Skip to main content
Log in

The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus

  • Overview
  • Published:
Experimental Brain Research Aims and scope Submit manuscript

Summary

In the mammalian visual system, the lateral geniculate nucleus is commonly thought to act merely as a relay for the transmission of visual information from the retina to the visual cortex, a relay without significant elaboration in receptive field properties or signal strength. However, many morphological and electrophysiological observations are at odds with this view. Only 10–20% of the synapses found on geniculate relay neurons are retinal in origin. Roughly half of all synapses derive from cells in layer VI of visual cortex; roughly one third are inhibitory and GABAergic, derived either from interneurons or from cells of the nearby perigeniculate nucleus. Most of the remaining synapses probably derive from cholinergic, noradrenergic, and serotonergic sites within the brainstem reticular formation. Moreover, recent biophysical studies have revealed several ionic currents present in virtually all thalamic neurons. One is a Ca2+-dependent K+ current underlying the afterhyperpolarization (or the IAHP), which may last up to 100–200 ms following an action potential. Activation of the IAHP leads to spike frequency adaptation in response to a sustained, suprathreshold input. Intracellular recordings from other neuronal preparations have shown that the IAHP can be blocked by noradrenalin or acetylcholine, leading to an increased cellular excitability. Another ionic current results from a voltage- and time-dependent Ca2+ conductance that produces a low threshold spike. Activation of this conductance transforms a geniculate neuron from a state of faithful relay of information to one of bursting behavior that bears little relationship to the activity of its retinal afférents. We propose that state-dependent gating of geniculate relay cells, which may represent part of the neuronal substrate involved in certain forms of selective visual attention, can be effected through at least three different mechanisms: (1) conventional GABAergic inhibition, which is largely controlled via brainstem and cortical afferents through interneurons and perigeniculate cells; (2) the IAHP, which is controlled via noradrenergic and cholinergic afferents from the brainstem reticular formation; and (3) the low threshold spike, which may be controlled by GABAergic inputs, cholinergic inputs, and/or the corticogeniculate input, although other possibilities also exist. Furthermore, it seems likely that gating functions involving the corticogeniculate pathway are suited to attentional processes within the visual domain (e.g., saccadic suppression), whereas brain-stem inputs seem more likely to have more global effects that switch attention between sensory systems. In any case, it is now abundantly clear that geniculate circuitry and the intrinsic electrophysiological properties of geniculate neurons are no longer compatible with the notion that the lateral geniculate nucleus serves as a simple relay.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Adams PR, Lancaster B (1985) Components of Ca-activated K current in rat hippocampal neurones in vitro. J Physiol (Lond) 362: 23

    Google Scholar 

  • Ahlsen G (1984) Brain stem neurones with differential projection to functional subregions of the dorsal lateral geniculate complex in the cat. Neuroscience 12: 817–838

    Google Scholar 

  • Ahlsen G, Grant K, Lindström S (1982) Monosynaptic excitation of principal cells in the lateral geniculate nucleus by corticofugal fibers. Brain Res 234: 454–458

    Google Scholar 

  • Ahlsen G, Lindström S (1982) Excitation of perigeniculate neurones via axon collaterals of principal cells. Brain Res 236: 477–481

    Google Scholar 

  • Ahlsen G, Lindström S, Lo F-S (1982) Functional distinction of perigeniculate and thalamic reticular neurons in the cat. Exp Brain Res 46: 118–126

    Google Scholar 

  • Anlsen G, Lindström S, Lo F-S (1984) Inhibition from the brain stem of inhibitory interneurones of the cat's dorsal lateral geniculate nucleus. J Physiol (Lond) 347: 593–609

    Google Scholar 

  • Ahlsen G, Lindström S, Lo F-S (1985) Interaction between inhibitory pathways to principal cells in the lateral geniculate nucleus of the cat. Exp Brain Res 58: 134–143

    Google Scholar 

  • Ahlsen G, Lo F-S (1982) Projection of brain stem neurones to the perigeniculate nucleus and lateral geniculate nucleus in the cat. Brain Res 238: 433–438

    Google Scholar 

  • Barker JL (1978) Evidence for diverse cellular roles of peptides in neuronal function. Neurosci Res Prog Bull 16: 535–555

