Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-26T07:05:05.822Z Has data issue: false hasContentIssue false

The brain-stem parabrachial region controls mode of response to visual stimulation of neurons in the cat’s lateral geniculate nucleus

Published online by Cambridge University Press:  02 June 2009

Shao-Ming Lu
Affiliation:
Department of Neurobiology, State University of New York, Stony Brook
William Guido
Affiliation:
Department of Neurobiology, State University of New York, Stony Brook
S. Murray Sherman
Affiliation:
Department of Neurobiology, State University of New York, Stony Brook

Abstract

We recorded the responses of neurons from the cat’s lateral geniculate nucleus to drifting sine-wave grating stimuli both before and during electrical stimulation of the parabrachial region of the midbrain. The parabrachial region provides a mostly cholinergic input to the lateral geniculate nucleus, and our goal was to study its effect on responses of geniculate cells to visual stimulation. Geniculate neurons respond to visual stimuli in one of two modes. At relatively hyperpolarized membrane potentials, low threshold (LT) Ca2+ spikes are activated, leading to high-frequency burst discharges (burst mode). At more depolarized levels, the low threshold Ca2+ spike is inactivated, permitting a more tonic response (relay or tonic mode). During our intracellular recordings of geniculate cells, we found that, at initially hyperpolarized membrane potentials, LT spiking in response to visual stimulation was pronounced, but that parabrachial activation abolished this LT spiking and associated burst discharges. Coupled with the elimination of LT spiking, parabrachial activation also led to a progressive increase in tonic responsiveness. Parabrachial activation thus effectively switched the responses to visual stimulation of geniculate neurons from the burst to relay mode. Accompanying this switch was a gradual depolarization of resting membrane potential by about 5–10 mV and a reduction in the hyperpolarization that normally occurs in response to the inhibitory phase of the visual stimulus. Presumably, the membrane depolarization was sufficient to inactivate the LT spikes. We were able to extend and confirm our intracellular observations on the effects of parabrachial activation to a sample of cells recorded extracellularly. This was made possible by adopting empirically determined criteria to distinguish LT bursts from tonic responses solely on the basis of the temporal pattern of action potentials. During parabrachial activation, every cell responded only in the relay mode, an effect that corresponds to our intracellular observations. We quantified the effects of parabrachial activation on various response measures. The fundamental Fourier response amplitude (Fl) was calculated separately for the total response, the tonic response component, and the LT burst component. Parabrachial activation resulted in an increased Fl amplitude for the total response. This increase was due to an increase in the tonic response component. For a subset of cells showing epochs of LT bursting, parabrachial activation concurrently reduced LT bursting and increased the amplitude of the tonic response. Parabrachial activation, by eliminating LT bursting, also caused cells to respond with more linearity. By keeping geniculate cells in the relay mode, the parabrachial region serves to maintain a more linear retinogeniculate transfer of information to cortex, and this may be important for detailed analysis of visual targets. However, when a geniculate neuron becomes hyperpolarized, as may occur during states of visual inattention, it would not respond well to visual stimuli without the sort of nonlinear amplification provided by the LT spike. Thus, the LT spike may permit hyperpolarized cells to relay to cortex the presence of a potentially salient or dangerous stimulus, but this is done at the expense of linearity. This may serve as a sort of “wake-up call” that redirects attention to a particular stimulus and eventually enhances activity of appropriate parabrachial inputs to switch the critical geniculate neurons into the relay mode.

