After-effects of stretch on the responses of cat soleus muscle spindles to static fusimotor stimulation

Summary Mammalian muscle spindles show persistent after-effects following conditioning stretch or fusimotor stimulation. Most previous observations have been carried out on primary endings of spindles and using dynamic fusimotor stimulation. We report here observations on after-effects produced either by conditioning stretch or by static fusimotor stimulation on the responses of primary and secondary endings to a slow test stretch during which a brief burst of static fusimotor stimulation is applied. We find that the response to the test burst is large if the muscle is kept short after conditioning but it becomes depressed if the muscle is held stretched for 3 s following conditioning. We attribute these effects to the presence of stable cross-bridges between actin and myosin filaments in intrafusal fibres. We conclude that, qualitatively, after-effects using static fusimotor testing are the same as with dynamic fusimotor testing and this must be taken into account when providing an explanation for the phenomenon.     

Slowing of the discharge of secondary endings of cat muscle spindles during fusimotor stimulation

Summary Responses of secondary endings of muscle spindles of the peroneus tertius muscle of the anaesthetized cat have been recorded during repetitive stimulation of functionally single fusimotor fibres that produced slowing of the discharge. In a sample of 125 pairs of single fusimotor fibres and secondary spindle afferents 5 examples of slowing were seen. The amount of slowing became less at longer muscle lengths. Conditioning the spindle by stimulating the muscle nerve at fusimotor strength, at a length 2.5 mm longer than the test length, and then returning to the test length 3 seconds later led to a greater degree of slowing of the discharge than after conditioning stimulation at the test length. With one exception, responses to muscle stretch were reduced during stimulation of a fusimotor fibre that produced slowing. On two occasions stimulating a fusimotor fibre that produced slowing of the response of one secondary ending, led to excitation of two other endings. Two possible explanations for the generation of slowing responses have been considered. The first is that the slowing is the result of contraction of the region of intrafusal fibre directly underlying the secondary sensory ending. The second, which we favour since it accounts for the facts more adequately, is that slowing is the result of shortening of the region of nuclear chain fibres on which the sensory ending lies, produced by movement in an adjacent nuclear bag fibre.     

Fusimotor activity and the tendon jerk in the anaesthetised cat

This is a study of the tendon jerk reflex elicited by a brief stretch applied to the triceps surae muscle group in the chloralose-anaesthetised cat. The size of the recorded reflex depended on stretch parameters (optimum at 300 μm amplitude at a rate of 100 mm/s) and on how the muscle had been conditioned. A reflex elicited after a conditioning contraction at the test length was often twice as large as after a contraction carried out at a length longer than the test length. This difference was attributed to the amount of slack introduced in the intrafusal fibres of muscle spindles by conditioning. The question was posed, did ongoing fusimotor activity exert any influence on the size of the tendon jerk? Depolarization indices (DPI) were calculated from responses of muscle spindles to stretch and correlated with the level of reflex tension. Values of DPI obtained from afferent responses with and without repetitive stimulation of identified fusimotor fibres suggested that with the stretch parameters used here the main influence of fusimotor activity was that it removed any pre-existing slack in muscle spindles and thereby increased reflex tension. In the absence of intrafusal slack, stimulation of static and dynamic fusimotor fibres had little additional influence on the size of the reflex. It is concluded that much of the variability typically seen with tendon jerks is due to muscle history effects. Since in muscles which have not been deliberately conditioned there is commonly some slack present in spindles, activity in fusimotor fibres is likely to reduce slack and therefore increase reflex size.     

