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[Influence of 100 Hz sinusoidal vibration on muscle spindle afferents of soleus muscles in suspended situation rat].

OBJECTIVE: To study influence of 100 Hz sinusoidal vibration on muscle spindle afferents discharges of rat soleus muscles in simulated-weightlessness situation. METHOD: The tail-suspended rat model was used to simulate weightlessness, and 100 Hz sinusoidal vibration was performed by a vibrator. Unit activity was recorded electrophysiologically from the centrally cut filaments of the spinal dorsal roots innervating muscle spindles of the rat soleus muscle; then observation on the changes in afferent discharges from muscle spindle in a rat soleus muscles were made after 7 d. RESULT: 1) Compared with control muscle spindle afferents discharges of rat soleus muscles decreased after 7 d tail-suspension (P<0.05). 2) Compared with suspension the afferent discharges from soleus muscle spindles increased after 7 d tail-suspension with 100 Hz sinusoidal vibration. CONCLUSION: Sinusoidal vibration (100 Hz; 300 micrometers) can selectively activate muscle spindles. Muscle spindle afferent input of the suspended rats increased after the application of 7 d 100 Hz sinusoidal vibration.

Afferent Pathways↗

Coactivity of secondary spindle afferents and alpha 2, alpha 3, gamma 1 and gamma 2-motoneurons innervating anal and urinary bladder sphincters in humans.

1. Mixed efferent action potential (Ap) activity of human dorsal lower sacral nerve roots which contained only a few alpha 1 and gamma beta-motoneurons was split up into single alpha 2, alpha 3 (extrafusal) and gamma 1,2-motoneuron (intrafusal) activities by recording with 2 pairs of wire electrodes, constructing conduction velocity frequency distribution histograms, identifying different nerve fibre groups by their conduction velocity distribution peaks and counting the number of occurring conduction velocities under a peak within certain distribution limits. alpha-motoneurons in the oscillatory firing mode were identified by their conduction velocity and firing pattern. The only existing secondary spindle afferents were identified by their continuous firing and their conduction velocity. 2. Following natural stimuli monosynaptic responses were not observed. 3. alpha 3-motoneurons (S-type) responded slowly and unspecifically and alpha 2-motoneurons (FR-type) responded faster, transiently and specifically in the occasional spike mode and oscillatory firing mode. 4. In the oscillatory firing mode alpha 2-motoneurons responded within 1 oscillation cycle period (110-170 msec) or after 2 sec and once additionally after about 4 sec. In the occasional spike mode activity levels of alpha 2-motoneurons increased within 0.5 sec after stimulation. 5. Activity levels of alpha 2 and alpha 3-motoneurons in the occasional spike mode varied between 0 and 3 Ap's/sec per fibre. In the continuous oscillatory firing mode the activity level of single alpha 2-motoneurons was in the range of 18 Ap's/sec and the one of a alpha 3-motoneuron was in the range of 30 Ap's/sec. 6. In the occasional spike mode alpha 2 and gamma 1-motoneurons showed coactivity following touch and pain application and the pulling of anal and bladder catheters. This coactivity lasted for about 3 sec, was not time locked and was not always in phase. 7. Secondary spindle afferents were transiently activated mainly by the gamma 1-motoneurons with a time course similar to that of the gamma 1-motoneurons. A very strong bladder catheter pull activated gamma 2-motoneurons over several seconds which resulted in a strong increase in secondary spindle afferent activity for more than 5 minutes (cumulative reaction). 8. The delay between secondary spindle afferent activity and gamma-motoneuron activity, mainly from gamma 1-fibres, was about 400 msec. Taking the conduction times of gamma 1-motoneurons and secondary spindle afferents into account, it was found that the spindle afferent activity lagged about 350 msec behind the gamma-motoneuron activity at the muscle spindle site.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗

Ultrastructural observations on muscle spindles in extraocular muscles of pig.

