J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 506, Number 3, 731-744, February 1, 1998
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 Maple, B. R.
Right arrow Articles by Wu, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Maple, B. R.
Right arrow Articles by Wu, S. M.
The Journal of Physiology (1998), 506.3, pp. 731-744
© Copyright 1998 The Physiological Society

Glycinergic synaptic inputs to bipolar cells in the salamander retina

Bruce R. Maple and Samuel M. Wu

Cullen Eye Institute, Baylor College of Medicine, Houston, TX 77030, USA

  1. Glycine activated strychnine-sensitive chloride conductances at both the dendrites and the axonal telodendria of most bipolar cells in the salamander retina.

  2. The chloride equilibrium potential of bipolar cells was found to be negative to -50 mV, indicating that glycinergic synapses on bipolar cells are inhibitory.

  3. Some bipolar cells exhibited discrete, strychnine-sensitive, chloride-mediated inhibitory postsynaptic currents (IPSCs). These were elicited by focal application of glutamate at the inner plexiform layer (IPL). Glycinergic synapses were localized using simultaneous focal application of calcium to retinal slices bathed in calcium-free media. Both dendritic and telodendritic glycinergic IPSCs were observed.

  4. The decay of the telodendritic IPSCs was well fitted by a single exponential with a time constant of 17·7 ± 8·7 ms. Similar kinetics were observed for dendritic IPSCs in some cells, but in one class of on-centre bipolar cell the decay of the dendritic IPSCs was better fitted by a sum of two exponentials with time constants 9·9 ± 4·3 and 51·3 ± 24·3 ms.

  5. The dendritic IPSCs were best driven by application of glutamate at the distal IPL (the off sublamina), while the telodendritic IPSCs were driven best by application near the telodendria. These results suggest that bipolar cell dendrites receive inhibitory glycinergic inputs from interplexiform cells that are excited by off-centre bipolar cells, whereas bipolar cell telodendria receive glycinergic amacrine cell inputs that are antagonistic to the photoreceptor inputs.

  6. Both inputs could be elicited in the presence of tetrodotoxin (TTX), but the dendritic IPSCs were sometimes abolished by TTX, suggesting that sodium-dependent spikes play an important role in the transmission of interplexiform cell signals to the outer plexiform layer.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
M. Greschner, A. Thiel, J. Kretzberg, and J. Ammermuller
Complex Spike-Event Pattern of Transient ON-OFF Retinal Ganglion Cells
J Neurophysiol, December 1, 2006; 96(6): 2845 - 2856.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
E. D. Eggers and P. D. Lukasiewicz
GABAA, GABAC and glycine receptor-mediated inhibition differentially affects light-evoked signalling from mouse retinal rod bipolar cells
J. Physiol., April 1, 2006; 572(1): 215 - 225.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
W. Shen
Repetitive Light Stimulation Inducing Glycine Receptor Plasticity in the Retinal Neurons
J Neurophysiol, September 1, 2005; 94(3): 2231 - 2238.
[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. Physiol.Home page
J.-J. Pang, F. Gao, and S. M. Wu
Stratum-by-stratum projection of light response attributes by retinal bipolar cells of Ambystoma
J. Physiol., July 1, 2004; 558(1): 249 - 262.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
F. Rieke
Temporal Contrast Adaptation in Salamander Bipolar Cells
J. Neurosci., December 1, 2001; 21(23): 9445 - 9454.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
G. B. Awatramani and M. M. Slaughter
Origin of Transient and Sustained Responses in Ganglion Cells of the Retina
J. Neurosci., September 15, 2000; 20(18): 7087 - 7095.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. M. Wu, F. Gao, and B. R. Maple
Functional Architecture of Synapses in the Inner Retina: Segregation of Visual Signals by Stratification of Bipolar Cell Axon Terminals
J. Neurosci., June 15, 2000; 20(12): 4462 - 4470.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
F. Gao, B. R. Maple, and S. M. Wu
I4AA-Sensitive Chloride Current Contributes to the Center Light Responses of Bipolar Cells in the Tiger Salamander Retina
J Neurophysiol, June 1, 2000; 83(6): 3473 - 3482.
[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. Neurophysiol.Home page
F. Gao and S. M. Wu
Characterization of Spontaneous Inhibitory Synaptic Currents in Salamander Retinal Ganglion Cells
J Neurophysiol, October 1, 1998; 80(4): 1752 - 1764.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. B. Cook, P. D. Lukasiewicz, and J. S. McReynolds
Action Potentials Are Required for the Lateral Transmission of Glycinergic Transient Inhibition in the Amphibian Retina
J. Neurosci., March 15, 1998; 18(6): 2301 - 2308.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1998 The Physiological Society.