1970
DOI: 10.3109/00016487009123353
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Effect of Ouabain on Cochlear Potentials and Endolymph Composition in Guinea Pigs

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1971
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Cited by 114 publications
(50 citation statements)
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“…Perilymphatic perfusion of ouabain, an inhibitor of the NKAα, causes a rapid reduction of the endocochlear potential (Konishi and Mendelsohn 1970;Kuijpers and Bonting 1970;Kusakari et al 1978), and researchers have identified NKAα1 in the strial marginal cells and NKAα2 in the lateral wall fibrocytes (McGuirt and Schulte 1994;Schulte and Steel 1994; reviewed in Wangemann 2006). The contribution of the NKAα1 and NKAα2 in maintaining the endocochlear potential is supported by the characterization of mice carrying deletions of these subunits.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Perilymphatic perfusion of ouabain, an inhibitor of the NKAα, causes a rapid reduction of the endocochlear potential (Konishi and Mendelsohn 1970;Kuijpers and Bonting 1970;Kusakari et al 1978), and researchers have identified NKAα1 in the strial marginal cells and NKAα2 in the lateral wall fibrocytes (McGuirt and Schulte 1994;Schulte and Steel 1994; reviewed in Wangemann 2006). The contribution of the NKAα1 and NKAα2 in maintaining the endocochlear potential is supported by the characterization of mice carrying deletions of these subunits.…”
Section: Discussionmentioning
confidence: 99%
“…Because inhibitors of the NKAα are known to reduce the endocochlear potential (Konishi and Mendelsohn 1970), previous research investigating the localization of the NKAα in the cochlea has focused on its expression in structures, like the stria vascularis and spiral ligament, responsible for maintaining the endocochlear potential (Wangemann 2006). Nonetheless, earlier work also reported expression of the NKAα in the neuronal elements of the mammalian cochlea using a variety of techniques, including enzyme cytochemistry (Kerr et al 1982), in situ hybridization (Ryan and Watts 1991), and immunohistochemistry (Schulte and Adams 1989;Iwano et al 1990;McGuirt and Schulte 1994;Schulte and Steel 1994;ten Cate et al 1994;Nakazawa et al 1995;Zuo et al 1995;Erichsen et al 1996;Peters et al 2001;Weber et al 2001).…”
Section: Introductionmentioning
confidence: 99%
“…Early metabolic studies demonstrated that the electrogenic mechanism is closely associated with both EP and cochlear cation gradients (Konishi and Mendelsohn, 1970;Kuijpers and Bonting, 1970;Johnstone, 1965;Davis et al, 1955) and described high Na,K-ATPase activity in stria vascularis and spiral ligament (Kuijpers and Bonting, 1969;Iinuma, 1967;Kuijpers et al, 1967 29425. for the a3-and P1-subunit isoforms. Subpopulations of fibroqtes in the spiral prominence, suprastrial and supralimbal regions, and vestibular system expressed either the al-or a2-isoform, or both.…”
Section: Introductionmentioning
confidence: 99%
“…Various ion transporters and channels that may be responsible for the generation of EP and endolymphatic high [K ϩ ] exist in these cells. Na ϩ ,K ϩ -ATPase and Na ϩ ,K ϩ ,2Cl Ϫ cotransporter that are localized at the basolateral membrane of marginal cells contribute to the generation of EP, because ouabain and furosemide, specific blockers of Na ϩ ,K ϩ -ATPase and Na ϩ ,K ϩ ,2Cl Ϫ cotransporter, respectively, depressed EP (Kusakari et al, 1978;Konishi and Mendelsohn, 1970). In vestibule, on the other hand, endovestibular fluid also contains 150 mM K ϩ , but its potential is ϳ0 mV, although dark cells, corresponding to cochlear marginal cells, also express both Na ϩ ,K ϩ -ATPase and Na ϩ ,K ϩ ,2Cl Ϫ cotransporter at their basolateral membrane (Schulte and Adams, 1989;Marcus et al, 1994).…”
mentioning
confidence: 99%