WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience PeproTech - Your Source for Neuroscience Research Reagents
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hawkins, R. D.
Right arrow Articles by Kandel, E. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hawkins, R. D.
Right arrow Articles by Kandel, E. R.

 Previous Article  |  Next Article 

Journal of Neuroscience, Vol 6, 1695-1701, Copyright © 1986 by Society for Neuroscience


ARTICLE

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

RD Hawkins, TJ Carew and ER Kandel

The siphon withdrawal reflex of Aplysia undergoes differential classical conditioning with cutaneous stimulation of the siphon or mantle shelf as the discriminative conditioned stimuli (CS+ and CS-) and shock to the tail as the unconditioned stimulus (US). The reflex has proved to be useful for analyzing the neural mechanisms of conditioning. To test the generality of this experimental system, we have begun to compare the properties of conditioning in Aplysia with those of conditioning in vertebrates. We first examined the effect of the interstimulus interval (ISI) by varying the time between presentation of the CS+ and the US in different groups of animals. Significant differential conditioning was obtained when the onset of the CS+ preceded the onset of the US by 0.5 sec, and marginal conditioning was obtained when the ISI was 1.0 sec. By contrast, no significant conditioning occurred when the CS+ preceded the US by 2, 5, or 10 sec, when the onsets of the stimuli were simultaneous, or when US onset preceded the CS+ by 0.5, 1.0, or 1.5 sec (backward conditioning). We next examined the effect of contingency by giving one group of animals normal differential conditioning, and a second group the same training but with additional USs inserted between the paired trials. Presentation of these additional USs reduced the degree to which the US was contingent on the CS+, but did not change the number of pairings. Animals receiving normal training again showed significant conditioning, whereas animals receiving additional USs showed no conditioning.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
J. Neurosci.Home page
S. A. Jami, W. G. Wright, and D. L. Glanzman
Differential Classical Conditioning of the Gill-Withdrawal Reflex in Aplysia Recruits Both NMDA Receptor-Dependent Enhancement and NMDA Receptor-Dependent Depression of the Reflex
J. Neurosci., March 21, 2007; 27(12): 3064 - 3068.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
B. A. Hoover, H. Nguyen, L. Thompson, and W. G. Wright
Associative memory in three aplysiids: Correlation with heterosynaptic modulation
Learn. Mem., November 1, 2006; 13(6): 820 - 826.
[Abstract] [Full Text] [PDF]


Home page
Biol. Bull.Home page
R. D. Hawkins, E. R. Kandel, and C. H. Bailey
Molecular Mechanisms of Memory Storage in Aplysia
Biol. Bull., June 1, 2006; 210(3): 174 - 191.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. D. Lent and H.-W. Kwon
Antennal movements reveal associative learning in the American cockroach Periplaneta americana
J. Exp. Biol., January 15, 2004; 207(2): 369 - 375.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
I. Antonov, I. Antonova, E. R. Kandel, and R. D. Hawkins
The Contribution of Activity-Dependent Synaptic Plasticity to Classical Conditioning in Aplysia
J. Neurosci., August 15, 2001; 21(16): 6413 - 6422.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
T W Abrams, Y Yovell, C U Onyike, J E Cohen, and H E Jarrard
Analysis of sequence-dependent interactions between transient calcium and transmitter stimuli in activating adenylyl cyclase in Aplysia: possible contribution to CS--US sequence requirement during conditioning.
Learn. Mem., January 1, 1998; 4(6): 496 - 509.
[Abstract] [PDF]


Home page
Adaptive BehaviorHome page
A. Mignault and A. A. J. Marley
A Real-Time Neuronal Model of Classical Conditioning
Adaptive Behavior, June 1, 1997; 6(1): 3 - 61.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
X. Y. Lin and D. L. Glanzman
Effect of Interstimulus Interval on Pairing-Induced LTP of Aplysia Sensorimotor Synapses in Cell Culture
J Neurophysiol, February 1, 1997; 77(2): 667 - 674.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
C Chen and R F Thompson
Temporal specificity of long-term depression in parallel fiber--Purkinje synapses in rat cerebellar slice.
Learn. Mem., January 1, 1995; 2(3-4): 185 - 198.
[Abstract] [PDF]


Home page
Learn. Mem.Home page
G A Clark, R D Hawkins, and E R Kandel
Activity-dependent enhancement of presynaptic facilitation provides a cellular mechanism for the temporal specificity of classical conditioning in Aplysia.
Learn. Mem., January 1, 1994; 1(4): 243 - 257.
[Abstract] [PDF]


Home page
ScienceHome page
S. Small, E. Kandel, and R. Hawkins
Activity-dependent enhancement of presynaptic inhibition in Aplysia sensory neurons
Science, March 24, 1989; 243(4898): 1603 - 1606.
[Abstract] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2008 by Society for Neuroscience ONLINE ISSN: 1529-2401
-