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A Gruart

Publications and source records attributed to A Gruart.

26 records · Page 2Linked to original sources

Kinematics of spontaneous, reflex, and conditioned eyelid movements in the alert cat.

1. Upper eyelid position and velocity, and the electromyographic (EMG) activity of the orbicularis oculi muscle, were recorded bilaterally in alert cats during spontaneous, reflexively evoked, and conditioned eyelid movements. 2. Spontaneous blinks appeared randomly (0.2-0.5 per min) and consisted of a fast, large downward lid movement followed by a slower up phase. Blinks of smaller amplitude and slower velocity were also observed mainly accompanying behavioral movements, such as during peering and grimacing. 3. Eyelid response to air puffs applied to the cornea and tarsal lid skin consisted of a short-latency (9-16 ms), fast (up to 2,000 degrees/s) downward movement that lasted for 25-30 ms, followed by late, small downward sags that were sometimes still evident after stimulus offset. Blinks outlasted the duration of the stimulus by approximately 150 ms. Blinks elicited by flashes of light or tones showed longer latency (47.3 +/- 6.3 and 53.7 +/- 8.0 ms, mean +/- SD; respectively), smaller amplitude, and a quicker habituation than air-puff-evoked lid responses. 4. For the down phase of the blink, the peak velocity, but not its duration, increased linearly with blink amplitude. Because the rise time of the down phase remained constant, changes in blink amplitude seemed to be the result of increased blink velocity. The down phase of a typical 10 degrees blink was 10 times faster than the up phase of the same blink or than upward and downward lid saccades of the same amplitude. The peak velocity and duration of the up phases of reflex blinks and upward and downward lid saccades increased linearly with lid movement amplitude. 5. The initial down phase of air-puff-evoked blinks decreased in latency, increased in amplitude and peak velocity, and maintained the same rise time for increasing puff pressure. None of these parameters was dependent on puff duration. The duration of the blink also increased linearly with air puff duration. 6. The amplitude of air-puff-evoked blinks was inversely related to lid position, decreasing with further lid positions in the closing direction. In contrast, neither peak nor integrated EMG activity of the orbicularis oculi muscle was affected by lid position, being only a function of stimulus parameters and of the animal's level of alertness. 7. Air puffs > 20 ms and > 1 kg/cm2 evoked two successive bursts (R(ap) 1 and R(ap) 2) in the EMG activity of the orbicularis oculi muscle. Shorter and/or weaker stimuli evoked only the R(ap) 1 response.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Kinematic analyses of classically-conditioned eyelid movements in the cat suggest a brain stem site for motor learning.

Upper eyelid movements were conditioned in the alert cat to the presentation of either tones or short, weak air puffs applied to the ipsi- or contralateral cornea followed by an unconditioned stimulus consisting of a long, strong air puff applied to the ipsilateral cornea. Eyelid movements were measured with the search-coil technique. Electromyographs of the orbicularis oculi muscle were also recorded. Quantitative analysis of the latencies and topographic profiles of eyelid conditioned responses suggests that the primary site for their initiation is the brain stem reflex circuit involved, depending on the sensory modality of and on the side where the conditioning stimulus was applied. However, the kinematic of the conditioned response indicates that other neural structures are involved in its acquisition and consolidation.

Animals↗

Signalling properties of identified deep cerebellar nuclear neurons related to eye and head movements in the alert cat.

1. The spike activity of deep cerebellar nuclear neurons was recorded in the alert cat during spontaneous and during vestibularly and visually induced eye movements. 2. Neurons were classified according to their location in the nuclei, their antidromic activation from projection sites, their sensitivity to eye position and velocity during spontaneous eye movements, and their responses to vestibular and optokinetic stimuli. 3. Type I EPV (eye position and velocity) neurons were located mainly in the posterior part of the fastigial nucleus and activated antidromically almost exclusively from the medial longitudinal fasciculus close to the oculomotor complex. These neurons, reported here for the first time, increased their firing rate during saccades and eye fixations towards the contralateral hemifield. Their position sensitivity to eye fixations in the horizontal plane was 5.3 +/- 2.6 spikes s-1 deg-1 (mean +/- S.D.). Eye velocity sensitivity during horizontal saccades was 0.71 +/- 0.52 spikes s-1 deg-1 s-1. Variability of their firing rate during a given eye fixation was higher than that shown by abducens motoneurons. 4. Type I EPV neurons increased their firing rate during ipsilateral head rotations at 0.5 Hz with a mean phase lead over eye position of 95.3 +/- 9.5 deg. They were also activated by contralateral optokinetic stimulation at 30 deg s-1. Their sensitivity to eye position and velocity in the horizontal plane during vestibular and optokinetic stimuli yielded values similar to those obtained for spontaneous eye movements. 5. Type II neurons were located in both fastigial and dentate nuclei and were activated antidromically from the restiform body, the medial longitudinal fasciculus close to the oculomotor complex, the red nucleus and the pontine nuclei. Type II neurons were not related to spontaneous eye movements. These neurons increased their firing rate in response to contralateral head rotation and during ipsilateral optokinetic stimulation, and decreased it with the oppositely directed movements. 6. Saccade-related neurons were located mostly in the fastigial and dentate nuclei. Fastigial neurons were activated antidromically from the medial longitudinal fasciculus, while dentate neurons were activated from the red nucleus. These neurons fired a burst of spikes whose duration was significantly related to saccade duration. Dentate neurons responded during the omni-directional saccades, while some fastigial neurons fired more actively during contralateral saccades. 7. These three types of neuron represent the output channel for oculomotor signals of the posterior vermis and paravermis. It is proposed that type I EPV neurons correspond to a group of premotor neurons directly involved in oculomotor control.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Very short-term potentiation of climbing fiber effects on deep cerebellar nuclei neurons by conditioning stimulation of mossy fiber afferents.

