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Evidence from the use of vibration that the human long-latency stretch reflex depends upon spindle secondary afferents.

The electromyographic activity of flexor pollicis longus has been recorded in normal human subjects on moving the tip of the thumb with the proximal phalanx clamped. Ramp and hold displacements (stretches) were compared with high-frequency sinusoidal movement (vibration). The subject exerted a constant flexor force between stimuli and made no voluntary response to them. On stretching the muscle by forcibly extending the thumb at various constant velocities the usual combination of short-latency (ca. 25-30 ms) and long-latency (ca. 40 ms) components of response were observed. The short-latency response progressively predominated as the velocity was increased (60-900 deg s-1, 9 deg joint displacement). One subject still showed only a long-latency response with the fastest stretch, arguing that it is a distinct reflex entity. On commencing vibration (143 Hz, 3 deg movement peak-to-peak) a short-latency response was regularly obtained, but any long-latency response was always small in relation to that elicited by stretch. This was equally so when the short-latency responses to the two types of stimulation were matched by using appropriate parameters of stimulation. The time course of the vibration response did not change appreciably with change of amplitude of vibration, so that its temporal profile was always quite different from that of the stretch response. The observed differences are in accordance with the hypothesis that the spindle group II afferents produce the long-latency excitation, with the time lost peripherally in afferent conduction rather than centrally. In relation to the strength of their Ia excitatory actions, stretch is known to excite secondary afferents more powerfully than does vibration. The findings are not readily accommodated on the hypothesis that the long-latency response is a transcortical reflex elicited by the initial Ia input, since vibration should then also have had a powerful long-latency action. Similar responses to vibration were obtained when it was applied percutaneously to the tendon of flexor pollicis longus 6 cm above the wrist. Also, those elicited by thumb vibration persisted largely unchanged when the thumb was anaesthetized. This confirms that they were dependent upon the excitation of receptors in flexor pollicis longus, presumably the Ia afferents, rather than upon cutaneous or joint receptors in the thumb. The stretch responses also depended upon muscle receptors, since they too survived anaesthesia.(ABSTRACT TRUNCATED AT 400 WORDS)

Adult↗

Modulation of the long-latency reflex to stretch by the supplementary motor area in humans.

Surface-recorded, electromyographic responses to 200-ms ramp stretches were studied in the wrist flexor muscles from both arms of a patient with clinical and radiographic evidence of infarction in the right supplementary motor area (SMA). They were compared with those from 8 age-matched control subjects. The latencies of the spinal component of the stretch reflex were slightly longer than normal in both arms of the patient (normal subjects: 28.5 +/- 2.6 ms; patient: 35 ms, right arm and 32 ms left arm). However, the amplitude and duration of the short-latency response were identical in both arms. The onset of the long-latency response to stretch was symmetrical in both the patient's arms and was slightly later than normal (normal subjects 55.5 +/- 4.0 ms, patient: 72 ms right arm and 70 ms left arm); however, its duration was considerably prolonged in the arm contralateral to the SMA lesion (normal subjects: 44.8 +/- 6.0 ms; patient: 48 ms right arm. 105 ms left arm). These results are consistent with the hypothesis that the long-latency stretch reflex is mediated via a transcortical loop.

Adult↗

Modulation of the functional stretch reflex by the segmental reflex pathway.

Electromyographic (EMG) reflex responses were examined in the biceps muscle of awake Cebus monkeys trained to resist perturbations of a handle with their forearm. In particular responses at latencies of 15-20 msec (M1) and 40-55 msec (M2), thought to correspond to segmental and suprasegmental reflex pathways respectively, were studied. The experiments demonstrated that the magnitude of the M1 response was large, as compared to M2, only when the muscle was tonically active and small perturbations were applied. For larger perturbations the magnitude of M1 saturated and the M2 response became functionally significant, its magnitude being directly related to the magnitude of the perturbation. By means of delayed reductions in torque, the magnitude of this M2 response was also shown to be very sensitive to changes in facilitatory drive provided by segmental pathways.

Afferent Pathways↗

Auxiliary spinal networks for signal focussing in the segmental stretch reflex system.

In continuation of a previous paper, the auxiliary signal focussing properties of more complicated spinal neuronal networks are considered here. Special emphasis is put on the distributive function of the recurrent feedback system of alpha-motoneurones, but also the inhomogeneous distribution of excitatory and inhibitor input to motoneurones is taken into account as an essential prerequisite for signal focussing. Simple hypothetical calculations for steady-state conditions yield a more vivid insight into the interaction of the two types of neuronal circuitry contributing to signal focussing.

Feedback↗

Modulation of slow and fast elbow extensor EMG tonic activity by stretch reflexes in man.

Reflex EMG responses to sudden passive flexion of the elbow were recorded from anconeus and triceps brachii in 5 human volunteers. While the subjects were required not to resist the flexion movement, they were required to maintain an extension torque of 3.5 or 7.0 Nm prior to its onset. Under these isotonic conditions, the latency and amplitude of the reflex activities from anconeus and triceps brachii did not differ significantly, in contrast to the findings of Le Bozec (1986) in actively relaxed subjects. The myotatic/postmyotatic EMG amplitude ratio did not provide a further quantitative way to distinguish between these muscles. The absence of a difference between the reflex activities of a slow (anconeus) and a fast (triceps brachii) muscle is interpreted as resulting from a strong drive of spindle activity on the whole extensor motoneuron pool, which outweights the differences in recruitment due to the differing relative amounts of type I and type II fibres in the two muscles. Differences like those described between finger and calf muscles by other authors are thought to be due to the relative degree of corticalization of these muscles. All short and long latency responses of the muscles increased in magnitude and decreased in latency with increasing background EMG activity as well as with increasing initial length. The position and tonic activity dependency of these responses is explained in terms of alpha-gamma coactivation.

Adult↗

Role of the stretch reflex in oxotremorine tremor.

Although the basic mechanism for parkinsonian tremor is known to be central, the case for the oscillator(s) of physiological tremor and shivering is still a matter of dispute. In this case, an important role has been proposed for muscle afferents. Oxotremorine tremor has in common with shivering its frequency range (10-28 Hz) and the co-contraction of flexors and extensors. On the other hand, in contradistinction, it can be blocked by atropine, as is the case with parkinsonian tremor. Thus it was of interest to analyze the role of muscle afferents in the production and maintenance of oxotremorine tremor in the acutely decorticated cat. This was studied with two experimental approaches. In one, either a front or hind limb of a cat was completely deafferented by dorsal rhizotomy and the tremor activity recorded electromyographycally in a pair of antagonistic muscles. In the other, the nerve and muscle electrical activity and force produced by the tremoring muscle (gastrocnemius) were recorded simultaneously. Tremor activity was induced by oxotremorine injection (200-750 micrograms/kg i.p.) given at different postoperative periods. The drug induced a regular tremor in the chronically deafferented animals (3 weeks to 5 months) but not in the acutely deafferented limb (3 hrs after dorsal rhizotomy). The tremor observed in the former group was very regular and had the same frequency range (10-28 Hz) for both normal and deafferentd sides. Section of all the muscle afferents of a given pool (agonist and its main synergist) did not have any effect on the regularity and frequency of the oscillation (tremor) of that pool. The role of other muscle and/or cutaneous afferents, although perhaps of some importance, remains unclear. A pure spinal mechanism to account for the regular oscillations (tremor) is proposed.

Animals↗