Responses of primary endings of cat muscle spindles to locally applied vibration

Summary Responses of muscle spindles in the cat soleus muscle have been studied during vibration applied locally to the belly of the muscle. Bursts of vibration at 170 Hz and with a peak amplitude of 200 m were applied to a site at which local pressure initiated impulses from the spindle. The response to vibration depended on the conditioning of the muscle immediately beforehand and the placement of the vibrator. The length at which the vibration was applied was called the test length; this was typically 10 mm less than the muscle's maximum length in the body. After a fusimotor strength contraction at a length 2–5 mm longer than the test length, vibration sensitivity, measured on return to the test length, was low. If the muscle was contracted at a length 2–5 mm shorter than the test length, vibration sensitivity was high. The low vibration sensitivity following conditioning at the longer length was attributed to the development of slack in intrafusal fibres. In the presence of slack, stimulation of some static fusimotor fibres was able to restore vibration sensitivity fully. It is suggested that the vibration sensitivity of passive spindles arises largely in bag₂ intrafusal fibres.     

Vibration sensitivity of cat muscle spindles at short muscle lengths

 Experiments are described in which the vibration sensitivity was tested for primary and secondary endings of soleus muscle spindles of the anaesthetised cat. The vibratory stimulus was applied longitudinally to the muscle tendon and, after locating the site of the spindle in the muscle, applied transversely to muscle fibres directly overlying the spindle. All measurements were made with the muscle slack, at 20 mm shorter than its maximum physiological length (L _m–20 mm). Spindles were separated into two groups: spontaneous spindles, which maintained background activity at this length, and silent spindles, which did not. Two forms of muscle conditioning were used: hold-long, in which the muscle was stretched by 5 mm, contracted and then returned to the test length, and hold-test, in which a conditioning contraction was given at the test length. After hold-test, most spindles responded to longitudinal vibration; after hold-long, most did not. This difference in responsiveness was attributed to the presence or absence of slack in intrafusal and extrafusal fibres, due to the muscle’s thixotropic property. When the vibration was applied transversely, at a site directly overlying the spindle, responses of silent spindles continued to show thixotropic behaviour, whereas responses of spontaneous spindles were almost independent of the form of muscle conditioning. It is proposed that the ability of spontaneous spindles to maintain background activity at short muscle lengths is due to connective tissue or elastic fibre links between the sensory ending and the spindle capsule. The vibratory stimulus, applied transversely, reaches the sensory ending via these strands which, as non-muscle tissue, do not alter their mechanical state as a result of muscle conditioning. Received: 23 March 1998 / Accepted: 4 August 1998     

The responses of secondary endings of cat soleus muscle spindles to succinyl choline

This report describes the effects of succinylcholine (SCh) on the secondary endings of cat soleus muscle spindles and attempts to explain them in terms of the action of the drug on intrafusal fibres. All but 2 of 41 secondary endings studied in detail showed a significant response to a single intravenous injection of 200 g kg^-1 SCh. This consisted of a rise in the resting rate or development of a resting discharge if the spindle had previously been silent and an increase in the response to stretch. The increases in the responses to stretch were weaker than those observed for primary endings of spindles, but were much larger than those of tendon organs, which showed very little effect with this concentration of drug. The response to SCh showed two features consistent with its action being mediated via an intrafusal muscle fibre contraction rather than a direct depolarising action on the afferent nerve ending. In the presence of SCh, secondary endings were able to maintain a discharge during muscle shortening at rates, on average, more than 5 times greater than under control conditions. Secondly, the increase in spindle discharge produced by SCh showed a length dependence similar to that for fusimotor stimulation. Further support for the action of SCh being principally via an intrafusal fibre contraction was provided by the observation that its effects were abolished by the neuromuscular blocker gallamine triethiodide. The time course of recovery of SCh responses, following their blockade by gallamine, was much slower than recovery of extrafusal tension and closely paralleled that for the recovery of fusimotor responses. In three separate experiments on the medial gastrocnemius muscle the possibility that SCh may exert an excitatory action on spindle sensory endings through the liberation of potassium ions from the muscle was tested by tetanic stimulation of the muscle. This had no detectable excitatory effect. Several observations were made on the effect of SCh on responses of cutaneous receptors. SCh did not change levels of spontaneous activity or responses to mechanical stimulation of either slowly or rapidly adapting mechanoreceptors. It was argued for both tendon organs and cutaneous receptors that if SCh had a direct action on the nerve ending at the concentrations used here, some responses of these receptors to the drug might have been expected. All of the above supports the view that secondary endings of spindles are able to respond to SCh by the development of an intrafusal fibre contracture. The question of the intrafusal fibre types involved is discussed.     

