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Efferents and afferents in an intact muscle nerve: background activity and effects of sural nerve stimulation in the cat
Author(s) -
Bessou P.,
Joffroy M.,
Pagès B.
Publication year - 1981
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1981.sp013936
Subject(s) - efferent , anatomy , tonic (physiology) , sural nerve , stimulation , reflex , efferent nerve , spinal cord , electrophysiology , chemistry , muscle spindle , motor unit , gastrocnemius muscle , neuroscience , biology , afferent , skeletal muscle
1. The background activity was observed in γ and α efferent fibres and in group I and II fibres innervating the muscle gastrocnemius lateralis or medialis. The reflex effects of ipsilateral and contralateral sural nerve stimulations on the muscle efferents were analysed together with their consequences upon the afferents of the same muscle. The observations were made in the decerebrated cat without opening the neural loops between the muscle and the spinal cord. 2. The multi‐unit discharges of each category of fibres were obtained, on line, by an original electronic device (Joffroy, 1975, 1980) that sorted the action potentials from the whole electrical activity of a small branch of gastrocnemius lateralis or medialis nerve according to the direction and velocity of propagation of the potentials. 3. The small nerve may be regarded as a representative sample of different functional groups of fibres conducting faster than 12 m.sec −1 and supplying gastrocnemius muscles. 4. Some γ efferents were always tonically firing except when a transient flaccid state developed. Usually the α efferents were silent, probably because the muscle was fixed close to the minimal physiological length. 5. Separate and selective stimulations of Aβ, Aδ and C fibres of ipsilateral and contralateral sural nerve showed that each group could induce the excitation of γ neurones. The reciprocal inhibition period of α efferents during a flexor reflex was only once accompanied by a small decrease in γ‐firing. 6. The reflex increase of over‐all frequency of γ efferents resulted from an increased firing rate of tonic γ neurones and from the recruitment of γ neurones previously silent. When the γ efferents in the small nerve naturally occurred in two subgroups, the slower‐conducting subgroup (mainly composed of tonic γ axons) was activated before the faster‐conducting subgroup (mostly composed by γ axons with no background discharge). Some rare exceptions were found, however. 7. The selective activation of γ efferents could be obtained with short‐and low‐frequency stimulation. When, with stronger stimulations, γ—α co‐activation was observed, the onset of the γ‐firing increase preceded by 100‐600 msec that of the α discharge in the small nerve. Likewise, the onset of the γ‐efferent response preceded the increase of over‐all electromyographic activity of the whole triceps muscle but only by 10‐100 msec. The discrepancy could be due to the soleus α motoneurones being activated earlier than the α‐motoneurones of gastrocnemius muscle, according to the size principle. In only one experiment, the α‐firing onset preceded the γ‐firing increase. 8. Stimulations of ipsilateral or contralateral nerve, whatever the α or γ reflex patterns, always led to increased firing rates of group I and II fibres of the small nerve. The origins of the discharge of group I and II muscle afferents and the excitation mechanisms of the receptors involved are considered. Some aspects of the mechanism of the reflex control of movement are discussed in the light of these results.

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