Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-26T08:10:29.535Z Has data issue: false hasContentIssue false

Brain-stem influence on visual response of lagged and nonlagged cells in the cat lateral geniculate nucleus

Published online by Cambridge University Press:  02 June 2009

E. Hartveit
Affiliation:
Department of Neurophysiology, University of Oslo, POB 1104 Blindern, N-0317 Oslo, Norway
P. Heggelund
Affiliation:
Department of Neurophysiology, University of Oslo, POB 1104 Blindern, N-0317 Oslo, Norway

Abstract

This study examined the influence of the pontomesencephalic peribrachial region (PBR) on the visual response properties of cells in the dorsal lateral geniculate nucleus (LGN). The response of single cells to a stationary flashing light spot was recorded with accompanying electrical stimulation of the PBR. The major objectives were to compare the effects of PBR stimulation on lagged and nonlagged cells, to examine how the visual response pattern of lagged cells could be modified by PBR stimulation and to examine whether the physiological criteria used to classify lagged and nonlagged cells are applicable during increased PBR input to the LGN. During PBR stimulation, the visual response was enhanced to a similar degree for lagged and nonlagged cells and the latency to half-rise of the visual response was reduced, particularly for the lagged X cells. The latency to half-fall of the visual response of lagged cells was not changed by PBR stimulation. Accordingly, the division of LGN cells into lagged and nonlagged cells based on visual response latencies was maintained during PBR stimulation. The initial suppression that a visual stimulus evokes in lagged cells was resistant to the effects of PBR stimulation. For the lagged cells, the largest response increase occurred for the initial part of the visual response. For the nonlagged cells, the largest increase occurred for the tonic part of the response. The results support the hypothesis that the differences in temporal response properties between lagged and nonlagged cells belong to the basic distinctions between these cell classes.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1993

