Abstract
1. We recorded with one electrode action potentials of single principal cells in the lateral geniculate nucleus (l.g.n.) of cats and monkeys, together with their retinal inputs, recorded as synaptic potentials (S potentials; Bishop, Burke & Davis, 1958; Cleland, Dubin & Levick, 1971; Kaplan & Shapley, 1984). 2. We studied the effect of stimulus contrast on the transmission of visual information from the retina to the l.g.n., compared the spontaneous discharge of l.g.n. cells with that of their retinal inputs, and studied the driven (modulated) and maintained (unmodulated) discharge of l.g.n. neurones and their retinal drives. 3. The spontaneous discharge of l.g.n. cells was considerably lower than that of their retinal drives. 4. The maintained (unmodulated) discharge of l.g.n. cells during stimulation was lower than that of their retinal drives, and was largely unaffected by the stimulus contrast. 5. The responses of both the retinal input and l.g.n. cells increased with contrast, but at different rates: a given increment of contrast caused a larger increment of response in the retinal input than in the l.g.n. target cells. 6. The transmission ratio (l.g.n. response/retinal response) for most cells depended upon the stimulus contrast. This dependence indicates the presence of a non-linear contrast gain control. 7. The amount by which the l.g.n. attenuated the retinal input depended upon the temporal frequency, and, to a lesser extent, upon the spatial frequency of the stimulus. 8. The effect of contrast on signal transmission between the retina and l.g.n. was essentially the same in the macaque monkey as in the cat. 9. The attenuation of the retinal input by the l.g.n. contrast gain control could serve to prevent saturation and extend the dynamic range of cortical units, which probably receive input from several l.g.n. units.
Full text
PDF





















Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ahlsén G., Lindström S., Lo F. S. Inhibition from the brain stem of inhibitory interneurones of the cat's dorsal lateral geniculate nucleus. J Physiol. 1984 Feb;347:593–609. doi: 10.1113/jphysiol.1984.sp015085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ahlsén G., Lindström S., Lo F. S. Interaction between inhibitory pathways to principal cells in the lateral geniculate nucleus of the cat. Exp Brain Res. 1985;58(1):134–143. doi: 10.1007/BF00238961. [DOI] [PubMed] [Google Scholar]
- Albrecht D. G., Farrar S. B., Hamilton D. B. Spatial contrast adaptation characteristics of neurones recorded in the cat's visual cortex. J Physiol. 1984 Feb;347:713–739. doi: 10.1113/jphysiol.1984.sp015092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BISHOP P. O., BURKE W., DAVIS R. Synapse discharge by single fibre in mammalian visual system. Nature. 1958 Sep 13;182(4637):728–730. doi: 10.1038/182728b0. [DOI] [PubMed] [Google Scholar]
- Burke W., Cole A. M. Extraretinal influences on the lateral geniculate nucleus. Rev Physiol Biochem Pharmacol. 1978;80:105–166. doi: 10.1007/3540084665_3. [DOI] [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]
- Coenen A. M., Vendrik A. J. Determination of the transfer ratio of cat's geniculate neurons through quasi-intracellular recordings and the relation with the level of alertness. Exp Brain Res. 1972;14(3):227–242. doi: 10.1007/BF00816160. [DOI] [PubMed] [Google Scholar]
- Dubin M. W., Cleland B. G. Organization of visual inputs to interneurons of lateral geniculate nucleus of the cat. J Neurophysiol. 1977 Mar;40(2):410–427. doi: 10.1152/jn.1977.40.2.410. [DOI] [PubMed] [Google Scholar]
- Enroth-Cugell C., Robson J. G., Schweitzer-Tong D. E., Watson A. B. Spatio-temporal interactions in cat retinal ganglion cells showing linear spatial summation. J Physiol. 1983 Aug;341:279–307. doi: 10.1113/jphysiol.1983.sp014806. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eysel U. T., Pape H. C., Van Schayck R. Excitatory and differential disinhibitory actions of acetylcholine in the lateral geniculate nucleus of the cat. J Physiol. 1986 Jan;370:233–254. doi: 10.1113/jphysiol.1986.sp015932. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Geisert E. E., Langsetmo A., Spear P. D. Influence of the cortico-geniculate pathway on response properties of cat lateral geniculate neurons. Brain Res. 1981 Mar 16;208(2):409–415. doi: 10.1016/0006-8993(81)90568-0. [DOI] [PubMed] [Google Scholar]
- HUBEL D. H., WIESEL T. N. Integrative action in the cat's lateral geniculate body. J Physiol. 1961 Feb;155:385–398. doi: 10.1113/jphysiol.1961.sp006635. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hirsch J. C., Fourment A., Marc M. E. Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat. Brain Res. 1983 Jan 24;259(2):308–312. doi: 10.1016/0006-8993(83)91264-7. [DOI] [PubMed] [Google Scholar]
