Maximum preservation of visual function is the main goal of glaucoma research. A patient cares little about his or her intraocular pressure or optic disc topography so long as their sight is normal. It may thus seem surprising that virtually nothing in known about the effect of glaucoma on the physiological properties of retinal ganglion cells, the very cells that provide the brain with visual input and that are targeted by the disease. The objective of the research project in to fill this important gap in our understanding of glaucoma. The research project proposes to do so by recording in vivo the visually-evoked activity of single optic tract fibers in the rat model of pressure-induced glaucoma and putting directly to test the hypothesis that the functional characteristics of retinal ganglion cells change in chronically hypertensive eyes before the cells die.
The specific aims are to quantitatively characterize: 1) the spatiotemporal response properties of ganglion cells in normal rats and 2) the spatiotemporal response properties of ganglion cells in rats with chronic ocular hypertension. ? ? One possible outcome of the research is that glaucoma has no ill effects on ganglion cell physiology. For all intensive purposes the cells behave normally up until the moment they receive the apoptotic signal to die. This would dampen the prospects of using non-invasive methods, like vision tests and electroretinograms, for glaucoma detection since cells would invariably have to die for these methods to detect the disease. The other possible outcome is that ocular hypertension alters the mean spike rate, receptive field size, or other response properties of surviving ganglion cells. The physiological effects might be confined to certain types of ganglion cell or shared by them all. This outcome would not only paint a more promising picture for early glaucoma detection but also suggest the kinds of vision test that would best reveal perceptual deficits, which would thereby help speed progress in the fight against the debilitating disease. ? ? Public Health: Glaucoma is an eye disease that kills the cells that provide visual input to the brain.
The aim of this research is determine how glaucoma affects the neural messages of these cells while the cells are still alive. This information could be used to design novel vision tests that detect the disease at an early stage. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY016849-01A1
Application #
7145349
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Liberman, Ellen S
Project Start
2006-09-30
Project End
2010-08-31
Budget Start
2006-09-30
Budget End
2007-08-31
Support Year
1
Fiscal Year
2006
Total Cost
$243,750
Indirect Cost
Name
Boston University
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
049435266
City
Boston
State
MA
Country
United States
Zip Code
02215
Heine, Walter F; Passaglia, Christopher L (2011) Spatial receptive field properties of rat retinal ganglion cells. Vis Neurosci 28:403-17
Freeman, Daniel K; GraƱa, Gilberto; Passaglia, Christopher L (2010) Retinal ganglion cell adaptation to small luminance fluctuations. J Neurophysiol 104:704-12
Passaglia, Christopher L; Freeman, Daniel K; Troy, John B (2009) Effects of remote stimulation on the modulated activity of cat retinal ganglion cells. J Neurosci 29:2467-76
Freeman, Daniel K; Heine, Walter F; Passaglia, Christopher L (2008) The maintained discharge of rat retinal ganglion cells. Vis Neurosci 25:535-48