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


     


J Neurophysiol 48: 968-980, 1982;
0022-3077/82 $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 Balkema, G. W.
Right arrow Articles by Pinto, L. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Balkema, G. W., Jr
Right arrow Articles by Pinto, L. H.

Journal of Neurophysiology, Vol 48, Issue 4 968-980, Copyright © 1982 by APS


ARTICLES

Electrophysiology of retinal ganglion cells in the mouse: a study of a normally pigmented mouse and a congenic hypopigmentation mutant, pearl

G. W. Balkema Jr and L. H. Pinto

1. The organization of the receptive fields of retinal ganglion cells in te normal mouse was studied qualitatively in recordings from 43 single axons in the optic nerve and optic tract, and the light sensitivity was studied quantitatively in 26 of these cells by measuring incremental sensitivity. 2. The receptive fields of normal animals were elliptical, had concentric center and peripheral subdivisions, and had an antagonistic center/surround organization; the receptive-field centers ranged from 1.95 to 83 degrees in diameter, with a median of 7 degrees. 3. The incremental sensitivity to white light was measured using a criterion response of 10 extra spikes; the most sensitive dark-adapted cell required a stimulus luminance of 3.5 x 10(-3) cd/m2 to generate a criterion response. 4. The action spectrum measured at seven different wavelengths (433-619 nm) from ganglion cells in the normally pigmented mouse resembled the CIE (International Commission on Illumination, CIE 1957 (11)) relative scotopic luminous efficiency function (41) and is consistent with a curve having a peak around 500 nm. 5. On light adaptation with blue light (less than 460 nm), the sensitivity to longer wavelength stimuli increased by 0.2-0.5 log units relative to the sensitivity to the shorter wavelengths; these results are compatible with the presence of a photoreceptor sensitive to long wavelengths in the normally pigmented mouse (C57BL/6J+/+). 6. The organization of the receptive fields of 48 retinal ganglion cells from the hypopigmentation mutant pearl (C57BL/6J-pe) was also studied qualitatively; the receptive field organization was similar to that of the normally pigmented mouse. 7. In 25 cells from dark-adapted pearl mice, the incremental sensitivity to white light was, on the average, 1.6 log units less than that for normal mice. 8. The dark-adapted action spectrum of pearl mice was similar to that of normally pigmented mice. However, a shift in sensitivity to longer wavelengths did not occur on selective light adaptation with the most luminous blue light (less than 460 nm) background that we could produce. 9. We conclude that pearl is one of the mammalian genes that codes for functions that affect dark-adapted retinal sensitivity. The results of this study and past studies suggest that the pearl gene's action on light sensitivity is predominantly within the retina and before (distal to) the ganglion cells.


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
S. F. Stasheff
Emergence of Sustained Spontaneous Hyperactivity and Temporary Preservation of OFF Responses in Ganglion Cells of the Retinal Degeneration (rd1) Mouse
J Neurophysiol, March 1, 2008; 99(3): 1408 - 1421.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. G. Gregg, M. Kamermans, J. Klooster, P. D. Lukasiewicz, N. S. Peachey, K. A. Vessey, and M. A. McCall
Nyctalopin Expression in Retinal Bipolar Cells Restores Visual Function in a Mouse Model of Complete X-Linked Congenital Stationary Night Blindness
J Neurophysiol, November 1, 2007; 98(5): 3023 - 3033.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
S. Augustinaite and P. Heggelund
Changes in firing pattern of lateral geniculate neurons caused by membrane potential dependent modulation of retinal input through NMDA receptors
J. Physiol., July 1, 2007; 582(1): 297 - 315.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
V. Porciatti, M. Saleh, and M. Nagaraju
The Pattern Electroretinogram as a Tool to Monitor Progressive Retinal Ganglion Cell Dysfunction in the DBA/2J Mouse Model of Glaucoma
Invest. Ophthalmol. Vis. Sci., February 1, 2007; 48(2): 745 - 751.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
B. Volgyi, M. R. Deans, D. L. Paul, and S. A. Bloomfield
Convergence and Segregation of the Multiple Rod Pathways in Mammalian Retina
J. Neurosci., December 8, 2004; 24(49): 11182 - 11192.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. S. Grubb and I. D. Thompson
Quantitative Characterization of Visual Response Properties in the Mouse Dorsal Lateral Geniculate Nucleus
J Neurophysiol, December 1, 2003; 90(6): 3594 - 3607.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
S. M. Carcieri, A. L. Jacobs, and S. Nirenberg
Classification of Retinal Ganglion Cells: A Statistical Approach
J Neurophysiol, September 1, 2003; 90(3): 1704 - 1713.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
G. H. Jacobs, J. C. Fenwick, J. B. Calderone, and S. S. Deeb
Human Cone Pigment Expressed in Transgenic Mice Yields Altered Vision
J. Neurosci., April 15, 1999; 19(8): 3258 - 3265.
[Abstract] [Full Text] [PDF]




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