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


     


J Neurophysiol 64: 1186-1198, 1990;
0022-3077/90 $5.00
This Article
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 White, G.
Right arrow Articles by Steward, O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by White, G.
Right arrow Articles by Steward, O.

Journal of Neurophysiology, Vol 64, Issue 4 1186-1198, Copyright © 1990 by APS


ARTICLES

Spatial overlap between populations of synapses determines the extent of their associative interaction during the induction of long-term potentiation and depression

G. White, W. B. Levy and O. Steward
Department of Neuroscience, University of Virginia Health Sciences Center, Charlottesville 22908.

1. This study evaluates the associative interactions between inputs that lead to long-term potentiation (LTP) and long-term depression (LTD) in the dentate gyrus (DG). Previous studies have revealed that when two inputs are coconditioned, the extent of LTP is greater than when each input is conditioned alone. Moreover, for a weak input that does not show LTP when conditioned alone, LTP can be induced in that weak input if it is coconditioned with a strong input. LTD results when one input is silent when another is conditioned. In the present study, we evaluate whether these associative interactions depend on the extent of overlap of the terminal fields of the different inputs. 2. The experiment took advantage of the topographical organization of the temporodentate pathway from the entorhinal cortex (EC) to the DG. Four stimulating electrodes were placed so as to activate ipsilateral and crossed components of the projections from medial and lateral portions of the EC. Recording electrodes were positioned unilaterally in the DG so as to record field potentials. The localization of the synaptic field that was activated by each electrode was determined by current source density (CSD) analysis. The extent of overlap between the terminal fields of ipsi- and contralateral pathways was assessed, and the pathways were divided into groups where the overlap between current sinks was 0-50 or 51-100%. 3. Conditioning stimulation (400-Hz trains of 8 pulses delivered 8 times) was delivered to pathways alone or in combination with other pathways. The extent of LTP was evaluated after coactivation of pathways that overlapped substantially (51-100%) or minimally (0-50%). The extent of LTD was evaluated in pathways that were silent during conditioning of other overlapping or nonoverlapping pathways. 4. The extent of associative LTP or LTD depended on the extent of overlap between the terminal fields of pathways. Coactivation of two pathways that overlapped by 51-100% led to LTP; coactivation of pathways that overlapped by 0-50% did not. Moreover, LTD was induced in a crossed pathway when an ipsilateral pathway that overlapped by 51-100% was activated, but not when a nonoverlapping (0-50% overlap) ipsilateral pathway was activated. The degree of associative LTP or LTD that was induced in crossed pathways was correlated with the percent overlap with the terminal field of the active ipsilateral pathway. 5. Evaluation of whether LTD was induced when one division (medial or lateral) of the ipsilateral pathway was silent when the other division was conditioned revealed similar relationships.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurosci.Home page
T. M. Reeves, M. L. Prins, J. Zhu, J. T. Povlishock, and L. L. Phillips
Matrix Metalloproteinase Inhibition Alters Functional and Structural Correlates of Deafferentation-Induced Sprouting in the Dentate Gyrus
J. Neurosci., November 12, 2003; 23(32): 10182 - 10189.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. J. Froc, B. Eadie, A. M. Li, K. Wodtke, M. Tse, and B. R. Christie
Reduced Synaptic Plasticity in the Lateral Perforant Path Input to the Dentate Gyrus of Aged C57BL/6 Mice
J Neurophysiol, July 1, 2003; 90(1): 32 - 38.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Kimura and C. Pavlides
Long-Term Potentiation/Depotentiation Are Accompanied by Complex Changes in Spontaneous Unit Activity in the Hippocampus
J Neurophysiol, October 1, 2000; 84(4): 1894 - 1906.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
W. R. Holmes and W. B. Levy
Quantifying the Role of Inhibition in Associative Long-Term Potentiation in Dentate Granule Cells With Computational Models
J Neurophysiol, July 1, 1997; 78(1): 103 - 116.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
V. Doyere, B. Srebro, and S. Laroche
Heterosynaptic LTD and Depotentiation in the Medial Perforant Path of the Dentate Gyrus in the Freely Moving Rat
J Neurophysiol, February 1, 1997; 77(2): 571 - 578.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. Schacher, F. Wu, and Z.-Y. Sun
Pathway-Specific Synaptic Plasticity: Activity-Dependent Enhancement and Suppression of Long-Term Heterosynaptic Facilitation at Converging Inputs on a Single Target
J. Neurosci., January 15, 1997; 17(2): 597 - 606.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
J. Magee and D Johnston
Synaptic activation of voltage-gated channels in the dendrites of hippocampal pyramidal neurons
Science, April 14, 1995; 268(5208): 301 - 304.
[Abstract] [PDF]




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