Human and some mammals such as the sheep, goat and domestic and wild pigs have more or less muscle spindles in the extrinsic eye muscles, especially the domestic pigs having abundant muscle spindles (Matsuyama, 1987). The muscle spindles play a large role in maintaining the stable visual posture of the eyeballs. To define the morphological properties of the muscle spindles relative to the eye movement, the ultrastructure of the spindles was investigated in 6 extraocular muscles of the pigs by electron microscopy. The muscle spindles in the pig extraocular muscles consist of 4 to 5 intrafusal muscle fibers, one of which is nuclear bag fiber and 3 to 4 are nuclear chain fibers. The outer capsule is thin, composing of few layers, and the inner capsule ramifying to enwrap the individual fiber, accompanied by the medullated and unmedullated nerve fibers and blood capillaries. The nuclear bag fiber, 14 micron in diameter, is innervated by the atypical annulospiral sensory terminals and the chain fiber by the typical annulospiral terminal packed with mitochondria and microvesicles. The intrafusal fibers are innervated by the flower-spray sensory terminals anchoring deeply into the sarcoplasma, having abundant neurotubules and few mitochondria. The gamma motor end-plates have a relatively smooth synaptic cleft with a width of 70 nm and synaptic boutons containing few synaptic vesicles, sometimes, revealing a shallow fold of postsynaptic sarcolemma and abundant synaptic vesicles. The alpha motor end-plates reveal a relatively smooth synaptic cleft with a width of 80 nm, sometimes with a rough postsynaptic infolding, and boutons containing few synaptic vesicles and small-sized mitochondria. The satellite cells are innervated by the sensory terminals in various ways. The muscle spindles in the pig extraocular muscles are found to be much simpler in structure than those in the other antigravity muscles of the body. Their ultrastructure seems to reflect the morphological adaptation relative to the eyebal movement.

Animals↗

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↗

Response of muscle spindle primary endings to static stretch in acute and chronic spinal cats.

To evaluate fusimotor activity, the response of muscle spindle primary endings to static stretch was recorded from group Ia fibers in 8 control cats and in 31 cats at 3, 6, 14, 30, and 60 days after lumbar spinal cord transection. The spindle responses and clinical status of each group were compared with those of the control group. At 3 days after transection, the cats were hypotonic and mildly hyperreflexic. Spindle responses were significantly depressed. By day 6, the cats were mildly hypertonic and significant spindle recovery had occurred, although the responses were still significantly depressed from control levels. Spindle responses, hypertonia, and hyperreflexia continued to increase to day 30. At this time, spindle responses remained significantly depressed, although the cats were markedly hypertonic and hyperreflexic. A significant change in spindle activity or clinical status did not occur from 30 to 60 days after transection.

Action Potentials↗

The computation of position sense from spindles in mono- and multiarticular muscles.

It is known that muscle spindles provide the majority of information about limb position, but little is known about how position sense is computed from their signals. We have developed a family of musculoskeletal models in order to determine some of the fundamental properties associated with transforming noisy spindle information into putative internal coordinate frames for position sense. A two-joint model was developed containing one biarticular and two monoarticular muscles with a total of 1000 sensors distributed among them. The sensors were assumed to function like spindle secondary afferents under fusimotor control designed to optimize their ability to encode static position in the presence of constant output noise. The optimal distribution of sensors was found to depend strongly on the coordinate frame in which position was measured (intersegmental angle, segment orientation, or end-point of the limb) and on the topology of the biarticular muscle with respect to the plane of motion. A similar analysis was performed for an anthropometric model of the human arm, using previously published counts of muscle spindles. In general, the actual distribution of spindles about the elbow and shoulder does not seem to favor any single coordinate frame for position sense. We also looked at the potential accuracy in detecting changes in joint angles based on the distribution of muscle spindles throughout the human body. The distribution of spindles about individual joints accounts well for psychophysical data showing a proximodistal descending gradient of angular resolution that partially reflects the relative importance of more proximal joints for determining the location of the end-point.

Extremities↗

Spindling artifact of urothelial cells in post-laser treatment urinary cytology.

We reviewed 22 post-laser (Nd:YAG laser) coagulation bladder washes collected immediately after treatment. All washes demonstrated a striking artifact of cellular spindling. These spindled cells occurred singly, in loose clusters, and in lamellar stacks and had elongated nuclei with dense chromatin and bipolar cytoplasm that was fused in the stacks. Concurrent biopsies demonstrated similar cytologic changes. The spindling is a nonspecific epithelial response to heat. Conventionally electrocauterized epithelia show this artifact in biopsies, but since only the base of the lesion and surrounding urothelium are subjected to heat with electrocautery, the relatively few spindled epithelial cells created presumably go undetected in cytology specimens. With laser treatment, however, the whole urothelial surface of the lesion is coagulated, producing a much greater number of spindled cells. It is important to avoid misinterpreting the spindled cells as cells from a mesenchymal neoplasm or a sarcomatoid carcinoma, mistakes that were made in some of our initial cases. Malignancy cannot be evaluated when cells exhibit spindling artifact; this judgement should be made on undistorted cells. Thus, pre-laser and post-laser washes should be submitted for evaluation of malignancy.

Artifacts↗

The spindle pole body duplicates in early G1 phase in the pathogenic yeast Exophiala dermatitidis: an ultrastructural study.