The responses of muscle spindles in the kitten to stretch and vibration

Summary Discharges of muscle spindle afferents from the soleus muscle were studied in kittens aged 1–21 days and in adult cats. Vibration applied longitudinally to the tendon elicited one impulse for each cycle of vibration over the range 1–200 Hz for the kittens and up to 450 Hz for the adult. Threshold amplitudes were generally higher in the kitten than in the adult. In response to large ramp and hold stretches applied at long muscle lengths kitten spindles showed rate saturation during the length change. Dynamic index, that is the peak rate during the length change minus the rate at the final length became progressively smaller at longer muscle lengths. No sign of saturation was seen at comparable muscle lengths in the adult. It is suggested that in the newborn the bag₁ intrafusal fibre is not functional and that the dynamic response is produced only by the afferent terminals on the bag₂ fibre. Another difference between kitten and adult was the length sensitivity measured under dynamic conditions. This increased much more steeply with stretch rate in the kitten. One possible explanation for the higher dynamic length sensitivity is a lack of elastic fibres surrounding intrafusal fibres of immature spindles.     

Motor and sensory innervation of muscle spindles in the neonatal rat

Summary Neural and muscular elements of three muscle spindles from the soleus muscles of 4-day-old rats were reconstructed by electron microscopy of skip-serial transverse ultrathin sections. Each spindle contained four encapsulated intrafusal fibers, including a minimum of one bag₁, one bag₂ and one chain fiber. The fibers were innervated by unmyelinated motor and sensory axons. The primary and secondary afferents approached the spindles as single axons and terminated on the central region of the intrafusal fibers. Single profiles of terminal axons occupied the sites of sensory neuromuscular junctions, similar to adult sensory endings. No morphological features suggested retraction of afferents from 4-day postnatal spindles. Motor axons approached spindles tightly packed in bundles of 5–20 axons and terminated in the juxtaequatorial and polar regions of both bag and chain fibers. Multiple profiles of terminal axons were visible for each intrafusal motor ending. More motor axons innervated 4-day postnatal spindles and a greater number of axon terminals were visible in immature intrafusal motor endings than in adult spindles. The data suggest that postnatal maturation of motor innervation to intrafusal fibers involves the elimination of supernumerary motor nerve inputs. Synapse elimination in the development of the fusimotor system might represent a mechanism whereby individual axons adjust the number of spindles they innervate.     

The responses of frog muscle spindles during stimulation of slow motor axons

Summary Responses of muscle spindles of the iliofibularis muscle of the frogLitoria aurea have been recorded during single shock and repetitive stimulation of single functional motor axons. Repetitive stimulation of axons which innervated slow muscle, and on four occasions, axons which innervated twitch muscle, produced a large increase in the dynamic response of the spindle to a ramp-and-hold stretch. While extrafusal slow muscle did not respond to a single motor volley, some spindles did, especially if at the same time the muscle was being stretched. In an explanation of the effect of muscle stretch on responses of spindles to slow motor volleys it was proposed that stretch acted to reduce the internal motion in muscle fibres produced by a non-uniform distribution of sarcomere lengths. It was proposed that this kind of effect may account for dynamic fusimotor actions in all vertebrate spindles.Financial assistance was provided by a grant from the National Health and Medical Research Council of Australia, Grant No. 78/5721     

Function and structure of atypical muscle spindles after neonatal nerve crush in rats

