Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “REFLEX”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 757 records · Page 42Linked to original sources

Enhancement of the intrinsic defecation reflex by mosapride, a 5-HT4 agonist, in chronically lumbosacral denervated guinea pigs.

The defecation reflex is composed of rectal distension-evoked rectal (R-R) reflex contractions and synchronous internal anal sphincter (R-IAS) reflex relaxations in guinea pigs. These R-R and R-IAS reflexes are controlled via extrinsic sacral excitatory nerve pathway (pelvic nerves), lumbar inhibitory nerve pathways (colonic nerves) and by intrinsic cholinergic excitatory and nitrergic inhibitory nerve pathways. The effect of mosapride (a prokinetic benzamide) on the intrinsic reflexes, mediated via enteric 5-HT(4) receptors, was evaluated by measuring the mechanical activity of the rectum and IAS in anesthetized guinea pigs using an intrinsic R-R and R-IAS reflex model resulting from chronic (two to nine days) lumbosacral denervation (PITH). In this model, the myenteric plexus remains undamaged and the distribution of myenteric and intramuscular interstitial cells of Cajal is unchanged. Although R-R and R-IAS reflex patterns markedly changed, the reflex indices (reflex pressure or force curve-time integral) of both the R-R contractions and the synchronous R-IAS relaxations were unchanged. The frequency of the spontaneous R and IAS motility was also unchanged. Mosapride (0.1-1.0 mg/kg) dose-dependently increased both intrinsic R-R (maximum: 1.82) and R-IAS reflex indices (maximum: 2.76) from that of the control (1.0) 6-9 days following chronic PITH. The dose-response curve was similar to that in the intact guinea pig, and had shifted to the left from that in the guinea pig after acute PITH. A specific 5-HT(4) receptor antagonist, GR 113808 (1.0 mg/kg), decreased both reflex indices by approximately 50% and antagonized the effect of mosapride 1.0 mg/kg. This was quite different from the result in the intact guinea pig where GR 113808 (1.0 mg/kg) did not affect either of the reflex indices. The present results indicate that mosapride enhanced the intrinsic R-R and R-IAS reflexes and functionally compensated for the deprivation of extrinsic innervation. The actions of mosapride were mediated through endogenously active, intrinsic 5-HT(4) receptors which may be post-synaptically located in the myenteric plexus of the anorectum.

Anal Canal↗

The stapedius reflex tests in retrocochlear hearing disorders.

The commonly used parameters of the stapedius reflex responses in the diagnosis of sensorineural hearing disorders are the reflex threshold level and the persistence of the reflex response on prolonged stimulation, i.e., the reflex decay test. With the object of establishing the sensitivity of these reflex parameters to identify tumours affecting the eighth nerve in the early stages, a series of 97 such cases were examined. The mean hearing loss of the affected ears was 32 dB; 28 of the cases still had normal thresholds of hearing; 95 of the ears demonstrated elevated reflex thresholds and/or pathologic reflex decay. To check the specificity of the test, a control series with sensorineural hearing loss and reflex threshold elevation or pathologic reflex decay was analysed with respect to clinical diagnoses. In every third case of reflex threshold elevation and in every second case of reflex decay, the medical diagnosis confirmed a disease known to be associated with retrocochlear dysfunction. It was also noted that none of the cases with brain stem lesion demonstrated reflex decay--an observation which supports the idea of the reflex decay phenomenon as specifically associated with eighth-nerve lesions.

Cranial Nerve Neoplasms↗

The inverse relationship between nonverbal intelligence and the latency of the Hoffmann reflex from the right and left thenar muscles in right- and left-handed subjects.