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adam, H.K., Glen, J.B. & Hoyle, P.A. (1980). Pharmacokinetics in laboratory animals of ICI 35 868, a new i.v. anaesthetic agent. British Journal of Anaesthesiology 52, 743746CrossRefGoogle ScholarPubMed
Ahlsén, G., Lindström, S. & Lo, F.-S. (1984). Inhibition from the brain stem of inhibitory interneurones of the cat’s dorsal lateral geniculate nucleus. Journal of Physiology 347, 593609Google Scholar
Beaulieu, C. & Cynader, M. (1992). Preferential innervation of immunoreactive choline acetyltransferase synapses on relay cells of the cat’s lateral geniculate nucleus: A double-labelling study. Neuroscience 47, 3344CrossRefGoogle ScholarPubMed
Brearley, J.C., Kellagher, R.E.B. & Hail, L.W. (1988). Propofol anaesthesia in cats. Journal of Small Animal Practice 29, 315322CrossRefGoogle Scholar
Cleland, B.G., Dubin, M.W. & Levick, W.R. (1971). Sustained and transient neurones in the cat’s retina and lateral geniculate nucleus. Journal of Physiology 217, 473496CrossRefGoogle ScholarPubMed
Cleland, B.G., Harding, T.H. & Tulunay-Keesey, U. (1979). Visual resolution and receptive field size: Examination of two kinds of cat retinal ganglion cells. Science 205, 10151017Google Scholar
Coenen, A.M.L. & Vendrik, A.J.H. (1972). Determination of the transfer ratio of cat’s geniculate neurones through quasi-intracellular recordings and the relation with level of alertness. Experimental Brain Research 14, 227242CrossRefGoogle ScholarPubMed
Dossi, R.Curró, Paré, D. & Steriade, M. (1991). Short-lasting nicotinic and long-lasting muscarinic depolarizing responses of thalamocortical neurons to stimulation of mesopontine cholinergic nuclei. Journal of Neurophysiology 65, 393406CrossRefGoogle Scholar
DeLima, A.D., Montero, V. & Singer, W. (1985). The cholinergic innervation of the visual thalamus: An EM immunocytochemical study. Experimental Brain Research 59, 206212Google Scholar
DeLima, A.D. & Singer, W. (1987). The brainstem projection to the lateral geniculate nucleus in the cat: Identification of cholinergic and monoaminergic elements. Journal of Comparative Neurology 259, 92121CrossRefGoogle Scholar
Fitzpatrick, D., Diamond, I.T. & Raczkowski, D. (1989). Cholinergic and monoaminergic innervation of the cat’s thalamus: Comparison of the lateral geniculate nucleus with other principal sensory nuclei. Journal of Comparative Neurology 288, 647675CrossRefGoogle ScholarPubMed
Francesconi, W., Muller, C.M. & Singer, W. (1988). Cholinergic mechanisms in the reticular control of transmission in the cat lateral geniculate nucleus. Journal of Neurophysiology 59, 16901718CrossRefGoogle ScholarPubMed
Glen, J.B., Hunter, S.C., Blackburn, T.P. & Wood, P. (1985). Interaction studies and other investigations of the pharmacology of propofol (‘Diprivan’). Postgraduate Medical Journal 61 (Suppl. 3), 714Google ScholarPubMed
Hartveit, E. (1992). Simultaneous recording of lagged and nonlagged cells in the cat lateral geniculate nucleus. Experimental Brain Research 88, 229232CrossRefGoogle Scholar
Hartveit, E. & Heggelund, P. (1990 a). Brainstem modulation of lagged and nonlagged cells in the cat lateral geniculate nucleus. Society for Neuroscience Abstracts 16, 159.Google Scholar
Hartveit, E. & Heggelund, P. (1990 b). Neurotransmitter receptors mediating excitatory input to cells in the cat lateral geniculate nucleus. II. Non-lagged cells. Journal of Neurophysiology 63, 13611372CrossRefGoogle Scholar
Hartveit, E. & Heggelund, P. (1992 a). Effects of acetylcholine on the visual response of lagged cells in the lateral geniculate nucleus of the cat. Society for Neuroscience Abstracts 18, 142.Google Scholar
Hartveit, E. & Heggelund, P. (1992 b). The effect of contrast on the visual response of lagged and nonlagged cells in the cat lateral geniculate nucleus. Visual Neuroscience 9, 515526CrossRefGoogle ScholarPubMed
Heggelund, P. (1981). Receptive field organization of simple cells in cat striate cortex. Experimental Brain Research 42, 8998Google ScholarPubMed
Heggelund, P. & Hartveit, E. (1990). Neurotransmitter receptors mediating excitatory input to cells in the cat lateral geniculate nucleus. I. Lagged cells. Journal of Neurophysiology 63, 13471360Google ScholarPubMed
Heggelund, P., Karlsen, H.E., Flugsrud, G. & Nordtug, T. (1989). Response to rates of luminance change of sustained and transient cells in the cat lateral geniculate nucleus and optic tract. Experimental Brain Research 74, 116130CrossRefGoogle ScholarPubMed
Hu, B., Steriade, M. & Deschênes, M. (1989). The effects of brainstem peribrachial stimulation on reticular thalamic neurons: The blockage of spindle waves. Neuroscience 31, 112CrossRefGoogle ScholarPubMed
Humphrey, A.L. & Saul, A.B. (1991). Stimulation of the brainstem reticular formation does not abolish the lagged/non-lagged cell distinction in the cat LGN. Society for Neuroscience Abstracts 17, 710.Google Scholar
