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Aminoglycoside antibiotics impair calcium entry but not viability and motility in isolated cochlear outer hair cells

✍ Scribed by D. Dulon; G. Zajic; J.-M. Aran; Dr. J. Schacht


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
907 KB
Volume
24
Category
Article
ISSN
0360-4012

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✦ Synopsis


Cochlear outer hair cells have been well established as primary targets of the ototoxic actions of aminoglycoside antibiotics. These cells, isolated from the guinea pig cochlea and maintained in short-term culture, were used as a model for evaluating the acute effects of gentamicin on cell viability, depolariizationinduced transmembrane calcium flux, and depolarization-induced motile responses.

On the basis of morphology and fluorochromasia, the presence of extracellular gentamicin as high as 5 mM did not affect the viability of the cells for up to 6 hr, the longest time tested. Viable cells showeid binding of fluorescently tagged gentamicin to their base but excluded the drug from their cytoplasm. In response to [K+]-depolarization, intracellular calcium levels (monitored with the fluorescent calciuni-sensitive dye fluo-3) increased from a resting value of 218 2 102 nM to 2,018 & 1,077 nM concomitant with a cell shortening of 0.7% & 1.3%. The depolarizationinduced calcium increase was apparently caused by calcium entry into the cell as it was inhibited by the calcium-channel blocker methoxyverapamil and prevented in the absence of extracellular calcium. Both gentamicin and neomycin blocked the [K+]-imduced calcium increase at an ICs0 of 50 pM. Despite the inhibition of calcium entry the ability of the outer hair cells to shorten under [K+]-depolarizatiion was not impaired; in fact, cell shortening was evein more pronounced in the absence of calcium influx (2.6% f 1.4%). This argues effectively against the existence of a calcium-dependent actomyosin-mediated component in [K+]-induced shape changes.

The results suggest the existence of voltage-gated calcium channels in outer hair cells and that calcium influx through these channels is impaired by the aminoglycoside antibiotics neomycin and gentamicin. This action may be part of the acute ototoxic mech-anism of these molecules. Furthermore, the results not only confirm the calcium independence of the depolarization-induced motility but also suggest that calcium influx into outer hair cells opposes cell shortening.