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


     


J Neurophysiol 83: 3509-3518, 2000;
0022-3077/00 $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 ISI Web of Science
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 ISI Web of Science (19)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Royer, S.
Right arrow Articles by Paré, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Royer, S.
Right arrow Articles by Paré, D.

The Journal of Neurophysiology Vol. 83 No. 6 June 2000, pp. 3509-3518
Copyright ©2000 by the American Physiological Society

Polarized Synaptic Interactions Between Intercalated Neurons of the Amygdala

Sébastien Royer, Marzia Martina, and Denis Paré

Laboratoire de Neurophysiologie, Département de Physiologie, Faculté de Médecine, Université Laval, Québec G1K 7P4, Canada

Royer, Sébastien, Marzia Martina, and Denis Paré. Polarized Synaptic Interactions Between Intercalated Neurons of the Amygdala. J. Neurophysiol. 83: 3509-3518, 2000. The intercalated (ITC) cell masses are small GABAergic cell clusters interposed between the basolateral (BL) complex and central (CE) nucleus of the amygdala. ITC cells receive excitatory afferents from the BL complex and generate feed-forward inhibition in the CE nucleus. Recently it was shown that ITC cells could gate impulse traffic between the BL complex and CE nucleus in a spatiotemporally differentiated manner. In addition, it was hypothesized that lateromedial inhibitory interactions between different ITC cell clusters played a critical role in this respect. Given the potential importance of such conditional computations, the present study aimed to characterize the connectivity existing among ITC cells. To this end, whole cell recordings of ITC neurons were obtained under visual guidance in coronal slices of the guinea pig amygdala. Electrical stimuli applied in the BL complex primarily elicited excitatory responses when they were applied at the same lateromedial level or more medially than the recorded ITC cells. As the stimulation site was moved laterally, the character of the response shifted toward inhibition. Both bicuculline and non-N-methyl-D-aspartate receptor antagonists abolished this BL-evoked inhibition, suggesting that it was not mediated by BL inhibitory cells projecting to ITC neurons. In keeping with this, local glutamate injections in and around the ITC clusters revealed that the most effective site to inhibit ITC cells were ITC clusters located laterally with respect to the recorded one. The activation of more medial ITC clusters evoked much smaller responses. Thus, connections between ITC clusters tend to run in a lateromedial direction. To identify the source of these directionally polarized synaptic interactions, the morphological features of ITC cells were analyzed by intracellular injection of Neurobiotin. This analysis revealed that the dendritic tree and axonal arbor of ITC cells are asymmetric in the lateromedial plane. In particular, their laterally directed dendrites were longer than the medial ones, whereas their laterally directed axon collaterals were shorter than the medial ones. It is concluded that the morphological asymmetry of ITC cells accounts for the directional polarization of inter-ITC connections. The significance of these findings for the gating of information transfer from the BL complex to the CE nucleus is discussed.




This article has been cited by other articles:


Home page
J. Physiol.Home page
R. Geracitano, W. A. Kaufmann, G. Szabo, F. Ferraguti, and M. Capogna
Synaptic heterogeneity between mouse paracapsular intercalated neurons of the amygdala
J. Physiol., November 15, 2007; 585(1): 117 - 134.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. E. Wilensky, G. E. Schafe, M. P. Kristensen, and J. E. LeDoux
Rethinking the Fear Circuit: The Central Nucleus of the Amygdala Is Required for the Acquisition, Consolidation, and Expression of Pavlovian Fear Conditioning
J. Neurosci., November 29, 2006; 26(48): 12387 - 12396.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. D. Samson and D. Pare
Activity-Dependent Synaptic Plasticity in the Central Nucleus of the Amygdala
J. Neurosci., February 16, 2005; 25(7): 1847 - 1855.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. Pare, G. J. Quirk, and J. E. Ledoux
New Vistas on Amygdala Networks in Conditioned Fear
J Neurophysiol, July 1, 2004; 92(1): 1 - 9.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
P. SAH, E. S. L. FABER, M. LOPEZ DE ARMENTIA, and J. POWER
The Amygdaloid Complex: Anatomy and Physiology
Physiol Rev, July 1, 2003; 83(3): 803 - 834.
[Abstract] [Full Text] [PDF]


Home page
Ann. N. Y. Acad. Sci.Home page
D. PARE, S. ROYER, Y. SMITH, and E. J. LANG
Contextual Inhibitory Gating of Impulse Traffic in the Intra-amygdaloid Network
Ann. N.Y. Acad. Sci., April 1, 2003; 985(1): 78 - 91.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. J. Delaney and P. Sah
Pathway-Specific Targeting of GABAA Receptor Subtypes to Somatic and Dendritic Synapses in the Central Amygdala
J Neurophysiol, August 1, 2001; 86(2): 717 - 723.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. Royer, M. Martina, and D. Pare
Bistable Behavior of Inhibitory Neurons Controlling Impulse Traffic through the Amygdala: Role of a Slowly Deinactivating K+ Current
J. Neurosci., December 15, 2000; 20(24): 9034 - 9039.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. Szinyei, T. Heinbockel, J. Montagne, and H.-C. Pape
Putative Cortical and Thalamic Inputs Elicit Convergent Excitation in a Population of GABAergic Interneurons of the Lateral Amygdala
J. Neurosci., December 1, 2000; 20(23): 8909 - 8915.
[Abstract] [Full Text] [PDF]




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