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At least 775 records · Page 43Linked to original sources
PubMed1975

Exteroceptive suppression and motor control of the masseter and temporalis muscles in normal man.

Single electrical stimuli to the gums and mucosa inside the mouth elicit two successive exteroceptive suppressions (ES1 and ES2) in the voluntary electromyogram of the masseter and temporalis muscles in normal man. The same afferent axons appear to be involved in the two effects, as indicated by the intensity function, the electrical excitability, the afferent conduction velocity and the lack of differential effect of Xylocaine infiltration of the inferior alveolar nerve. Two similar phases of inhibition involve the monosynaptic masseter reflex and the synchronized electromyographical spikes induced by jaw vibration. Exteroceptive suppression is thought to be mediated, in the brain stem, by both an oligosynaptic (ES1) and a multisynaptic (ES2) mechanism.

Action Potentials↗
PubMed1982

Localization of proprioceptive reflexes in the splenius muscle of the cat.

Activity of the cat splenius muscle was modulated by sinusoidal rotation of the head around the C1-C2 joint in decerebrate cats with labyrinth intact or with all semicircular canals plugged, or, in one intact and alert cat, by rotation of the body with the head fixed in space. EMG modulation, recorded from the areas of splenius innervated by the C1-C4 nerves, was due to the cervicocollic reflex. Modulation was not uniform, but decreased with progressively more caudal recording locations; with stimuli of small amplitude it was often possible to obtain modulation of the rostral part of the muscle only. The results demonstrate localization of proprioceptive reflexes, including the stretch reflex, within the splenius muscle.

Animals↗
PubMed1984

Natural cutaneous stimulation induces late and long-lasting facilitation of extensor motoneurons in the cat.

An investigation was made of the effects of physiological cutaneous stimulation on the excitability of extensor motoneurons in spinal unanesthetized cats. The time course of changes in the monosynaptic reflex (MSR) amplitude of the soleus (Sol) and gastrocnemius medialis (GM) and lateralis (GL) was studied after conditioning stimulation with air jets (delivered to different regions of the skin of the ipsilateral hind limb), pinpricks, or stretching of the skin of the heel induced by passive rotation of the tibio-tarsal joint. Low-intensity electrical stimulation of the sural or saphenous nerves was also employed in order to condition the MSRs of the triceps surae muscles. Hair bending, skin indentation or stretching, as well as electrical nerve stimulation, can induce a similar biphasic excitability cycle of the extensor MSRs, characterized by an early inhibition followed by a late facilitatory period (LFP). The LFP started approximately 20 ms after the arrival of the cutaneous afferent volley, and lasted about 80 ms. Conditioned MSRs could attain values corresponding to 200% or more of controls. The receptive field of the LFP evoked by the air jet proved to be as large as the whole leg and foot skin surface. No significant differences were found in the extent of the late facilitation in the MSRs of Sol, GM and GL, conditioned by electrical stimulation. The LFP was also present, after conditioning stimulation of the same types as above, in intact (and spinal) chloralose-anesthetized cats.

Anesthesia, Intravenous↗
PubMed1985

Acute effects of lead at central synapses in vitro.

The acute effects of lead in the rat CNS in vitro were studied on synaptic transmission in the isolated hemisected spinal cord from newborn rats and on the transport of exogenous GABA, acetylcholine and cis-3-aminocyclohexane carboxylic acid (ACHC) from slices of cerebral cortex from adult rats. Lead had quite variable effects on monosynaptic reflexes and synaptic potentials. When it occurred, the depression of synaptic transmission by lead (typically at 18.5 mumol/liters of added lead acetate) was reversible provided exposure times were less than 15 min; furthermore, depression could be antagonised by increasing the external calcium concentration. Lead had no effect on the postsynaptic responses of motoneurons to the putative transmitters L-glutamate, GABA and glycine or to eledoisin-related peptide. The effects of lead on uptake and release of exogenous GABA and ACHC were dependent on the perfusion buffer employed: minimal effects were seen in solutions buffered with either phosphate or carbonate. When Tris HCl was used as buffer, lead inhibited the uptake of GABA and potentiated the spontaneous release of GABA with an EC50 = 50 mumol/liters as added lead acetate. In Tris HCl buffer, lead acetate (100 mumol/liters) produced a two-fold enhancement in the spontaneous release of acetylcholine under conditions where choline and acetylcholine re-uptake was blocked by hemicholinium. The availability of free lead cations in solution is highly dependent on the concentrations of other ions (particularly phosphates) and the pH. Under the appropriate conditions, lead can inhibit CNS synaptic function acutely in a manner consistent with lead competing with calcium ions in transmitter release processes as has been established for acetylcholine release at peripheral synapses.

Acetylcholine↗
PubMed1985

Topographic studies relating distribution of Ia- and gamma-fibres in spinal cord and position of muscle spindles in cat tibialis anterior muscle.