Type
Research Articles
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

Ahlsén, G. (1984). Brainstem neurones with differential projection to functional subregions of the dorsal lateral geniculate complex in the cat. Neuroscience 12, 817838.CrossRefGoogle ScholarPubMed
Ahlsén, G., Lindström, S. & Lo, F.-S. (1984). Inhibition from the brainstem of inhibitory interneurones of the cat’s dorsal lateral geniculate nucleus Journal of Physiology (London) 347, 593609.CrossRefGoogle ScholarPubMed
Berman, A.I. (1968). The brainstem of the Cat. A Cytoarchitectonic Atlas with Stereotaxic Coordinates. Madison, Wisconsin: University of Wisconsin Press.Google Scholar
Bloomfield, S.A., Hamos, J.E. & Sherman, S.M. (1987). Passive cable properties and morphological correlates of neurones in the lateral geniculate nucleus of the cat Journal of Physiology (London) 383, 653692.CrossRefGoogle ScholarPubMed
Bloomfield, S.A. & Sherman, S.M. (1988). Postsynaptic potentials recorded in neurons of the cat’s lateral geniculate nucleus following electrical stimulation of the optic chiasm. Journal of Neurophysiology 60, 19241945.CrossRefGoogle ScholarPubMed
Burke, W. & Cole, A.M. (1978). Extraretinal influence on the lateral geniculate nucleus. Reviews in Physiology, Biochemistry and Pharmacology 80, 105166.CrossRefGoogle ScholarPubMed
Crick, F. (1984). Function of the thalamic reticular complex: The searchlight hypothesis. Proceedings of the National Academy of Sciences of the U.S.A. 81, 45864590.CrossRefGoogle ScholarPubMed
Cucchiaro, J.B., Uhlrich, D.J. & Sherman, S.M. (1988). Parabrachial innervation of the cat’s dorsal lateral geniculate nucleus: An electron microscopic study using the tracer Phaseolus vulgaris leucoagglutinin (PHA-L). Journal of Neuroscience 8, 45764588.CrossRefGoogle ScholarPubMed
De Lima, A.D., Montero, V.M. & Singer, W. (1985). The cholinergic innervation of the visual thalamus: An EM immunocytochemical study. Experimental Brain Research 59, 206212.CrossRefGoogle ScholarPubMed
De Lima, 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, 92121.CrossRefGoogle Scholar
Deschênes, M. & Hu, B. (1990). Membrane resistance increase induced in thalamic neurons by stimulation of brainstem cholinergic afferents. Brain Research 513, 339342.CrossRefGoogle ScholarPubMed
Deschênes, M., Paradis, M., Roy, J.P. & Steriade, M. (1984). Electrophysiology of neurons of lateral thalamic nuclei in cat: Resting properties and burst discharges. Journal of Neurophysiology 51, 11961219.CrossRefGoogle ScholarPubMed
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, 647675.CrossRefGoogle ScholarPubMed
Fourment, A., Hirsch, J.C. & Marc, M.E. (1988). Reticular control of thalamic transmission during behavioral states: A study in dorsal lateral geniculate nucleus relay neurons of the cat. Experimental Neurology 100, 305321.CrossRefGoogle Scholar
Francesconi, W., Müller, C.M. & Singer, W. (1988). Cholinergic mechanisms in the reticular control of transmission in the cat lateral geniculate nucleus. Journal of Neurophysiology 59, 16901718.CrossRefGoogle ScholarPubMed
Funke, K. & Eysel, U.T. (1992). EEG-dependent modulation of response dynamics of cat dLGN relay cells and the contribution of corticogeniculate feedback. Brain Research 573, 217227.CrossRefGoogle ScholarPubMed
Guido, W., Lu, S.-M. & Sherman, S.M. (1992). Relative contributions of burst and tonic responses to the receptive-field properties of lateral geniculate neurons in the cat. Journal of Neurophysiology 68, 21992211.CrossRefGoogle Scholar
Hall, W.C., Fitzpatrick, D., Klatt, L.L. & Raczkowski, D. (1989). Cholinergic innervation of the superior colliculus in the cat. Journal of Comparative Neurology 287, 495514.CrossRefGoogle ScholarPubMed
Hockstein, S. & Shapley, R.M. (1976). Quantitative analysis of retinal ganglion cell classifications Journal of Physiology (London) 262, 237264.CrossRefGoogle Scholar
Hu, B., Steriade, M. & Deschênes, M. (1989). The effects of brainstem peribrachial stimulation on neurons of the lateral geniculate nucleus. Neuroscience 31, 1324.CrossRefGoogle ScholarPubMed