    Google Scholar 

  • Beaulieu C, Colonnier M (1983) The number of neurons in the different laminae of the binocular and monocular regions of area 17 in the cat. J Comp Neurol 217: 337–344

    Google Scholar 

  • Belcher G, Ryall RW (1977) Substance P selectively blocks nicotinic receptors on Renshaw cells: a new concept of inhibitory synaptic interaction. J Physiol (Lond) 272: 105–119

    Google Scholar 

  • Berardi N, Morrone MC (1984) The role of γ-aminobutyric acid mediated inhibition in the response properties of cat lateral geniculate nucleus neurones. J Physiol (Lond) 357: 505–524

    Google Scholar 

  • Bishop PO, Jeremy D, McLeod JG (1953) The phenomenon of repetitive firing in the lateral geniculate nucleus of the cat. J Neurophysiol 16: 437–447

    Google Scholar 

  • Bizzi E (1966) Discharge patterns of single geniculate neurons during the rapid eye movements of sleep. J Neurophysiol 16: 437–447

    Google Scholar 

  • Bloomfield SA, Hamos JE, Sherman SM (1985) Passive electrical properties of X- and Y-cells in the cat's lateral geniculate nucleus. Soc Neurosci Abstr 11: 232

    Google Scholar 

  • Bowery NG, Doble A, Hill DR, Hudson AL, Shaw JS, Turnbull MJ, Warrington R (1981) Bicuculline-insensitive GABA receptors on peripheral autonomic nerve terminals. Eur J Pharmacol 71: 53–70

    Google Scholar 

  • Bowery NG, Hill DR, Hudson AL (1983) Characteristics of GABAB receptor binding sites on rat whole brain synaptic membranes. Br J Pharmacol 78: 191–206

    Google Scholar 

  • Bowery NG, Hudson AL, Price GW (1985) Comparative autoradiographic studies with [3H]-GABA and [3H]-(−)-baclofen in rat brain in vivo. Br J Pharmacol 85: 234

    Google Scholar 

  • Bowery GP, Price GW, Hudson AL, Hill DR, Wilkin GP, Turnbull MJ (1984) GABA receptor multiplicity. Visualization of different receptor types in the mammalian CNS. Neuropharmacology 23: 219–232

    Google Scholar 

  • Boycott BB, Wässle H (1974) The morphological types of ganglion cells of the domestic cat's retina. J Physiol (Lond) 240: 397–419

    Google Scholar 

  • Burke W, Cole AM (1978) Extraretinal influences on the lateral geniculate nucleus. Rev Physiol Biochem Pharmacol 80: 105–166

    Google Scholar 

  • Burr DC, Holt J, Johnstone JR, Ross J (1982) Selective depression of motion sensitivity during saccades. J Physiol (Lond) 333: 1–15

    Google Scholar 

  • Chu N-S, Bloom FE (1973) Norepinephrine-containing neurons: changes in spontaneous discharge patterns during sleeping and waking. Science 179: 908–910

    Google Scholar 

  • Cleland BG, Dubin MW, Levick WR (1971) Sustained and transient neurones in the cat's retina and lateral geniculate nucleus. J Physiol (Lond) 217: 473–496

    Google Scholar 

  • Coenen AMI, Vendrik AJH (1972) 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 14: 227–242

    Google Scholar 

  • Cole AE, Nicoll RA (1983) Acetylcholine mediates a slow synaptic potential in hippocampal pyramidal cells. Science 221: 1299–1301

    Google Scholar 

  • Cole AE, Nicoll RA (1984) Characterization of a slow cholinergic postsynaptic potential recorded in vitro from rat hippocampal cells. J Physiol (Lond) 352: 173–188

    Google Scholar 

  • Crick F (1984) The function of the thalamic reticular complex: the searchlight hypothesis. Proc Natl Acad Sci USA 81: 4586–4590

    Google Scholar 

  • Cucchiaro J, Uhlrich DJ, Hamos JE, Sherman SM (1985) Perigeniculate input to the cat's lateral geniculate nucleus: a light- and electron microscopic study of single, HRP-filled cells. Soc Neurosci Abstr 11: 231