Summary During the early postnatal period, the differentiation and maturation of muscle spindles in the rat is still dependent on their sensory innervation. When a nerve is crushed during this period, most spindles in the denervated muscles degenerate and after reinnervation only occasional spindles of atypical structure are to be found in these muscles. We determined the basic functional properties of these atypical spindles in adult rats and attempted to correlate them with their structural characteristics. The discharge rates of 13 afferent units from the soleus or lateral gastrocnemius muscles were evaluated in response to stretch. These units were capable of a slowly adapting response to 2–4 mm stretches. Their mean discharge frequencies at any point of the ramp-and-hold stretch were, however, on an average 50% lower than normal values. The conduction velocities of afferents from the atypical spindles were in the range of 10–40 m/s. Histological examinations revealed that 90% of the atypical muscle spindles found in the soleus or lateral gastrocnemius muscles had only 1 or 2 intrafusal fibres without any nuclear accumulations as compared to four intrafusal fibres in normal muscle spindles in the rat. The proportional decrease of the discharge rate in both the dynamic and static part of the response of these atypical spindles could be due to the decreased synaptic area between the sensory terminals and the intrafusal fibres and/or to altered structural properties of the intrafusal fibres.     

Postembedding light- and electron microscopic immunocytochemistry of amino acids: description of a new model system allowing identical conditions for specificity testing and tissue processing

Summary Responses of soleus muscle afferents were studied in anaesthetised kittens, after intravenous injection of succinyl choline (SCh), a drug which in adult spindles, at low doses, produces a contracture preferentially of bag₁ intrafusal muscle fibres and so mimics the effect of dynamic fusimotor stimulation. Following injection of SCh in kittens aged between 1 and 57 days the integrated discharge recorded in large portions of dorsal root during muscle stretch showed a smaller increase than in the adult. Recordings from functionally single afferents of muscle spindles showed that in the youngest animals SCh induced a resting discharge from all spindles, which were normally silent. The response to a ramp-and-hold stretch showed an abrupt rise in firing rate at the start of the stretch followed by a slow decline. The abrupt fall at the end of the ramp, typical of the adult dynamic response, was almost absent in spindles of animals 2–5 days old. In the younger animals SCh allowed primary and secondary spindle endings to be distinguished on the basis of their response to stretch. Conduction velocity of developing Group I nerve fibres was found to increase from 9.5 ms^–1 on day 2 to 51.6 ms^–1 on day 57, an increase of 0.77 ms^–1 per day, while Group II increased from 5.0 ms^–1 to 23.2 ms^–1 over the same period, an increase of 0.33 ms^–1 per day. The two groups appeared to be separate even in the youngest animals. It is concluded that although spindles in the newborn kitten respond vigorously to SCh, the pattern of discharge is quite different from that seen in older animals.     

Motor control of nuclear bag and nuclear chain intrafusal fibres in isolated living muscle spindles from the cat.

1. The behaviour of nuclear bag and nuclear chain intrafusal fibres in isolated cat muscle spindles was studied by direct observation during repetitive stimulation of the muscle nerve at different stimulus strengths. Contraction of intrafusal fibres and stretch of sensory endings was recorded on film. 2. Tenuissimus spindles are usually operated by a total of four or five fusimotor axons, and the individual action of all of them was studied in many cases. 3. The great majority of fusimotor axons produce activity at one spindle pole only. 4. In about 60% of spindles nuclear bag and nuclear chain intrafusal fibres are selectively controlled by different fusimotor axons, while in one third of these spindles the individual nuclear bag fibres are themselves controlled independently. The remaining 40% of spindles, in addition to some selective innervation, receive one non-selective axon which operates both nuclear chain and nuclear bag fibres though usually only one of the nuclear bag fibres is involved. Selective control is demonstrated in photographs. 5. The thresholds of fusimotor axons selectively innervating nuclear bag and nuclear chain fibres, and of non-selective fusimotor axons are not significantly different. 6. It is suggested that in spindles in which the nuclear bag fibres are controlled by the same axon, it is a 'dynamic' gamma, or occasionally beta, axon. Where one nuclear bag fibre is operated along with the nuclear chain fibres it is controlled by 'static' gamma axon(s), and the other nuclear bag fibre is selectively controlled by 'dynamic' gamma, and perhaps beta, axon(s). Where two nuclear bag fibres are separately operated one may be controlled by 'dynamic' axon(s) and the other by 'static' gamma axon(s). Nuclear chain fibres are always controlled by 'static' gamma axons.     

