“…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.…”