The relationship between nonverbal reasoning ability and the latency of the Hoffmann (H) reflex was studied in right- and left-handed subjects. The nonverbal reasoning ability was assessed by the Cattell's Culture Fair Intelligence test. Hand preference was assessed by the Edinburgh Handedness Inventory. Hoffmann reflex was recorded from thenar muscles of the right and left thumbs. In left-handers (total sample), IQ was found to be significantly and negatively linearly related to the H-reflex latency from the left side. In strong left-handers, there was a significant negative linear relationship between IQ and the H-reflex latency from right and left sides, but with a higher correlation for the left side. In weak left-handers, IQ did not show any significant relation to the H-reflex latencies from the right and left sides. In right-handers (total sample), there was a significant negative linear correlation between IQ and the H-reflex latency from the right side. In right-handed women without familial sinistrality (FS-), IQ was found to be inversely related to the H-reflex latency from the right and left side, but with a higher correlation for the right side. In right-handed women with FS, IQ did not show any significant relation to the H-reflex latency from the right and left sides. In right-handed men with right eye preference and FS-, IQ was found to be negatively linearly related to the H-reflex latency from the right and left sides equally. In right-handed men with right eye FS+, mixed eye FS-, +, mixed eye-right foot (FS-), mixed eye-mixed foot, and left eye preference there was no significant relationship between IQ and the H-reflex latency from the right and left sides. Only in strong left-handers there was a significant, positive linear correlation between IQ and the right minus left (R-L) difference of latencies. The H-reflex latency from the right and left sides was not significantly correlated with the R-L difference of latencies in left-handers. In right-handed women with right eye preference FS-, and in right-handed men with right eye preferences FS-, The H-reflex latency from the right side was found to be positively linearly correlated with the R-L difference of latencies. In right-handed women FS+, and in right-handed men FS+, and mixed or left eye preference, the H-reflex latency from the left side was found to be negatively linearly related to the R-L difference of latencies.(ABSTRACT TRUNCATED AT 400 WORDS)

Female↗

The reliability of H-reflex recordings in standing subjects.

OBJECTIVE: Several studies have used the H-reflex to investigate the effect of upright stances and locomotion on spinal reflex excitability. The reliability of eliciting this reflex during weight-bearing has however yet to be addressed. This study was undertaken to determine the reliability of individual differences in the H-reflex recorded from healthy subjects during quiet standing. Secondary aims of the study were to evaluate individual reliability during prolonged standing, and to establish the minimum number of trials required to provide reliable measurements of the H-reflex. DESIGN AND PARTICIPANTS: Twenty neurologically healthy volunteers participated in a repeated measures design consisting of 8 blocks of 20 trials evenly distributed over two testing sessions. H-reflex recordings were elicited from the subject's dominant side soleus muscle by percutaneously stimulating the posterior tibial nerve. Stimuli were presented every 10 s, with 2 min seated rest provided between blocks of trials. Peak-to-peak amplitude of H-reflexes and m-responses determined for individual trials were used for subsequent analysis. RESULTS: It was found that the reliability of measuring the H-reflex and m-response during quiet standing was extremely robust (r = .97 for both measures). This pattern of individual differences remained consistent over 80 trials confirming the stability of the measures. High reliabilities (r = .96 and .87 for the H-reflex and m-responses respectively) were also observed when as few as four trials were analysed. When measures obtained during the first session of testing were compared with those obtained for session two, the correlation coefficients were generally of a lower order (r = .54 to .90). DISCUSSION: The results demonstrate that the H-reflex in quiet standing provides high intra-individual reliability, suggestive of a stable reflex resistant to potentially confounding postural influences, or other sources of biological variation. The between-session reliability underscores the difficulty in reproducing conditions between sessions, and emphasises the need for within-session comparisons of H-reflex amplitudes. Given the functional challenge of maintaining an upright posture, the H-reflex appears to be a well maintained and stable phenomenon.

Adolescent↗

The effect of elbow position on biceps tendon reflex.

BACKGROUND: Testing of tendon (T) reflex is the basic method used in the diagnostic procedure of clinical neurology. Measurement of T reflexes precisely can be a valuable adjunct to clinical examination. Quantification of T reflexes may provide more accurate results. AIMS: To analyze the effect of elbow position on biceps T reflex. SETTINGS AND DESIGN: A self-controlled clinical trial of biceps T reflex testing at the Electrophysiology Unit of the Department of Physical Medicine and Rehabilitation. METHODS AND MATERIALS: Biceps T reflex was obtained utilizing a hand-held electronic reflex hammer in 50 extremities of 25 healthy volunteers and the effect of elbow position (at 90 degrees , 120 degrees and 150 degrees ) on reflex response was evaluated. STATISTICAL ANALYSIS: Repeated-measures analysis of variance by the General Linear Model and Pearson correlation test procedures. RESULTS: Onset latency was significantly shorter at 120 degrees of elbow position. The maximum amplitude value of biceps T reflex was obtained at 90 degrees of elbow position. Onset latency of the reflex correlated significantly with the height and arm length but not with age. CONCLUSIONS: The electrophysiological measurement of T reflexes is an easy and useful method in the quantification of reflexes, supplying more objective data. However, when performing T reflex studies, the position of the extremity should be taken into consideration to achieve more reliable results.