Muscle spindles in rheumatoid arthritis

Summary Ultrastructural features of muscle spindles were studied in biopsy material from 100 patients suffering from classical rheumatoid arthritis. Thickening of the outer capsule, increased amount of extracellular ground substance within the inner capsule, and marked thickening of the basement membrane of capillary blood vessels supplying the muscle spindles were observed. Chronic inflammatory cells and macrophages were present within the spindles. Changes affecting the intrafusal muscle fibres were also seen. They were manifest as atrophy and degeneration of the intrafusal muscle fibres, absence of the specialised junctional complexes, and of the intercellular bridges, microladders and satellite cells. It is suggested that the changes affecting the intrafusal muscle fibres are probably secondary. Damage to the myelinated nerves was present, while the sensory and motor nerve endings were well preserved.Temporary Research Fellow the Rotterdam Centre for Rheumatic Disease Present address: Division of Pathology, Department of Obstetrics and Gynaecology, University of Chicago, Chicago, Illinois 60637, USA     

The regularity of primary and secondary muscle spindle afferent discharges

1. The patterns of nerve impulses in the afferent fibres from muscle spindles have been studied using the soleus muscle of the decerebrate cat. Impulses from up to five single units were recorded simultaneously on magnetic tape, while the muscle was stretched to a series of different lengths. Various statistics were later determined by computer analysis.2. After the ventral roots were cut to eliminate any motor outflow to the muscle spindles, both primary and secondary spindle endings discharged very regularly. At frequencies around 30 impulses/sec the coefficient of variation of the interspike interval distributions had a mean value of only 0.02 for the secondary endings and 0.058 for the primary endings. The values obtained for the two kinds of ending did not overlap.3. When the ventral roots were intact, the ;spontaneous' fusimotor activity considerably increased the variability of both kinds of endings. Secondary endings still discharged much more regularly than primary endings, even when the fusimotor activity increased the frequency of firing equally for the two kinds of endings. At frequencies around 30/sec the average coefficient of variation of the interval distributions was then 0.064 for the secondary endings and 0.25 for the primary endings.4. When the ventral roots were intact there was usually an inverse relation between the values of successive interspike intervals. The first serial correlation coefficient often had values down to - 0.6 for both kinds of ending. Higher order serial correlation coefficients were also computed.5. Approximate calculations, based on the variability observed when the ventral roots were intact, suggested that when the length of the muscle was constant an observer analysing a 1 sec period of discharge from a single primary ending would only be able to distinguish about six different lengths of the muscle. The corresponding figure for a secondary ending was twenty-five lengths.6. The increase in variability with fusimotor activity, and the pattern of serial correlations, were probably caused by static fusimotor fibres firing at rates below the fusion frequency of the intrafusal muscle fibres that they supply.     

Fusimotor stimulation and the dynamic sensitivity of the secondary ending of the muscle spindle

The response of secondary endings of de-efferented muscle spindles in the soleus muscle of the anaesthetized cat was recorded during stretching of the muscle at velocities of 5-30 mm/sec. Stimulation of single fusimotor fibres, most and probably all of which were static fusimotor fibres, produced no appreciable change in the normally small dynamic sensitivity of these endings.     

