Sensory gating mechanisms of the thalamus

The thalamus is an obligatory station through which nearly all sensory information must pass before reaching the cerebral cortex. One of the major functions of the thalamus is the selective control of the flow of sensory-motor information to the cerebral cortex during different states of the sleep-wake cycle and arousal, and is controlled through the actions of various neurotransmitter systems in the brainstem, hypothalamus, and cerebral cortex. Recent investigations have detailed the cellular mechanisms, including the role of GABAA and GABAB receptors, involved in the generation of both normal (e.g. spindle waves) and abnormal (e.g. generalized seizures) patterns of activity in thalamocortical circuits. In addition, in vivo investigations have also revealed that the dense projection from the cerebral cortex to the thalamus may synchronize thalamocortical activity in a manner useful for sensory analysis. Together, these data suggest that oscillations and synchronization are important for both normal and abnormal function in thalamocortical circuits.

[1]  David A. McCormick,et al.  Cellular mechanisms underlying cholinergic and noradrenergic modulation of neuronal firing mode in the cat and guinea pig dorsal lateral geniculate nucleus , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  Vincenzo Crunelli,et al.  A role for GABAB receptors in excitation and inhibition of thalamocortical cells , 1991, Trends in Neurosciences.

[3]  S. Sherman,et al.  Electron‐microscopic analysis of synaptic input from the perigeniculate nucleus to the A‐laminae of the lateral geniculate nucleus in cats , 1991, The Journal of comparative neurology.

[4]  O. Snead Evidence for GABAB-mediated mechanisms in experimental generalized absence seizures. , 1992, European journal of pharmacology.

[5]  David A. McCormick,et al.  Acetylcholine induces burst firing in thalamic reticular neurones by activating a potassium conductance , 1986, Nature.

[6]  R. Llinás,et al.  Electrophysiological properties of guinea‐pig thalamic neurones: an in vitro study. , 1984, The Journal of physiology.

[7]  P. Ohara,et al.  Thalamic reticular nucleus: anatomical evidence that cortico-reticular axons establish monosynaptic contact with reticulo-geniculate projection cells , 1981, Brain Research.

[8]  E. G. Jones,et al.  Thalamic oscillations and signaling , 1990 .

[9]  R. Llinás,et al.  Ionic basis for the electro‐responsiveness and oscillatory properties of guinea‐pig thalamic neurones in vitro. , 1984, The Journal of physiology.

[10]  D. McCormick,et al.  A model of the electrophysiological properties of thalamocortical relay neurons. , 1992, Journal of neurophysiology.

[11]  D. McCormick,et al.  Cellular mechanisms of a synchronized oscillation in the thalamus. , 1993, Science.

[12]  T. Morrow,et al.  Corticofugal influences of S1 cortex on ventrobasal thalamic neurons in the awake rat , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  D. Contreras,et al.  The slow (< 1 Hz) oscillation in reticular thalamic and thalamocortical neurons: scenario of sleep rhythm generation in interacting thalamic and neocortical networks , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  M. Steriade,et al.  Brainstem Control of Wakefulness and Sleep , 1990, Springer US.

[15]  D. McCormick,et al.  Corticothalamic activation modulates thalamic firing through glutamate "metabotropic" receptors. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Brain stem modulation of spatial receptive field properties of single cells in the dorsal lateral geniculate nucleus of the cat. , 1993, Journal of neurophysiology.

[17]  T. Tsumoto,et al.  Three groups of cortico‐geniculate neurons and their distribution in binocular and monocular segments of cat striate cortex , 1980, The Journal of comparative neurology.

[18]  T. Sejnowski,et al.  Simulations of cortical pyramidal neurons synchronized by inhibitory interneurons. , 1991, Journal of neurophysiology.

[19]  H. Pape,et al.  Nitric oxide controls oscillatory activity in thalamocortical neurons , 1992, Neuron.

[20]  J R Huguenard,et al.  A fast transient potassium current in thalamic relay neurons: kinetics of activation and inactivation. , 1991, Journal of neurophysiology.

[21]  D. Prince,et al.  Slow inactivation of a TEA-sensitive K current in acutely isolated rat thalamic relay neurons. , 1991, Journal of neurophysiology.

[22]  A. L. Humphrey,et al.  Functionally distinct groups of X‐cells in the lateral geniculate nucleus of the cat , 1988, The Journal of comparative neurology.

[23]  D. McCormick,et al.  Mechanisms of oscillatory activity in guinea‐pig nucleus reticularis thalami in vitro: a mammalian pacemaker. , 1993, The Journal of physiology.

[24]  David A. McCormick,et al.  Acetylcholine inhibits identified interneurons in the cat lateral geniculate nucleus , 1988, Nature.

[25]  J. Gotman,et al.  A study of the transition from spindles to spike and wave discharge in feline generalized penicillin epilepsy: Microphysiological features , 1981, Experimental Neurology.