The spindle pole body of the pathogenic yeast Exophiala dermatitidis was observed during the cell cycle using freeze-substitution and serial ultrathin sectioning electron microscopy. The spindle pole body was located on the outer membrane of the nuclear envelope and consisted of two disk elements connected by an intervening midpiece in G1 through G2 phases. Each disk element was composed of filamentous materials and measured 150 nm in diameter and 100 nm in thickness. The midpiece had higher electron density and measured 60 nm in length and 40 nm in thickness. At the beginning of prophase, each disk element of the spindle pole body enlarged to more than double in size. They were separated on the nuclear envelope, and associated with numerous cytoplasmic microtubules. At mitosis, the spindle pole body entered the nuclear envelope, associated with numerous nuclear microtubules, and was located at the spindle poles. At the end of telophase, it was extruded back into the cytoplasm from the nuclear envelope. Three-dimensional analysis of cells in different cell cycles suggested that duplication of the spindle pole body took place in early G1 phase. Thus, the location, structure, and duplication cycle of the E. dermatitidis spindle pole body were different from those of Saccharomyces cerevisiae.

Ascomycota↗

The influence of extrafusal muscle activity on discharge patterns of primary muscle spindle endings.

The influence of extrafusal muscle activity in anaemically decerebrate cats upon discharge patterns of primary spindle endings was ascertained by simultaneously recording spike trains from several Ia afferents and muscle tension fluctuations of the triceps-surae muscle. 1. Tension fluctuations were averaged with respect to spikes from primary endings yielding tension "trajectories" of specific shape for each spindle and probably reflecting frequently recurring mechanical events in the spindles' surroundings. 2. Spindles situated in close vicinity and influenced by similar mechanical events as evidenced by similar average tension trajectories are correlated in their discharge patterns to a degree depending on the strength of their mechanical coupling. 3. The modulation of spindle discharge frequency in response to average tension changes at the muscle tendon is very different in amplitude for different spindles; this response may show a high sensitivity. It is usually phase advanced by 90-180 degrees with respect to the "internal length" changes; between spindles ther may be phase differences of up to 180 degrees. 4. It is concluded that primary endings react very sensitively to local extrafusal events. The CNS receives much more accurate information about these events in the correlation of several Ia afferents than in the discharge of a single fibre.

Anemia↗

Spindle cell ductal carcinoma in situ. An unusual variant of ductal intra-epithelial neoplasia that simulates ductal hyperplasia or a myoepithelial proliferation.

Seventeen examples of a variant of ductal carcinoma in situ (DCIS) composed exclusively or predominantly of spindle cells arranged in fascicles, whorls, and solid sheets are described. The fascicular arrangement of the spindle cells simulates the "streaming" phenomenon associated with ordinary intraductal epithelial hyperplasia (IDH). This process also resembles the myoid, solid form of intraductal myoepithelial proliferation. The women ranged in age from 38 years to 79 years with a mean age of 59.3 years. Five patients presented with a palpable mass. The remaining tumors were discovered using mammography. The radiological appearances of the lesions raised concern for carcinoma, but there were no distinctive mammographic findings to suggest an unusual variant of DCIS. Cytological preparations were suspicious for malignancy in two patients and were reported as malignant in another case. Sixteen patients were treated with wide local excision, and one woman had a partial mastectomy. The tumors measured from 3 mm to 15 mm (mean 8.65 mm). In three cases, minute foci of stromal invasion were associated with the spindle cell DCIS. In another specimen, a 2.7-cm invasive ductal carcinoma of no special type was identified in an area away from the foci of the spindle cell DCIS. None of the patients has experienced recurrence or metastasis during the relatively short mean follow-up period of 16.2 months (range 4-77 months). Spindle cell DCIS is distinguished from the streaming pattern of ordinary IDH by its solid growth pattern, lack of secondary spaces or peripheral fenestrations, uniformity of appearance and distribution of nuclei, cytological atypia in the range of low to intermediate-grade DCIS, and negative immunoreaction with CK-34betaE12 (HMW-CK903). When fenestrations are present, they are evident in areas of cribriform DCIS that merge with the solid, spindle cell areas in hybrid ducts harboring both patterns. This admixture, with conventional cribriform DCIS, and the association with foci of invasive ductal carcinoma in some cases further help recognition and confirmation of this lesion as in situ carcinoma. When there is no transition from the spindle cells to recognizable cribriform DCIS, distinction from intraductal myoepithelial hyperplasia (myoepitheliosis) requires immunostains for actin and S-100 protein. Recognition of this pattern of DCIS is important in order to avoid its frequent misclassification as a benign lesion.