Morphological and histochemical differentiation of intrafusal fibres in the posterior latissimus dorsi muscle of the developing chick

Summary Morphological and histochemical differentiation of neuromuscular spindles was studied in the posterior latissimus dorsi (PLD) of the chick during embryonic and post-hatching development. A rapid increase in the number of spindles takes place between the 13th and 15th of embryonic life. By the 15th day in ovo, the spindle capsule appears filled with numerous contiguous cells. Large sensory endings and small primitive motor endings are observed on intrafusal fibres. Ultrastructural observations of the nerve supply of the spindles confirm that each developing spindle receives one thick Ia axon with one to three thin axons. The intracapsular space differentiates by the 17th day of embryonic development. All intrafusal fibres are morphologically of the nuclear-chain type, while two fibre types are distinguished as early as the 14th day of embryonic life, when myofibrillar ATPase activity is demonstrated after acid preincubation. These two histochemical types of intrafusal fibres are also described in the adult. The relation between these two histochemical types and different functional activity of intrafusal fibres is suggested.     

Innervation of developing intrafusal muscle fibers in the rat

The chronology of development of spindle neural elements was examined by electron microscopy in fetal and neonatal rats. The three types of intrafusal muscle fiber of spindles from the soleus muscle acquired sensory and motor innervation in the same sequence as they formed—bag₂, bag₁, and chain. Both the primary and secondary afferents contacted developing spindles before day 20 of gestation. Sensory endings were present on myoblasts, myotubes, and myofibers in all intrafusal bundles regardless of age. The basic features of the sensory innervation—first-order branching of the parent axon, separation of the primary and secondary sensory regions, and location of both primary and secondary endings beneath the basal lamina of the intrafusal fibers—were all established by the fourth postnatal day. Cross-terminals, sensory terminals shared by more than one intrafusal fiber, were more numerous at all developmental stages than in mature spindles. No afferents to immature spindles were supernumerary, and no sensory axons appeared to retract from terminations on intrafusal fibers. The earliest motor axons contacted spindles on the 20th day of gestation or shortly afterward. More motor axons supplied the immature spindles, and a greater number of axon terminals were visible at immature intrafusal motor endings than in adult spindles; hence, retraction of supernumerary motor axons accompanies maturation of the fusimotor system analogous to that observed during the maturation of the skeletomotor system. Motor endings were observed only on the relatively mature myofibers; intrafusal myoblasts and myotubes lacked motor innervation in all age groups. This independence of the early stages of intrafusal fiber assembly from motor innervation may reflect a special inherent myogenic potential of intrafusal myotubes or may stem from the innervation of spindles by sensory axons.     

Cinematographic analysis of contractile events produced in intrafusal muscle fibres by stimulation of static and dynamic fusimotor axons.

1. Muscle spindles with an intact blood supply and uninterrupted connexions with ventral and dorsal spinal roots (Bessou & Pagés, 1967, 1972) have been prepared in cat's tenuissimus muscles with the aim of cinephotographically recording intrafusal movements induced by the stimulation of single static or dynamic gamma axons; the time cours of these movements and the morphological kind of activated intrafusal muscle fibres have been established. 2. Displacements of spindle guiding marks in the equatorial region elicited by stimulating single static gamma axons are 4-20 times greater in amplitude than the ones elicited by stimulating dynamic gamma axons at the same frequency. 3. The dynamic gamma axons induced a contraction only in nuclear bag fibres which, in addition, never received any static gamma innervation. The static gamma axons evoked contractions either in nuclear bag fibres alone, or in nuclear chain fibres alone, or in both types of intrafusal fibres. Two thirds of static gamma axons supplied nuclear bag fibres. For various reasons, one half only of static gamma axons innervating nuclear bag fibres could be shown to simultaneously innervate nuclear chain fibres. Consequently, about one third of static gamma axons supplied both nuclear bag fibres and nuclear chain fibres, but it is highly probable that this latter figure is an underestimate. One third of static gamma axons produced contraction in nuclear chain fibres only. In this work, the distribution of fusimotor axons has been established in only one muscle spindle of the cluster of muscle spindles that each fusimotor axon is generally innervating. 4. Generally speaking, a static gamma axon elicits contraction of several intrafusal fibres whereas a dynamic gamma axon innervates only one intrafusal fibre and frequently only one pole of the fibre. 5. One third of static gamma axons evoked contractions in nuclear chain fibres that seemed to involve the whole pole. The other static gamma axons and all dynamic gamma axons produced, in the intrafusal fibres that they supplied, one or several foci of localized contractions. 6. The nuclear chain fibres contract and relax faster than nuclear bag fibres. The contractions of nuclear bag fibres supplied by static gamma axons are stronger and faster than those of nuclear bag fibres innervated by dynamic gamma axons. Nearly all nuclear bag fibres innervated by static gamma axons, like the nuclear chain fibres, show transient contractions at each pulse of a stimulation at low frequency (2-20/sec). 7. The results are discussed taking into account the available anatomical and physiological data on the muscle spindle. Their consequences with regard to intrafusal working are briefly considered.     

