spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Bastian, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bastian, J.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Journal of Experimental Biology, Vol 202, Issue 10 1327-1337, Copyright © 1999 by Company of Biologists


JOURNAL ARTICLES

Plasticity of feedback inputs in the apteronotid electrosensory system

J Bastian
Department of Zoology, University of Oklahoma, Norman, OK 73019, USA. jbastian@ou.edu

Weakly electric fish generate an electric field surrounding their body by means of an electric organ typically located within the trunk and tail. Electroreceptors scattered over the surface of the body encode the amplitude and timing of the electric organ discharge (EOD), and central components of the electrosensory system analyze the information provided by the electroreceptor afferents. The electrosensory system is used for electrolocation, for the detection and analysis of objects near the fish which distort the EOD and for electrocommunication. Since the electric organ is typically located in the tail, any movement of this structure relative to the rest of the body alters the EOD field, resulting in large changes in receptor afferent activity. The amplitude of these reafferent stimuli can exceed the amplitudes of near-threshold electrolocation signals by several orders of magnitude. This review summarizes recent studies of the South American weakly electric fish Apteronotus leptorhynchus aimed at determining how the animals differentiate self-generated or reafferent electrosensory stimuli from those that are more behaviorally relevant. Cells within the earliest stages of central electrosensory processing utilize an adaptive filtering technique which allows the system preferentially to attenuate reafferent as well as other predictable patterns of sensory input without degrading responses to more novel stimuli. Synaptic plasticity within the system underlies the adaptive component of the filter and enables the system to learn to reject new stimulus patterns if these become predictable. A Ca2+-mediated form of postsynaptic depression contributes to this synaptic plasticity. The filter mechanism seen in A. leptorhynchus is surprisingly similar to adaptive filters described previously in mormyrid weakly electric fish and in elasmobranchs, suggesting that this mechanism may be a common feature of sensory processing systems.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
Z. Zhang and D. Bodznick
Plasticity in a cerebellar-like structure: suppressing reafference during episodic behaviors
J. Exp. Biol., December 1, 2008; 211(23): 3720 - 3728.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. J. Chacron and J. Bastian
Population Coding by Electrosensory Neurons
J Neurophysiol, April 1, 2008; 99(4): 1825 - 1835.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. E. Lewis, B. Lindner, B. Laliberte, and S. Groothuis
Control of neuronal firing by dynamic parallel fiber feedback: implications for electrosensory reafference suppression
J. Exp. Biol., December 15, 2007; 210(24): 4437 - 4447.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
W. H. Mehaffey, F. R. Fernandez, L. Maler, and R. W. Turner
Regulation of Burst Dynamics Improves Differential Encoding of Stimulus Frequency by Spike Train Segregation
J Neurophysiol, August 1, 2007; 98(2): 939 - 951.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. J. Chacron, L. Maler, and J. Bastian
Feedback and Feedforward Control of Frequency Tuning to Naturalistic Stimuli
J. Neurosci., June 8, 2005; 25(23): 5521 - 5532.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. E. Lewis and L. Maler
Synaptic Dynamics on Different Time Scales in a Parallel Fiber Feedback Pathway of the Weakly Electric Fish
J Neurophysiol, February 1, 2004; 91(2): 1064 - 1070.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
A. A. Caputi, P. A. Aguilera, and M. E. Castello
Probability and amplitude of novelty responses as a function of the change in contrast of the reafferent image in G. carapo
J. Exp. Biol., March 15, 2003; 206(6): 999 - 1010.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. Harvey-Girard and R. J. Dunn
Excitatory Amino Acid Receptors of the Electrosensory System: The NR1/NR2B N-Methyl-D-Aspartate Receptor
J Neurophysiol, February 1, 2003; 89(2): 822 - 832.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. Doiron, L. Noonan, N. Lemon, and R. W. Turner
Persistent Na+ Current Modifies Burst Discharge By Regulating Conditional Backpropagation of Dendritic Spikes
J Neurophysiol, January 1, 2003; 89(1): 324 - 337.
[Abstract] [Full Text] [PDF]


Home page
Biol. Bull.Home page
J. Montgomery, G. Carton, and D. Bodznick
Error-Driven Motor Learning in Fish
Biol. Bull., October 1, 2002; 203(2): 238 - 239.
[Full Text] [PDF]


Home page
J. Neurosci.Home page
J. Bastian, M. J. Chacron, and L. Maler
Receptive Field Organization Determines Pyramidal Cell Stimulus-Encoding Capability and Spatial Stimulus Selectivity
J. Neurosci., June 1, 2002; 22(11): 4577 - 4590.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A.-M. M. Oswald, J. E. Lewis, and L. Maler
Dynamically Interacting Processes Underlie Synaptic Plasticity in a Feedback Pathway
J Neurophysiol, May 1, 2002; 87(5): 2450 - 2463.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
N. Berman, R. J. Dunn, and L. Maler
Function of NMDA Receptors and Persistent Sodium Channels in a Feedback Pathway of the Electrosensory System
J Neurophysiol, October 1, 2001; 86(4): 1612 - 1621.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
M. MacIver, N. Sharabash, and M. Nelson
Prey-capture behavior in gymnotid electric fish: motion analysis and effects of water conductivity
J. Exp. Biol., January 2, 2001; 204(3): 543 - 557.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
J. Bastian and J. Nguyenkim
Dendritic Modulation of Burst-Like Firing in Sensory Neurons
J Neurophysiol, January 1, 2001; 85(1): 10 - 22.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
R. Turner and L Maler
Oscillatory and burst discharge in the apteronotid electrosensory lateral line lobe
J. Exp. Biol., January 5, 1999; 202(10): 1255 - 1265.
[Abstract] [PDF]




© The Company of Biologists Ltd 1999