Literature DB >> 2798428

Classical conditioning of the Aplysia siphon-withdrawal reflex exhibits response specificity.

R D Hawkins1, N Lalevic, G A Clark, E R Kandel.   

Abstract

The gill- and siphon-withdrawal reflex of Aplysia undergoes classical conditioning of its amplitude and duration when siphon stimulation (the conditioned stimulus, CS) is paired with tail or mantle shock (the unconditioned stimulus, US). This conditioning of a preexisting response exhibits both temporal and stimulus specificities, which can be accounted for by activity-dependent enhancement of presynaptic facilitation of the siphon sensory neurons. To test whether conditioning of the reflex also exhibits response specificity (development of a new type of response to the CS that often resembles the response to the US), we measured the direction of siphon withdrawal in response to siphon stimulation (the CS) with tail or mantle shock as the US. The unlearned response to siphon stimulation is straight contraction, the response to tail shock is backward bending, and the response to mantle shock is forward bending. In the first experiment, we trained different animals with the tail or mantle US paired or unpaired with the CS; in a second experiment, we trained each animal with two CSs, one of which was paired with the US; in a third experiment, we varied US intensity; and in a fourth experiment, we trained each animal with two USs, one of which was paired with the CS. There was a significant, pairing-specific tendency for the direction of the response to the CS to resemble the response to the US after training in each experiment, demonstrating response specificity in conditioning of the withdrawal reflex. This feature of conditioning could in principle be accounted for by an elaboration of activity-dependent facilitation.

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Year:  1989        PMID: 2798428      PMCID: PMC298118          DOI: 10.1073/pnas.86.19.7620

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


  24 in total

1.  Branch-specific heterosynaptic facilitation in Aplysia siphon sensory cells.

Authors:  G A Clark; E R Kandel
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

2.  Differential expression of pseudoconditioning and sensitization by siphon responses in Aplysia: novel response selection after training.

Authors:  M T Erickson; E T Walters
Journal:  J Neurosci       Date:  1988-08       Impact factor: 6.167

3.  Local, reflex, and central commands controlling gill and siphon movements in Aplysia.

Authors:  I Kupfermann; T J Carew; E R Kandel
Journal:  J Neurophysiol       Date:  1974-09       Impact factor: 2.714

4.  Changes in unit activity and thresholds to electrical microstimulation at coronal-pericruciate cortex of cat with classical conditioning of different facial movements.

Authors:  C D Woody; J Engel
Journal:  J Neurophysiol       Date:  1972-03       Impact factor: 2.714

Review 5.  Cellular analysis of associative learning.

Authors:  J H Byrne
Journal:  Physiol Rev       Date:  1987-04       Impact factor: 37.312

6.  Is there a cell-biological alphabet for simple forms of learning?

Authors:  R D Hawkins; E R Kandel
Journal:  Psychol Rev       Date:  1984-07       Impact factor: 8.934

7.  Interneurons involved in mediation and modulation of gill-withdrawal reflex in Aplysia. I. Identification and characterization.

Authors:  R D Hawkins; V F Castellucci; E R Kandel
Journal:  J Neurophysiol       Date:  1981-02       Impact factor: 2.714

8.  A cellular mechanism of classical conditioning in Aplysia: activity-dependent amplification of presynaptic facilitation.

Authors:  R D Hawkins; T W Abrams; T J Carew; E R Kandel
Journal:  Science       Date:  1983-01-28       Impact factor: 47.728

9.  A test of Hebb's postulate at identified synapses which mediate classical conditioning in Aplysia.

Authors:  T J Carew; R D Hawkins; T W Abrams; E R Kandel
Journal:  J Neurosci       Date:  1984-05       Impact factor: 6.167

10.  Effects of interstimulus interval and contingency on classical conditioning of the Aplysia siphon withdrawal reflex.

Authors:  R D Hawkins; T J Carew; E R Kandel
Journal:  J Neurosci       Date:  1986-06       Impact factor: 6.167

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  5 in total

1.  The contribution of activity-dependent synaptic plasticity to classical conditioning in Aplysia.

Authors:  I Antonov; I Antonova; E R Kandel; R D Hawkins
Journal:  J Neurosci       Date:  2001-08-15       Impact factor: 6.167

2.  Involvement of presynaptic and postsynaptic mechanisms in a cellular analog of classical conditioning at Aplysia sensory-motor neuron synapses in isolated cell culture.

Authors:  J X Bao; E R Kandel; R D Hawkins
Journal:  J Neurosci       Date:  1998-01-01       Impact factor: 6.167

Review 3.  Associative learning in invertebrates.

Authors:  Robert D Hawkins; John H Byrne
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-04-15       Impact factor: 10.005

4.  Transformation of siphon responses during conditioning of Aplysia suggests a model of primitive stimulus-response association.

Authors:  E T Walters
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

Review 5.  Separate effects of a classical conditioning procedure on respiratory pumping, swimming, and inking in Aplysia fasciata.

Authors:  M Levy; A J Susswein
Journal:  Learn Mem       Date:  1999 Jan-Feb       Impact factor: 2.460

  5 in total

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