JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 72: 402-420, 1994;
0022-3077/94 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Spear, P. D.
Right arrow Articles by Tumosa, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Spear, P. D.
Right arrow Articles by Tumosa, N.

Journal of Neurophysiology, Vol 72, Issue 1 402-420, Copyright © 1994 by APS


ARTICLES

Effects of aging on the primate visual system: spatial and temporal processing by lateral geniculate neurons in young adult and old rhesus monkeys

P. D. Spear, R. J. Moore, C. B. Kim, J. T. Xue and N. Tumosa
Department of Psychology, Wisconsin Regional Primate Research Center, Madison.

1. Visual abilities decline during normal aging, and many of these declines are due to neural changes in the retina or central visual pathways. We have begun studies of the primate visual system to investigate the location and nature of these changes as well as to answer general questions about the effects of aging on neural function. We began with the dorsal lateral geniculate nucleus (LGN) because it is the main structure through which visual information passes on the way to cortex and because the parallel parvocellular and magnocellular pathways, which may be affected differently by aging, are anatomically distinct there. 2. Single-cell recordings were made in the LGN of young adult (5-16 yr) and old (25-28 yr) rhesus monkeys. We made quantitative measures of a wide variety of response properties for a large number of parvocellular (n = 257) and magnocellular (n = 113) neurons in the two groups of animals. As a result, in addition to studying the effects of aging, we were able to make quantitative comparisons between parvocellular and magnocellular neurons using larger samples than have been studied previously and for some properties that have not been studied before. 3. We found that magnocellular neurons have significantly higher maximal response rates and signal-to-noise ratios than parvocellular neurons. However, response latencies to visual stimulation were similar for neurons in the two types of layers. In agreement with previous studies, magnocellular neurons had higher maximal contrast sensitivity and higher contrast gain than parvocellular neurons. However, the sensitivity difference occurred because nearly all of the neurons with low sensitivities (< 10) were in the parvocellular layers, not because neurons in the magnocellular layers had the highest sensitivities. 4. Neurons with the smallest receptive-field centers, the highest spatial-frequency resolutions, and the highest optimal spatial frequencies were found in the parvocellular layers. However, the overall distributions of each of these properties overlapped substantially for neurons in the two types of layers, and the mean values were not significantly different. The mean high temporal-frequency cutoff was significantly higher for magnocellular than parvocellular neurons, but the difference was small (only 3 Hz), and it occurred because many parvocellular neurons had lower cutoffs than any seen in the magnocellular layers, not because magnocellular neurons had the highest temporal-frequency cutoffs. Parvocellular neurons also had narrower temporal-frequency tuning than magnocellular neurons. However, there was no significant difference in optimal temporal frequency.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
BrainHome page
B. C. Skottun and J. Skoyles
A few remarks on assessing magnocellular sensitivity in Schizophrenic patients
Brain, November 1, 2007; 130(11): e83 - e83.
[Full Text] [PDF]


Home page
BrainHome page
P. D. Butler, A. Martinez, J. J. Foxe, D. Kim, V. Zemon, G. Silipo, J. Mahoney, M. Shpaner, M. Jalbrzikowskil, and D. C. Javitt
Reply: A few remarks on assessing magnocellular sensitivity in patients with schizophrenia
Brain, November 1, 2007; 130(11): e84 - e84.
[Full Text] [PDF]


Home page
IOVSHome page
A. M. McKendrick, G. P. Sampson, M. J. Walland, and D. R. Badcock
Contrast Sensitivity Changes Due to Glaucoma and Normal Aging: Low-Spatial-Frequency Losses in Both Magnocellular and Parvocellular Pathways
Invest. Ophthalmol. Vis. Sci., May 1, 2007; 48(5): 2115 - 2122.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. B Saul, P. L Carras, and A. L Humphrey
Temporal Properties of Inputs to Direction-Selective Neurons in Monkey V1
J Neurophysiol, July 1, 2005; 94(1): 282 - 294.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
Y. Wang, Y. Zhou, Y. Ma, and A. G. Leventhal
Degradation of Signal Timing in Cortical Areas V1 and V2 of Senescent Monkeys
Cereb Cortex, April 1, 2005; 15(4): 403 - 408.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
W. Bair and J. A. Movshon
Adaptive Temporal Integration of Motion in Direction-Selective Neurons in Macaque Visual Cortex
J. Neurosci., August 18, 2004; 24(33): 7305 - 7323.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. C. Reid and R. M. Shapley
Space and Time Maps of Cone Photoreceptor Signals in Macaque Lateral Geniculate Nucleus
J. Neurosci., July 15, 2002; 22(14): 6158 - 6175.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. B. Levitt, R. A. Schumer, S. M. Sherman, P. D. Spear, and J. A. Movshon
Visual Response Properties of Neurons in the LGN of Normally Reared and Visually Deprived Macaque Monkeys
J Neurophysiol, May 1, 2001; 85(5): 2111 - 2129.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. P. O'Keefe, J. B. Levitt, D. C. Kiper, R. M. Shapley, and J. A. Movshon
Functional Organization of Owl Monkey Lateral Geniculate Nucleus and Visual Cortex
J Neurophysiol, August 1, 1998; 80(2): 594 - 609.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online