We propose to explore two novel metabotropic G-protein coupled receptors (GPCRs): one that is sensitive to sweet taste ligands and another that is activated by glycine. GPCRs represent a diverse family of proteins involved in neuronal function. The importance of GPCRs in retina is obvious because a pair of these receptors are responsible for phototransduction (rhodopsin) and for the formation of ON responses (mGluR6) throughout the visual pathway. Furthermore, two of the primary retinal neurotransmitters, GABA and glutamate, activate GPCRs throughout the neural retina. We found two taste receptor proteins in rat retina that are identical to those in the tongue. Unlike the tongue, a key third protein subunit is missing in retina. Surprisingly, the two subunits that are present are sufficient to detect sweet tastants, they detect some sweet tastants not detected in rat tongue, and they are more sensitive to sweet tastants than the tongue. We propose to test the hypothesis that retinal neurons possess a novel system that responds to extracellular glucose and that this system can influence synaptic transmission. Taste receptors may be important in normal retinal function and in diabetes. We have also recently found evidence for a metabotropic glycine receptor in retina. This is the first evidence that glycine activates metabotropic as well as ionotropic receptors. Since glycine is one of the three major neurotransmitter systems in retina, we will test the hypotheses that glycine regulates bipolar and amacrine cell outputs and acts in opposition to GABA activated metabotropic receptors.

Public Health Relevance

This grant proposal will address the function of novel "sweet taste receptors" in retina. We hypothesize that these newly discovered receptors can influence how the normal retina functions and how that might change in diabetic conditions. We will also explore a new glycine receptor that controls inhibition in the retina.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005725-29
Application #
8304870
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Greenwell, Thomas
Project Start
1984-08-01
Project End
2014-08-31
Budget Start
2012-09-01
Budget End
2014-08-31
Support Year
29
Fiscal Year
2012
Total Cost
$372,377
Indirect Cost
$132,377
Name
State University of New York at Buffalo
Department
Physiology
Type
Schools of Medicine
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
Sethuramanujam, Santhosh; Slaughter, Malcolm M (2014) Disinhibitory recruitment of NMDA receptor pathways in retina. J Neurophysiol 112:193-203
Duan, Lei; Yang, Jaeyoung; Slaughter, Malcolm M (2009) Caffeine inhibition of ionotropic glycine receptors. J Physiol 587:4063-75
Frolov, R V; Slaughter, M M; Singh, S (2008) Effects of celecoxib on ionic currents and spontaneous firing in rat retinal neurons. Neuroscience 154:1525-32
Shen, W; Slaughter, M M (2001) Multireceptor GABAergic regulation of synaptic communication in amphibian retina. J Physiol 530:55-67
Tian, N; Slaughter, M M (1994) Pharmacological similarity between the retinal APB receptor and the family of metabotropic glutamate receptors. J Neurophysiol 71:2258-68
Tian, N; Slaughter, M M (1994) Pharmacology of the GABAB receptor in amphibian retina. Brain Res 660:267-74
Gurevich, L; Slaughter, M M (1993) Comparison of the waveforms of the ON bipolar neuron and the b-wave of the electroretinogram. Vision Res 33:2431-5
Bai, S H; Slaughter, M M (1989) Effects of baclofen on transient neurons in the mudpuppy retina: electrogenic and network actions. J Neurophysiol 61:382-90
Slaughter, M M; Bai, S H (1989) Differential effects of baclofen on sustained and transient cells in the mudpuppy retina. J Neurophysiol 61:374-81
Stockton, R A; Slaughter, M M (1989) B-wave of the electroretinogram. A reflection of ON bipolar cell activity. J Gen Physiol 93:101-22

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