    Google Scholar 

  • Curtis DR, Johnston GAR (1974) Amino acid transmitters in the mammalian central nervous system. Ergebn Physiol Biol Chem Exp Pharmakol 69: 97–188

    Google Scholar 

  • Deschenes M, Paradis M, Roy JP, Steriade M (1984) Electrophysiology of neurons of lateral thalamic nuclei in cat: resting properties and burst discharges. J Neurophysiol 51:1196–1219

    Google Scholar 

  • Dingledine R, Langmoen IA (1980) Conductance changes and inhibitory actions of hippocampal recurrent IPSPs. Brain Res 185: 277–287

    Google Scholar 

  • Dowling JE (1970) Organization of vertebrate retinas. Invest Ophthalmol 9: 655–680

    Google Scholar 

  • Dubin MW, Cleland BG (1977) Organization of visual inputs to interneurons of lateral geniculate nucleus of the cat. J Neurophysiol 40: 410–427

    Google Scholar 

  • Egan TM, North RA (1986) Acetylcholine hyperpolarizes central neurones by acting on an M2 muscarinic receptor. Nature 319: 405–407

    Google Scholar 

  • Eysel UTh (1976) Quantitative studies of intracellular postsynaptic potentials in the lateral geniculate nucleus of the cat with respect to optic tract stimulus response latencies. Exp Brain Res 25: 469–486

    Google Scholar 

  • Ferster D, LeVay S (1978) The axonal arborization of lateral geniculate neurons in the striate cortex of the cat. J Comp Neurol 182: 923–944

    Google Scholar 

  • Fibiger HC (1982) The organization and some projections of cholinergic neurons of the mammalian forebrain. Brain Res Rev 4: 327–388

    Google Scholar 

  • Fitzpatrick D, Penny GR, Schmechel DE (1984) Glutamic acid decarboxylase-immunoreactive neurons and terminals in the lateral geniculate nucleus of the cat. J Neurosci 4: 1809–1829

    Google Scholar 

  • Foote SL, Aston-Jones G, Bloom FE (1980) Impulse activity of locus coeruleus neurons in awake rats and monkeys is a function of sensory stimulation and arousal. Proc Natl Acad Sci USA 77: 3033–3037

    Google Scholar 

  • Foote WE, Maciewicz RJ, Mordes JP (1974) Effect of midbrain raphe and lateral mesencephalic stimulation on spontaneous and evoked activity in the lateral geniculate of the cat. Exp Brain Res 19: 124–130

    Google Scholar 

  • Friedlander MJ, Lin C-S, Stanford LR, Sherman SM (1981) Morphology of functionally identified neurons in the lateral geniculate nucleus of the cat. J Neurophysiol 46: 80–129

    Google Scholar 

  • Fukuda Y, Stone J (1976) Evidence of differential inhibitory influences on X- and Y-type relay cells in the cat's lateral geniculate nucleus. Brain Res 113: 188–196

    Google Scholar 

  • Geisert EE, Langsetmo A, Spear PD (1981) Influence of the corticogeniculate pathway on response properties of cat lateral geniculate neurons. Brain Res 208: 409–415

    Google Scholar 

  • Gilbert C (1977) Laminar differences in receptive field properties of cells in cat primary visual cortex. J Physiol (Lond) 268: 391–421

    Google Scholar 

  • Gilbert C (1983) Microcircuitry of the visual cortex. Ann Rev Neurosci 6: 217–247

    Google Scholar 

  • Gilbert CD, Kelly JP (1975) The projections of cells in different layers of the cat's visual cortex. J Comp Neurol 163: 81–106

    Google Scholar 

  • Guillery RW (1967) Patterns of fiber degeneration in the dorsal lateral geniculate nucleus of the cat following lesions in the visual cortex. J Comp Neurol 130: 197–222

    Google Scholar 

  • Guillery RW (1971) Patterns of synaptic interconnections in the dorsal lateral geniculate nucleus of the cat and monkey: a brief review. Vision Res Suppl 3: 211–227

    Google Scholar 

  • Hamos JE, Van Horn SC, Raczkowski D, Uhlrich DJ, Sherman SM (1985) Synaptic connectivity of a local circuit neuron in the cat's lateral geniculate nucleus. Nature 317: 618–621

