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PubMed1971

Rhythmic leaf movements in biloxi soybean and their relation to flowering.

The rhythmic leaf movement of Biloxi soybean (Glycine max) and its relationship to the rhythmic flowering response were studied. The movements of fully expanded trifoliate leaves were recorded with kymographs and time lapse photography in growth chambers. A comparison between the leaf movement rhythm and the rhythmic flowering response indicates that a high degree of similarity exists between the two rhythms. A definite relationship was shown to exist between the direction of the leaf movement and the photophil-photophobe phases of the rhythmic flowering response.Short light perturbations may affect flowering by interacting directly with the flowering process while not affecting the basic endogenous rhythm. Long light perturbations may affect flowering by phase shifting the basic endogenous rhythm. Thus, light perturbations appear to have a dual effect on the flowering response of Biloxi soybean. The hypothesis that both the flowering rhythm and the leaf movement rhythm are coupled to the same basic oscillator is supported by the similarity of the phase shifts induced in the two rhythms by identical light perturbations.

Journal Article↗

PubMed1998

Neuronal activity related to spontaneous and capsaicin-induced rhythmical jaw movements in the rat.

Intraoral capsaicin induced rhythmical jaw movements (RJM) in anesthetized rats. Neurons in the trigeminal spinal nucleus caudalis or the cortico-peduncular (CP) axons were extracellularly recorded. Capsaicin excited dose-dependently most caudalis neurons, which were activated by stimulation of the oral cavity and/or the tooth pulp and activated during spontaneous or induced RJM. Ten of 55 CP axons were antidromically activated by stimulation of the contralateral trigeminal motor nucleus. All antidromic and 29 other CP axons discharged prior to the spontaneous RJM, but most of them did not during capsaicin-induced RJM. These neuronal activities possibly initiate spontaneous RJM although the activities of caudalis neurons are necessary for capsicin-induced RJM.

Animals↗

PubMed2001

Involuntary rhythmic leg movements time-locked with the respiratory cycle.

Involuntary rhythmic leg movements in childhood is an uncommon condition, the generators of which remain unknown. We report on a male 3 years of age with distinct features providing important clues concerning the location of one of these generators. At the age of 7 months, the previously healthy young male started with low frequency, rhythmic, and continuous (both during wakefulness and sleep) flexion/extension movements of the lower limbs. Movements interfered significantly with gait acquisition, and, despite normal cognitive development, he was able to walk only at age 2 years, 4 months. The neurologic examination revealed the absence of automatic stepping in the neonatal period, but was otherwise normal. A polygraphic electroencephalogram/electromyogram (EEG/EMG) recording, at the age of 2 years, 9 months, revealed rhythmic and synchronous legs with EMG activity at 0.5 Hz. A more complete polygraphic recording at the age of 3 years, 10 months, showed a lower frequency (0.35 Hz) for the movements, which were time-locked with the respiratory cycle. Magnetic resonance imaging (MRI) of the brain revealed an increased T(2) signal in the upper medulla-lower pons regions. The generator of the rhythmic legs movements is postulated to be the respiratory center, connecting with the reticulospinal projecting neurons through an aberrant pathway.

Child, Preschool↗

PubMed1982

Brainstem mechanisms underlying variations in the occurrence of experimentally elicited rhythmic oral movements in the rat.

Mechanical stimulation of the oral cavity of the decerebrate rat induces rhythmic oral movements in some animals but not in others. Reasons for this difference were sought using electrical stimulation of the lip to elicit a variety of responses which were capable of accurate quantification. Neither the digastric reflex threshold, size of suprathreshold response nor the ability to generate rhythmic activity within the brainstem differed in the two groups. Depression of the digastric reflex by an electrical stimulus applied 30-150 ms previously was, however, significantly greater in those animals not showing rhythmic oral movements. It is suggested that the two groups differed in their ability to produce rhythmic oral movements because of differences in the level of stimulus related inhibition rather than any tonic effects on trigeminal neuronal activity.

Animals↗

PubMed2005

Energy efficient and robust rhythmic limb movement by central pattern generators.