Ikeda, H. & Wright, M. J. (1974). Sensitivity of neurons in the visual cortex (area 17) under different levels of anesthesia. Experimental Brain Research 20, 471484.CrossRefGoogle Scholar
Jahnsen, H. & Llinás, R. (1984 a). Electrophysiological properties of guinea-pig thalamic neurones: An in vitro study Journal of Physiology (London) 349, 205226.CrossRefGoogle ScholarPubMed
Jahnsen, H. & Llinás, R. (1984 b). Ionic basis for the electroresponsiveness and oscillatory properties of guinea-pig thalamic neurones in vitro. Journal of Physiology (London) 349, 227247.CrossRefGoogle ScholarPubMed
Koch, C. (1987). The action of the corticofugal pathway on sensory thalamic nuclei: A hypothesis. Neuroscience 23, 399406.CrossRefGoogle ScholarPubMed
Livingstone, M.S. & Hubel, D.H. (1981). Effects of sleep and arousal on the processing of visual information in the cat. Nature 291, 554561.CrossRefGoogle ScholarPubMed
Lo, F.-S., Lu, S.-M. & Sherman, S.M. (1991). Intracellular and extracellular in vivo recording of different response modes for relay cells of the cat’s lateral geniculate nucleus. Experimental Brain Research 83, 317328.CrossRefGoogle ScholarPubMed
Lu, S.-M., Guido, W. & Sherman, S.M. (1992). Effects of membrane voltage on receptive-field properties of lateral geniculate neurons in the cat: Contributions of the low threshold Ca2+ conductance. Journal of Neuroscience 68, 21852198.Google ScholarPubMed
McCarley, R.W., Benoit, O. & Barrionuevo, G. (1983). Lateral geniculate nucleus unitary discharge in sleep and waking: State- and rate-specific aspects. Journal of Neurophysiology 50, 798818.CrossRefGoogle ScholarPubMed
McCormick, D.A. (1992). Cellular mechanisms underlying cholinergic and noradrenergic modulation of neuronal firing mode in the cat and guinea pig dorsal lateral geniculate nucleus. Journal of Neuroscience 12, 278289.CrossRefGoogle Scholar
McCormick, D.A. & Feeser, H.R. (1990). Functional implications of burst firing and single spike activity in lateral geniculate relay neurons. Neuroscience 39, 103113.CrossRefGoogle ScholarPubMed
McCormick, D.A. & Pape, H.-C. (1988). Acetylcholine inhibits identified interneurons in the cat lateral geniculate nucleus. Nature 334, 246248.CrossRefGoogle 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 (London) 392, 147165.CrossRefGoogle 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, 676690.CrossRefGoogle ScholarPubMed
Sherman, S.M. & Koch, C. (1986). The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus. Experimental Brain Research 63, 120.CrossRefGoogle ScholarPubMed
Sherman, S.M. & Koch, C. (1990). Thalamus. In Synoptic Organization of the Brain, 3rd edition, ed. Shepherd, G.M., pp. 246278. New York: Oxford University Press.Google Scholar
Singer, W. (1977). Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system. Physiological Reviews 57, 386420.CrossRefGoogle ScholarPubMed
Smith, Y., Paré, D., Deschênes, M., Parent, A. & Steriade, M. (1988). Cholinergic and non-cholinergic projections from the upper brainstem core to the visual thalamus in the cat. Experimental Brain Research 70, 166180.CrossRefGoogle Scholar
Steriade, M. & Deschênes, M. (1988). Intrathalamic and brainstemthalamic networks involved in resting and alert states. In Cellular Thalamic Mechanisms, ed. Bentivoglio, M. & Spreafico, R., pp. 3762. Amsterdam: Elsevier.Google Scholar
Steriade, M. & Llinás, R. (1988). The functional states of the thalamus and the associated neuronal interplay. Physiological Reviews 68, 649742.CrossRefGoogle ScholarPubMed
Steriade, M. & McCarley, R.W. (1990). Brainstem Control of Wakefulness and Sleep. New York: Plenum Press.CrossRefGoogle Scholar
Uhlrich, D.J., Cucchiaro, J.B. & Sherman, S.M. (1988). The projection of individual axons from the parabrachial region of the brain stem to the dorsal lateral geniculate nucleus in the cat. Journal of Neuroscience 8, 45654575.CrossRefGoogle Scholar
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, 25602563.CrossRefGoogle ScholarPubMed