2009
DOI: 10.1523/jneurosci.0581-09.2009
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The Role of the Monkey Dorsal Pontine Nuclei in Goal-Directed Eye and Hand Movements

Abstract: Prevailing concepts on the control of goal-directed hand movements (HM) have focused on a network of cortical areas whose early parieto-occipital stages are thought to extract and integrate information on target and hand location, involving subsequent stages in frontal cortex forming and executing movement plans. The substantial experimental results supporting this "cortical network" concept for hand movements notwithstanding, the concept clearly needs refinement to account for the surprisingly mild HM disturb… Show more

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Cited by 20 publications
(21 citation statements)
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“…This ability to predict ON and OFF states is in agreement with previous modeling (albeit with a different feature) work [23] and conforms with experimental work [51] showing that single neurons can encode state transitions, and PFC neurons in particular, can categorize signals in vivo at the onset of stimulus presentation [52]. This information is readily available to downstream regions [53], [54], presumably contributing to the preparation of a specific movement.…”
Section: Discussionsupporting
confidence: 89%
“…This ability to predict ON and OFF states is in agreement with previous modeling (albeit with a different feature) work [23] and conforms with experimental work [51] showing that single neurons can encode state transitions, and PFC neurons in particular, can categorize signals in vivo at the onset of stimulus presentation [52]. This information is readily available to downstream regions [53], [54], presumably contributing to the preparation of a specific movement.…”
Section: Discussionsupporting
confidence: 89%
“…Both the DPN and the NRTP contribute to saccades as well as to SPEMs, deploying oculomotor neurons that vary regarding the degree of sensitivity for either type of visually guided eye movements (Crandall and Keller, 1985;Dicke et al, 2004;Suzuki et al, 1999;Thier and Mock, 2006;Thier et al, 1988;Tziridis et al, 2009). In view of this input, it is not surprising that also the OMV sports saccadeas well as pursuit-related PCs-the only output neuron of cerebellar cortex.…”
Section: Anatomical Considerationsmentioning
confidence: 99%
“…Precerebellar mossy fiber neurons are remarkably diverse with respect to both the stimuli they respond to and their firing responses in vivo (Eccles et al, 1971; Lisberger and Fuchs, 1978; Noda, 1986; van Kan et al, 1993; Zhang et al, 1995; Cheron et al, 1996; Escudero et al, 1996; Garwicz et al, 1998; Mackie et al, 1999; Rancz et al, 2007; Bengtsson and Jorntell, 2009; Tziridis et al, 2009; Tziridis et al, 2011). For example, neurons in the external cuneate nucleus fire transient, high frequency bursts in response to direct sensory (cutaneous) stimulation (Bengtsson and Jorntell, 2009), while those in the prepositus hypoglossi exhibit graded modulations in firing rate that are proportional to eye position (Escudero et al, 1996).…”
Section: Introductionmentioning
confidence: 99%
“…For example, neurons in the external cuneate nucleus fire transient, high frequency bursts in response to direct sensory (cutaneous) stimulation (Bengtsson and Jorntell, 2009), while those in the prepositus hypoglossi exhibit graded modulations in firing rate that are proportional to eye position (Escudero et al, 1996). Neurons in pontine nuclei are driven by complex cortical signals and exhibit a wide range of firing responses even during simple sensory-motor tasks (Tziridis et al, 2009, 2011). …”
Section: Introductionmentioning
confidence: 99%