Abstract
Both the "on" and the "on-off" ganglion cells in the mudpuppy retina generate graded responses over a narrow range of log test intensities. Sustained full field or surround backgrounds change the range of center log test intensities that elicits the graded response for both cell types. The on-off, but not the on ganglion cells are further affected by moving or flashing surround backgrounds. These cells are hyperpolarized, threshold is elevated, and the entire graded range of response is elicited by a higher range of log center test intensities. Depolarizing activity is elicited in amacrine cells by moving backgrounds that affect the on-off ganglion cells, but bipolar activity is unaffected. These results suggest that the amacrine cells at the inner plexiform layer mediate a third stage of sensitivity control in the retina, increasing threshold for response to change specifically in the on-off ganglion cells.
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Selected References
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- Ames A., 3rd, Pollen D. A. Neurotransmission in central nervous tissue: a study of isolated rabbit retina. J Neurophysiol. 1969 May;32(3):424–442. doi: 10.1152/jn.1969.32.3.424. [DOI] [PubMed] [Google Scholar]
- Barlow H. B., Levick W. R. The mechanism of directionally selective units in rabbit's retina. J Physiol. 1965 Jun;178(3):477–504. doi: 10.1113/jphysiol.1965.sp007638. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cleland B. G., Dubin M. W., Levick W. R. Sustained and transient neurones in the cat's retina and lateral geniculate nucleus. J Physiol. 1971 Sep;217(2):473–496. doi: 10.1113/jphysiol.1971.sp009581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dowling J. E., Werblin F. S. Organization of retina of the mudpuppy, Necturus maculosus. I. Synaptic structure. J Neurophysiol. 1969 May;32(3):315–338. doi: 10.1152/jn.1969.32.3.315. [DOI] [PubMed] [Google Scholar]
- Dubin M. W. The inner plexiform layer of the vertebrate retina: a quantitative and comparative electron microscopic analysis. J Comp Neurol. 1970 Dec;140(4):479–505. doi: 10.1002/cne.901400406. [DOI] [PubMed] [Google Scholar]
- Enroth-Cugell C., Robson J. G. The contrast sensitivity of retinal ganglion cells of the cat. J Physiol. 1966 Dec;187(3):517–552. doi: 10.1113/jphysiol.1966.sp008107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KUFFLER S. W., EYZAGUIRRE C. Synaptic inhibition in an isolated nerve cell. J Gen Physiol. 1955 Sep 20;39(1):155–184. doi: 10.1085/jgp.39.1.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LEVICK W. R., OYSTER C. W., DAVIS D. L. EVIDENCE THAT MCILWAIN'S PERIPHERY EFFECT IS NOT A STRAY LIGHT ARTIFACT. J Neurophysiol. 1965 May;28:555–559. doi: 10.1152/jn.1965.28.3.555. [DOI] [PubMed] [Google Scholar]
- MATURANA H. R., FRENK S. DIRECTIONAL MOVEMENT AND HORIZONTAL EDGE DETECTORS IN THE PIGEON RETINA. Science. 1963 Nov 15;142(3594):977–979. doi: 10.1126/science.142.3594.977. [DOI] [PubMed] [Google Scholar]
- MATURANA H. R., LETTVIN J. Y., MCCULLOCH W. S., PITTS W. H. Anatomy and physiology of vision in the frog (Rana pipiens). J Gen Physiol. 1960 Jul;43(6):129–175. doi: 10.1085/jgp.43.6.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MCILWAIN J. T. RECEPTIVE FIELDS OF OPTIC TRACT AXONS AND LATERAL GENICULATE CELLS: PERIPHERAL EXTENT AND BARBITURATE SENSITIVITY. J Neurophysiol. 1964 Nov;27:1154–1173. doi: 10.1152/jn.1964.27.6.1154. [DOI] [PubMed] [Google Scholar]
- Matsumoto N., Naka K. I. Identification of intracellular responses in the frog retina. Brain Res. 1972 Jul 13;42(1):59–71. doi: 10.1016/0006-8993(72)90042-x. [DOI] [PubMed] [Google Scholar]
- Michael C. R. Receptive fields of single optic nerve fibers in a mammal with an all-cone retina. I: contrast-sensitive units. J Neurophysiol. 1968 Mar;31(2):249–256. doi: 10.1152/jn.1968.31.2.249. [DOI] [PubMed] [Google Scholar]
- Saito H. A., Shimahara T., Fukada Y. Four types of responses to light and dark spot stimuli in the cat optic nerve. Tohoku J Exp Med. 1970 Oct;102(2):127–133. doi: 10.1620/tjem.102.127. [DOI] [PubMed] [Google Scholar]
- Teller D. Y., Matter C., Phillips W. D., Alexander K. Sensitization by annular surrounds: sensitization and masking. Vision Res. 1971 Dec;11(12):1445–1458. doi: 10.1016/0042-6989(71)90065-4. [DOI] [PubMed] [Google Scholar]
- Werblin F. S., Dowling J. E. Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. J Neurophysiol. 1969 May;32(3):339–355. doi: 10.1152/jn.1969.32.3.339. [DOI] [PubMed] [Google Scholar]
- Werblin F. S. Lateral interactions at inner plexiform layer of vertebrate retina: antagonistic responses to change. Science. 1972 Mar 3;175(4025):1008–1010. doi: 10.1126/science.175.4025.1008. [DOI] [PubMed] [Google Scholar]
- Werblin F. S. Response of retinal cells to moving spots: intracellular recording in Necturus maculosus. J Neurophysiol. 1970 May;33(3):342–350. doi: 10.1152/jn.1970.33.3.342. [DOI] [PubMed] [Google Scholar]
- West R. W., Dowling J. E. Synapses onto different morphological types of retinal ganglion cells. Science. 1972 Nov 3;178(4060):510–512. doi: 10.1126/science.178.4060.510. [DOI] [PubMed] [Google Scholar]