Adult↗

[Functional characteristics and topography of spinal tracts involved in low- and high-threshold startle reflexes].

Electrophysiological and topographical properties of the spinal tract systems involved in two functional types of startle reflexes were studied in chloralose anesthetized cats: a high threshold reflex evoked by intense peripheral nerve stimulation (spino-bulbo-spinal, SBS, reflex) and low threshold evoked by tactile (T-reflex) and acoustic (A-reflex) stimulation. It was found that the mean maximal conduction velocity of descending transmission of SBS-reflexes was much less (30 m/s) than that of T- (85 m/s) and A-reflexes (100 m/s). Ascending conduction velocities for SBS- and T-reflexes were 70.8 and 40.2 m/s, respectively. It was established by partial spinal cord lesions that ascending tracts for T-reflex passed in dorsal and dorso-lateral funiculi; those for SBS reflexes were found not only in the latter but also in ventro-lateral and partially in ventral funiculi. Descending pathways for SBS reflex passed mainly in ventro-lateral funiculi and partially in the ventral ones. Descending pathways of T- and A-reflexes had a similar organization and were located mainly in the ventral and ventro-lateral funiculi. Functional organization of spinal tracts of all studied types of startle reflexes is discussed.

Acoustic Stimulation↗

Altered patterns of reflex excitability subsequent to contusion injury of the rat spinal cord.

1. The present study investigated regulation of reflex excitability after experimental contusion injury of the spinal cord. 2. Four measures of H-reflex excitability were evaluated in normal rats and at 6, 28, and 60 days after contusion injury at the T8 level: 1) reflex thresholds, 2) slope of the reflex recruitment curves, 3) maximal plantar H-reflex/maximal plantar M-response (Hmax/Mmax) ratios, and 4) rate-sensitive depression (i.e., the decrease in reflex magnitude relative to repetition rate). 3. Tested as a function of the afferent volley magnitude, the thresholds for reflex initiation fell progressively subsequent to contusion injury. No change was observed at 6 days postinjury, and the decrease at 28 days was not significant. However, by 60 days postinjury, the threshold had decreased by 23% of the maximal afferent volley, and this decrease was significant, [analysis of variance (ANOVA, P < or = 0.01)]. 4. Hmax/Mmax ratios elicited in postcontusion animals at 0.3 Hz were not significantly different from those recorded in normal animals. 5. The slopes of the recruitment curves were markedly reduced subsequent to contusion injury. The decrease was greatest at 6 days postinjury. Although some recovery toward normal occurred at 28 and 60 days postinjury, the slopes of recruitment curves in postcontusion animals remained significantly decreased. 6. H-reflexes elicited at 1-5 Hz were less sensitive to rate depression in postcontusion animals than in normal animals at the same respective frequencies. The decrease was progressive in onset, becoming significant by 28 days postinjury, and of an enduring nature, i.e., still significantly different from normal in the reflexes tested 60 days postinjury. 7. Rate sensitivity of the tibial nerve monosynaptic reflex (MSR) was also compared in normal and postcontusion animals. Rate sensitivity of the tibial MSRs was significantly reduced at 28 and 60 days post-contusion, compared with normal animals. 8. These data indicate that significant changes in lumbar reflex excitability result from midthoracic contusion injury of the spinal cord. These changes include reflex threshold, slope of recruitment, and rate-sensitive depression. Although recruitment slope was most altered in the shortest postinjury interval tested, followed by some recovery, the other changes were progressive in onset and enduring in duration.

Animals↗

Roles of neuronal NK1 and NK3 receptors in synaptic transmission during motility reflexes in the guinea-pig ileum.

