Literature DB >> 2363838

Classical nictitating membrane conditioning in rabbits with varying interstimulus intervals and direct activation of cerebellar mossy fibers as the CS.

J E Steinmetz1.   

Abstract

The rate and level of classical nictitating membrane (NM)/eyelid conditioning in rabbits established by pairing a pontine nucleus stimulation conditioned stimulus (CS) with an air puff unconditioned stimulus (US) were studied at 6 interstimulus intervals (ISIs). Similar to earlier studies which used peripheral CSs, an inverted U-shaped function relating ISI and conditioning was generated. Interstimulus intervals of 250 and 500 ms produced the highest levels of conditioning, 100, 1000 and 2000 ms ISIs resulted in lower levels of conditioning, and no conditioning was established with a 50 ms ISI. These results demonstrate that a normal ISI function can be established when direct activation of cerebellar mossy fibers is used as a CS instead of conventional peripheral CSs.

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Year:  1990        PMID: 2363838     DOI: 10.1016/0166-4328(90)90008-3

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  14 in total

1.  A biophysical model of synaptic delay learning and temporal pattern recognition in a cerebellar Purkinje cell.

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2.  Toward a reconstructive understanding of behavior: A response to Reese.

Authors:  D Bullock
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3.  Purkinje cell activity during classical conditioning with different conditional stimuli explains central tenet of Rescorla–Wagner model [corrected].

Authors:  Anders Rasmussen; Riccardo Zucca; Fredrik Johansson; Dan-Anders Jirenhed; Germund Hesslow
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4.  Metabotropic glutamate receptor activation in cerebellar Purkinje cells as substrate for adaptive timing of the classically conditioned eye-blink response.

Authors:  J C Fiala; S Grossberg; D Bullock
Journal:  J Neurosci       Date:  1996-06-01       Impact factor: 6.167

5.  Small-Volume Effect Enables Robust, Sensitive, and Efficient Information Transfer in the Spine.

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6.  Medial auditory thalamic nuclei are necessary for eyeblink conditioning.

Authors:  Hunter E Halverson; John H Freeman
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7.  Evaluation of bidirectional interstimulus interval (ISI) shift in auditory delay eye-blink conditioning in healthy humans.

Authors:  Adam B Steinmetz; Patrick D Skosnik; Chad R Edwards; Amanda R Bolbecker; Joseph E Steinmetz; William P Hetrick
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Review 8.  Neural circuitry and plasticity mechanisms underlying delay eyeblink conditioning.

Authors:  John H Freeman; Adam B Steinmetz
Journal:  Learn Mem       Date:  2011-10-03       Impact factor: 2.460

9.  Medial auditory thalamus inactivation prevents acquisition and retention of eyeblink conditioning.

Authors:  Hunter E Halverson; Amy Poremba; John H Freeman
Journal:  Learn Mem       Date:  2008-07-11       Impact factor: 2.460

10.  Stimulation of the lateral geniculate, superior colliculus, or visual cortex is sufficient for eyeblink conditioning in rats.

Authors:  Hunter E Halverson; Erin M Hubbard; John H Freeman
Journal:  Learn Mem       Date:  2009-04-24       Impact factor: 2.460

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