JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 80: 3148-3162, 1998;
0022-3077/98 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mcintosh, A. R.
Right arrow Articles by Gonzalez-Lima, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mcintosh, A. R.
Right arrow Articles by Gonzalez-Lima, F.

The Journal of Neurophysiology Vol. 80 No. 6 December 1998, pp. 3148-3162
Copyright ©1998 The American Physiological Society

Large-Scale Functional Connectivity in Associative Learning: Interrelations of the Rat Auditory, Visual, and Limbic Systems

A. R. Mcintosh1 and F. Gonzalez-Lima2

1 Rotman Research Institute of Baycrest Centre and Department of Psychology, University of Toronto, Toronto, Ontario M6A 2E1, Canada; and 2 Department of Psychology and Institute for Neuroscience, University of Texas, Austin, Texas, 78712

McIntosh, A. R. and F. Gonzalez-Lima. Large-scale functional connectivity in associative learning: interrelations of the rat auditory, visual, and limbic systems. J. Neurophysiol. 80: 3148-3162, 1998. Functional relations between specialized parts of the brain may be important determinants of learned behaviors. To study this, we examined the interrelations of the auditory system with several extraauditory structures in two groups of rats having different behavioral histories. Both groups were trained to associate a tone conditional stimulus (CS) with an aversive unconditional stimulus (US). For one group, a light presented with the tone predicted the absence of the US (group TL-). In the other group, the light was a neutral stimulus (group TL0). Fluorodeoxyglucose (FDG) incorporation was measured in the presence of the tone-light compound. Because the tone-light compound was physically identical for both groups, neural differences between groups reflected differences in the learned associative properties of the stimuli. Covariances of FDG uptake in the auditory system and extraauditory structures were examined using partial least squares. Three strong covariance or functional connectivity patterns were identified. The first pattern mainly reflected similarities between groups, with strong interrelations between the subcortical auditory system and the thalamocortical visual system, cerebellum, deep cerebellar nuclei, and midline thalamus. This pattern of interactions may represent part of a common circuit for relaying the associative value of the tone CS to the cerebellum and the midline thalamus. The external nucleus of the inferior colliculus and medial division of the medial geniculate nucleus were associated more strongly with this pattern for group TL-, which was interpreted as representing the change of the associative value of the tone by the light, mediated through extraauditory influences on these two regions. A second pattern involved midbrain auditory regions, superior colliculus, zona incerta, and subiculum and was stronger for group TL0. The relations between midbrain structures may represent the excitatory conditioned response (CR) evoked by the tone in this group. The final pattern was strongest in group TL- and involved interrelations of the thalamocortical auditory system with hippocampus, basolateral amygdala, and hypothalamus. This pattern may represent the learned inhibition of the CR to the tone in the presence of the light. These findings are consistent with behavioral studies suggesting that at least two types of associations are formed during associative learning. One is the sensory relation of the stimuli and another is the relation between the CS and the affective components of the US. These behavioral associations are mapped to the patterns of functional connectivity between auditory and extraauditory regions.




This article has been cited by other articles:


Home page
Learn. Mem.Home page
D. Talmi, A. K. Anderson, L. Riggs, J. B. Caplan, and M. Moscovitch
Immediate memory consequences of the effect of emotion on attention to pictures
Learn. Mem., March 5, 2008; 15(3): 172 - 182.
[Abstract] [Full Text] [PDF]


Home page
J. Neuropsychiatry Clin. Neurosi.Home page
A. Anand, Y. Li, Y. Wang, K. Gardner, and M. J. Lowe
Reciprocal Effects of Antidepressant Treatment on Activity and Connectivity of the Mood Regulating Circuit: An fMRI Study
J Neuropsychiatry Clin Neurosci, August 1, 2007; 19(3): 274 - 282.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
V. Della-Maggiore and A. R. McIntosh
Time Course of Changes in Brain Activity and Functional Connectivity Associated With Long-Term Adaptation to a Rotational Transformation
J Neurophysiol, April 1, 2005; 93(4): 2254 - 2262.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
A. Solodkin, P. Hlustik, E. E. Chen, and S. L. Small
Fine Modulation in Network Activation during Motor Execution and Motor Imagery
Cereb Cortex, November 1, 2004; 14(11): 1246 - 1255.
[Abstract] [Full Text] [PDF]


Home page
Behav Cogn Neurosci RevHome page
J. Shumake and F. Gonzalez-Lima
Brain Systems Underlying Susceptibility to Helplessness and Depression
Behav Cogn Neurosci Rev, September 1, 2003; 2(3): 198 - 221.
[Abstract] [PDF]


Home page
J. Neurosci.Home page
A. R. McIntosh, M. N. Rajah, and N. J. Lobaugh
Functional Connectivity of the Medial Temporal Lobe Relates to Learning and Awareness
J. Neurosci., July 23, 2003; 23(16): 6520 - 6528.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Vazdarjanova
Chasing "fear memories" to the cerebellum
PNAS, June 11, 2002; 99(12): 7814 - 7815.
[Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. Jones and F. Gonzalez-Lima
Mapping Pavlovian Conditioning Effects on the Brain: Blocking, Contiguity, and Excitatory Effects
J Neurophysiol, August 1, 2001; 86(2): 809 - 823.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
H. P. Nair, J. D. Berndt, D. Barrett, and F. Gonzalez-Lima
Maturation of Extinction Behavior in Infant Rats: Large-Scale Regional Interactions with Medial Prefrontal Cortex, Orbitofrontal Cortex, and Anterior Cingulate Cortex
J. Neurosci., June 15, 2001; 21(12): 4400 - 4407.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
V. Della-Maggiore, A. B. Sekuler, C. L. Grady, P. J. Bennett, R. Sekuler, and A. R. McIntosh
Corticolimbic Interactions Associated with Performance on a Short-Term Memory Task Are Modified by Age
J. Neurosci., November 15, 2000; 20(22): 8410 - 8416.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
C. Schauz and M. Koch
Blockade of NMDA Receptors in the Amygdala Prevents Latent Inhibition of Fear-Conditioning
Learn. Mem., November 1, 2000; 7(6): 393 - 399.
[Abstract] [Full Text]


Home page
J. Cogn. Neurosci.Home page
L. Nyberg, R. Habib, E. Tulving, R. Cabeza, S. Houle, J. Persson, and A. R. McIntosh
Large Scale Neurocognitive Networks Underlying Episodic Memory
J. Cogn. Neurosci., January 1, 2000; 12(1): 163 - 173.
[Abstract] [Full Text]


Home page
ScienceHome page
A. R. McIntosh, M. N. Rajah, and N. J. Lobaugh
Interactions of Prefrontal Cortex in Relation to Awareness in Sensory Learning
Science, May 28, 1999; 284(5419): 1531 - 1533.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online