1973
DOI: 10.1007/bf00234725
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Mesencephalic control of lateral geniculate nucleus in primates. III. Modifications with state of alertness

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Cited by 29 publications
(4 citation statements)
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“…With such pronounced depression of activity, secondary burst-pause sequences followed that were closely correlated with cortical afterdischarge responses in the VER; the late negative wave and afterdischarges appear in this context to have similar origins. Thus, in line with multiunit data in cats (Gijsbers & Melzack, 1972) and with other observations on shifts in LG excitability with changes in alertness (Bartlett, Doty, Saavedra, & Wilson, 1973;Malcolm, Bruce, & Burke, 1970), LG multiunit patterns of response to flashes in rats showed phasic movement-related fluctuations.…”
Section: Discussionsupporting
confidence: 89%
“…With such pronounced depression of activity, secondary burst-pause sequences followed that were closely correlated with cortical afterdischarge responses in the VER; the late negative wave and afterdischarges appear in this context to have similar origins. Thus, in line with multiunit data in cats (Gijsbers & Melzack, 1972) and with other observations on shifts in LG excitability with changes in alertness (Bartlett, Doty, Saavedra, & Wilson, 1973;Malcolm, Bruce, & Burke, 1970), LG multiunit patterns of response to flashes in rats showed phasic movement-related fluctuations.…”
Section: Discussionsupporting
confidence: 89%
“…Photic responses of maximal amplitude were obtained with the OX electrode in Horsely-Clark's coordinates at AP 20, LM 2, and 32 mm below the cortical surface. Adequate placement of the LGN electrodes was verified by monitoring typical postsynaptic waves induced by single OX shocks: When the electrode tip reached the surface of the LGN, a lame negative wave (Bartlett et al, 1973) appeared, further deep into the magnoc&ular laminas, another negative wave of short latency appeared. In each monkey, the tip of the LGN electrode was carefully adiusted in between the pa-rvo-and magnocellular laminas by recording both fast and slow potentials from the OX electrode (Schiller and Malneli.…”
Section: Group III Experimentsmentioning
confidence: 99%
“…Such modulation is seen in anesthetized subjects, where the EEG is activated by reticular stimulation (Castro-Alamancos and Oldford, 2002; Castro-Alamancos 2002), and in awake subjects that momentarily shift between alert and non-alert states (Swadlow and Weyand, 1987; Bezdudnaya et al, 2004; Cano et al, 2004). Some of the cortical changes are clearly due to changes occurring at the thalamus (Maffei et al, 1965; Coenen and Vendrik, 1972; Bartlett et al, 1973; Singer, 1977; Livingstone and Hubel, 1981), where EEG state-changes are associated with shifts between tonic and burst mode (Sherman and Guillery, 2002; Weyand et al, 2001). These shifts in thalamic mode occur even in awake subjects that shift their level of arousal (Bezdudnaya et al, 2006; Cano et al, 2006).…”
Section: Introductionmentioning
confidence: 99%