Humphrey, A.L. & Weller, R.E. (1988 a). Functionally distinct groups of X-cells in the lateral geniculate nucleus of the cat. Journal of Comparative Neurology 268, 429447CrossRefGoogle ScholarPubMed
Humphrey, A.L. & Weller, R.E. (1988 b). Structural correlates of functionally distinct groups of X-cells in the lateral geniculate nucleus of the cat. Journal of Comparative Neurology 268, 448468CrossRefGoogle ScholarPubMed
Kwon, Y.H., Esguerra, M. & Sim, M. (1991). NMDA and non-NMDA receptors mediate visual responses of neurons in the cat’s lateral geniculate nucleus. Journal of Neurophysiology 66, 414428Google ScholarPubMed
Levick, W.R. (1972). Another tungsten microelectrode. Medical Electronics and Biological Engineering 10, 510515CrossRefGoogle ScholarPubMed
Lindström, S. & Wróbel, A. (1990). Private inhibitory systems for the X and Y pathways in the dorsal lateral geniculate nucleus of the cat. Journal of Physiology 429, 259280Google Scholar
Livingstone, M.S. & Hubel, D.H. (1981). Effects of sleep and arousal on the processing of visual information in the cat. Nature 291, 554561Google ScholarPubMed
Mastronarde, D.N. (1987 a). Two classes of single-input X-cells in cat lateral geniculate nucleus. I. Receptive field properties and classification of cells. Journal of Neurophysiology 57, 357380CrossRefGoogle ScholarPubMed
Mastronarde, D.N. (1987 b). Two classes of single-input X-cells in cat lateral geniculate nucleus. II. Retinal inputs and the generation of receptive field properties. Journal of Neurophysiology 57, 381413CrossRefGoogle ScholarPubMed
Mastronarde, D.N. (1988). Branching of X- and Y-functional pathways in cat lateral geniculate nucleus. Society for Neuroscience Abstracts 14, 309.Google Scholar
Mastronarde, D.N., Humphrey, A.L. & Saul, A.B. (1991). Lagged Y cells in the cat lateral geniculate nucleus. Visual Neuroscience 7, 191200CrossRefGoogle ScholarPubMed
McCormick, D.A. & Pape, H.-C. (1988). Acetylcholine inhibits identified interneurons in the cat lateral geniculate nucleus. Nature 334, 246248CrossRefGoogle ScholarPubMed
McCormick, D.A. & Prince, D.A. (1987). Actions of acetylcholine in the guinea-pig and cat medial and lateral geniculate nuclei, in vitro. Journal of Physiology 392, 147165Google ScholarPubMed
Peichl, L. & Wässle, H. (1979). Size, scatter and coverage of ganglion cell receptive field centres in the cat retina. Journal of Physiology 291, 117141CrossRefGoogle ScholarPubMed
Raczkowski, D. & Fitzpatrick, D. (1989). Organization of cholinergic synapses in the cat’s dorsal lateral geniculate and perigeniculate nuclei. Journal of Comparative Neurology 288, 676690CrossRefGoogle ScholarPubMed
Robson, J.G. (1986). Neurophysiology of retinal ganglion cells and optic nerve. In Optical Neuritis, ed. Hess, R.F. & Plant, G., pp. 1941. Cambridge, UK: Cambridge University Press.Google Scholar
Rodieck, R.W., Pettigrew, J.D., Bishop, P.O. & Nikara, T. (1967). Residual eye movements in receptive field studies of paralyzed cats. Vision Research 7, 107110Google ScholarPubMed
Saul, A.B. & Humphrey, A.L. (1990). Spatial and temporal response properties of lagged and nonlagged cells in cat lateral geniculate nucleus. Journal of Neurophysiology 64, 206224CrossRefGoogle ScholarPubMed
Sawai, H., Morigiwa, K. & Fukuda, Y. (1988). Effects of EEG synchronization on visual responses of the cat’s geniculate relay cells: A comparison among Y, X and W cells. Brain Research 455, 394400CrossRefGoogle Scholar
Sestokas, A.K. & Lehmkuhle, S. (1986). Visual response latency of X- and Y-cells in the dorsal lateral geniculate nucleus of the cat. Vision Research 26, 10411054CrossRefGoogle ScholarPubMed
Singer, W. (1973). The effect of mesencephalic reticular stimulation on intracellular potentials of cat lateral geniculate neurons. Brain Research 61, 3554CrossRefGoogle ScholarPubMed
Steriade, M. & McCarley, R.W. (1990). Brainstem Control of Wake-fulness and Sleep. New York: Plenum Press.CrossRefGoogle Scholar
Steriade, M., Paré, D., Hu, B. & Deschênes, M. (1990 a). The Visual Thalamocortical System and Its Modulation by the Brain Stem Core. Berlin: Springer.CrossRefGoogle Scholar
Steriade, M., Datta, S., Paré, D., Oakson, G. & Dossi, R.Curró (1990 b). Neuronal activities in brainstem cholinergic nuclei related to tonic activation processes in thalamocortical systems. Journal of Neuroscience 10, 25412559CrossRefGoogle ScholarPubMed
Steriade, M., Paré, D., Datta, S., Oakson, G. & Dossi, R.Curró (1990 c). Different cellular types in mesopontine cholinergic nuclei related to ponto-geniculo-occipital waves. Journal of Neuroscience 10, 25602579CrossRefGoogle ScholarPubMed
Uhlrich, D.J., Tamamaki, N. & Sherman, S.M. (1990). Brainstem control of response modes in neurons of the cat’s lateral geniculate nucleus. Proceedings of the National Academy of Sciences of the U.S.A. 87, 25602563CrossRefGoogle ScholarPubMed