Humans show great energy efficiency and robustness in rhythmic tasks, such as walking and arm swinging. In this study a mathematical model of rhythmic limb movement is presented, which shows that tight local coupling of Central Pattern Generators (CPGs) to limbs could explain part of this behavior. Afferent feedback to flexor and extensor centers of the CPG is crucial in providing energy efficiency by means of resonance tuning. Feedback of positional information provides resonance tuning above the endogenous frequency of the CPG. Integral feedback provides resonance tuning at and below the endogenous frequency. Feedback of velocity information is necessary to compensate for the time delay in the loop, coupling limb to CPG; without velocity feedback bi-stability occurs and resonance tuning is not possible at high movement frequencies. The concepts of energy efficient and robust control of rhythmic limb movements are also applicable to robotics. It is the first CPG model, which provides resonance tuning at natural limb frequencies above and below its endogenous frequency.

Brain↗

PubMed1991

Centrally generated rhythmic and non-rhythmic behavioural responses in Rana temporaria embryos.

Embryos of the frog Rana temporaria up to and around the time of hatching show a range of rhythmic and non-rhythmic movements. These may occur spontaneously or in response to lightly touching the skin of the trunk or head. The first response to touching one side is usually on the opposite side. Non-rhythmic movements range from weak twitches centred on the mid trunk to strong flexions along much of one side of the body and part of the tail, which result in the animal becoming tightly coiled. Rhythmic movements range from slow, high-amplitude 'lashing' movements to faster, lower-amplitude 'swimming' movements. During rhythmic movements, a wave of bending passes along the animal from head to tail. The longitudinal phase delay in bending is constant for a range of cycle periods (88-193 ms) but is not uniform along the whole body. Bending is maximal along the body and rostral part of the tail, decreases towards the tip of the tail and is lowest at the head. Lateral displacement during rhythmic movements is lowest 0.2 body lengths from the snout, increases rostral and caudal to this level and is highest at the tip of the tail. In animals immobilised with curare, a range of patterns of motor discharge can be recorded in response to stimulation. Non-rhythmic responses range from single spikes to prolonged bursts, usually on the opposite side to the stimulus. Stronger bursts can alternate briefly between the two sides and are never synchronous on both. Episodes of sustained rhythmic activity can be evoked by touch, electrical stimulation of the skin or, rarely, dimming the lights. Cycle periods within each episode can vary considerably but often shorten as activity proceeds. Discharge on the two sides alternates (phase is approximately 0.5). Motor root burst duration correlates with cycle period, bursts being longer at longer cycle periods. Burst onset is delayed caudally, this delay being longer at longer cycle periods. Stimulating one side of the head evokes a large burst of discharge on the opposite side, often followed by sustained rhythmic discharge. These responses in immobilised animals are judged to constitute centrally generated correlates of the main behavioural responses of R. temporaria embryos.

Animals↗

PubMed1993

[Rhythmical involuntary movement at rest associated with olivo-ponto-cerebellar atrophy (OPCA)].

The authors analyzed rhythmical involuntary movements at rest, which appeared as complications in 12 (sporadic 11, hereditary 1) out of a total of 139 cases (sporadic 99, hereditary 40) of olivo-ponto-cerebellar atrophy. These movements tended to be seen in patients with sporadic OPCA of longer illness duration and at more advanced stages. They were distributed over the face, neck and extremities. Palatal myoclonus was observed in only one case. The movements were exacerbated by maintenance of a fixed posture, motion and mental stress, and stopped during sleep. In some cases, clonazepam, trihexyphenidyl or 1-Dopa was effective. In the surface electromyogram, rhythmical grouped discharges of 2-4 Hz were recorded only on agonist muscles or on both agonist and antagonist muscles synchronously, which is characteristic of skeletal myoclonus. However, pathological study of 3 cases with involuntary movements revealed marked putaminal degenerations as compared with 3 uncomplicated cases. This suggests that these rhythmical movements might be related to parkinsonian tremor.

Adolescent↗

PubMed2006

Influence of predominant patterns of coordination on the exploitation of interaction torques in a two-joint rhythmic arm movement.

