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  • 1
    ISSN: 1432-0878
    Keywords: Key words Neurotrophins ; Ear development ; trk receptors ; Mutants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Analyses of single and double mutants of members of the neurotrophin family and their receptors are reviewed. These data demonstrate that the two neurotrophins, brain-derived neurotrophic factor (BDNF) and neurotrophin 3 (NT-3), and their high-affinity receptors trkB and trkC, are the sole support for the developing afferent innervation of the ear. Neurotrophins are first expressed in the otocyst around the time afferent sensory neurons become postmitotic. They are crucial for the survival of certain topologically distinct populations of sensory neurons. BDNF supports all sensory neurons to the semicircular canals, most sensory neurons to the saccule and utricle, and many sensory neurons to the apex and middle turn of the cochlea. In contrast, NT-3 supports few sensory neurons to the utricle and saccule, all sensory neurons to the basal turn of the cochlea and most sensory neurons to the middle and apical turn. Some topologically restricted effects reflect the pattern of neurotrophin distribution as revealed by in situ hybridization (e.g., loss of all innervation to the semicircular canal sensory epithelia in BDNF or trkB mutants). However, other topologically restricted effects cannot be explained on the basis of current knowledge of neurotrophin or neurotrophin receptor distribution. Data on mutants also support the notion that BDNF may play a role in neonatal plastic reorganization of the pattern of innervation in the ear and possibly the brainstem. In contrast, data obtained thus far on the ability of neurotrophins to rescue adult sensory neuron after insults to cochlear hair cells are less compelling. The ear is a model system to test the interactions of the two neurotrophins, BDNF and NT-3, with their two high-affinity receptors, trkB and trkC.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European archives of oto-rhino-laryngology and head & neck 234 (1982), S. 157-161 
    ISSN: 1434-4726
    Keywords: Menière's disease ; Sudden deafness ; Neurectomy ; Cochlear nerve ; Fiber counts ; Audiometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Surgical biopsy specimens of the cochlear nerve from 19 patients with Menière's disease and six patients with sudden deafness were studied. The total number of myelinated nerve fibers in the transverse fascicular area of each nerve were counted and the results were correlated with the clinical and preoperative audiological data. The total number of cochlear neurons in patients with Menière's disease ranged from 5,760 to 27,722 and in patients with sudden deafness from 8,500 to 22,714. The long duration of the disease or absent speech discrimination appeared not to be connected with lower numbers of neurons than preserved speech discrimination or short history of the disease.
    Type of Medium: Electronic Resource
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