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Biomedical subjects

Y Laporte

Publications and source records attributed to Y Laporte.

At least 37 records · Page 2Linked to original sources
PubMed1986

[Glycogen depletion produced in intrafusal nuclear bag muscle fibers by brief large-amplitude muscle stretches].

The glycogen content of the three types of intrafusal muscle fibre was studied with histochemical techniques in cat muscle spindles of superficial lumbrical muscles after a very large number of brief large stretches. Zones of glycogen depletion were observed in a high proportion of nuclear bag fibres, notably in bag 1 fibres, but not in chain fibres. These observations suggest that stretching of bag fibres by itself may activate these fibres.

Animals↗
PubMed1985

Fusimotor after-effects on responses of primary endings to test dynamic stimuli in cat muscle spindles.

Conditioning stimulation of individual dynamic fusimotor axons, either gamma or beta, leaves after-effects which enhance the responses of primary endings to test stimulation of the same axon applied during slow ramp stretch. These after-effects have a long duration, persisting well over 5 min, but are abolished by stretch of large amplitude. The dynamic after-effects also enhance frequencygrams elicited by low-frequency repetitive stimulation during slow ramp stretch, causing single stimuli to become much more effective. When several dynamic axons to the same spindle are isolated, conditioning stimulation of one leaves an after-effect to test stimulation of itself and of all other dynamic axons. When two dynamic axons are used for conditioning stimulation, facilitation or occlusion can be demonstrated in their interaction, indicating that they converge on the same intrafusal element. Dynamic after-effects persist during background static fusimotor activity of considerable amplitude, suggesting that static and dynamic actions are quite independent. Dynamic after-effects appear to result from residual changes in the bag fibre, probably from a persistent increase in the number of cross-bridges between thick and thin filaments. These after-effects produce a large increase in the response of primary endings to dynamic fusimotor activity and probably have an important functional role.

Action Potentials↗
PubMed1985

Effects of stretch on dynamic fusimotor after-effects in cat muscle spindles.

Conditioning stimulation of dynamic fusimotor axons leaves persistent after-effects which increase the responses of primary endings to test dynamic stimuli. Such after-effects are abolished by muscle stretch. Destruction of these after-effects depends on the following. (a) Amplitude of stretch: with symmetrical triangular stretches of moderate velocity, an extension of soleus by 4-5 mm totally abolishes the after-effects. Lesser stretches cause a graded reduction. (b) Velocity of relaxation: for a given amplitude of stretch there is greater destruction of after-effects when it is followed by a slow rate of relaxation than after rapid relaxation. (c) After-effects tested late in ramp stretch are more resistant to destruction by stretch than those increasing test dynamic responses early in ramp stretch. Stretch itself produces after-effects which enhance test responses to dynamic but not to static fusimotor stimulation. Interactions between conditioning dynamic stimulation and stretch suggest that both these effects occur in the same intrafusal elements, the bag fibres.

Action Potentials↗
PubMed1984

Some effects of sympathetic stimulation and isoprenaline on fatigued tetanic contractions of skeletal muscle in the cat.

In anaesthetized cats, stimulation of the lumbar sympathetic trunk inconsistently elicited small increases in the contraction of fatigued Peroneus Longus muscles (Orbeli phenomenon). Facilitation of this anti-fatigue effect was regularly observed following close intra-arterial injection of isoprenaline, a beta-adrenergic agonist. Injection of the drug by itself exerted a marked anti-fatigue effect on muscle contraction.

Animals↗
PubMed1984

Glycogen depletion elicited in tenuissimus intrafusal muscle fibres by stimulation of static gamma-axons in the cat.