In this study we investigate the coordination between rhythmic flexion-extension (FE) and supination-pronation (SP) movements at the elbow joint-complex, while manipulating the intersegmental dynamics by means of a 2-degrees of freedom (df) robot arm. We hypothesized that constraints imposed by the structure of the neuromuscular-skeletal system would (1) result in predominant pattern(s) of coordination in the absence of interaction torques and (2) influence the capabilities of participants to exploit artificially induced interaction torques. Two experiments were conducted in which different conditions of interaction torques were applied on the SP-axis as a function of FE movements. These conditions promoted different patterns of coordination between the 2-df. Control trials conducted in the absence of interaction torques revealed that both the in-phase (supination synchronized with flexion) and the anti-phase (pronation synchronized with flexion) patterns were spontaneously established by participants. The predominance of these patterns of coordination is explained in terms of the mechanical action of bi-articular muscles acting at the elbow joint-complex, and in terms of the reflexes that link the activity of the muscles involved. Results obtained in the different conditions of interaction torques revealed that those neuromuscular-skeletal constraints either impede or favor the exploitation of intersegmental dynamics depending on the context. Interaction torques were indeed found to be exploited to a greater extent in conditions in which the profiles of interaction torques favored one of the two predominant patterns of coordination (i.e., in-phase or anti-phase) as opposed to other patterns of coordination (e.g., 90 degrees or 270 degrees). Those results are discussed in relation to recent studies reporting exploitation of interaction torques in the context of rhythmic movements.

Adult↗

PubMed2005

Neural control of rhythmic human movement: the common core hypothesis.

Rhythmic motor patterns are ubiquitous in the animal kingdom. Walking, cycling, and swimming are examples of rhythmic locomotor tasks that humans perform routinely. This paper outlines the common core hypothesis that rhythmic motor patterns in human locomotion share common central neural control mechanisms. This is subserved by presumed central pattern generators that regulate arm and leg movements during locomotion.

Arm↗

PubMed2002

Correlations between response properties of periodontal mechanosensitive neurones in the primary somatosensory cortex of the rabbit and cortically induced rhythmical jaw movements.

The response properties of incisor- and molar-sensitive periodontal mechanosensitive (PM) neurones in the primary somatosensory (SI) cortex of rabbits were examined and rhythmical jaw movements induced by repetitive electrical stimulation of the recording sites of cortical PM neurones were observed. PM units were recorded from the rostromedial (RM) and rostrolateral (RL) areas of the SI cortex. In the RM area, most PMs (85%) were lower incisor-sensitive. Electrical stimulation of the RM area produced chopping-type rhythmical jaw movements. In the RL area, both incisor- and molar-sensitive PM units were recorded, and molar-sensitive units were located more rostromedially than incisor-sensitive units. More than half (66%) of the incisor-sensitive PM units were upper incisor-sensitive. The incidences of sustained-response type units were 8 and 10% for upper incisor- and lower incisor-sensitive units and 28 and 34% for upper molar- and lower molar-sensitive units, respectively. The optimal stimulus directions for the upper molar-sensitive units were predominantly labial or lingual, whereas those for most of the lower molar-sensitive units were lingual. Electrical stimulation of the PM unit-recording sites in the RL area induced grinding-type rhythmical jaw movements. Based on these findings, the lower incisor-sensitive neurones in the RM area of the SI cortex might mainly contribute to a neural network that controls jaw movements during ingestion. Furthermore, the response properties of molar-sensitive cortical neurones might be useful for discriminating the magnitude and direction of the biting force during grinding. Further studies are needed to clarify the role of upper incisor-sensitive neurones in the RL area in triggering grinding-type rhythmical jaw movements.

Animals↗

PubMed1995

Modification of rhythmical jaw movements by noxious pressure applied to the periosteum of the zygoma in decerebrate rabbits.

The purpose of this study was to describe and quantify changes in the movement and EMG patterns caused by tonic noxious pressure on the periosteum of the zygoma during electrically induced rhythmic jaw movements in the decerebrate rabbit. Eight New Zealand rabbits were anesthetized with urethane. EMG electrodes were placed in the masseter and digastric muscles and a light was attached to the mandibular symphysis to track jaw movements. The animals were decerebrated and the anesthetic was discontinued. Rhythmic jaw movements were evoked by electrically stimulating the corticobulbar tracts (1-msec rectangular pulses, 50 Hz), in the absence and presence of tonic noxious pressure applied bilaterally to the zygomatic periosteum (range: 400-1500 kPa). The overall response to tonic noxious pressure was a statistically significant decrease in the frequency and amplitude of the rhythmic jaw movements and in the mandibular velocity during opening and closing. The slowing of the frequency was associated with a significant increase in the duration between muscle bursts. In those animals in which the jaw closing muscles were most active, there was a significant decrease in the area of the masseter muscle bursts during jaw closure. The changes in motor activity in response to the application of tonic noxious pressure are similar to those that have been reported for patients experiencing musculoskeletal pain, suggesting that pain modifies motor programs at the segmental level. Our data support the pain-adaptation model.

