1967
DOI: 10.3109/05384916709074285
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Cerebellifugal Fibres to the Cochlear Nuclei and Superior Olivary Complex

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Cited by 4 publications
(5 citation statements)
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“…Subsequent physiological studies have confirmed the same result across different animal species [Aitikin and Boyd, 1975;Huang and Liu, 1990;Sun et al, 1983;Wolfe and Kos, 1975;Xi et al, 1994]. It has also been demonstrated anatomically that the cochlear nucleus, the first relay nucleus along the auditory pathway, sends efferents directly to the cerebellum [Huang et al, 1982] and together with the ᭜ Petacchi et al ᭜ ᭜ 124 ᭜ superior olive directly receives retrograde cerebellifugal projections [Gacek, 1973;Rossi et al, 1967]. Although the functional significance of this direct cerebellar projection close to the auditory periphery has been little considered, it has been shown that the cerebellum can exert an inhibitory effect on the auditory nerve action potentials and on cochlear microphonics [Velluti and Crispino, 1979].…”
Section: Anatomical and Physiological Support For The Cerebellar Imagsupporting
confidence: 53%
“…Subsequent physiological studies have confirmed the same result across different animal species [Aitikin and Boyd, 1975;Huang and Liu, 1990;Sun et al, 1983;Wolfe and Kos, 1975;Xi et al, 1994]. It has also been demonstrated anatomically that the cochlear nucleus, the first relay nucleus along the auditory pathway, sends efferents directly to the cerebellum [Huang et al, 1982] and together with the ᭜ Petacchi et al ᭜ ᭜ 124 ᭜ superior olive directly receives retrograde cerebellifugal projections [Gacek, 1973;Rossi et al, 1967]. Although the functional significance of this direct cerebellar projection close to the auditory periphery has been little considered, it has been shown that the cerebellum can exert an inhibitory effect on the auditory nerve action potentials and on cochlear microphonics [Velluti and Crispino, 1979].…”
Section: Anatomical and Physiological Support For The Cerebellar Imagsupporting
confidence: 53%
“…However, the extent to which these would have been removed was assessed by evaluating the extent of the transection of the olivocochlear bundle as it traverses the brainstem, at a location distal to where its strial branch exits but definitely before the exit of the ventral branch connections to the cochlear nucleus. Connections from the cerebellum to the cochlear nucleus were not specifically cut, but these appear to connect mostly to the ventral cochlear nucleus (VCN; Rasmussen, 1967; Rossi et al, 1967; Gacek, 1973). Based on the degree of transection of descending projections, both control and exposed animals were divided into the following three experimental subgroups: 1) animals without sectioning (no surgical sectioning was performed to separate the DCN from its adjacent brainstem structures), 2) animals with partial sectioning (incomplete transection of brainstem tracts near the DCN was achieved), and 3) animals with complete or nearly complete sectioning (the DCN was completely or nearly completely isolated from the adjacent brainstem structures).…”
Section: Methodsmentioning
confidence: 99%
“…Sources of these auditory inputs include the contralateral cochlear nucleus (Adams and Warr, 1976; Cant and Gaston, 1982; Wenthold, 1987; Shore et al, 1992; Alibardi, 2000; Arnott et al, 2004), superior olivary complex (Starr and Wernick, 1968; Brown et al, 1988; Sherriff and Henderson, 1994; Ostapoff et al, 1997), inferior colliculi (Rasmussen, 1960; Conlee and Kane, 1982; Faye‐Lund, 1988; Caicedo and Herbert, 1993), nuclei of the lateral lemniscus (Rasmussen, 1960; Kane, 1977), and primary auditory cortex (Weedman and Ryugo, 1996). Sources of nonauditory inputs include the mesencephalic reticular formation (Gonzalez‐Lima and Scheich, 1984), locus coeruleus (Kromer and Moore, 1980; Ebert, 1996), cuneate nucleus (Weinberg and Rustioni, 1987; Wright and Ryugo, 1996), trigeminal nucleus (Itoh et al, 1987; Li and Mizuno, 1997; Zhou and Shore, 2004), trigeminal ganglion (Shore, 2005), dorsal raphe nucleus (Thompson and Thompson, 2001; Ye and Kim, 2001), and cerebellum (Rasmussen, 1967; Rossi et al, 1967; Gacek, 1973). The purpose of the current study was to test whether DCN hyperactivity is dependent on any of these descending inputs to the DCN.…”
mentioning
confidence: 99%
“…The connections between the cerebellum and the cerebral cortex are composed of feedforward (the corticopontine-pontocerebellar circuit) and feedback (the cerebellothalamic-thalamocortical circuit) loops, which are the anatomic foundations of the involvement of the cerebellum in sensory perception (Baumann et al, 2015 ). The cerebellum is structurally connected to the cochlear nucleus (Huang et al, 1982 ), superior olivary nucleus (Rossi et al, 1967 ), inferior colliculus (Ruchalski and Hathout, 2012 ), medial geniculate body (Keifer et al, 2015 ) and the auditory cortex (Huffman and Henson, 1990 ), either directly or indirectly. This suggests that the cerebellum could impact the signal from the peripheral hearing organs or modulate the activity of the acoustic center.…”
Section: Introductionmentioning
confidence: 99%