Field potentials induced in deep cerebellar nuclei by the electrical stimulation of contralateral red, pontine and reticularis tegmenti pontis oralis nuclei, the restiform body and the inferior olive were recorded in the alert cat. Recording sites in interpositus and fastigial nuclei were selected with the aid of antidromic field potentials induced by red nucleus and restiform body stimulation, respectively. Pontine and reticularis tegmenti pontis oralis nuclei stimulation induced small, but constant amplitude, field potentials consisting of one or two negative waves. Control field potentials induced by inferior olive stimulation consisted of a negative wave at 2-3 ms followed by a late (4-6 ms) positivity. Conditioning stimuli applied to the pontine and reticularis tegmenti pontis oralis nuclei greatly enhanced the amplitude of the inferior olive-evoked synaptic field potential for a time window of about 40 ms. In contrast, inferior olive conditioning stimulation failed to modify the field potentials induced by pontine nuclei stimulation. These facilitatory effects on field potential amplitude showed no long-lasting modifications. The transient modification of inferior olive-induced field potentials could be related to attentional movements made by the animal to natural or electrically-induced sensory cues.

Afferent Pathways↗

Discharge of identified deep cerebellar nuclei neurons related to eye blinks in the alert cat.

The activity of identified cerebellar nuclear neurons was recorded in the alert cat during blinks induced by corneal air puffs, light flashes and tones. Eyelid response to air puffs consisted of an early (16.5 +/- 2.7 ms) downward movement followed by two to three late downward steps. Blinks induced by flashes or tones presented longer latencies (52.6 +/- 4.8 and 50.1 +/- 8.0 ms). Type A neurons (n = 86) increased their spike activity in coincidence with the beginning of the blink, regardless of the stimulus modality. The late eyelid downward responses were accompanied by corresponding increases in the firing rate of the neuron. Type A neurons were activated mostly from the red nucleus (48/86) or the restiform body (24/86). Type B neurons (n = 30) fired a brief burst of spikes slightly preceding the blink, followed by a noticeable decrease in their firing rate. As for type A, the discharge response of type B neurons was always the same regardless of the sensory modality. These neurons were activated from the red nucleus (18/30), oculomotor complex (6/30) and restiform body (6/30). Although no precise temporal coupling was found between the beginning of the neuronal response and the start of either the stimulus or the motor response, linear regression analysis demonstrated significant relationships between mean firing rate of type A and B neurons and eyelid position, velocity and/or acceleration. Deep cerebellar nuclei neurons presented here seem to be directly involved in the execution of reflexively induced blinks following the smaller details of eyelid motor performance. The opposite behavior of type A and B cells suggests an interplay of reciprocal actions to determine the ongoing displacements of the lid. Finally, the cerebellum seems to influence blinks through a spread action on many brainstem sites and not exclusively on the red nucleus.

Acoustic Stimulation↗

Response diversity of pontine and deep cerebellar nuclear neurons to air puff stimulation of the eye in the alert cat.

The discharge of antidromically identified brainstem and cerebellar nuclear neurons involved in the corneal reflex was recorded in the alert cat during corneal air puffs. Eye movements were measured with the search coil technique. Recorded sensory, motor, reticular formation and cerebellar nuclear neurons showed a wide diversity in latencies and patterns of response to air puff stimulation. This diversity suggests that each part of the circuit may contribute different properties to information processing for the corneal reflex, for sustained eyelid closure and, possibly, for the classical conditioning of the nictitating membrane response.

Abducens Nerve↗

Respiration-related neurons recorded in the deep cerebellar nuclei of the alert cat.

The activity of deep cerebellar nuclei neurons was recorded in the alert cat and related to the respiratory cycle. Respiration-related neurons (RRNs, n = 29), located in the rostral fastigial and interpositus nuclei, were classified as inspiratory (24%) or expiratory (76%). Nine RRNs were antidromically activated from the red nucleus, but none from the inferior olive. Half of the RRNs showed well defined proprioceptive inputs of a rather broad origin. Other RRNs (27%) showed a respiration-related pattern independent of respiratory movement performance. Repeated electrical stimulation of the inferior olive exerted a synchronizing effect on the firing rate of 24% of the RRNs. It is proposed that cerebellar nuclear RRNs are involved in locomotor re-adjustments of the respiratory musculature.

Animals↗

[Neuronal regeneration and functional recovery following peripheral nervous system lesions].

INTRODUCTION: The complete traumatic sectioning of peripheral nerves start subcellular and molecular processes in the involved sensory and motor neurons that ends, in many cases, with a complete reinnervation of the sensory or muscular target. Nevertheless, the process is frequently disturbed, from a functional point of view, by the improper reinnervation of targets different from the original ones, a fact implying a partial or total lost of the involved sensory or motor function. METHOD AND AIMS: Results obtained with several types of axotomy and of experimental anastomosis carried out with the different brainstem motor nerves are shown. The aim was to analyze the capabilities of the different brainstem centers to adapt their physiology to the functional characteristics of a new motor target, with respect to their affinity with the motor tasks carried out by the new target. CONCLUSIONS: It is concluded that there is a gradient of functional adaptability in motoneurons to the role of new motor targets depending on their affinity in embryologic origins and functional properties. It is remarked the importance that, for a proper recovery of the lost function, have the compensatory processes started by synergistic motor systems not affected directly by the lesion.

Adaptation, Physiological↗