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Biomedical subjects

Y Laporte

Publications and source records attributed to Y Laporte.

At least 55 records · Page 3Linked to original sources

On the subdivision of static and dynamic fusimotor actions on the primary ending of the cat muscle spindle.

1. Using large ramp and triangular stretches a survey has been made of the effect of stimulating single gamma fusimotor fibres on primary endings of muscle spindles in the peroneus brevis to see whether 'intermediate' types of fusimotor action could be recognized, falling between the well known static and dynamic types. 2. Responses were classified into six groups, as detailed on pp. 844-846, ranging from apparently 'pure' dynamic action (category I) to apparently 'pure' static action (category IV). Models for a putative mixed action were produced by combining the stimulation of a static and of a dynamic fibre to the same spindle. The clearest sign of static action was firing on the releasing phase of the stretch. The essential sign of dynamic action, which survived combination with the more dominant static action, was the low adaptive decay of firing with a time constant of about 0-5 sec that occurs on the plateau of the ramp stretch. 3. Out of 153 responses, each elicited from a primary ending on stimulation of a single fusimotor fibre, 67% were apparently 'pure' examples of dynamic and static action. The remaining 33% of responses were to some degree suggestive of an admixture, in various proportions, of static and dynamic actions. For only 18% of them was there firm indication of such admixture. 4. When a given fibre was tested on more than one ending then, with one exception out of thirty-six instances, its action always proved to be either predominantly static or predominantly dynamic. There was no special tendency for an axon with a mixed action on one spindle to have a similarly mixed action on other endings so that individual fusimotor fibres were best classified as static or dynamic without intermediate grades. 5. Simultaneous stimulation of two fusimotor fibres eliciting apparently 'pure static and dynamic actions, could mimic all the intermediate types of action. 6. The results are discussed in relation to recent studies, especially those based on glycogen depletion. It was concluded that dynamic action arises from activation of the bag1 intrafusal muscle fibre, and that static action arises from the bag2 and chain fibres, whether acting individually or collaboratively. The intermediate actions are suggested to arise from an overlap of motor innervation to contrasting types of intrafusal muscle fibre. 7. On the basis of effects on the regularity of the afferent discharge the findings support the view that a given static action axon can innervate bag2 and chain fibres in various proportions in different spindles, so that they do not provide separable effector pathways. 8. Responses to large amplitude sinusoidal stretching were also studied in relation to our classification.

Action Potentials↗

Fast-conducting skeletofusimotor axons supplying intrafusal chain fibers in the cat peroneus tertius muscle.

1. In six experiments on cat peroneus tertius muscle, from 12 to 23 motor axons with conduction velocities above 85 m/s were repetitively stimulated so as to produce glycogen depletion in the muscle fibers they innervated. 2. The whole muscle was then quick-frozen, serially cut, stained to demonstrate glycogen, and examined for intrafusal glycogen depletion. 3. Zones of glycogen depletion were found in 27 of the 99 examined spindles: they were almost invariably located on chain fibers and specifically on the longest of the chain fibers in affected spindles. 4. Since it was shown that there are no purely fusimotor fast axons in the motor supply to peroneus tertius, it is concluded that skeletofusimotor axons are present among the fastest motor axons to this muscle.

Animals↗

Distribution of fusimotor axons to intrafusal muscle fibres in cat tenuissimus spindles as determined by the glycogen-depletion method.

