Abstract
Place an electrode on the surface or in the depth of nearly any neuronal structure in the brain of either vertebrates or invertebrates. Record the fluctuations of voltage produced by the flow of current, and what you are likely to observe is an irregular sequence of rhythmic changes of potential having a multitude of frequencies (Bullock and Başar, 1988). If your electrode happens to be within one of many structures responsive to sensory stimuli, the presentation of a stimulus will in many cases evoke a sustained rhythmic fluctuation of potential outlasting the stimulus. This propensity for neural structures to generate oscillatory waves of activity has come to be termed an “induced rhythm”. It is a general property of sensory as well as many other neuronal networks that is expressed during periods of activation. In this chapter we describe some of our recent observations of induced rhythms in the mammalian visual cortex and discuss the evidence for several neuronal mechanisms thought to underlie their generation.
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Munemori J, Hara K, Kimura M, Sato R (1984): Statistical features of impulse trains in cat’s lateral geniculate neurons. Biol Cybern 50:167–172
Perez-Borja C, Tyce FA, McDonald C, Uihlein A (1961): Depth electrographic studies of a focal fast response to sensory stimulation in the human Electroencephalogr Clin Neurophysiol 13: 695–702
Raether A, Gray CM, Singer W (1989): Intercolumnar interactions of oscillatory neuronal responses in the visual cortex of alert cats. Eur Neurosci Assoc Abst 72.5
Rougeul A, Bouyer JJ, Dedet L, Debray O (1979): Fast somato-parietal rhythms during combined focal attention and immobility in baboon and squirrel monkey. Electroencephalogr Clin Neurophysiol 46: 310–319
Schwindt PC, Spain WJ, Foehring RC, Stafstrom CE, Chubb MC, Crill WE (1988): Multiple potassium conductances and their functions in neurons from cat sensorimotor cortex in vitro. J Neurophysiol 59(2): 424–449
Sem-Jacobsen CW, Petersen MC, Dodge HW, Lazarte JA, Holman CB (1956): Electroencephalographic rhythms from the depths of the parietal, occipital and temporal lobes in man. Electroencephalogr Clin Neurophysiol. 8: 263–278
Sheer DE, (1976): Focused arousal and 40-Hz EEG. In: The Neuropsychology of Learning Disorders, Knights RM, Bakker DJ, eds., Baltimore: University Park Press, pp 71–78
Singer W (1979): Central-core control of visual cortex functions. In: The Neurosciences Fourth Study Program, Schmitt FO, Worden FG, Cambridge, MA: eds. MIT Press, pp 1093–1109
Sporns O, Gally JA, Reeke GN, Edelman GM (1989) Reentrant signaling among simulated neuronal groups leads to coherency in their oscillatory activity. Proc Natl Acad Sci 86: 7265–7269
Thommesen G. (1978) The spatial distribution of odor-induced potentials in the olfactory bulb of char and trout (Salmonidae). Acta Physiol Scand 102: 205–217
Vianna Di Prisco G, Freeman WJ (1985): Odor-related bulbar EEG spatial pattern analysis during appetitive conditioning in rabbits. Behav Neurosci 99(5): 964–978
Wilson HR, Cowan JD (1972): Excitatory and inhibitory interactions in localized populations of model neurons. Biophys J 12: 1–24
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Gray, C.M., Engel, A.K., König, P., Singer, W. (1992). Mechanisms Underlying the Generation of Neuronal Oscillations in Cat Visual Cortex. In: Başar, E., Bullock, T.H. (eds) Induced Rhythms in the Brain. Brain Dynamics. Birkhäuser, Boston, MA. https://doi.org/10.1007/978-1-4757-1281-0_2
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DOI: https://doi.org/10.1007/978-1-4757-1281-0_2
Publisher Name: Birkhäuser, Boston, MA
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