Literature DB >> 12708526

Covariation of alternative measures of responding in rabbit (Oryctolagus cuniculus) eyeblink conditioning during acquisition training and tone generalization.

Keith S Garcia1, Michael D Mauk, Gabrielle Weidemann, E James Kehoe.   

Abstract

The likelihood, size, and speed of eyelid movements are thought to covary during the acquisition and expression of conditioning in rabbits (Oryctolagus cuniculus) and are generally accepted as interchangeable measures of the associative strength activated by the conditioned stimulus (CS). To test this assumption, the authors examined the patterns of covariation in these eyelid movement measures in acquisition and stimulus generalization in the upper eyelid and nictitating membrane. Rather than the expected covariation among these measures, eyelid movement magnitudes during the CS were distributed in approximately a bimodal manner. That is, eyelid activity consisted largely of a mixture of very small (< 0.125 mm) baseline measurements and larger (> 1 mm) movements. The results are discussed with respect to their implications for real-time models of eyelid conditioning.

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Year:  2003        PMID: 12708526     DOI: 10.1037/0735-7044.117.2.292

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


  27 in total

1.  Stimulus generalization of conditioned eyelid responses produced without cerebellar cortex: implications for plasticity in the cerebellar nuclei.

Authors:  Tatsuya Ohyama; William L Nores; Michael D Mauk
Journal:  Learn Mem       Date:  2003 Sep-Oct       Impact factor: 2.460

2.  Unpaired extinction: implications for treating post-traumatic stress disorder.

Authors:  Bernard G Schreurs; Carrie A Smith-Bell; Lauren B Burhans
Journal:  J Psychiatr Res       Date:  2010-11-12       Impact factor: 4.791

3.  Eyeblink conditioning in the developing rabbit.

Authors:  Kevin L Brown; Diana S Woodruff-Pak
Journal:  Dev Psychobiol       Date:  2011-09-27       Impact factor: 3.038

Review 4.  Neuroscience and learning: lessons from studying the involvement of a region of cerebellar cortex in eyeblink classical conditioning.

Authors:  Ronald P Villarreal; Joseph E Steinmetz
Journal:  J Exp Anal Behav       Date:  2005-11       Impact factor: 2.468

5.  Stimulus specificity of concurrent recovery in the rabbit nictitating membrane response.

Authors:  Gabrielle Weidemann; E James Kehoe
Journal:  Learn Behav       Date:  2005-08       Impact factor: 1.986

6.  Repeated acquisitions and extinctions in classical conditioning of the rabbit nictitating membrane response.

Authors:  E James Kehoe
Journal:  Learn Mem       Date:  2006-05-16       Impact factor: 2.460

7.  Delayed unpaired extinction as a treatment for hyperarousal of the rabbit nictitating membrane response and its implications for treating PTSD.

Authors:  Bernard G Schreurs; Carrie A Smith-Bell; Lauren B Burhans
Journal:  J Psychiatr Res       Date:  2018-01-12       Impact factor: 4.791

8.  Sex differences in a rabbit eyeblink conditioning model of PTSD.

Authors:  Bernard G Schreurs; Carrie Smith-Bell; Lauren B Burhans
Journal:  Neurobiol Learn Mem       Date:  2018-04-24       Impact factor: 2.877

9.  Systematic variation of acquisition rate in delay eyelid conditioning.

Authors:  Hunter E Halverson; Loren C Hoffmann; Yujin Kim; Eszter A Kish; Michael D Mauk
Journal:  Behav Neurosci       Date:  2016-05-19       Impact factor: 1.912

10.  Ontogeny of trace eyeblink conditioning to shock-shock pairings in the rat pup.

Authors:  Bernard G Schreurs; Lauren B Burhans; Carrie A Smith-Bell; Sylwia W Mrowka; Desheng Wang
Journal:  Behav Neurosci       Date:  2012-12-17       Impact factor: 1.912

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