Literature DB >> 20410355

Behavioral characteristics, associative learning capabilities, and dynamic association mapping in an animal model of cerebellar degeneration.

Elena Porras-García1, Raudel Sánchez-Campusano, David Martínez-Vargas, Eduardo Domínguez-del-Toro, Jan Cendelín, Frantisek Vozeh, José M Delgado-García.   

Abstract

Young adult heterozygous Lurcher mice constitute an excellent model for studying the role of the cerebellar cortex in motor performance-including the acquisition of new motor abilities-because of the early postnatal degeneration of almost all of their Purkinje and granular cells. Wild-type and Lurcher mice were classically conditioned for eyelid responses using a delay paradigm with or without an electrolytic lesion in the interpositus nucleus. Although the late component of electrically evoked blink reflexes was smaller in amplitude and had a longer latency in Lurcher mice than that in controls, the two groups of animals presented similar acquisition curves for eyeblink conditioning. The lesion of the interpositus nucleus affected both groups of animals equally for the generation of reflex and conditioned eyelid responses. Furthermore, we recorded the multiunitary activity at the red and interpositus nuclei during the same type of associative learning. In both nuclei, the neural firing activity lagged the beginning of the conditioned response (determined by orbicularis oculi muscle response). Although red nucleus neurons and muscle activities presented a clear functional coupling (strong correlation and low asymmetry) across conditioning, the coupling between interpositus neurons and either red nucleus neurons or muscle activities was slightly significant (weak correlation and high asymmetry). Lurcher mice presented a nonlinear coupling (high asymmetry) between red nucleus neurons and muscle activities, with an evident compensatory adjustment in the correlation of firing between interpositus and red nuclei neurons (a coupling with low asymmetry), aimed probably at compensating the absence of cerebellar cortical neurons.

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Year:  2010        PMID: 20410355     DOI: 10.1152/jn.00180.2010

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


  20 in total

1.  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

2.  Dynamic changes in the cerebellar-interpositus/red-nucleus-motoneuron pathway during motor learning.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Cerebellum       Date:  2011-12       Impact factor: 3.847

Review 3.  Mini-review: synaptic integration in the cerebellar nuclei--perspectives from dynamic clamp and computer simulation studies.

Authors:  Dieter Jaeger
Journal:  Cerebellum       Date:  2011-12       Impact factor: 3.847

Review 4.  Oscillations, Timing, Plasticity, and Learning in the Cerebellum.

Authors:  G Cheron; J Márquez-Ruiz; B Dan
Journal:  Cerebellum       Date:  2016-04       Impact factor: 3.847

Review 5.  Consensus paper: current views on the role of cerebellar interpositus nucleus in movement control and emotion.

Authors:  Vincenzo Perciavalle; Richard Apps; Vlastislav Bracha; José M Delgado-García; Alan R Gibson; Maria Leggio; Andrew J Carrel; Nadia Cerminara; Marinella Coco; Agnès Gruart; Raudel Sánchez-Campusano
Journal:  Cerebellum       Date:  2013-10       Impact factor: 3.847

6.  Inactivation of the interpositus nucleus blocks the acquisition of conditioned responses and timing changes in conditioning-specific reflex modification of the rabbit eyeblink response.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Neurobiol Learn Mem       Date:  2018-07-24       Impact factor: 2.877

7.  Motor learning of mice lacking cerebellar Purkinje cells.

Authors:  M Elena Porras-García; Rocío Ruiz; Eva M Pérez-Villegas; José Á Armengol
Journal:  Front Neuroanat       Date:  2013-04-23       Impact factor: 3.856

8.  Age-dependent impairment of eyeblink conditioning in prion protein-deficient mice.

Authors:  Yasushi Kishimoto; Moritoshi Hirono; Ryuichiro Atarashi; Suehiro Sakaguchi; Tohru Yoshioka; Shigeru Katamine; Yutaka Kirino
Journal:  PLoS One       Date:  2013-04-10       Impact factor: 3.240

9.  Intracerebellar application of P19-derived neuroprogenitor and naive stem cells to Lurcher mutant and wild type B6CBA mice.

Authors:  Zbyněk Houdek; Jan Cendelín; Vlastimil Kulda; Václav Babuška; Miroslava Cedíková; Milena Králíčková; Jiří Pacherník; George B Stefano; František Vožeh
Journal:  Med Sci Monit       Date:  2012-05

10.  A Variable Oscillator Underlies the Measurement of Time Intervals in the Rostral Medial Prefrontal Cortex during Classical Eyeblink Conditioning in Rabbits.

Authors:  C Rocío Caro-Martín; Rocío Leal-Campanario; Raudel Sánchez-Campusano; José M Delgado-García; Agnès Gruart
Journal:  J Neurosci       Date:  2015-11-04       Impact factor: 6.167

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