In this study the experimental conditions used to elicit glycogen depletion in tenuissimus intrafusal muscle fibres were different from those used by Barker, Emonet-Dénand, Harker, Jami & Laporte (1976): the tenuissimus was left in situ; several (4-6) static gamma-axons were stimulated together; the blood flow through the muscle was not reduced during the periods of gamma stimulation except in two experiments; very much longer periods (up to 9 h) of intermittent stimulation by bursts at 50-500/s were used. Bag1 and bag2 fibres were identified by their different ATPase activities in the B region. In two experiments with normal circulation, test responses of several primary endings to short periods of stimulation at 50-100/s were still very strong after stimulation of several static gamma-axons for 5 and 9 h, respectively. Glycogen depletion was observed in a large number of chain and bag2 poles but in only one of nineteen bag1 poles examined. In two other experiments with normal circulation, there was a very pronounced reduction of the test responses after stimulation of several static gamma-axons for 7 and 9 h, respectively. Out of twenty-four bag1 poles examined, nineteen exhibited zones of depletion. In an experiment in which stimulation was conducted as in Barker et al. (1976), i.e. with reduction of muscle blood flow during 1 min periods of stimulation at 50-100/s, the primary endings still gave a strong response after fifteen periods of stimulation in contrast with the marked 'fatigue' that was constantly observed in the former study. No depleted intrafusal fibres were found in the spindles of this muscle. In a last experiment, after an initial pattern of stimulation similar to that described above, the new pattern of stimulation, but with periodical reduction of blood flow, was applied, leading to a 'fatigue' of the test responses in 2 h. In the spindles of this muscle three out of ten bag1 poles were depleted. The variability of glycogen depletion in bag1 fibres appears to be linked to the degree of spindle 'fatigue' which may develop after static gamma stimulation. It seems that in 'fatigued' spindles some factor or factors liberated by the contraction of neighbouring fibres may deplete glycogen in bag1 fibres by a non-neural mechanism. When, in spite of a prolonged stimulation of static gamma-axons, no fatigue of the test responses develops, zones of depletion in bag1 fibres--possibly of neural origin--are very rare, although a large proportion of bag2 and chain fibres are depleted.

Animals↗
PubMed1983

[Not Available].

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France↗
PubMed1982

Effects of stimulating the lumbar sympathetic trunk on cat hindlimb muscle spindles.

1. The effect of stimulating the lumbar sympathetic trunk has been observed on cat lumbrical and tenuissimus muscle spindles. 2. Spindle afferent discharges were recorded either from single Ia fibers in teased dorsal root filaments or from a large number of spindles by integrating their discharges led from muscles nerves. 3. Blood flow in small arteries supplying the muscle was observed through a microscope during and after the stimulation of the sympathetic trunk. 4. In some spindles repetitive stimulation of the sympathetic trunk elicited, after a few seconds delay, a small increase in firing rate. This can be ascribed to a direct action of sympathetic axons on the spindles because it precedes by about 20-30 sec the reduction of blood flow observed in the muscle arteries. This effect is not accompanied by a change in dynamic sensitivity of the primary ending. 5. This early effect is followed, after 20-30 sec, by a later rise in firing frequency which still progresses after the end of stimulation and eventually terminates in an abrupt fall in firing often leading to interruption of the ending activity. Recovery takes places at a variable time after the blood flow has bee reestablished. These long lasting effects can be ascribed to reduction of blood flow in muscle spindles since they are always associated with changes in blood flow in muscle arteries and since they are mimicked by occlusion of the muscle circulation. 6. In some spindles, the amplitudes of frequencygrams elicited by stimulation of static gamma axons were slightly increased suggesting a weak facilitatory effect on the contraction of some intrafusal muscle fibers.

Adrenergic Fibers↗
PubMed1980

Effects of slow muscle stretch on the responses of primary and secondary endings to small amplitude periodic stretches in de-efferented soleus muscle spindles.

The responses of primary and secondary endings of de-efferented soleus spindles to small amplitude periodic stretches superimposed on slow ramp stretches have been studied. For primary endings, the responses become progressively larger especially during the last period of the ramp whereas for secondary endings, after an initial period of moderate growth, the amplitude of the responses display a relative reduction precisely when the responses of the primary endings are the largest. These differences can be interpreted in terms of progressive increase in stiffness of the striated polar portions of the intrafusal muscle fibers.

Afferent Pathways↗
PubMed1980

Identifications of the intrafusal endings of skeletofusimotor axons in the cat.

Direct identification of the endings of skeletofusimotor (beta) axons has been made in muscle spindles deprived for their gamma innervation by degeneration. Hindlimb muscles were prepared in which 1--5 fast-conducting motor axons were left intact while the rest of the motor supply was cut and allowed to degenerate for a period of 7 days. In 3 experiments a single beta axons survived supplying tenuissimus, and in 2 experiments beta axons were among 4 or 5 surviving axons that supplied superficial lumbrical and abductor digiti quinti medius muscles. Motor endings identified as p1 plates were found in teased, silver preparations of all experimental muscles, a total of 35 such plates being located in 15 spindles. The plates were all supplied to bag1 fibres. The experiments show that if a spindle innervated by a beta axon is deprived of its gamma supply by degeneration the motor endings that remain intact are p1 plates.