1. The role of NK1 and NK3 receptors in synaptic transmission between myenteric neurons during motility reflexes in the guinea-pig ileum was investigated by recording intracellularly the reflex responses of the circular muscle to distension or compression of the mucosal villi. Experiments were performed in a three-chambered organ bath that enabled drugs to be selectively applied to different sites along the reflex pathways. 2. When applied in the recording chamber, an NK1 receptor antagonist, SR140333 (100 nM), reduced by 40-50% the amplitudes of inhibitory junction potentials (i.j.ps) evoked in the circular muscle by activation of descending reflex pathways. This effect was abolished when synaptic transmission in the stimulus region was blocked with physiological saline containing 0.1 mM Ca2+ plus 10 mM Mg2+, leaving only the component of the descending reflex pathway conducted via long anally directed collaterals of intrinsic sensory neurons. 3. SR140333 (100 nM) had no effect on descending reflex i.j.ps when applied to the stimulus region. Ascending reflexes were also unaffected by SR140333 in the stimulus region or between the stimulus and recording sites. 4. Septide (10 nM), an NK1 receptor agonist, enhanced descending reflexes by 30-60% when in the recording chamber. [Sar9,Met(O2)11]substance P had no effect at 10 nM, but potentiated distension-evoked reflexes at 100 nM. 5. A selective NK3 receptor antagonist, SR142801 (100 nM), when applied to the stimulus region, reduced the amplitude of descending reflex responses to compression by 40%, but had no effect on responses to distension. SR142801 (100 nM) had no effect when applied to other regions of the descending reflex pathways. 6. SR142801 (100 nM) only inhibited ascending reflexes when applied at the recording site. However, after nicotinic transmission in the stimulus region was blocked, SR142801 (100 nM) at this site reduced responses to compression. 7. Contractions of the circular muscle of isolated rings of ileum evoked by low concentrations of septide, but not [Sar9,Met(O2)11]substance P, were potentiated by tetrodotoxin (300 nM). 8. Contractile responses evoked by an NK3 receptor agonist, senktide, were non-competitively inhibited by SR142801. After excitatory neuromuscular transmission was blocked, senktide produced inhibitory responses that were also antagonised by SR142801, but to a lesser extent and in an apparently competitive manner. 9. These results indicate that tachykinins acting via NK1 receptors partly mediate transmission to inhibitory motor neurons. NK3 receptors play a role in transmission from intrinsic sensory neurons and from ascending interneurons to excitatory motor neurons during motility reflexes.

Animals↗

Differential Effects of a Distant Noxious Stimulus on Hindlimb Nociceptive Withdrawal Reflexes in the Rat.

Recent studies indicate that the nociceptive withdrawal reflexes to individual muscles are evoked by separate reflex pathways. The present study examines whether nociceptive withdrawal reflexes to different muscles are subject to differential supraspinal control in rats. A distant noxious stimulus was used to activate a bulbospinal system which selectively inhibits 'multireceptive' neurons (i.e. neurons receiving excitatory tactile and nociceptive inputs) in the dorsal horn of the spinal cord. Withdrawal reflexes, recorded with electromyographic techniques in single hindlimb muscles, were evoked by standardized noxious pinch. Thirty-seven rats, anaesthetized with halothane and nitrous oxide, were used. Whereas withdrawal reflexes to the extensor digitorum longus and brevis, tibialis anterior and biceps posterior muscles were strongly inhibited, reflexes to interossei muscles were potentiated during noxious pinch of the nose. Reflexes to peronei muscles were not significantly changed. The effects on the reflexes usually had an onset latency of <0.5 s and outlasted the conditioning stimulation by up to 2 s. The monosynaptic la reflex to the deep peroneal nerve, innervating dorsiflexors of the digits and ankle, was not significantly changed during noxious pinch of the nose. Hence, the inhibitory effects on the hindlimb withdrawal reflexes induced by the conditioning stimulation were presumably exerted on reflex interneurons. It is concluded that nociceptive withdrawal reflexes to different hindlimb muscles are differentially controlled by descending pathways activated by a distant noxious stimulus. The results support our previous conclusion that there are separate nociceptive withdrawal reflex pathways to different hindlimb muscles.

Journal Article↗

[Generalized nocifensive reflexes. I. Methodologic bases].

Normal protective and defence reflexes show that the nocifensive system is intact. Nocifensive reflexes can be modified by various brainstem disturbances, and in the case of lesions the symptoms may appear in the afferent or efferent section of the reflex arc. The purpose of our study was to find a method for evoked generalized nocifensive reflexes so that inferences regarding the course of the reflex could be drawn from a reflex pattern obtained from the latent periods of various lead regions during nocifensive stimulation. The stimulus is provided by a painful train of electrical pulses applied to a superficial nerve (N. medianus, N. fibularis). As a rule, the leads are connected symmetrically to the flexors of the upper and lower extremities. The results shown, as expected, that nocifensive reactions fulfill the conditions of a conditioned reflex with increasing habituation and sensitization. The reflex arc passes through the formatio reticularis, and it is here in particular that cerebral influences can have a modulatory effect. These conclusions are based on the length of the latent times, which are longer than those associated with spinal reflexes, but shorter than the reaction times shown by the voluntary innervation. Moreover, the reflex patterns observed for the upper and lower extremities are identical for different stimulation sites, so the reflex circuit must be supraspinal. Since, in addition, the reflex pattern associated with acoustic stimulation is similar to that of an electrically evoked reflex, the formatio reticularis can be considered a nocifensive centre.

