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Selective inhibition by methysergide of the monosynaptic reflex discharge in the isolated spinal cord of the newborn rat.

In the isolated spinal cord of the newborn rat, methysergide and LSD-25 depressed the monosynaptic reflex discharge selectively. Cyproheptadine and dimethothiazine did not inhibit the monosynaptic reflex. The selective inhibitory effect of methysergide on the monosynaptic reflex was not due to a presumptive low safety factor of this reflex. The inhibition was restored under a condition such as the compound action potential in the dorsal root was enhanced by 4-aminopyridine. Methysergide did not decrease the sensitivity of the motoneuron to substance P and L-glutamic acid. It is suggested that methysergide acts at the presynaptic terminal of Ia afferent fibers and depresses evoked transmitter release.

Action Potentials↗

Effect of nucleus raphe magnus stimulation on recurrent inhibition of the monosynaptic reflex in the cat.

Experiments were performed on 8 cats anesthetized with urethan-chloralose. The effects of nucleus raphe magnus (NRM) conditioning stimulation on recurrent inhibition of posterior biceps semitendinosus nerve (PBSt) monosynaptic reflex elicited by electric stimulation of a part of L7 ventral root were investigated in the cat. It was found that (1) the PBSt monosynaptic reflex was facilitated by NRM conditioning stimulation at 30, 50 and 80 ms conditioning-test stimulus intervals, but that (2) the inhibited monosynaptic reflex by recurrent inhibition was further inhibited by NRM conditioning stimulation at the same conditioning-test stimulus intervals, and that (3) the activity of Renshaw cells as recorded by glass microelectrode was enhanced by NRM conditioning stimulation. These facts indicated that recurrent inhibition pathways are enhanced by NRM conditioning stimulation.

Animals↗

Depressive effect of coughing on spinal monosynaptic reflexes in conscious man.

1. The relationship between coughing and spinal monosynaptic reflexes (SMR) in extensors and flexors was investigated in eight healthy subjects by using the Hoffmann technique. Coughing exerted major depression (81% in extensor and 83% in flexor SMR). This depressant effect began simultaneously with the first cough and lasted through the coughing phase. Complete recovery to initial values occurred an average of 40 s thereafter. 2. In comparison, mental tasks induced only a slight decrease in SMR amplitude. In contrast, the Mueller and Valsalva manoeuvres induced facilitation. 3. During coughing, large variations in extensor amplitudes were observed that were coupled with the ventilatory cycle. Slight facilitation was observed during inspiration, but expiration induced pronounced depression, occurring 0.20 s after the beginning of the expiratory period. Experiments performed during baseline breathing failed to show any change throughout inspiratory or expiratory phases. 4. Chemical stimulation of irritant receptors (inhalation of citric acid) produced no specific modification of extensor responses compared with the effect of placebo inhalation (distilled water). 5. These data suggest that coughing exerts a major depressant effect on motor activity via a loop that possibly includes cardiopulmonary receptors and inhibitory supraspinal descending pathways.

Adult↗

A comparison of homonymous and heteronymous connectivity in the spinal monosynaptic reflex arc of the cat.

Multi-unit spike triggered averaging was used to determine functional connectivity between spindle afferent fibers from the medial gastrocnemius muscle and the motoneurons innervating the medial (homonymous connections) and the lateral gastrocnemius-soleus muscle (heteronymous connections). As many as 288 possible connections between 24 motoneurons and 12 afferent fibers were studied in single, acute experiments. The influences of morphological and topographical factors, as well as of motoneuron species on functional connectivity were analysed. The probability that a motoneuron would receive functional connections from a given population of afferent fibers was related to its size and its proximity to the spinal entry level of the afferent fibers. The faster the axonal conduction velocity of the motoneuron (i.e. the larger the motoneuron) and the closer its location to the entry zone of the afferent fibers, the higher was its probability of receiving functional connections. The greater the conduction velocity (i.e. diameter) of a stretch receptor afferent fiber, the higher was its probability of making functional connections with motoneurons. These relationships were qualitatively similar for homonymous and heteronymous connections. 58% (233/399) of the Ia and group II afferents (combined) had functional connections with homonymous motoneurons, 32% (75/234) with heteronymous motoneurons. However, homonymous and heteronymous motoneurons of similar sizes were equally likely to receive functional connections when located at the same craniocaudal level. Differences in the locations and mean sizes of homonymous and heteronymous motoneurons however, cannot account completely for the observed overall differences in homonymous and heteronymous connectivity.

Action Potentials↗