    Google Scholar 

  • Harth E, Unnikrishnan KP (1985) Brainstem control of sensory information: a mechanism for perception. Int J Psychophysiol 3: 101–119

    Google Scholar 

  • Harvey AR (1980) A physiological analysis of subcortical and commissural projections of area 17 and 18 of the cat. J Physiol (Lond) 302: 507–534

    Google Scholar 

  • von Helmholtz H (1866) Handbuch der physiologischen Optik. Translated by Southall JP. Dover, New York, 1925

    Google Scholar 

  • Hendry SHC, Jones EG, DeFelipe J, Schmechel D, Brandon C, Emson PC (1984) Neuropeptide-containing neurons of the cerebral cortex are also GABAergic. Proc Natl Acad Sci USA 81: 6526–6530

    Google Scholar 

  • Hoffmann K-P, Stone J, Sherman SM (1972) Relay of receptivefield properties in dorsal lateral geniculate nucleus of the cat. J Neurophysiol 35: 518–531

    Google Scholar 

  • Hoover DB, Jacobowitz DM (1979) Neurochemical and histochemical studies of the effect of a lesion of nucleus cuneiformis on the cholinergic innervation of discrete areas of the rat brain. Brain Res 170: 113–122

    Google Scholar 

  • Hubel DH, Wiesel TN (1961) Integrative action in the cat's lateral geniculate body. J Physiol (Lond) 155: 385–398

    Google Scholar 

  • Hubel DH, Wiesel TN (1977) Functional architecture of the macaque monkey visual cortex. Proc R Soc B 196: 1–59

    Google Scholar 

  • Hughes HC, Mullikin WH (1984) Brainstem afferents to the lateral geniculate nucleus of the cat. Exp Brain Res 54: 253–258

    Google Scholar 

  • Humphrey AL, Sur M, Uhlrich DJ, Sherman SM (1985a) Projection patterns of individual X- and Y-cell axons from the lateral geniculate nucleus to cortical area 17 in the cat. J Comp Neurol 233: 159–189

    Google Scholar 

  • Humphrey AL, Sur M, Uhlrich DJ, Sherman SM (1985b) Termination patterns of individual X- and Y-cell axons in the visual cortex of the cat: projections to area 18, to the 17–18 border region, and to both areas 17 and 18. J Comp Neurol 233: 190–212

    Google Scholar 

  • Ide LS (1982) The fine structure of the perigeniculate nucleus in the cat. J Comp Neurol 210: 317–334

    Google Scholar 

  • Ikeda H, Wright MJ (1972) Receptive field organization of sustained and transient retinal ganglion cells which subserve different functional roles. J Physiol (Lond) 227: 769–800

    Google Scholar 

  • Jahnsen H, Llinas R (1984a) Electrophysiological properties of guinea-pig thalamic neurones: an in vitro study. J Physiol (Lond) 349: 205–226

    Google Scholar 

  • Jahnsen H, Llinas R (1984b) Ionic basis for the electroresponsiveness and oscillatory properties of guinea-pig thalamic neurones in vitro. J Physiol (Lond) 349: 227–247

    Google Scholar 

  • Jan YN, Jan LY (1983) A LHRH-like peptidergic neurotransmitter capable of “action at a distance” in autonomic ganglia. Trends Neurosci 6: 320–325

    Google Scholar 

  • Jones EG (1975) Some aspects of the organization of the thalamic reticular complex. J Comp Neurol 162: 285–308

    Google Scholar 

  • Jones EG, Powell TPS (1969) An electron microscopic study of the mode of termination of cortico-thalamic fibres within the sensory relay nuclei of the thalamus. Proc R Soc B 172: 173–185

    Google Scholar 

  • Kalil RE, Chase R (1970) Corticofugal influence on activity of lateral geniculate neurons in the cat. J Neurophysiol 33: 459–474

    Google Scholar 

  • Kayama Y (1985) Ascending, descending and local control of neuronal activity in the rat lateral geniculate nucleus. Vision Res 25: 339–347

    Google Scholar 

  • Kayama Y, Negi T, Sugitani M, Iwama K (1982) Effects of locus coeruleus stimulation on neuronal activities of dorsal lateral geniculate nucleus and perigeniculate reticular nucleus of the rat. Neuroscience 7: 655–666