Adolescent↗

An explanation for reflex blink hyperexcitability in Parkinson's disease. II. Nucleus raphe magnus.

Hyperexcitable reflex blinks are a cardinal sign of Parkinson's disease. The first step in the circuit linking the basal ganglia and brainstem reflex blink circuits is the inhibitory nigrostriatal pathway (Basso et al., 1996). The current study reports the circuits linking the superior colliculus (SC) to trigeminal reflex blink circuits. Microstimulation of the deep layers of the SC suppresses subsequent reflex blinks at a latency of 5.4 msec. This microstimulation does not activate periaqueductal gray antinociceptive circuits. The brainstem structure linking SC to reflex blink circuits must suppress reflex blinks at a shorter latency than the SC and produce the same effect on reflex blink circuits as SC stimulation, and removal of the structure must block SC modulation of reflex blinks. Only the nucleus raphe magnus (NRM) meets these requirements. NRM microstimulation suppresses reflex blinks with a latency of 4.4 msec. Like SC stimulation, NRM microstimulation reduces the responsiveness of the spinal trigeminal nucleus. Finally, blocking the receptors for the NRM transmitter serotonin eliminates SC modulation of reflex blinks, and muscimol inactivation of the NRM transiently prevents SC modulation of reflex blinks. Thus, the circuit through which the basal ganglia modulates reflex blinking is (1) the substantia nigra pars reticulata inhibits SC neurons, (2) the SC excites tonically active NRM neurons, and (3) NRM neurons inhibit spinal trigeminal neurons involved in reflex blink circuits.

Animals↗

Stretch and H reflexes in triceps surae are similar during tonic and rhythmic contractions in high decerebrate cats.

During locomotion in decerebrate and spinal cats the group Ia afferents from hind leg muscles are depolarized rhythmically. An earlier study concluded that this locomotor-related primary afferent depolarization (PAD) does not contribute to modulation of monosynaptic reflex pathways during locomotion. This finding indicated that the neural network generating the locomotor rhythm, the central pattern generator (CPG), does not presynaptically inhibit monosynaptic reflexes. In this investigation we tested this prediction in decerebrate cats by measuring the magnitude of reflexes evoked in ankle extensor muscles during periods of tonic contractions and during sequences of rhythmic contractions. The latter occurred when the animal was induced to walk on a treadmill. At the similar levels of activity in the soleus muscle there was no significant difference in the magnitude of the soleus H reflex in these two behavioral situations. Similar results were obtained for reflexes evoked by brief stretches of the soleus muscle. We also examined the reflexes evoked by ramp-and-hold stretches during periods of rhythmic and tonic activity of the isolated medial gastrocnemius (MG) muscle. At similar levels of background activity, the reflexes evoked in the MG muscle were the same during rhythmic and tonic contractions. Our failure to observe a reduction in the magnitude of H reflexes and stretch reflexes during rhythmic contractions, compared with reflexes evoked at the same level of background activity during tonic contractions, is consistent with the notion that the CPG for stepping does not presynaptically inhibit monosynaptic reflexes during the extension phase of locomotor activity. Our results indicate that presynaptic inhibition of the monosynaptic reflex associated with normal locomotion in cats or humans arises from sources other than the extensor burst generating system of the central pattern generator.

Animals↗

Reflex modification as a test for sensory function.

Reflex modification is a versatile procedure for the assessment of sensory function because it can provide information about the responses of several sensory systems to both weak and intense stimuli. The procedure has two elements: The elicitation of some reflex, such as the acoustic startle reflex, and the modification of that reflex by preliminary stimuli. In these experiments we used reflex modification and reflex elicitation procedures to examine the normal development of auditory function in rats and to evaluate alterations in auditory function produced by physical and toxic insult. Adult rats exposed to octave bands of noise demonstrated frequency-specific deficits on a test of reflex modification, but not reflex elicitation. In the studies of developing rats, reflex elicitation appeared by postnatal day 12 and modification around day 14. Frequency-specific increases in both measures suggested that the phenomena were sensitive to auditory development and, not simply, motor development. Exposure to kanamycin on postnatal days 8 to 16 produced dose-related deficits in the ability to detect stimuli at 32 and 16 kHz, but not 4 and 0.8 kHz. These effects were observed in the absence of changes in reflex elicitation. The results demonstrate that reflex modification procedures provide more sensitive and specific information than that provided by the use of reflex elicitation alone.

