In the vertebrate retina, two distinct lateral inhibitory mechanisms contribute to the shaping of ganglion cell responses and their receptive field organization. Sustained lateral inhibition is activated by steady illumination and transient lateral inhibition by stimuli that are changing in intensity or are moving. These lateral inhibitory mechanisms are mediated by separate synaptic pathways in the retina. Both mechanisms undergo significant, but different, changes between light- and dark- adapted conditions. The proposed research will investigate the synaptic pathways involved in each of these two lateral inhibitory mechanisms and how they are modulated during changes in the state of adaptation. Intracellular recordings will be made from ganglion cells in intact retinas in superfused eyecup preparations from the tiger salamander, a well-studied animal model of the vertebrate retina. Ganglion cell responses to illumination of different parts of the receptive field with various stationary and moving light stimuli will be made under different conditions of adaptations. Pharmacological treatments with agonists and antagonists to specific neurotransmitters, drugs which block action potential generation, and putative neuromodulator substances will be used to dissect the contributions of different synaptic pathways to components are modulated by light adaptation. These studies should contribute to our understanding of visual information processing in the retina and how the synaptic pathways are modulated during light and dark adaptation to optimize the output of retinal ganglion cells for differing visual conditions.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY001653-25
Application #
6476289
Study Section
Visual Sciences C Study Section (VISC)
Program Officer
Hunter, Chyren
Project Start
1979-05-01
Project End
2003-11-30
Budget Start
2001-12-01
Budget End
2003-11-30
Support Year
25
Fiscal Year
2002
Total Cost
$257,846
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Physiology
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Cook, P B; Lukasiewicz, P D; McReynolds, J S (2000) GABA(C) receptors control adaptive changes in a glycinergic inhibitory pathway in salamander retina. J Neurosci 20:806-12
Cook, P B; Lukasiewicz, P D; McReynolds, J S (1998) Action potentials are required for the lateral transmission of glycinergic transient inhibition in the amphibian retina. J Neurosci 18:2301-8
Ball, A K; McReynolds, J S (1998) Localization of gap junctions and tracer coupling in retinal Muller cells. J Comp Neurol 393:48-57
Cook, P B; McReynolds, J S (1998) Lateral inhibition in the inner retina is important for spatial tuning of ganglion cells. Nat Neurosci 1:714-9
Cook, P B; McReynolds, J S (1998) Modulation of sustained and transient lateral inhibitory mechanisms in the mudpuppy retina during light adaptation. J Neurophysiol 79:197-204
Myhr, K L; McReynolds, J S (1996) Cholinergic modulation of dopamine release and horizontal cell coupling in mudpuppy retina. Vision Res 36:3933-8
Myhr, K L; Dong, C J; McReynolds, J S (1994) Cones contribute to light-evoked, dopamine-mediated uncoupling of horizontal cells in the mudpuppy retina. J Neurophysiol 72:56-62
Dong, C J; McReynolds, J S (1992) Comparison of the effects of flickering and steady light on dopamine release and horizontal cell coupling in the mudpuppy retina. J Neurophysiol 67:364-72
Dong, C J; McReynolds, J S (1992) An intensity-dependent biphasic neuron in mudpuppy retina. Vision Res 32:1405-8
Akopian, A; McReynolds, J; Weiler, R (1991) Short-term potentiation of off-responses in turtle horizontal cells. Brain Res 546:132-8

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