    Google Scholar 

  • Kemp JA, Roberts H, Sillito AM (1982) Further studies on the action of 5-hydroxytryptamine in the dorsal lateral geniculate nucleus of the cat. Brain Res 246: 334–337

    Google Scholar 

  • Kemp JA, Sillito AM (1982) The nature of the excitatory transmitter mediating X and Y cell inputs to the cat dorsal lateral geniculate neucleus. J Physiol (Lond) 323: 377–391

    Google Scholar 

  • Kimura H, McGeer PL, Peng JH, McGeer EG (1981) The central cholinergic system studied by choline acetyltransferase immunohistochemistry in the cat. J Comp Neurol 200: 151–201

    CAS  PubMed  Google Scholar 

  • Koch C (1985) Understanding the intrinsic circuitry of the cat's LGN: electrical properties of the spine-triad arrangement. Proc R Soc B: 391–398

  • Koch C, Poggio T (1983) A theoretical analysis of electrical properties of spines. Proc R Soc 218: 455–477

    Google Scholar 

  • Koch C, Poggio T, Torre V (1982) Retinal ganglion cells: a functional interpretation of dendritic morphology. Philos Trans R Soc 298: 227–264

    Google Scholar 

  • Koch C, Poggio T, Torre V (1983) Nonlinear interactions in a dendritic tree: localization, timing, and role in information processing. Proc Natl Acad Sci USA 80: 2799–2802

    Google Scholar 

  • Kromer LF, Moore RY (1980) A study of the organization of the locus coeruleus projections to the lateral geniculate nuclei in the albino rat. Neuroscience 5: 255–271

    Google Scholar 

  • Lancaster B, Adams PR (1986) Calcium-dependent current generating the afterhyperpolarization of hippocampal neurons. J Neurophysiol (in press)

  • de Lima AD, Montero VM, Singer W (1985) The cholinergic innervation of the visual thalamus: an EM immunocytochemical study. Exp Brain Res 59: 206–212

    Google Scholar 

  • Lindström S (1982) Synaptic organization of inhibitory pathways to principal cells in the lateral geniculate nucleus of the cat. Brain Res 234: 447–453

    Google Scholar 

  • Livingstone MS, Hubel DH (1981) Effects of sleep and arousal on the processing of visual information in the cat. Nature 291: 554–561

    Google Scholar 

  • Madison DV, Lancaster B, Nicoll RA, Adams PR (1985) Voltage clamp analysis of slow cholinergic synaptic transmission in the hippocampus. Soc Neurosci Abstr 11: 466

    Google Scholar 

  • Madison DV, Nicoll RA (1982) Noradrenalin blocks accommodation of pyramidal cell discharge in the hippocampus. Nature 299: 636–638

    Google Scholar 

  • Madison DV, Nicoll RA (1984) Control of the repetitive discharge of rat CA1 pyramidal neurones in vitro. J Physiol (Lond) 354: 319–334

    Google Scholar 

  • Madison DV, Nicoll RA (1986a) Actions of noradrenaline recorded intracellularly in rat hippocampal CA1 pyramidal neurones, in vitro. J Physiol (Lond) 372: 221–244

    Google Scholar 

  • Madison DV, Nicoll RA (1986b) Cyclic adenosine 3′, 5′-monophosphate mediates β-receptor actions of noradrenaline in rat hippocampal pyramidal cells. J Physiol (Lond) 372: 245–259

    Google Scholar 

  • McBride RL, Sutin J (1976) Projections of the locus coeruleus and adjacent pontine tegmentum in the cat. J Comp Neurol 165: 265–284

    Google Scholar 

  • McCarley RW, Benoit O, Barrionuevo G (1983) Lateral geniculate nucleus unitary discharge in sleep and waking: state- and rate-specific aspects. J Neurophysiol 50: 798–818

    Google Scholar 

  • McCormick DA, Prince DA (1986) Acetylcholine induces burst firing in thalamic reticular neurones by activating a potassium conductance. Nature 319: 402–405

    Google Scholar 

  • McIlwain JT, Creutzfeldt OD (1967) Microelectrode study of synaptic excitation and inhibition in the lateral geniculate nucleus of the cat. J Neurophysiol 30: 1–21