Animals↗

PubMed1993

Resetting of cortically induced rhythmical jaw movements by stimulation of the cerebellar interpositus nucleus in the guinea pig.

Effects of stimulation of the cerebellar interpositus nucleus on fictive rhythmical jaw movements induced by stimulation of the cortical masticatory area were studied in ketamine-anesthetized, paralyzed guinea pigs. A short pulse-train applied to the interpositus nucleus caused a phase shift in cortically induced rhythmical jaw movements. A phase transition curve indicated that interpositus stimulation can reset the cortically induced rhythmical jaw movements.

Animals↗

PubMed2001

Analysis of rhythmical jaw movements produced by taste stimulation in rats.

Taste stimulation of the mouth induces various oral movements. Sucrose or salt solution induces rhythmical jaw movements (RJM) or tongue protrusion as an ingestive behavior. Bitter taste induces a gaping or tongue retraction as an aversive behavior. There is no report that describes the precise pattern of jaw movements induced by taste stimulation. The purpose of the present study is to clarify the pattern of the taste-induced RJM with electromyographic activities of the masticatory muscles in the anesthetized rat. When water was injected into the mouth of the rat, an RJM was induced. In this type of RJM, the lower jaw swung right and left side in each open-close cycle alternately. The anterior digastric muscle was active in every opening phase, while activities of the jaw closing muscles were generally weak. The RJM induced by water was opening-dominant movements. Sucrose or salt solution induced a similar pattern of RJM to water-induced RJM. When acetic acid was injected, amplitude of the alternate lateral jaw movement was significantly larger than that in the water-induced RJM. The activity of the superficial temporalis muscle was large in those closing phases with ipsilateral side movement, while it was small in the closing phases with contralateral movement. The pattern of quinine-induced RJM was characterized by small lateral, large open-close and large antero-posterior movements. Tastes which are reported to induce ingestive behavior such as sweet or salty don't alter the pattern of RJM; however, the tastes which induce aversive behavior make the pattern of RJM different from the water-induced RJM.

Animals↗

PubMed1985

The effects of a glycine antagonist (strychnine) on cortically induced rhythmical jaw movements in the anesthetized guinea pig.

We have investigated the effects of systemic administration of a glycine antagonist, strychnine, on rhythmical jaw movements (RJMs) induced by repetitive stimulation of the masticatory area of the guinea pig cerebral cortex. It was found that after strychnine administration (0.4 mg/kg), the frequency of the cortically induced RJMs was minimally affected, whereas the burst durations of the digastric EMG during the jaw opening phase of the RJM cycle were dramatically increased. These data suggest that the neuronal network (central pattern generator (CPG)) which is responsible for the production of rhythmical jaw movements is not critically dependent upon glycine for the genesis of the basic oscillatory rhythm. On the other hand, glycine synapses are involved with the neuronal mechanisms which are responsible for controlling the burst durations of the digastric muscle during the jaw opening phase of each rhythmic jaw movement cycle.

Animals↗

PubMed2004

Facilitation of soleus H-reflex amplitude evoked by cutaneous nerve stimulation at the wrist is not suppressed by rhythmic arm movement.

Neural connections between the cervical and lumbosacral spinal cord may assist in arm and leg coordination during locomotion. Currently the extent to which arm activity can modulate reflex excitability of leg muscles is not fully understood. We showed recently that rhythmic arm movement significantly suppresses soleus H-reflex amplitude probably via modification of presynaptic inhibition of the IA afferent pathway. Further, during walking reflexes evoked in leg muscles by stimulation of a cutaneous nerve at the wrist (superficial radial nerve; SR) are phase and task dependent. However, during walking both the arms and legs are rhythmically active thus it is difficult to identify the locus of such modulation. Here we examined the influence of SR nerve stimulation on transmission through the soleus H-reflex pathway in the leg during static contractions and during rhythmic arm movements. Nerve stimulation was delivered with the right shoulder in flexion or extension. H-reflexes were evoked alone (unconditioned) or with cutaneous conditioning via stimulation of the SR nerve (also delivered alone without H-reflex in separate trials). SR nerve stimulation significantly facilitated H-reflex amplitude during static contractions with the arm extended and countered the suppression of reflex amplitude induced by arm cycling. The results demonstrate that cutaneous feedback from the hand on to the soleus H-reflex pathway in the legs is not suppressed during rhythmic arm movement. This contrasts with the observation that rhythmic arm movement suppresses facilitation of soleus H-reflex when cutaneous nerves innervating the leg are stimulated. In conjunction with other data taken during walking, this suggests that the modulation of transmission through pathways from the SR nerve to the lumbosacral spinal cord is partly determined by rhythmic activity of both the arms and legs.

