Much of the power of the retina to process and package information is derived from the properties of retinal synapses. It is known, from anatomical studies, that retinal synapses have structural features suggesting they work differently from more familiar synapses elsewhere in the nervous system. Presently though, the physiology of retinal synapses is very imperfectly understood. This proposal describes electrophysiological experiments to investigate the normal working of retinal synapses, concentrating in particular, on the first synapse of the visual system: the synapse between photoreceptors and bipolar cells. Four sets of questions are addressed here, each of which is a continuation of our present work. A first set of questions concerns the properties of channels, on bipolar cells, that are opened by the photoreceptor transmitter, glutamate. We have recently discovered that these channels have some unorthodox and surprising properties that we intend to examine in more detail. A second set of questions is concerned with the presynaptic mechanisms involved in the release of transmitter from photoreceptors. To tackle these questions we have developed the sparse culture of chick retinal cells as a preparation that avoids the technical problems associated with the intact retina. The third group of questions centers on the role of the peptide, somatostatin, in the outer retina. This peptide, which in the amphibian retina is probably the neurotransmitter of an interplexiform cell, has been shown to have diverse, modulatory actions in other parts of the nervous system. We propose to describe somatostatin's effects in the intact retina and uncover the underlying mechanisms by examining isolated retinal neurons. Lastly, we want to find out more about two important membrane currents found in chick cone cells. One of these currents is the calcium current involved in transmitter release.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004112-11
Application #
3258596
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1982-04-01
Project End
1996-09-29
Budget Start
1992-09-30
Budget End
1993-09-29
Support Year
11
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Wilson, Martin; Nacsa, Nick; Hart, Nathan S et al. (2011) Regional distribution of nitrergic neurons in the inner retina of the chicken. Vis Neurosci 28:205-20
Wilson, Martin; Lindstrom, Sarah H (2011) What the bird's brain tells the bird's eye: the function of descending input to the avian retina. Vis Neurosci 28:337-50
Lindstrom, Sarah H; Azizi, Nason; Weller, Cynthia et al. (2010) Retinal input to efferent target amacrine cells in the avian retina. Vis Neurosci 27:103-18
Lindstrom, S H; Nacsa, N; Blankenship, T et al. (2009) Distribution and structure of efferent synapses in the chicken retina. Vis Neurosci 26:215-26
Weller, Cynthia; Lindstrom, Sarah H; De Grip, Willem J et al. (2009) The area centralis in the chicken retina contains efferent target amacrine cells. Vis Neurosci 26:249-54
Borges, Salvador; Lindstrom, Sarah; Walters, Cameron et al. (2008) Discrete influx events refill depleted Ca2+ stores in a chick retinal neuron. J Physiol 586:605-26
Warrier, Ajithkumar; Wilson, Martin (2007) Endocannabinoid signaling regulates spontaneous transmitter release from embryonic retinal amacrine cells. Vis Neurosci 24:25-35
Green, Daniel G; Kapousta-Bruneau, Natalia V (2007) Evidence that L-AP5 and D,L-AP4 can preferentially block cone signals in the rat retina. Vis Neurosci 24:9-15
Warrier, Ajithkumar; Borges, Salvador; Dalcino, David et al. (2005) Calcium from internal stores triggers GABA release from retinal amacrine cells. J Neurophysiol 94:4196-208
Hurtado, Jose; Borges, Salvador; Wilson, Martin (2002) Na(+)-Ca(2+) exchanger controls the gain of the Ca(2+) amplifier in the dendrites of amacrine cells. J Neurophysiol 88:2765-77

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