[26]  D. McCormick,et al.  Serotonin and noradrenaline excite GABAergic neurones of the guinea‐pig and cat nucleus reticularis thalami. , 1991, The Journal of physiology.

[27]  M. Deschenes,et al.  The thalamus as a neuronal oscillator , 1984, Brain Research Reviews.

[28]  W. A. Wilson,et al.  The role of GABAB receptor activation in absence seizures of lethargic (lh/lh) mice. , 1992, Science.

[29]  A L Humphrey,et al.  Action of brain stem reticular afferents on lagged and nonlagged cells in the cat lateral geniculate nucleus. , 1992, Journal of neurophysiology.

[30]  S. Andersson,et al.  Physiological basis of the alpha rhythm , 1968 .

[31]  S. Sherman,et al.  Relative contributions of burst and tonic responses to the receptive field properties of lateral geniculate neurons in the cat. , 1992, Journal of neurophysiology.

[32]  R. Kalil,et al.  Synaptic connections between corticogeniculate axons and interneurons in the dorsal lateral geniculate nucleus of the cat , 1989, The Journal of comparative neurology.

[33]  D. McCormick Neurotransmitter actions in the thalamus and cerebral cortex and their role in neuromodulation of thalamocortical activity , 1992, Progress in Neurobiology.

[34]  S. Sherman,et al.  N-methyl-D-aspartate receptors contribute to excitatory postsynaptic potentials of cat lateral geniculate neurons recorded in thalamic slices. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[35]  D. McCormick,et al.  Functional implications of burst firing and single spike activity in lateral geniculate relay neurons , 1990, Neuroscience.

[36]  D. McCormick,et al.  Properties of a hyperpolarization‐activated cation current and its role in rhythmic oscillation in thalamic relay neurones. , 1990, The Journal of physiology.

[37]  D. Prince,et al.  A novel T-type current underlies prolonged Ca(2+)-dependent burst firing in GABAergic neurons of rat thalamic reticular nucleus , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[38]  M. Steriade,et al.  Electrophysiology of a slow (0.5‐4 Hz) intrinsic oscillation of cat thalamocortical neurones in vivo. , 1992, The Journal of physiology.

[39]  H. Pape,et al.  Different Types of Potassium Outward Current in Relay Neurons Acutely Isolated from the Rat Lateral Geniculate Nucleus , 1992, The European journal of neuroscience.

[40]  H. Pape Adenosine promotes burst activity in guinea‐pig geniculocortical neurones through two different ionic mechanisms. , 1992, The Journal of physiology.

[41]  D. Hubel,et al.  Effects of sleep and arousal on the processing of visual information in the cat , 1981, Nature.

[42]  G Avanzini,et al.  Intrinsic properties of nucleus reticularis thalami neurones of the rat studied in vitro. , 1989, The Journal of physiology.

[43]  S. Sherman,et al.  Evidence that cholinergic axons from the parabrachial region of the brainstem are the exclusive source of nitric oxide in the lateral geniculate nucleus of the cat , 1993, The Journal of comparative neurology.

[44]  George L. Gerstein,et al.  Feature-linked synchronization of thalamic relay cell firing induced by feedback from the visual cortex , 1994, Nature.

[45]  S. Sherman,et al.  Brainstem control of response modes in neurons of the cat's lateral geniculate nucleus. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[46]  P. Heggelund,et al.  Brain-stem influence on visual response of lagged and nonlagged cells in the cat lateral geniculate nucleus , 1993, Visual Neuroscience.

[47]  T. Sejnowski,et al.  Thalamocortical oscillations in the sleeping and aroused brain. , 1993, Science.

[48]  I. Soltesz,et al.  Two inward currents and the transformation of low‐frequency oscillations of rat and cat thalamocortical cells. , 1991, The Journal of physiology.

[49]  D. McCormick,et al.  Noradrenergic and serotonergic modulation of a hyperpolarization‐activated cation current in thalamic relay neurones. , 1990, The Journal of physiology.

[50]  P. Gloor,et al.  A study of the transition from spindles to spike and wave discharge in feline generalized penicillin epilepsy: EEG features , 1981, Experimental Neurology.

[51]  D. McCormick,et al.  Simulation of the currents involved in rhythmic oscillations in thalamic relay neurons. , 1992, Journal of neurophysiology.

[52]  A. Depaulis,et al.  Involvement of intrathalamic GABA b neurotransmission in the control of absence seizures in the rat , 1992, Neuroscience.

[53]  D. Hubel,et al.  Integrative action in the cat's lateral geniculate body , 1961, The Journal of physiology.

[54]  J. Hirsch,et al.  Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat , 1983, Brain Research.

[55]  James E. Vaughn,et al.  GABA neurons are the major cell type of the nucleus reticularis thalami , 1980, Brain Research.