Adult↗

PubMed2006

Mathematical model for rhythmic protoplasmic movement in the true slime mold.

The plasmodium of the true slime mold Physarum polycephalum is a large amoeboid organism that displays "smart" behavior such as chemotaxis and the ability to solve mazes and geometrical puzzles. These amoeboid behaviors are based on the dynamics of the viscoelastic protoplasm and its biochemical rhythms. By incorporating both these aspects, we constructed a mathematical model for the dynamics of the organism as a first step towards understanding the relation between protoplasmic movement and its unusual abilities. We tested the validity of the model by comparing it with physiological observation. Our model reproduces fundamental characteristics of the spatio-temporal pattern of the rhythmic movement: (1) the antiphase oscillation between frontal tip and rear when the front is freely extending; (2) the asynchronous oscillation pattern when the front is not freely extending; and (3) the formation of protoplasmic mounds over a longer time scale. Both our model and physiological observation suggest that cell stiffness plays a primary role in plasmodial behaviors, in contrast to the conventional theory of coupled oscillator systems.

Algorithms↗

PubMed1994

[Modulation of spinal monosynaptic reflexes during rhythmical jaw movements and its central neural mechanisms].

The present study was carried out to investigate whether there was any modulation of the spinal monosynaptic reflexes during mastication in the healthy humans and urethane-anesthetized rabbits and to elucidate the central neural mechanisms responsible for the modulation in the urethane-anesthetized rabbits. 1. Human soleus H-reflex was significantly facilitated during the rhythmical jaw movements and rhythmical gum chewing. 2. There was no significant difference in the magnitude of the facilitation between the jaw-opening and -closing phases. 3. In the rabbits, monosynaptic reflex (MSR) volleys recorded from the tibial nerve (TIB) innervating the crural extensors and the common peroneal nerve (CP) innervating the crural flexors tonically increased in amplitude during the masticatory movements induced by either intraoral stimulation or repetitive stimulation of the cortical masticatory area (CMA). 4. Antidromic field potentials in the anterior horn of the lumbar cord evoked by the stimulation of TIB and CP increased during the CMA-induced actual and fictive mastication. 5. There was no significant change in the amplitude of the directly evoked antidromic potential in the primary afferents by intraspinal stimulation during the CMA-induced mastication compared with the resting state. It was concluded that (1) the MSR of the crural muscles undergoes a tonic non-reciprocal facilitation during mastication, (2) the stomatognathic afferents induced during mastication are not essential for the facilitation, and (3) an increase in the excitability of motoneurons is mainly involved in the facilitation of the MSR during mastication.

Adult↗

PubMed1977

Modification of cortically evoked rhythmic jaw movements by reflex deglutition in rabbits.

In rabbits, lightly anesthetized with ether, tetanic stimulation of the superior laryngeal nerve (SLN) displaced the jaw toward opening and reduced the amplitude of cortically evoked rhythmic jaw movements. With increased intensity of stimulus, the effects became remarkable and the opened jaw movement ultimately ceased. Reflex swallowing in reaction to weak electrical stimuli of SLN or to a small amount of water squirted into the oropharynx yielded a brief and instantaneous cessation of rhythmic jaw movements with the jaw open. Strong electrical stimuli to the nerve or a squirt of relatively large amount of water into the oropharynx prolonged the duration of both swallowing and the cessation of rhythmic jaw movements for about 1.0 sec. Reflex swallowing yielded a burst of activity for about 300 msec in the mylohyoideus and silence for a longer period in the masseter. Spontaneous activity of the masseter was moderately decreased during the nerve stimulation and, when swallowing occurred, this decrease became prominent for a short period.

Animals↗