1978
DOI: 10.1007/bf00237385
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Properties and connections of cat fastigiospinal neurons

Abstract: 1. Neurons in the cat fastigial nucleus that project to the upper cervical spinal segments (fastigiospinal neurons) were fired by antidromic stimulation of the contralateral spinal cord. Dye ejection from the recording electrode was used to show that most neurons were in the rostral half of the fastigial nucleus. 2. Fastigiospinal neurons can be excited and/or inhibited by stimulation of forelimb and hindlimb nerves and by stimulation of the vestibular nerve. These inputs converge on many neurons. 3. Antidromi… Show more

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Cited by 43 publications
(16 citation statements)
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“…Neurons in the vestibular nerve and nuclei of the rhesus monkey encode motion of the head during passive motion (Roy and Cullen, 2001; Cullen and Minor, 2002), despite early vestibular-neck convergence in sensory processing (Boyle and Pompeiano, 1981; Anastasopoulos and Mergner, 1982; Wilson et al, 1990; Wilson, 1991). The significant convergence of vestibular and proprioceptive inputs within the next stage of processing in the rostral FN nucleus of the cerebellum (Furuya et al, 1975; Wilson et al, 1978; Matsushita and Tanami, 1987; Matsushita and Xiong, 2001), make this area a likely candidate for encoding body motion. Indeed, given that the rostral FN constitutes a major output of the anterior vermis (Verburgh et al, 1989) and nodulus/uvula (Voogd et al, 1996), both of which have been implicated in vestibular-proprioceptive interactions for limb and postural control; our findings suggest that the body motion signals encoded by rostral FN play an important role in the production of accurate motor behaviors.…”
Section: Discussionmentioning
confidence: 99%
“…Neurons in the vestibular nerve and nuclei of the rhesus monkey encode motion of the head during passive motion (Roy and Cullen, 2001; Cullen and Minor, 2002), despite early vestibular-neck convergence in sensory processing (Boyle and Pompeiano, 1981; Anastasopoulos and Mergner, 1982; Wilson et al, 1990; Wilson, 1991). The significant convergence of vestibular and proprioceptive inputs within the next stage of processing in the rostral FN nucleus of the cerebellum (Furuya et al, 1975; Wilson et al, 1978; Matsushita and Tanami, 1987; Matsushita and Xiong, 2001), make this area a likely candidate for encoding body motion. Indeed, given that the rostral FN constitutes a major output of the anterior vermis (Verburgh et al, 1989) and nodulus/uvula (Voogd et al, 1996), both of which have been implicated in vestibular-proprioceptive interactions for limb and postural control; our findings suggest that the body motion signals encoded by rostral FN play an important role in the production of accurate motor behaviors.…”
Section: Discussionmentioning
confidence: 99%
“…The cerebellum asserts control over muscle tone through a relatively direct action on spinal motor neurons and reflex mechanisms (Pompeiano, 1967;Thomas, Kaufman, Sprague, & Chambers, 1956;Wilson, Uchino, Maunz, Susswein, & Fukushima, 1978). At the same time, it influences higher levels of sensorimotor organization through direct inputs to brain· stem postural mechanisms (Brodal, 1957;Sherrington, 1906;Sprague & Chambers, 1953, 1959.…”
mentioning
confidence: 99%
“…The paleocerebellum, as described by Larsell (1934Larsell ( , 1967, includes portions of the anterior lobe and vermal cortex. In addition to interactions with the vestibular system, the paleocerebellum establishes extensive descending connections, directly and via the fastigial nucleus, to widespread areas of the brainstem reticular formation (Bharos, Kuypers, Lemon, & Muir, 1981;Larsell & Jansen, 1972;Martin, King, & Dom, 1974; and to the spinal cord (Batton, Jayaraman, Ruggiero, & Carpenter, 1977;Thomas, Kaufman, Sprague, & Chambers, 1956;Wilson, Uchino, Maunz, Susswein, & Fukushima, 1978). In addition, the paleocerebellum contributes direct and indirect projections to multiple areas within the limbic system (Angaut & Bowsher, 1970;Heath, 1976a;Snider, 1967;.…”
mentioning
confidence: 99%
“…Second, the rFN is a principle outflow nucleus of the cerebellar vermis, and neurons in the vermal regions of the anterior and posterior cerebellum are responsive to hindlimb movement (Oscarsson 1969; Gray et al 1993). Furthermore, the activity of rFN neurons is modulated during mechanical manipulations of the hindlimb (toe taps and pressure to foot pads) and electrical stimulation of hindlimb nerves (Eccles et al 1974a; Eccles et al 1974b; Wilson et al 1978). Third, rFN neuronal activity is modulated by vestibular afferent activation (Ghelarducci 1973; Ghelarducci et al 1974; Stanojevic et al 1980; Stanojevic 1981; Siebold et al 1997; Shaikh et al 2005; Miller et al 2008).…”
Section: Introductionmentioning
confidence: 99%