Adult↗

Degeneration and alteration of axons and intrafusal muscle fibers in spindles following tenotomy.

The effect of tenotomy (cutting of distal and proximal tendons) on the spindles in soleus muscle of adult rats was examined by light and electron microscopy in tissue obtained 1, 2, 3, 4, 5, 6, 7, and 14 days after surgery. Degenerative changes in the spindles progressed with time; also, the degree of alteration observed in a spindle varied with its position in the muscle, i.e., the earliest and most extensive changes occurred in spindles situated near the tendons. The disorganization and breakdown of myofibrils in the intrafusal muscle fibers were observed 3 days after tenotomy and continued with longer periods after surgery. The progression of morphological changes included alteration in fiber outline and the external lamina of the intrafusal muscle fibers and changes in the extracellular environment within the spindle capsule. The intrafusal muscle fibers of some spindles were shortened, apparently due to the loss of their polar ends, and degenerated axons which apparently supplied the intrafusal muscle fibers were also observed. Completely necrotic intrafusal fibers were absent. A possible relationship between the observed morphologic alterations and an adjustment of the spindle to muscle shortening is discussed.

Animals↗

Cholinergic effects on arousal and cocaine-induced olfactory-amygdala spindling and seizures in cats.

Effects of intravenous cholinergic and dopaminergic agents on pre-cocaine olfactory bulb (OB) spindling and behavioral arousal, and on cocaine-induced OB-amygdala spindling and behavioral seizures were evaluated in seven cats with stereotaxically implanted electrodes. Spindle data were computer analyzed using a special program for spindle detection and averaging. The number, duration and amplitude of pre-cocaine OB spindles were increased by physostigmine and decreased by atropine. Physostigmine augmented pre-cocaine behavioral arousal levels and this effect was associated with the absence of cocaine seizures. Cocaine-induced amygdala spindle number was increased by physostigmine. Changes in seizure duration following cholinergic drugs suggest cholinergic inhibitory effects. These data, in accord with previous studies showing cholinergic effects on reticulocortical arousal and seizures, suggest a cholinergic mechanism which is excitatory on OB-amygdala arousal spindling and inhibitory on cocaine-induced seizures.

Amygdala↗

EEG slow waves and sleep spindles: windows on the sleeping brain.

Slow waves and sleep spindles are prominent features of the EEG in non-REM sleep and some of the neurophysiological mechanisms underlying their genesis have been elucidated. In humans, slow-wave activity in non-REM sleep increases and EEG activity in the frequency range of sleep spindles decreases when wakefulness prior to sleep is varied from 2 to 40 h. The opposite changes are observed in the course of sleep, even when sleep is scheduled out of phase with the circadian rhythm of sleep propensity. Within non-REM sleep episodes the association between slow waves and sleep spindles is bi-phasic: both activities are correlated positively at the beginning and end of non-REM sleep episodes whereas in the middle part of non-REM sleep episodes high values of slow-wave activity coincide with low levels of spindle activity. An extension of wakefulness enhances the rise rate of slow-wave and spindle activity at the onset of sleep. Since macroscopic slow waves and sleep spindles both are dependent on hyperpolarization and synchronization of neurons in thalamo-cortical and cortical circuits, the sleep deprivation induced changes in these EEG activities may be related to reduced activating input to thalamo-cortical and cortical neurons, local facilitation of their hyperpolarization or facilitation of their synchronization. The precise regulation of slow-wave and spindle activity as a function of the duration and intensity of prior sleep and wakefulness demonstrates that these EEG oscillations are accurate indicators of non-REM-sleep homeostasis and suggests that they are fundamental to the sleeping brain.

Animals↗

Characterization of high voltage spindles and spatial memory in young, mature and aged rats.

EEG was recorded from rats of three age groups, and high voltage spindles (HVS) were measured during waking immobility. Total mean spindling times in 4- (young), 10- (mature) and 22- (aged) month-old rats were 0.3 +/- 0.1, 20.4 +/- 7.4 and 33.4 +/- 14.9 s, respectively. Spatial memory was assessed in these rats using a discrimination version of the Morris water maze. Performance (as measured by number of choice errors) was compared with the extent of HVS activity by characterizing rats as "spindling" if the total average duration of HVS discharges exceeded 5 s, and "non-spindling" if these discharges averaged less than 5 s. Spindling and nonspindling rats had similar performance during training; however, on a 14-day retention trial, spindling rats had a significantly higher mean error score of 2.8 +/- 0.5 compared with 1.2 +/- 0.3 for nonspindling rats (p = 0.011). These results show that spindling activity increases in mature and aged rats, and that HVS discharges may be an electrophysiological change that parallels the progression of brain dysfunction associated with memory impairment.

