Literature DB >> 3365316

Reflex facilitation of the nictitating membrane response remains after cerebellar lesions.

D J Weisz1, J J LoTurco.   

Abstract

Reflex facilitation and associated properties were investigated during classical conditioning of the nictitating membrane (NM) response in rabbit. In the first experiment, the role of the cerebellum was examined by comparing the unconditioned responses of animals with bilateral lesions of the deep cerebellar nuclei with those of operated controls during counterbalanced tone/light (T/L) discrimination training. Both T and L facilitated unconditioned NM responses when used as the CS+ (conditioned stimulus), but neither facilitated when used as the CS-. There were no significant differences in the amount of reflex facilitation exhibited by animals with lesions compared with control animals. Animals with lesions, however, failed to acquire conditioned responses after 10 days of training, whereas all control animals met acquisition criterion within 4 days. In the second experiment, reflex facilitation was shown to decrement in a stimulus-specific manner when nonreinforced presentations of an auditory stimulus were given. The discussion of results focuses on the relation between reflex facilitation and classical conditioning in terms of behavioral properties and underlying neural systems.

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Year:  1988        PMID: 3365316     DOI: 10.1037//0735-7044.102.2.203

Source DB:  PubMed          Journal:  Behav Neurosci        ISSN: 0735-7044            Impact factor:   1.912


  8 in total

1.  The M1 muscarinic agonist CI-1017 facilitates trace eyeblink conditioning in aging rabbits and increases the excitability of CA1 pyramidal neurons.

Authors:  C Weiss; A R Preston; M M Oh; R D Schwarz; D Welty; J F Disterhoft
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

2.  Evoking blinks with natural stimulation and detecting them with a noninvasive optical device: a simple, inexpensive method for use with freely moving animals.

Authors:  Craig Weiss; John F Disterhoft
Journal:  J Neurosci Methods       Date:  2008-06-13       Impact factor: 2.390

3.  The effects of two forms of physical activity on eyeblink classical conditioning.

Authors:  John T Green; Amy C Chess; Montana Burns; Kira M Schachinger; Alexandra Thanellou
Journal:  Behav Brain Res       Date:  2011-01-14       Impact factor: 3.332

4.  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

5.  Learned modification of the nictitating membrane reflex by auditory stimuli in the barn owl.

Authors:  Avinash D S Bala; Terry T Takahashi
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2005-06-25       Impact factor: 1.836

6.  Inactivation of the interpositus nucleus during unpaired extinction does not prevent extinction of conditioned eyeblink responses or conditioning-specific reflex modification.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Behav Neurosci       Date:  2019-03-14       Impact factor: 1.912

7.  Delay eyeblink classical conditioning is impaired in Fragile X syndrome.

Authors:  Michael J Tobia; Diana S Woodruff-Pak
Journal:  Behav Neurosci       Date:  2009-06       Impact factor: 1.912

8.  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

  8 in total

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