The segmental distribution of 115 Ia- and 115 paired gamma-fibres of the tibialis anterior muscle was studied in anaesthetized cats. All Ia-fibres recorded were found in the lumbar segments L6 and L7, from caudal L6 to middle L7. The paired gamma-axons were also mainly found in these parts of the spinal cord, only 7 gamma-fibres were localized in caudal L7. A total of 70% of all fibres was found in L7. Of the fibres constituting 'muscle spindle units' of the tibialis anterior 92.2% enter the same segment (a 'muscle spindle unit' is here defined as a muscle spindle with its Ia-fibres and one gamma-fibre innervating it). More than that, 88% of the afferent and efferent fibres of muscle spindle units were found in the same part of the segment. For the first time, the position of the muscle spindles was related to the location of their Ia- and gamma-fibres in the spinal cord. In general, the muscle spindles located in the proximal muscle region project to the more cranial part of the spinal cord and the muscle spindles localized distally in the muscle project to the more caudal part of the spinal cord. The topographic pattern of the muscle spindle units is discussed with respect to the topographically arranged monosynaptic reflex loop.

Animals↗
PubMed1987

Suppression of the recurrent inhibitory pathway in lumbar cord segments during locus coeruleus stimulation in cats.

The present study revealed a consistent reduction of ventral root-induced recurrent inhibition of monosynaptic reflexes in both extensor (gastrocnemius-soleus) and flexor (common peroneal) motonuclei upon delivery of preconditioning stimuli to the locus coeruleus (LC) in decerebrate cats. The magnitudes of the LC-induced decrease in recurrent inhibition, functionally disinhibition, and of recurrent inhibition were significantly correlated. Direct recordings from Renshaw cells have indicated that LC conditioning stimuli cause a decrease in the number of spikes and the duration of firing in response to single antidromic (ventral root) volleys. These results suggest that the LC depression of the recurrent inhibitory pathway is attributed, in part at least, to inhibition of Renshaw cell activity.

Animals↗
PubMed1989

Changes in extracellular calcium and magnesium and synaptic transmission in isolated mouse spinal cord.

Hemisected mouse spinal cords were maintained in vitro and the concentrations of calcium [CA2+] and of magnesium [Mg2+] in the bath were varied. In control solution containing 1.2 mM of both [Ca2+] and [Mg2+] stimulation of a dorsal root (DR) evoked in an adjacent DR an initial fiber volley representing 'input'; a postsynaptic compound spike recorded by volume conduction from dorsal gray matter, the dorsal horn response (DHR); and a slow dorsal root potential (DRP). In the ventral root of the stimulated segment a monosynaptic reflex (VRR1) was evoked. The fiber volley was enhanced by lowering [Ca2+] or [Mg2+] and depressed when either ion concentration was raised. The DRP, DHR and VRR1 were enhanced in low [Mg2+] and in moderately elevated [Ca2+]. At 1.8 mM [Ca2+] and above, the 'classical' dorsal root reflex (DRR) and a GABA-dependent delayed VR reflex (VRR2) appeared. Transmission of reflexes was maximal between 2.4 and 3.6 mM [Ca2+], while DRP was maximal at about 4.8 mM. In elevated [Mg2+] and in low [Ca2+] all synaptically transmitted responses (DRR, DRP and VRR) were depressed. The influence of both [Ca2+] and [Mg2+] was stronger on DRP, DRR and VRR2 than on DHR and VRR1. The effects of simultaneous changes of [Ca2+] and [Mg2+] partially cancelled each other. We conclude that low to moderately elevated [Ca2+] mainly influences the release of transmitter from presynaptic terminals; at very high [Ca2+] the depression of neuronal excitability dominates. The effects of Ca2+ and Mg2+ on GABAergic transmission are especially marked.

Action Potentials↗
PubMed1996

Changes in sensitivity of vestibular nucleus neurons induced by cross-axis adaptation of the vestibulo-ocular reflex in the cat.

In alert, chronically-prepared cats, we studied response characteristics of well-isolated vestibular nucleus neurons (n = 9) while pairing yaw rotation with a pitch optokinetic stimulus, resulting in cross-axis adaptation of the horizontal vestibulo-ocular reflex. Each neuron's sensitivity to whole body rotation in a variety of axes in three-dimensional space was determined. When tested in darkness following adaptation, neurons showed statistically significant increases in sensitivity to yaw but not vertical plane rotations, suggesting participation in reflex plasticity.

Animals↗
PubMed1975

Startle responses recorded in the leg of man.

The EMG pattern of startle reactions in the leg was studied in man using a 100 msec, 1 kc/sec squre wave tone burst of 114 dB as the auitory stimulus. At rest, 74 responses were recorded in the ankle flexor tibialis anterior (TA) and 23 in the ankle extensor gastrocnemius (G) with a significantly different mean latency of 151 and 123 msecrespectively. During tonic extension or flexion of the ankle, the EMG response in TA or G consisted in a burst of activity superimposed on the voluntary EMG at a latency of approximately 150 msec after the onset of the tone burst and followed, at 200 msec, by a period of EMG silence lasting close to 100 msec. Similar periods of silence also occurred as the sole EMG modulation in response to sound. Although predominant in flexors, startle reactions are significant in extensors during or after tonic ankle extension suggesting that audiospinal influences may be channelled to one or the other group depending on their functional state. The silent period of EMG following an excitatory startle or appearing on its own suggests an important inhibitory component in audiospinal mechanisms particularly related to startle since it had not been disclosed in a previous study of the modulation of the H-reflex by non-startling auditory stimulus. From the distribution and EMG pattern of startle, it is inferred that audiospinal influences may be meaningfully integrated through the reticulospinal system in sound guided behaviour.

Acoustic Stimulation↗