Literature DB >> 7472326

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

A Gruart1, P Blázquez, J M Delgado-García.   

Abstract

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)

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Year:  1995        PMID: 7472326     DOI: 10.1152/jn.1995.74.1.226

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  43 in total

1.  A kinetic study of blinking responses in cats.

Authors:  José Alberto Trigo; Laura Roa; Agnès Gruart; José María Delgado-García
Journal:  J Physiol       Date:  2003-03-28       Impact factor: 5.182

Review 2.  Consensus paper: roles of the cerebellum in motor control--the diversity of ideas on cerebellar involvement in movement.

Authors:  Mario Manto; James M Bower; Adriana Bastos Conforto; José M Delgado-García; Suzete Nascimento Farias da Guarda; Marcus Gerwig; Christophe Habas; Nobuhiro Hagura; Richard B Ivry; Peter Mariën; Marco Molinari; Eiichi Naito; Dennis A Nowak; Nordeyn Oulad Ben Taib; Denis Pelisson; Claudia D Tesche; Caroline Tilikete; Dagmar Timmann
Journal:  Cerebellum       Date:  2012-06       Impact factor: 3.847

Review 3.  The role of interpositus nucleus in eyelid conditioned responses.

Authors:  J M Delgado-García; A Gruart
Journal:  Cerebellum       Date:  2002-12       Impact factor: 3.847

4.  Gene-environment interplay in affect and dementia: emotional modulation of cognitive expression in personal outcomes.

Authors:  T Palomo; R J Beninger; R M Kostrzewa; T Archer
Journal:  Neurotox Res       Date:  2004       Impact factor: 3.911

5.  Timing and causality in the generation of learned eyelid responses.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Front Integr Neurosci       Date:  2011-08-30

6.  Cholinergic septo-hippocampal innervation is required for trace eyeblink classical conditioning.

Authors:  Angela Fontán-Lozano; Julieta Troncoso; Alejandro Múnera; Angel Manuel Carrión; José María Delgado-García
Journal:  Learn Mem       Date:  2005-11-14       Impact factor: 2.460

7.  Role of cerebellar interpositus nucleus in the genesis and control of reflex and conditioned eyelid responses.

Authors:  Lydia Jiménez-Díaz; Juan de Dios Navarro-López; Agnès Gruart; José M Delgado-García
Journal:  J Neurosci       Date:  2004-10-13       Impact factor: 6.167

8.  An experimental model for the study of cognitive disorders: the hippocampus and associative learning in mice.

Authors:  José M Delgado-García; Agnès Gruart
Journal:  Neurotox Res       Date:  2008-12       Impact factor: 3.911

9.  Examination of bilateral eyeblink conditioning in rats.

Authors:  Matthew M Campolattaro; John H Freeman
Journal:  Behav Neurosci       Date:  2009-12       Impact factor: 1.912

10.  The use of alert behaving mice in the study of learning and memory processes.

Authors:  Antonio Rodríguez-Moreno; Eduardo Domínguez Del Toro; Elena Porras-García; José M Delgado-García
Journal:  Neurotox Res       Date:  2004       Impact factor: 3.911

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