1987
DOI: 10.1016/s0006-3495(87)83256-3
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Tetrodotoxin-sensitive, voltage-dependent sodium currents in hair cells from the alligator cochlea

Abstract: We have used whole-cell patch clamp techniques to record from tall hair cells isolated from the apical half of the alligator cochlea. Some of these cells gave action potentials in response to depolarizing current injections. When the same cells were voltage clamped, large transient inward currents followed by smaller outward currents were seen in response to depolarizing steps. We studied the transient inward current after the outward current had been blocked by external tetraethylammonium (20 mM) or by replac… Show more

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Cited by 44 publications
(29 citation statements)
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“…I Na is downregulated during the first postnatal week, decreasing the sodium-based excitability in mature hair cells. This developmental excitability, also observed in the mouse utricle (Geleoc et al, 2004), has also been reported in other sensory organs of the higher vertebrates, such as the cochlea (Evans and Fuchs, 1987;Kros et al, 1998) and the retina (Pan and Hu, 2000;Kawai et al, 2001). Although, in most cases, the physiological relevance of the I Na remains unknown, we first reported that I Na was involved in the activity-dependent secretion of brain-derived neurotrophic factor (BDNF) in the neonate rat utricle (Chabbert et al, 2003).…”
Section: Introductionsupporting
confidence: 60%
“…I Na is downregulated during the first postnatal week, decreasing the sodium-based excitability in mature hair cells. This developmental excitability, also observed in the mouse utricle (Geleoc et al, 2004), has also been reported in other sensory organs of the higher vertebrates, such as the cochlea (Evans and Fuchs, 1987;Kros et al, 1998) and the retina (Pan and Hu, 2000;Kawai et al, 2001). Although, in most cases, the physiological relevance of the I Na remains unknown, we first reported that I Na was involved in the activity-dependent secretion of brain-derived neurotrophic factor (BDNF) in the neonate rat utricle (Chabbert et al, 2003).…”
Section: Introductionsupporting
confidence: 60%
“…Similarly, there were increased amounts of the sodium channel transcript SCN3B in the LF end and of SCNN1A in the HF end. While sodium channels have not been observed in the chicken, hair cells from the LF end of alligator BP were found to contain TTX-sensitive currents (Evans and Fuchs 1987). Actin was detected by our array but found not to be tonotopically expressed (data not shown), a finding that is intuitive given that the total amount of actin per hair cell does not vary tonotopically in chickens (Tilney and Tilney 1988).…”
Section: Discussionmentioning
confidence: 60%
“…A third Na ϩ current type, TTX-sensitive (like I Na,2 ) but negatively inactivating (like I Na,1 ), is reported from hair cells of diverse juvenile and mature hair cell organs (Evans and Fuchs 1987;Masetto et al 2003;Sugihara and Furukawa 1989;Witt et al 1994). The channel composition may change with maturation or, because most of these are nonmammals, differ between vertebrate classes.…”
Section: Two Na ϩ Currents In Hair Cellsmentioning
confidence: 99%
“…Information on voltagegated sodium (Na ϩ ) channels is more fragmentary. By the classic properties of voltage range of inactivation and sensitivity to tetrodotoxin (TTX), voltage-gated Na ϩ currents in hair cells fall into three classes: TTX-sensitive currents that inactivate at very negative potentials (Evans and Fuchs 1987;Masetto et al 2003;Sugihara and Furukawa 1989;Witt et al 1994); TTX-sensitive currents that inactivate at less negative potentials (Chabbert et al 2003;Marcotti et al 2003); and TTX-insensitive currents that inactivate at very negative potentials (Géléoc et al 2004;Oliver et al 1997;Rüsch and Eatock 1997).…”
Section: Introductionmentioning
confidence: 99%