Animals↗
PubMed1980

Glycogen depletion of bag1 fibers elicited by stimulation of static gamma axons in cat peroneus brevis muscle spindles.

1. The distribution of static fusimotor axons to intrafusal muscle fibres in cat peroneus brevis spindles has been studied with the glycogen depletion method. 2. In each of six experiments three to seven static axons were stimulated. The muscle was subsequently quick-frozen and cut in serial transverse sections that were stained for glycogen. In each muscle, nearly all the spindles were examined for depletion. 3. Intrafusal muscle fibres displaying zones of complete glycogen depletion were observed in fifty-two whole spindles and seven half-spindles. Chain fibres were depleted in forty-eight (92%) of the whole spindles, bag2 fibres in thirty-five spindles (67%) and bag1 fibres in nineteen spindles (36%). 4. Seven other experiments were performed to test whether small amplitude sinusoidal stretching (30--100 Hz) of the muscle might produce glycogen depletion in bag1 fibres. Two hundred and seven spindles were examined. In nearly all of them the glycogen content of the intrafusal muscle fibres was normal. Two muscles had limited atrophic portions within which a few depleted spindles were found. 5. These experiments show that the intrafusal distribution of static gamma axons is not restricted to chain and bag2 fibres but that in a significant number of spindles the bag1 fibres are also supplied by static gamma axons.

Animals↗
PubMed1978

[Heterogeneous effects of sinusoidal muscular stretching on frequency grams of primary endings due to stimulation of static gamma axons].

The action of sinusoidal stretching at 1,5 Hz on primary ending frequencygrams due to repetitive stimulation of static gamma axons has been studied, in nembutalized cats, on flexor hallucis longus muscle spindles. Whenever, in static conditions, driving is elicited by the repetitive stimulation of gamma axons, the elementary components of the frequencygrams increase in amplitude during muscle stretch. This effect is not observed when the stimulation of the gamma axons gives a regular acceleration of the primary endings without "driving".

Animals↗
PubMed1978

[Frequencygrams due to the stimulation of dynamic gamma axons exerting type II effects].

Frequencygrams are graphs giving indirect information on the contraction of intrafusal muscle fibres. Frequencygrams of Cat spindle primary endings (flexor hallucis longus, soleus and peroneus brevis muscles) were recorded during repetitive stimulation of dynamic gamma axons exerting type II effects. The features of these frequencygrams (periodic increments whose frequency is equal to that of the stimulation and "driving") show that they can be ascribed to a relatively strong and fast intrafusal contraction. Two interpretations are considered.

Action Potentials↗
PubMed1977

Types of intra- and extrafusal muscle fibre innervated by dynamic skeleto-fusimotor axons in cat peroneus brevis and tenuissimus muscles, as determined by the glycogen-depletion method.

1. The types of intra- and extrafusal muscle fibre innervated by dynamic skeleto-fusimotor (beta) axons were determined by using a modification of the glycogen-depletion method of Edström & Kugelberg (1968) combined with histochemical tests for various enzyme reactions. A single beta axon was prepared in each of the experiments, which were carried out on six peroneus brevis and two tenuissimus muscles. 2. The intrafusal distribution of dynamic beta axons is almost exclusively restricted to bag1 fibres. The bags fibre was depleted in each of twenty-four beta-innervated spindle poles; the only fibres of a different type depleted intrafusally were a bag2 fibre in one pole and a long chain in another. 3. Depletion in the bag1 fibres was usually restricted to one zone in one pole, generally in a mid-polar location. 4. The extrafusal muscle fibres depleted by dynamic beta axons belong to the slow oxidative type as defined by Ariano, Armstrong & Edgerton (1973). The number of such fibres in each motor unit could not be accurately determined, but is almost certainly small. 5. The slow oxidative muscle fibres innervated by dynamic beta axons were not depleted over their entire length. Since there is no reason to assume that they are not twitch fibres, it would seem that the localized depletions result from the conditions required to obtain glycogen depletion, i.e. long periods of motor stimulation applied during the occlusion of the muscle's blood supply. Under similar experimental conditions depletion of glycogen was also restricted to portions of fibres in fast oxidative-glycolytic motor units, but extended over most of the length of the fibres in fast glycolytic units.

Action Potentials↗