- Hochstein S., Shapley R. M. Quantitative analysis of retinal ganglion cell classifications. J Physiol. 1976 Nov;262(2):237–264. doi: 10.1113/jphysiol.1976.sp011594. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hámori J., Pasik P., Pasik T. Differential frequency of P-cells and I-cells in magnocellular and parvocellular laminae of monkey lateral geniculate nucleus. An ultrastructural study. Exp Brain Res. 1983;52(1):57–66. doi: 10.1007/BF00237149. [DOI] [PubMed] [Google Scholar]
- Kalil R. E., Chase R. Corticofugal influence on activity of lateral geniculate neurons in the cat. J Neurophysiol. 1970 May;33(3):459–474. doi: 10.1152/jn.1970.33.3.459. [DOI] [PubMed] [Google Scholar]
- Kaplan E., Shapley R. M. The primate retina contains two types of ganglion cells, with high and low contrast sensitivity. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2755–2757. doi: 10.1073/pnas.83.8.2755. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kaplan E., Shapley R. The origin of the S (slow) potential in the mammalian lateral geniculate nucleus. Exp Brain Res. 1984;55(1):111–116. doi: 10.1007/BF00240504. [DOI] [PubMed] [Google Scholar]
- Krüger J. The shift-effect in the lateral geniculate body of the rhesus monkey. Exp Brain Res. 1977 Sep 28;29(3-4):387–392. doi: 10.1007/BF00236177. [DOI] [PubMed] [Google Scholar]
- Lee B. B., Virsu V., Creutzfeldt O. D. Linear signal transmission from prepotentials to cells in the macaque lateral geniculate nucleus. Exp Brain Res. 1983;52(1):50–56. doi: 10.1007/BF00237148. [DOI] [PubMed] [Google Scholar]
- Levine M. W., Troy J. B. The variability of the maintained discharge of cat dorsal lateral geniculate cells. J Physiol. 1986 Jun;375:339–359. doi: 10.1113/jphysiol.1986.sp016120. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Livingstone M. S., Hubel D. H. Effects of sleep and arousal on the processing of visual information in the cat. Nature. 1981 Jun 18;291(5816):554–561. doi: 10.1038/291554a0. [DOI] [PubMed] [Google Scholar]
- McClurkin J. W., Marrocco R. T. Visual cortical input alters spatial tuning in monkey lateral geniculate nucleus cells. J Physiol. 1984 Mar;348:135–152. doi: 10.1113/jphysiol.1984.sp015103. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ohzawa I., Sclar G., Freeman R. D. Contrast gain control in the cat visual cortex. Nature. 1982 Jul 15;298(5871):266–268. doi: 10.1038/298266a0. [DOI] [PubMed] [Google Scholar]
- Rodieck R. W., Dreher B. Visual suppression from nondominant eye in the lateral geniculate nucleus: a comparison of cat and monkey. Exp Brain Res. 1979 May 2;35(3):465–477. doi: 10.1007/BF00236765. [DOI] [PubMed] [Google Scholar]
- Schmielau F., Singer W. The role of visual cortex for binocular interactions in the cat lateral geniculate nucleus. Brain Res. 1977 Jan 21;120(2):354–361. doi: 10.1016/0006-8993(77)90914-3. [DOI] [PubMed] [Google Scholar]
- Shapley R. M., Victor J. D. The effect of contrast on the transfer properties of cat retinal ganglion cells. J Physiol. 1978 Dec;285:275–298. doi: 10.1113/jphysiol.1978.sp012571. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sherman S. M., Koch C. The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus. Exp Brain Res. 1986;63(1):1–20. doi: 10.1007/BF00235642. [DOI] [PubMed] [Google Scholar]
- Sillito A. M., Kemp J. A. The influence of GABAergic inhibitory processes on the receptive field structure of X and Y cells in cat dorsal lateral geniculate nucleus (dLGN). Brain Res. 1983 Oct 24;277(1):63–77. doi: 10.1016/0006-8993(83)90908-3. [DOI] [PubMed] [Google Scholar]
- Singer W. Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system. Physiol Rev. 1977 Jul;57(3):386–420. doi: 10.1152/physrev.1977.57.3.386. [DOI] [PubMed] [Google Scholar]
- So Y. T., Shapley R. Spatial tuning of cells in and around lateral geniculate nucleus of the cat: X and Y relay cells and perigeniculate interneurons. J Neurophysiol. 1981 Jan;45(1):107–120. doi: 10.1152/jn.1981.45.1.107. [DOI] [PubMed] [Google Scholar]
- Tanaka K. Cross-correlation analysis of geniculostriate neuronal relationships in cats. J Neurophysiol. 1983 Jun;49(6):1303–1318. doi: 10.1152/jn.1983.49.6.1303. [DOI] [PubMed] [Google Scholar]
- Tolhurst D. J., Movshon J. A., Thompson I. D. The dependence of response amplitude and variance of cat visual cortical neurones on stimulus contrast. Exp Brain Res. 1981;41(3-4):414–419. doi: 10.1007/BF00238900. [DOI] [PubMed] [Google Scholar]