Acoustic Stimulation↗

Human jaw reflexes.

Although the jaw reflexes are analogous in many ways to the corresponding limb reflexes, important differences do exist. The myotatic reflex appears to contribute more stiffness to the jaw-closing muscles than to limb muscles. The jaw tends to swing up and down during locomotion, and, to maintain a stable position in relationship to the skull, it is necessary that the muscles be made stiff by tonic contraction and/or through a powerful servoreflex. The short conduction pathway and rapid contraction of jaw muscles allow reflex effects to act with little phase lag and to provide efficient compensation. If limb muscle reflexes were equally powerful, their effects could be of more nuisance than help in overcoming expected loads because they occur so late. Perhaps the lack of Renshaw cell inhibition of trigeminal MNs and the potentiation of the jaw jerk reflex by chin vibration are features designed to maintain the strength of the myotatic reflex during locomotion. The jaw-opening reflex (including exteroceptive suppression of jaw-closer muscle activity) is bilaterally symmetrical rather than bilaterally reciprocal, as are the analogous spinal flexor withdrawal reflexes. Bilateral braking is necessary to stop closure, because the mandible crosses the midline, whereas withdrawal of a limb often needs to be compensated for by extension of the other to maintain balance. It has recently been shown in animals that limb and jaw reflex responses are highly context dependent: the size and direction of limb reflexes depend on the phase of locomotion (Forssberg et al., 1977), and the gain of the jaw-opening reflex is increased during the closing phase of mastication (Lund et al., 1981).

Electromyography↗

Hand muscle reflexes following air puff stimulation.

Hand muscle reflexes following muscle stretch and electrical nerve stimulation show a typical pattern consisting of short- and long-latency reflexes. The present investigation was designed to test reflexes following pure cutaneous stimulation. Air puffs were delivered to the palmar tip and the nail bed of the first, second and fifth fingers during isotonic contraction of hand muscles. The EMGs from the thenar muscles, the first dorsal interosseous muscle and the hypothenar muscles were recorded. Reflexes were obtained in all muscles, with a typical configuration consisting of a short-latency excitatory component (cutaneous long-latency reflex I, cLLR I) and a second excitatory component (cutaneous long-latency reflex II, cLLR II), with an inhibitory component between them. The size of cLLR II differed depending on the area stimulated and the muscle recorded. We found the largest responses always in the muscle acting on the stimulated finger. The reflex size depended on the strength of air puff stimulation. Allowing small displacements of the fingers led to an additional increase in the size of the reflex. The pattern of reflexes was identical independent of whether the finger tip or the nail bed was stimulated, but the size of the reflexes was smaller following nail bed stimulation. Following blockade of the cutaneous nerve branches of the thumb with local anaesthetics, air puff stimulation of the thumb no longer elicited this reflex pattern. Hence, under our experimental conditions, cutaneous receptors were the only source of afferent input for these reflexes.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗

A task dependent change in the medium latency component of the soleus stretch reflex.

In comparison to the H-reflex, the task dependency of the human stretch reflex during locomotive and postural tasks has not received a great deal of attention in the literature. The few studies on reflex task dependency that have been performed to date have concentrated on either the group Ia mediated H-reflex or the short latency stretch reflex. In the present study the medium latency component of a mechanically evoked stretch reflex is investigated during walking, pedalling, and sitting. Stretch reflexes were evoked in the soleus muscle using dorsiflexion perturbations generated with a portable stretching device. Perturbations of equal amplitude and velocity (8 deg, 300 deg/s) were presented to 16 healthy subjects while they walked on a treadmill and pedalled a cycle ergometer. For eight of these subjects, an additional set of data was collected as they sat on the ergometer holding a steady posture. Perturbations were presented in the early to mid stance phase of walking and the downstroke of the pedal cycle. During all three conditions, the background soleus muscle activity was matched. The short (SLR) and medium (MLR) components of the soleus reflex responses were quantified by calculating the area of each burst in a 15-ms window centred on the peak of the respective burst. In addition, the stretch velocity-stretch reflex input-output curve was examined for the two locomotion tasks over a range of velocities from 100 to 400 deg/s. Peak latencies for the two reflex responses were observed at 52+/-5/77+/-6 ms (SLR/MLR) for walking, 51+/-3/76+/-6 ms (SLR/MLR) for pedalling, and 50+/-3/76+/-7 ms for sitting. A statistically significant increase in the magnitude of the MLR was observed during walking compared with pedalling and sitting ( P=0.007), whereas no difference in magnitude was observed between the three tasks for the SLR ( P=0.616). Furthermore, no difference was observed in the stretch velocity-stretch reflex input-output relationship between walking and pedalling. It is suggested that the medium component of the stretch reflex response is modulated to provide increased control for the postural demands of walking.