Action Potentials↗

Mps1 phosphorylation by MAP kinase is required for kinetochore localization of spindle-checkpoint proteins.

The spindle checkpoint delays anaphase onset until all chromosomes have achieved bipolar attachment to the spindle microtubules. Unattached kinetochores activate the spindle checkpoint by recruiting several spindle-checkpoint proteins, including Mps1, Mad1, Mad2, Bub1, Bub3, and BubR1 (Mad3 in yeast). In vertebrate cells, active MAP kinase (MAPK) is also enriched at unattached kinetochores and is required for the spindle checkpoint. It has been shown that the kinase activity of Mps1 is required for the spindle checkpoint and for kinetochore localization of Bub1, Bub3, Mad1, and Mad2 . We herein demonstrate that MAPK phosphorylates Mps1 at S844 in Xenopus egg extracts. Interestingly, changing S844 to unphosphorylatable alanine (S844A) has no effect on the kinase activity of Mps1, although it abolishes the checkpoint function of Mps1. Biochemical and immunofluorescence studies show that S844A mutation perturbs kinetochore localization of Mps1 and other spindle-checkpoint proteins, whereas the phosphorylation-mimicking S844D mutant restores their functions. Our studies suggest that Mps1 phosphorylation by MAPK at S844 might create a phosphoepitope that allows Mps1 to interact with kinetochores. In addition, our results indicate that active Mps1 must localize to kinetochores in order to execute its checkpoint function.

Animals↗

Determination of dominant simulated spindle frequency with different methods.

Accurate analysis of EEG sleep spindle frequency is challenging. The frequency content of true sleep spindles is not known. Therefore, simulated spindle activity was studied in the present work. Five types of simulated test signals were designed, all containing a dominant spindle represented by a 13-Hz sine wave as such or with a waxing and waning pattern accompanied by a secondary spindle activity in three test signals. Background EEG was included in four test signals, modeled either as small additional sinusoids across the spindle frequency range or as filtered Gaussian noise segments. The purpose of this study was to investigate how accurately the dominant spindle frequency of 13 Hz could be resolved with different methods in the presence of the interfering waveforms. A matching pursuit (MP) based approach, discrete Fourier transform (DFT) with Hanning windowing with and without zero padding, Hankel total least squares (HTLS) and wavelet methods were compared in the analyses. MP method provided best overall performance, followed closely by DFT with zero padding. Comparative studies like this are important to decide the method of choice in clinical sleep EEG analysis.

Algorithms↗

Transitory sleep spindles impairment in deep cerebral venous thrombosis.

Sleep spindles may be affected by thalamic or hemispheric ischemic stroke. However, spindles reduction and their relationship with K-complexes following deep cerebral venous thrombosis have not been reported. An 18-year-old woman suffered from a deep cerebral venous thrombosis with vasogenic oedema located predominantly in the thalami. Stage 2 sleep EEG recorded in acute setting showed preservation of K-complexes but absent 12-14 Hz sleep spindles, which were replaced by spindle-like theta oscillations. One month later, the patient having completely recovered, sleep spindles were normally seen on the control EEG. This case illustrates that deep cerebral venous thrombosis, through a vasogenic oedema, may transiently affect thalamic functions such as spindles generation. Furthermore, thalamic impairment may lead to dissociation of spindle and K-complex activity.

Adolescent↗

Disintegration of the peritrophic membrane of silkworm larvae due to spindles of an entomopoxvirus.

Mode of action by which entomopoxvirus (EPV) spindles enhance nucleopolyhedrovirus (NPV) infection remains unclear. Spindles of Anomala cuprea entomopoxvirus (AcEPV), a coleoptran EPV, are known to enhance Bombyx mori NPV (BmNPV) infection in silkworm larvae. AcEPV spindles were orally administered to silkworm larvae with or without BmNPV polyhedra, and the peritrophic membranes (PMs) were observed using a binocular microscope. Soon after the larvae's access to spindles with or without the polyhedra had been terminated, some PMs disappeared wholly and some were observed in partial form. Some of the partial PMs observed were very fragile. The disintegration of the PM due to spindles also was observed by the histological sectioning of the midgut. However, a day after the larvae had terminated their access to the spindles, the PM regenerated partially or wholly. In contrast, the administration of AcEPV spheroids caused neither the disintegration of PMs nor the enhancement of BmNPV infection in silkworm larvae. These findings strongly suggest that the enhancement of NPV infection occurs due to that a greater number of NPV virions reaching the microvilli of midgut susceptible to NPV, since spindles lead to the disintegration of the PM as a barrier against NPV virions.

Animals↗