Origin of ascending auditory projections to the nucleus mesencephalicus lateralis pars dorsalis in the chicken
Reference (42)
Technical considerations on the use of horseradish peroxidase as a neuronal marker
Neuroscience
(1977)- et al.
Organization of ascending auditory pathways in the pigeon (Columbia livia) as determined by autoradiographic methods
Brain Research
(1982) - et al.
Auditory centers in the elasmobranch brain stem: deoxyglucose autoradiography and evoked potential recording
Brain Research
(1982) - et al.
The autoradiographic demonstration of axonal connections in the central nervous system
Brain Research
(1972) - et al.
Infrasound responses in the midbrain of the guinea fowl
Neurosci. Lett.
(1984) Fiber degeneration following lesions in the anteroventral cochlear nucleus of the cat
Exp. Neurol.
(1966)Fiber degeneration following lesions in the posteroventral cochlear nucleus of the cat
Exp. Neurol.
(1969)Ascending projections to the inferior colliculus
J. Comp. Neurol.
(1979)- et al.
Inferior colliculus. I. Comparison of response properties of neurons in central, precentral and external nuclei of adult cat
J. Neurophysiol.
(1975) - et al.
Auditory responses of neurons in the lateral mesencephalic nucleus (inferior colliculus) of the barbary dove
J. Physiol.
Ascending projections form the primary cochlear nuclei and nucleus laminaris in the pigeon
J. Comp. Neurol.
The distribution of primary lagenar fibers within the vestibular nuclear complex of the pigeon
Brain Behav. Evol.
Central auditory pathways of nonmammalian vertebrates
Morphology and physiology of the auditory system
A comparison of the size of an auditory nucleus (n. mesencephalicus lateralis, pars dorsalis) with the size of the optic lobe in twenty-seven species of birds
J. Comp. Neurol.
The response properties of auditory neurones in the midbrain of the domestic fowl (Gallus gallus) to monaural and binaural stimuli
J. Comp. Physiol.
Ascending projections from the cochlear nuclei and nucleus laminaris to nucleus mesencephalicus lateralis pars dorsalis in the chicken
Anat. Rec.
The afferent connections of the main and the accessory olfactory bulb formations in the rat: an experimental HRP study
J. Comp. Neurol.
The course of the stria of Monakow and Held in the cat
J. Comp. Neurol.
The organization of central auditory pathways in a reptile,Iguana iguana
J. Comp. Neurol.
Cited by (80)
Avian adeno-associated virus as an anterograde transsynaptic vector
2021, Journal of Neuroscience MethodsCitation Excerpt :To that end, we next chose the nucleus mesencephalicus lateralis pars dorsalis (MLd) as the injection target. MLd is the pivot of the avian auditory pathway; it receives input fibers from various brainstem auditory nuclei and sends output fibers to the auditory thalamus, nucleus ovoidalis (Ov), which in turn send axons to the pallium, field L (FL) (Conlee and Parks, 1986; Ito and Atoji, 2016; Krutzfeldt et al., 2010a, b; Wang and Karten, 2010; Wang et al., 2017; Wild et al., 1993, 2010) (Fig. 2). In the ascending pathway from MLd, Ov is monosynaptic (second-order), and FL is disynaptic (third-order) from the MLd in the shortest route.
Intrinsic properties of avian interaural level difference sound localizing neurons
2021, Brain ResearchCitation Excerpt :In birds, the first nucleus that encodes ILD is the posterior portion of the dorsal nucleus of the lateral lemniscus (LLDp, formerly known as VLVp, the nucleus ventralis lemnisci lateralis pars posterior) (Mogdans and Knudsen, 1994). LLDp neurons receive excitatory input from the contralateral cochlear nucleus angularis (NA) (Conlee and Parks, 1986; Takahashi and Konishi, 1988), and receive inhibitory input primarily from the other LLDp, which is driven by excitatory input originating from the ipsilateral NA (Manley et al., 1988; Takahashi and Keller, 1992). A number of in vivo studies have demonstrated the roles of LLDp neurons in ILD processing (Adolphs, 1993; Sato et al., 2010; Takahashi and Keller, 1992).
2.19 - Evolution of Central Pathways
2020, The Senses: A Comprehensive Reference: Volume 1-7, Second EditionConserved mechanisms of vocalization coding in mammalian and songbird auditory midbrain
2013, Hearing ResearchCitation Excerpt :The avian auditory midbrain is traditionally called the lateral dorsal mesencephalon (MLd) because of its anatomical location, but this nucleus is homologous to the mammalian central nucleus of the inferior colliculus (ICc; Grothe et al., 2004; Covey and Carr, 2005). The ICc and MLd receive inputs directly from contralateral and ipsilateral cochlear nuclei, from lateral lemniscal nuclei and from the contralateral auditory midbrain (Conlee and Parks, 1986; Krutzfeldt et al., 2010; see Fig. 1 for details). The IC and MLd also receive ascending input from other brainstem nuclei, including the superior olivary complex and superior paraolivary nucleus in mammals (Winer and Schreiner, 2005 for review), and the superior olivary nucleus in songbirds (Wild et al., 2010).
Neuronal morphology in subdivisions of the inferior colliculus of chicken (Gallus gallus)
2012, Journal of Chemical NeuroanatomyCitation Excerpt :The IC is the most prominent neuronal midbrain structure medially to the optic tectum (TeO) and lies enveloped within the intercollicular complex (ICo; Knudsen, 1983; Conlee and Parks, 1986; Kingsbury et al., 2011). The boundaries of this nucleus were already defined by means of hodological and histological analysis in a large number of studies in several avian species such as pigeon (Karten, 1967), barn owl (Knudsen, 1983; Wagner et al., 2003) and chicken (Conlee and Parks, 1986; Sorenson et al., 1989; Puelles et al., 1994; Zeng et al., 2008). Karten (1967) referred to this nucleus as the MLd and suggested this structure to be homologous to the mammalian inferior colliculus (IC).