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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European archives of oto-rhino-laryngology and head & neck 245 (1988), S. 300-301 
    ISSN: 1434-4726
    Keywords: Cochlea ; Stria vascularis ; Vestibular organ (secretory epithelium) ; Autoradiography ; Menière's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Atrial natriuretic peptide (ANP) is a cardiac hormone known to mediate increased capillary permeability, vasodilation, and natriuresis. Since specific receptors for ANP exist in both the eye and brain, possibly playing a role in ocular and cerebrospinal fluid regulation, we postulated that ANP might also be involved in inner ear fluid dynamics. Autoradiography was used to evaluate whether and where ANP receptors are present in the inner ear. Frozen sections of the cochlea and vestibular organ from guinea pigs (n=18) were incubated in either 125J-ANP alone or together with an excess of unlabeled ANP (as control). ANP receptors were demonstrated in the stria vascularis of the cochlea and in the secretory epithelium of the ampulla and the utriculus, but not in the region of the sensory cells. These results indicate that (1) specific ANP receptors are present in the inner ear, and (2) their local distribution is congruent with those parts thought to regulate labyrinthine fluid composition and volume. We speculate that ANP contributes to the homeostasis of the inner ear fluids and may even play a role in the pathophysiology of Menière's disease.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European archives of oto-rhino-laryngology and head & neck 253 (1996), S. 470-474 
    ISSN: 1434-4726
    Keywords: Stria vascularis ; Spiral ganglion ; Organ of Corti ; Collagen ; Transgenic mouse strain animal model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The Mpv l7 mouse strain is a recessive transgenic mouse mutant that develops glomerulosclerosis and nephrotic syndrome at a young age. The phenotype results from a loss of function of a gene coding for a hydrophobic peroxisomal protein of 176 amino acids of 20 kDa following its destruction by retroviral integration. To investigate a potential effect of the missing Mpv 17 function on the inner ear light and electron microscopic investigations were performed on the inner ears of Mpv 17 mice and controls. These revealed degeneration of the stria vascularis and spiral ligament, loss of cochlear neurons and degeneration of the organ of Corti. The alterations observed here were similar to those described for Alport's syndrome, an inherited disorder characterized by progressive nephritis and neurosensory deafness. These findings indicate that although the molecular cause is different, the Mpv17 mouse model may share pathological mechanisms involved in patients with Alport's syndrome. At present the Mpv17 mouse appears to be a suitable animal model for this disease and may help to further elucidate the relationship between the kidney and the inner ear.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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