    Google Scholar 

  • Montero VM, Scott GL (1981) Synaptic terminals in the dorsal lateral geniculate nucleus from neurons of the thalamic reticular nucleus: a light and electron microscopic autoradiographic study. Neuroscience 6: 2561–2577

    Google Scholar 

  • Montero VH, Singer W (1984) Ultrastructure and synaptic relations of neural elements containing glutamic acid decarboxylase (GAD) in the perigeniculate nucleus of the cat. Exp Brain Res 56: 115–125

    Google Scholar 

  • Moore RY, Bloom FE (1979) Central catecholamine neuron systems: anatomy and physiology of the norepinephrine and epinephrine systems. Ann Rev Neurosci 2: 113–168

    Google Scholar 

  • Nakai Y, Takaori S (1974) Influence of norepinephrine-containing neurons derived from the locus coeruleus on lateral geniculate neuronal activities of cats. Brain Res 71: 47–60

    Google Scholar 

  • Newberry NR, Nicoll RA (1984) A bicuculline-resistant inhibitory postsynaptic potential in rat hippocampal pyramidal cells in vitro. J Physiol (Lond) 348: 239–254

    Google Scholar 

  • Newberry NR, Nicoll RA (1985) Comparison of the action of baclofen with γ-aminobutyric acid on rat hippocampal pyramidal cells in vitro. J Physiol (Lond) 360: 161–185

    Google Scholar 

  • Noda H (1975) Depression in the excitability of relay cells of lateral geniculate nucleus following saccadic eye movements in the cat. J Physiol (Lond) 249: 87–102

    Google Scholar 

  • O'Donnell P, Koch C, Poggio T (1985) Demonstrating the nonlinear interaction between excitation and inhibition on dendritic trees using computer-generated color graphics: a film. Soc Neurosci Abstr 11: 465

    Google Scholar 

  • Oertel WH, Graybiel AM, Mugnaibi E, Elde RP, Schmechel DE, Kopin IJ (1983) Coexistence of glutamic acid decarboxylase- and somatostatin-like immunoreactivity in neurons of the feline nucleus reticularis thalami. J Neurosci 3: 1322–1332

    Google Scholar 

  • O'Hara PT, Lieberman AR, Hunt SP, Wu J-Y (1983) Neural elements containing glutamic acid decarboxylase (GAD) in the dorsal lateral geniculate nucleus of the rat: immunohistochemical studies by light and electron-microscopy. Neuroscience 8: 189–211

    Google Scholar 

  • O'Hara PT, Sefton AJ, Lieberman AR (1980) Mode of termination of afferents from the thalamic reticular nucleus in the dorsal lateral geniculate nucleus of the rat. Brain Res 197: 503–506

    Google Scholar 

  • Orban GA (1984) Neuronal operations in the visual cortex. Springer Berlin Heidelberg New York Tokyo

    Google Scholar 

  • Pasquier DA, Villar MJ (1982) Specific serotonergic projections to the lateral geniculate body from the lateral cell groups of the dorsal raphe nucleus. Brain Res 249: 142–146

    Google Scholar 

  • Pennefather P, Lancaster B, Adams PR, Nicoll RA (1986) Two distinct CA-dependent K currents in bullfrog sympathetic ganglion cells. Proc Natl Acad Sci USA 82: 3040–3044

    Google Scholar 

  • Robson JA (1983) The morphology of corticofugal axons to the dorsal lateral geniculate nucleus in the cat. J Comp Neurol 216: 89–103

    Google Scholar 

  • Rogawski MA, Aghajanian GK (1980) Modulation of lateral geniculate neurone excitability by noradrenalin microiontophoresis or locus coeruleus stimulation. Nature 287: 731–734

    Google Scholar 

  • Sakai K (1980) Some anatomical and physiological properties of pontomesencephalic tegmental neurons with special reference to the PGO waves and postural atonia during paradoxical sleep in the cat. In: Hobson JA, Brazier MAB (eds) The reticular formation revisited. Raven Press, New York, pp 427–447

    Google Scholar 

  • Sanderson KJ (1971) Visual field projection columns and magnification factors in the lateral geniculate nucleus of the cat. Exp Brain Res 13: 159–177

