WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience MBF Bioscience Autoneuron
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text
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 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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (47)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cook, P. B.
Right arrow Articles by McReynolds, J. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cook, P. B.
Right arrow Articles by McReynolds, J. S.

 Previous Article

The Journal of Neuroscience, March 15, 1998, 18(6):2301-2308

Action Potentials Are Required for the Lateral Transmission of Glycinergic Transient Inhibition in the Amphibian Retina

Paul B. Cook1, Peter D. Lukasiewicz2, and John S. McReynolds1

1 Department of Physiology, University of Michigan, Ann Arbor, Michigan 48109, and 2 Department of Ophthalmology and Visual Science, Washington University, St. Louis, Missouri 63110

Transient lateral inhibition (TLI), the suppression of responses of a ganglion cell to light stimuli in the receptive field center by changes in illumination in the receptive field surround, was studied in light-adapted mud puppy and tiger salamander retinas using both eyecup and retinal slice preparations. In the eyecup, TLI was measured in on-off ganglion cells as the ability of rotating, concentric windmill patterns of 500-1200 µm inner diameter to suppress the response to a small spot stimulus in the receptive field center. Both the suppression of the spot response and the hyperpolarization produced in ganglion cells by rotation of the windmill were blocked in the presence of 2 µM strychnine or 500 nM tetrodotoxin (TTX), but not by 150 µM picrotoxin. In the slice preparation in which GABA-mediated currents were blocked with picrotoxin, IPSCs elicited by diffuse illumination were blocked by strychnine and strongly reduced by TTX. The TTX-resistant component was probably attributable to illumination of the receptive field center. TTX had a much greater effect in reducing the glycinergic inhibition elicited by laterally displaced stimulation versus nearby focal electrical stimulation. Strychnine enhanced light-evoked excitatory currents in ganglion cells, but this was not mimicked by TTX. The results suggest that local glycinergic transient inhibition does not require action potentials and is mediated by synapses onto both ganglion cell dendrites and bipolar cell terminals. In contrast, the lateral spread of this inhibition (at least over distances >250 µm) requires action potentials and is mainly onto ganglion cell dendrites.

Key words: retina; ganglion cell; receptive field; lateral inhibition; glycine; action potentials


Copyright © 1998 Society for Neuroscience  0270-6474/98/1862301-08$05.00/0


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
K. A. Zaghloul, M. B. Manookin, B. G. Borghuis, K. Boahen, and J. B. Demb
Functional Circuitry for Peripheral Suppression in Mammalian Y-Type Retinal Ganglion Cells
J Neurophysiol, June 1, 2007; 97(6): 4327 - 4340.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. Ichinose and P. D. Lukasiewicz
Ambient Light Regulates Sodium Channel Activity to Dynamically Control Retinal Signaling
J. Neurosci., April 25, 2007; 27(17): 4756 - 4764.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. F. Miller, N. P. Staff, and T. J. Velte
Form and Function of ON-OFF Amacrine Cells in the Amphibian Retina
J Neurophysiol, May 1, 2006; 95(5): 3171 - 3190.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. K. Dhingra, M. A. Freed, and R. G. Smith
Voltage-Gated Sodium Channels Improve Contrast Sensitivity of a Retinal Ganglion Cell
J. Neurosci., August 31, 2005; 25(35): 8097 - 8103.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. Ichinose and P. D. Lukasiewicz
Inner and outer retinal pathways both contribute to surround inhibition of salamander ganglion cells
J. Physiol., June 1, 2005; 565(2): 517 - 535.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. Ichinose, C. R. Shields, and P. D. Lukasiewicz
Sodium Channels in Transient Retinal Bipolar Cells Enhance Visual Responses in Ganglion Cells
J. Neurosci., February 16, 2005; 25(7): 1856 - 1865.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. B. Demb, P. Sterling, and M. A. Freed
How Retinal Ganglion Cells Prevent Synaptic Noise From Reaching the Spike Output
J Neurophysiol, October 1, 2004; 92(4): 2510 - 2519.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. R. Shields and P. D. Lukasiewicz
Spike-Dependent GABA Inputs to Bipolar Cell Axon Terminals Contribute to Lateral Inhibition of Retinal Ganglion Cells
J Neurophysiol, May 1, 2003; 89(5): 2449 - 2458.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. Ichinose and P. D. Lukasiewicz
GABA Transporters Regulate Inhibition in the Retina by Limiting GABAC Receptor Activation
J. Neurosci., April 15, 2002; 22(8): 3285 - 3292.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Koizumi, S.-I. Watanabe, and A. Kaneko
Persistent Na+ Current and Ca2+ Current Boost Graded Depolarization of Rat Retinal Amacrine Cells in Culture
J Neurophysiol, August 1, 2001; 86(2): 1006 - 1016.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. L. Passaglia, C. Enroth-Cugell, and J. B. Troy
Effects of Remote Stimulation on the Mean Firing Rate of Cat Retinal Ganglion Cells
J. Neurosci., August 1, 2001; 21(15): 5794 - 5803.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. Flores-Herr, D. A. Protti, and H. Wassle
Synaptic Currents Generating the Inhibitory Surround of Ganglion Cells in the Mammalian Retina
J. Neurosci., July 1, 2001; 21(13): 4852 - 4863.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. D. Cohen
Light-Evoked Excitatory Synaptic Currents of X-Type Retinal Ganglion Cells
J Neurophysiol, June 1, 2000; 83(6): 3217 - 3229.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
B. Roska, E. Nemeth, L. Orzo, and F. S. Werblin
Three Levels of Lateral Inhibition: A Space-Time Study of the Retina of the Tiger Salamander
J. Neurosci., March 1, 2000; 20(5): 1941 - 1951.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. B. Cook, P. D. Lukasiewicz, and J. S. McReynolds
GABAC Receptors Control Adaptive Changes in a Glycinergic Inhibitory Pathway in Salamander Retina
J. Neurosci., January 15, 2000; 20(2): 806 - 812.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. C. Bieda and D. R. Copenhagen
Sodium Action Potentials Are Not Required for Light-Evoked Release of GABA or Glycine From Retinal Amacrine Cells
J Neurophysiol, June 1, 1999; 81(6): 3092 - 3095.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. H. Higgs and P. D. Lukasiewicz
Glutamate Uptake Limits Synaptic Excitation of Retinal Ganglion Cells
J. Neurosci., May 15, 1999; 19(10): 3691 - 3700.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. D. Cohen
Interactions of Inhibition and Excitation in the Light-Evoked Currents of X Type Retinal Ganglion Cells
J Neurophysiol, December 1, 1998; 80(6): 2975 - 2990.
[Abstract] [Full Text] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

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