Literature DB >> 7761454

Inactivation of the superior cerebellar peduncle blocks expression but not acquisition of the rabbit's classically conditioned eye-blink response.

D J Krupa1, R F Thompson.   

Abstract

The localization of sites of memory formation within the mammalian brain has proven to be a formidable task even for simple forms of learning and memory. Recent studies have demonstrated that reversibly inactivating a localized region of cerebellum, including the dorsal anterior interpositus nucleus, completely prevents acquisition of the conditioned eye-blink response with no effect upon subsequent learning without inactivation. This result indicates that the memory trace for this type of learning is located either (i) within this inactivated region of cerebellum or (ii) within some structure(s) efferent from the cerebellum to which output from the interpositus nucleus ultimately projects. To distinguish between these possibilities, two groups of rabbits were conditioned (by using two conditioning stimuli) while the output fibers of the interpositus (the superior cerebellar peduncle) were reversibly blocked with microinjections of the sodium channel blocker tetrodotoxin. Rabbits performed no conditioned responses during this inactivation training. However, training after inactivation revealed that the rabbits (trained with either conditioned stimulus) had fully learned the response during the previous inactivation training. Cerebellar output, therefore, does not appear to be essential for acquisition of the learned response. This result, coupled with the fact that inactivation of the appropriate region of cerebellum completely prevents learning, provides compelling evidence supporting the hypothesis that the essential memory trace for the classically conditioned eye-blink response is localized within the cerebellum.

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Year:  1995        PMID: 7761454      PMCID: PMC41855          DOI: 10.1073/pnas.92.11.5097

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  39 in total

1.  A theory of cerebellar cortex.

Authors:  D Marr
Journal:  J Physiol       Date:  1969-06       Impact factor: 5.182

2.  Accessory abducens nucleus and conditioned eye retraction/nictitating membrane extension in rabbit.

Authors:  J F Disterhoft; K J Quinn; C Weiss; M T Shipley
Journal:  J Neurosci       Date:  1985-04       Impact factor: 6.167

3.  Cerebellum: essential involvement in the classically conditioned eyelid response.

Authors:  D A McCormick; R F Thompson
Journal:  Science       Date:  1984-01-20       Impact factor: 47.728

4.  Red nucleus lesions disrupt the classically conditioned nictitating membrane response in rabbits.

Authors:  M E Rosenfield; J W Moore
Journal:  Behav Brain Res       Date:  1983-12       Impact factor: 3.332

5.  Neuronal responses of the rabbit cerebellum during acquisition and performance of a classically conditioned nictitating membrane-eyelid response.

Authors:  D A McCormick; R F Thompson
Journal:  J Neurosci       Date:  1984-11       Impact factor: 6.167

6.  Red nucleus lesions impair acquisition of the classically conditioned nictitating membrane response but not eye-to-eye savings or unconditioned response amplitude.

Authors:  M E Rosenfield; J W Moore
Journal:  Behav Brain Res       Date:  1985-09       Impact factor: 3.332

7.  Superior cerebellar peduncle lesions selectively abolish the ipsilateral classically conditioned nictitating membrane/eyelid response of the rabbit.

Authors:  D A McCormick; P E Guyer; R F Thompson
Journal:  Brain Res       Date:  1982-07-29       Impact factor: 3.252

8.  Effects of lesions of cerebellar nuclei on conditioned behavioral and hippocampal neuronal responses.

Authors:  G A Clark; D A McCormick; D G Lavond; R F Thompson
Journal:  Brain Res       Date:  1984-01-16       Impact factor: 3.252

9.  Effects of muscimol inactivation of the cerebellar interposed-dentate nuclear complex on the performance of the nictitating membrane response in the rabbit.

Authors:  V Bracha; M L Webster; N K Winters; K B Irwin; J R Bloedel
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

10.  Brachium conjuntivum and rubrobulbar tract: brain stem projections of red nucleus essential for the conditioned nictitating membrane response.

Authors:  M E Rosenfield; A Dovydaitis; J W Moore
Journal:  Physiol Behav       Date:  1985-05
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  20 in total

1.  Learning about pain: the neural substrate of the prediction error for aversive events.

Authors:  A Ploghaus; I Tracey; S Clare; J S Gati; J N Rawlins; P M Matthews
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-01       Impact factor: 11.205

2.  Acquisition of eyeblink conditioning is critically dependent on normal function in cerebellar cortical lobule HVI.

Authors:  P J Attwell; S Rahman; C H Yeo
Journal:  J Neurosci       Date:  2001-08-01       Impact factor: 6.167

Review 3.  Parallel neural systems for classical conditioning: support from computational modeling.

Authors:  M T Allen; C E Myers; M A Gluck
Journal:  Integr Physiol Behav Sci       Date:  2001 Jan-Mar

Review 4.  Memory systems in the brain and localization of a memory.

Authors:  R F Thompson; J J Kim
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-26       Impact factor: 11.205

5.  Multiple components in direction learning in smooth pursuit eye movements of monkeys.

Authors:  Nathan J Hall; Yan Yang; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2018-08-01       Impact factor: 2.714

6.  Inactivation of cerebellar output axons impairs acquisition of conditioned eyeblinks.

Authors:  W U Nilaweera; G D Zenitsky; V Bracha
Journal:  Brain Res       Date:  2006-10-24       Impact factor: 3.252

7.  Learning induces a CDC2-related protein kinase, KKIAMRE.

Authors:  H Gomi; W Sun; C E Finch; S Itohara; K Yoshimi; R F Thompson
Journal:  J Neurosci       Date:  1999-11-01       Impact factor: 6.167

8.  The role of the cerebellar interpositus nucleus in short and long term memory for trace eyeblink conditioning.

Authors:  Narawut Pakaprot; Soyun Kim; Richard F Thompson
Journal:  Behav Neurosci       Date:  2009-02       Impact factor: 1.912

9.  Blockade of GABAA receptors in the interpositus nucleus modulates expression of conditioned excitation but not conditioned inhibition of the eyeblink response.

Authors:  Brian C Nolan; Daniel A Nicholson; John H Freeman
Journal:  Integr Physiol Behav Sci       Date:  2002 Oct-Dec

10.  Reversible inactivations of the cerebellum with muscimol prevent the acquisition and extinction of conditioned nictitating membrane responses in the rabbit.

Authors:  M J Hardiman; N Ramnani; C H Yeo
Journal:  Exp Brain Res       Date:  1996-07       Impact factor: 1.972

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