    Google Scholar 

  • Scheibel ME, Scheibel AB (1966) The organization of the nucleus of the reticularis thalami: a Golgi study. Brain Res 1: 43–62

    Google Scholar 

  • Schmielau F, Singer W (1977) The role of visual cortex for binocular interactions in the cat lateral geniculate nucleus. Brain Res 120: 354–361

    Google Scholar 

  • Segal M, Barker JL (1984) Rat hippocampal neurons in culture: properties of GABA-activated Cl ion conductance. J Neurophysiol 51: 500–515

    Google Scholar 

  • Shapley R, Lennie P (1985) Spatial frequency analysis in the visual system. Ann Rev Neurosci 8: 547–583

    Google Scholar 

  • Sherman SM (1979) The functional significance of X- and Y-cells in normal and visually deprived cats. Trends Neurosci 2: 192–195

    Google Scholar 

  • Sherman SM (1985) Functional organization of the W-, X-, and Y- cell pathways: a review and hypothesis. In: Sprague JM, Epstein AN (eds) Progress in psychobiology and physiological psychology, Vol 11. Academic Press, New York, pp 233–314

    Google Scholar 

  • Sherman SM, Spear PD (1982) Organization of the visual pathways in normal and visually deprived cats. Physiol Rev 62: 738–855

    Google Scholar 

  • Sillito AM, Kemp JA (1983) The influence of GABAergic inhibitory processes on the receptive field structure of X and Y cells in the cat dorsal lateral geniculate nucleus (dLGN). Brain Res 277: 63–77

    Google Scholar 

  • Sillito AM, Kemp JA, Berardi N (1983) The cholinergic influence on the function of the cat dorsal lateral geniculate nucleus (dLGN). Brain Res 280: 299–307

    Google Scholar 

  • Simmonds MA (1983) Multiple GABA receptors and associated regulatory sites. Trends Neurosci 6: 279–281

    Google Scholar 

  • Singer W (1973) The effect of mesencephalic reticular stimulation on intracellular potentials of cat lateral geniculate neurons. Brain Res 61: 35–54

    Google Scholar 

  • Singer W (1977) Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system. Physiol Rev 57: 386–420

    Google Scholar 

  • Singer W, Creutzfeldt OD (1970) Reciprocal lateral inhibition of On- and Off-Center neurones in the lateral geniculate body of the cat. Exp Brain Res 10: 311–330

    Google Scholar 

  • Steriade M, Deschenes M (1985) The thalamus as a neuronal oscillator. Brain Res Rev 8: 1–63

    Google Scholar 

  • Stockmeier CA, Martino AM, Kellar KJ (1985) A strong influence of serotonin axons on β-adrenergic receptors in rat brain. Science 220: 323–325

    Google Scholar 

  • Stone J, Dreher B (1973) Projection of X- and Y-cells of the cat's lateral geniculate nucleus to areas 17 and 18 of visual cortex. J Neurophysiol 36: 551–567

    Google Scholar 

  • Stone J, Dreher B, Leventhal A (1979) Hierarchical and parallel mechanisms in the organization of visual cortex. Brain Res Rev 1: 345–394

    Google Scholar 

  • Tsumoto T, Creutzfeldt OD, Legendy CR (1978) Functional organization of the corticofugal system from visual cortex to lateral geniculate nucleus in the cat. Exp Brain Res 32: 345–364

    Google Scholar 

  • Tusa RJ, Palmer LA, Rosenquist AC (1978) The retinotopic organization of area 17 (striate cortex) in the cat. J Comp Neurol 177: 213–236

    Google Scholar 

  • Uhlrich DJ, Cucchiaro JB, Sherman SM (1985) Terminal patterns of the brainstem projection to the lateral geniculate nucleus in the cat: an anterograde tracer study using Phaseolus vulgaris leucoagglutinin (PHA-L). Soc Neurosci Abstr 11: 232

    Google Scholar 

  • Wilson JR, Friedlander MJ, Sherman SM (1984) Ultrastructural morphology of identified X- and Y-cells in the cat's lateral geniculate nucleus. Proc R Soc B 221: 411–436

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sherman, S.M., Koch, C. The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus. Exp Brain Res 63, 1–20 (1986). https://doi.org/10.1007/BF00235642

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00235642

Key words

Navigation