Activity patterns in individual hindlimb primary and secondary muscle spindle afferents during normal movements in unrestrained cats.

1. Chronically implanted microelectrode wires in the L7 and S1 dorsal root ganglia were used to record unit activity from cat hindlimb primary and secondary muscle spindle afferents. Units could be reliably recorded for several days, permitting comparison of their activity with homonymous muscle EMG and length during a variety of normal, unrestrained movements. 2. The general observation was that among both primary and secondary endings there was a broad range of different patterns of activity depending on the type of muscle involved and the type of movement performed. 3. During walking, the activity of a given spindle primary was usually consistent among similar step cycles. However, the activity was usually poorly correlated with absolute muscle length, apparently unrealted to velocity of muscle stretch, and could change markedly for similar movements performed under different conditions. 4. Spindle activity modulation not apparently related to muscle length changes was assumed to be influenced by fusimotor activity. In certain muscles, this presumption leads to the conclusion that gamma-motoneurons may be activated out of phase with homonymous alpha-motoneurons as well as by more conventional alpha-gamma-motoneuron coactivation. 5. Simultaneous recordings of two spindle primary afferents from extensor digitorum longus indicated that spindles within the same muscle may differ considerably with respect to this presumed gamma-motoneuron drive. 6. Spindle secondary endings appeared to be predominantly passive indicators of muscle length during walking, but could demonstrate apparently strong fusimotor modulation during other motor activities such as postural changes and paw shaking. 7. Both primary and secondary endings were observed to undergo very rapid modulation of firing rates in response to presumed reflexly induced intrafusal contractions. 8. It is suggested that the pattern of fusimotor control of spindles may be tailored to the specific muscle and task being performed, rather than necessarily dominated by rigid alpha-gamma coactivation.     

“Fast” and “slow” skeleto-fusimotor innervation in cat tenuissimus spindles; a study with the glycogen-depletion method

The glycogen-depletion method was used to investigate the motor supply to tenuissimus with respect to the presence of fast β axons and to assess the total proportion of both fast and slow β-innervated spindles in this muscle. In a first series of 5 expts., groups of motor axons with conduction velocities higher than 85 m/s were repetitively stimulated so as to produce glycogen depletion in the muscle fibres they innervated. The whole muscle was then quick-frozen, serially cut, stained to demonstrate glycogen and examined for intrafusal glycogen depletion. Zones of glycogen depletion were found in 16 of the 46 examined spindles; they were most frequently located in the longest of the chain intrafusal muscle fibres. Since it is known that there are no purely fusimotor axons to tenuissimus with conduction velocities above 50 m/s, it was concluded that β axons are present among the fastest axons to this muscle. In a second series of 5 expts. as many motor axons as possible with conduction velocities above 60 m/s were stimulated. Zones of glycogen depletion were found in 19 of the 47 examined spindles. They affected chain fibres in about half of the instances and bag₂ fibres in the others. As this latter location is characteristic of slow dynamic β axons, it was concluded that both slow and fast β axons occur regularly in the motor supply to tenuissimus. β-innervation is present in at least 40% of tenuissimus spindles with almost no convergence of fast and slow β axons onto the same spindle.