,et al.  The convergence of monosynaptic excitatory afferents on to many different species of alpha motoneurones , 1957, The Journal of physiology.