1. The distribution of fusimotor axons to bag1, bag2 and chain muscle fibres in cat tenuissimus spindles has been studied using a modification of the glycogen-depletion technique of Edstrrom & Kugelberg (1968). Single fusimotor axons were stimulated intermittently at 40-100/sec for long periods (30-90 sec) during blood occlusion. Portions of muscle containing the activated spindles were quick-frozen, fixed in absolute ethanol during freeze-substitution, and then embedded in paraffin wax. Serial transverse sections were stained for glycogen using the periodic acid-Schiff method, and examined for depletion. 2. Dynamic gamma axons (i.e. those that increase the dynamic index of primary-ending responses to ramp stretches of large amplitude) depleted bag1 fibres almost exclusively. 3. Static gamma axons (i.e. those that reduce or abolish the dynamic index) depleted both bag and chain fibres. Bag1 and bag2 fibres were depleted about equally. 4. A single static gamma axon may activate both bag and chain fibres in one spindle (the most common pattern), chain fibres only in another, and bag fibres only in a third spindle. 5. Static gamma axons with conduction velocities less than 25 m/sec also had a non-selective distribution, but no depletion was observed in bag2 fibres. 6. The zones of depletion produced by dynamic gamma axons were distributed more or less equally in the intra- and extracapsular parts of spindle poles, whereas those produced by static gamma axons were mainly intracapsular. 7. The results are compared with the glycogen-depletion studies of Brown & Butler (1973, 1975) and our own study of the distribution of static gamma axons to spindles in which all other motor axons had degenerated (Barker, Emonet-Dénand, Laporte, Proske & Stacey, 1973). The implications of the finding that both static gamma and dynamic gamma axons activate bag1 fibres are discussed.

Animals↗

Skeleto-fusimotor axons in the hind-limb muscles of the cat.

1. Motor axons supplying various hind-limb muscles of the cat (flexor hallucis lingus, peroneus brevis, peroneus digiti quinti, tibialis anterior, soleus and tenuissimus) were identified as skeleto-fusimotor or beta axons because their repetitive stimulation elicited both the contraction of extrafusal muscle fibres and an increase in the rate of discharge of spindle primary endings which perisited after selective blockade of extrafusal neuromuscular junctions. 2. The conduction velocity of these axons ranged from 39 to 92 m/sec. 3. Of seventy-six beta axons, seventy-two had a dynamic action on the sensitivity to velocity of stretching of primary endings, four had a static action. 4. The dynamic action of six beta axons was observed only after the contraction of extrafusal muscle fibres was selectively suppressed. 5. Tendon organs can be activated by beta motor units.

Action Potentials↗

Proportion of muscles spindles supplied by skeletofusimotor axons (beta-axons) in peroneus brevis muscle of the cat.

Of 32 cat peroneus brevis spindles, 23 (72%) were found to be supplied by a least 1 skeletofusimotor or beta-axon. A motor axon was identified as skeletofusimotor when repetitive stimulation of it elicited both the contraction of extrafusal muscle fibers and as acceleration of the discharge of primary ending, which persisted after selective block of the neuromuscular junctions of extrafusal muscle fibers. The block was obtained by stimulating single axons at 400-500/s for a few seconds. Of 135 axons supplying extrafusal muscle fibers, 24 (18%) were shown to be beta-axons; 22 beta-axons had conduction velocities ranging from 45 to 75 m/s. All but three beta-axons increased the dynamic sensitivity of primary endings. Beta-innervated spindles may also be supplied by dynamic gamma-axons.

Animals↗

Morphological identification and intrafusal distribution of the endings of static fusimotor axons in the cat.

1. Tenuissimus muscles of the cat were prepared in which the motor innervation was reduced to a single gamma axon by cutting all the other motor axons and allowing them to degenerate during a period of 7-12 days. The function of the surviving gamma axon was then determined, and the distribution of its endings ascertained in teased, silver preparations.2. In the ten muscles successfully prepared the function of the surviving gamma axon was static and the motor innervation distributed to the spindles consisted of trail endings. The conduction velocities of the axons ranged from 33 to 48 m/sec.3. A detailed histological analysis was made of thirty spindles innervated by six of the surviving static axons.4. The six static axons distributed trail endings to both bag and chain muscle fibres in the poles of thirty spindles with about twice the frequency of supplying them to poles in which the distribution was restricted exclusively to one type of muscle fibre or the other.5. The density of trail innervation supplied to the bag fibres, in terms of the mean number of terminals per fibre, was typically from one and a half to twice that supplied to the chain fibres. On the other hand, whereas the number of bag fibres supplied with trail endings in a spindle pole was seldom more than one, the number of chain fibres innervated was usually two in a range of one to four.6. The possible effects that partial denervation might have had on the spindles are discussed, but it is concluded that they are unlikely to have affected the results.

Action Potentials↗