Adult↗

Diurnal changes in the amplitude of the Hoffmann reflex in the human soleus but not in the flexor carpi radialis muscle.

Changes in the reflex amplitude throughout the day have been observed in non-human mammals. The present experiment tested whether diurnal fluctuations also occur in humans. Hoffmann reflex (H-reflex) amplitude was measured in soleus and flexor carpi radialis (FCR) muscles from the data collected over a 12-h period between 7:00-9:00 a.m. and 7:00-9:00 p.m. At 4-h intervals, M/H recruitment curves were obtained, and two measures of H-reflex excitability were calculated. The maximal H-reflex (H (max)) was calculated as the average of the three largest H-reflexes. H-reflexes were also sampled from the ascending limb of the M/H recruitment curve (H (A), n=10), with a corresponding M-wave of 5% M (max). All values were normalized to the maximal M-wave (M (max)). Soleus H-reflex amplitude and plantar flexion maximal voluntary isometric contraction force (MVIC) were significantly smaller (p<0.05) in the morning (H (max)=57.2% M (max), H (A)=42.3%, M (max), MVIC=162.1 Nm) than in the evening (H (max)=69.1% M (max), a 20.1% increase, H (A)=54.1% M (max), a 27.4% increase and MVIC=195.8 Nm, a 20.8% increase). In contrast, FCR H-reflex amplitude and FCR MVIC were unchanged across all testing sessions. The data show that diurnal fluctuations are present in the amplitude of the human soleus but not in the FCR H-reflex. Diurnal fluctuation in the human soleus H-reflex amplitude must be considered when interpreting H-reflex data, especially when a repeated measures design spanning several days is utilized.

Adult↗

Vestibulospinal reflexes: quantitative effects of sensory feedback and postural task.

Vestibulospinal and vestibulocollic reflexes evoked by galvanic stimulation were studied in 20 normal volunteers. In an initial "baseline" study, subjects stood unsupported on a flat surface and a narrow base with their eyes shut and with their heads rotated to the left. The effects of vision, external support and increasing stance width were examined both individually and in combination. In a second series, the effects of the same factors were examined while subjects stood on a compliant surface. Short latency (SL) and medium latency (ML) vestibulospinal reflex responses were evoked using 4 mA/20 ms galvanic vestibular stimulation (GVS) and measured from the right soleus muscle. Vestibulocollic reflexes to short duration galvanic stimulation (4 mA/2 ms) were also measured under similar conditions. Both SL and ML vestibulospinal reflexes decreased significantly and to a similar degree with vision, external support and increasing stance width on a flat surface. On the compliant surface, stance width did not result in a decrease in the ML reflex. Reflex amplitudes further decreased in a non-linear fashion with each additional sensory modality ("factor") that was made available; the degree of attenuation due to the addition of a second and third factor closely approximated the product of the effect of each factor in isolation. Standing on a compliant surface resulted in enhancement of average SL and ML reflexes under all conditions. Vestibulocollic reflexes in contrast showed no significant modulation with vision, external support and stance width. The dissociation between vestibulocollic and vestibulospinal reflexes indicates that the modulation of vestibulospinal reflexes with task occurs proximal to the primary vestibular afferents. Vestibulospinal reflexes were largest when subjects stood on a narrow base, on a compliant surface, deprived of vision and external support, consistent with the importance of vestibular function under these conditions. Although attenuated, vestibulospinal reflexes were preserved in most subjects even when vision and external support were available and a wider stance width was adopted. The combination of different factors caused a multiplicative attenuation of the initial response.

Adult↗