TY - JOUR
T1 - Quinoxaline protects zebrafish lateral line hair cells from cisplatin and aminoglycosides damage
AU - Sanchez, Sonia M.Rocha
AU - Fuson, Olivia
AU - Tarang, Shikha
AU - Goodman, Linda
AU - Pyakurel, Umesh
AU - Liu, Huizhan
AU - He, David Z.
AU - Zallocchi, Marisa
N1 - Funding Information:
We thank J. Taylor and J. Talaska for providing assistance with microscopy. Support for the UNMC Advanced Microscopy Core Facility was provided by the Nebraska Research Initiative, the Fred and Pamela Buffett Cancer Center Support Grant (P30CA036727), an Institutional Development Award (IDeA) from the NIGMS of the NIH (P30GM106397), the Nebraska Research Initiative Grant and Nebraska Center for Cellular Signaling CoBRE (NIH P30GM106397). We thank D. Delimont for genotyping and S. Kennedy for figure preparation. This work was supported by National Institutes of Health (grant 5P20RR018788) and the Tobacco Settlement Fund from the State of Nebraska to M.Z. and NIH R01 DC016807 from the NIDCD to D.Z.H. This work received past support through an NIH/NCRR 5P20RR018788/NIH/NIGMS 8P20GM103471 COBRE grant (S.M.R.-S.), and NIH/ ORIP R21OD019745-01A1 (S.M.R.-S.). The content of this research is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Hair cell (HC) death is the leading cause of hearing and balance disorders in humans. It can be triggered by multiple insults, including noise, aging, and treatment with certain therapeutic drugs. As society becomes more technologically advanced, the source of noise pollution and the use of drugs with ototoxic side effects are rapidly increasing, posing a threat to our hearing health. Although the underlying mechanism by which ototoxins affect auditory function varies, they share common intracellular byproducts, particularly generation of reactive oxygen species. Here, we described the therapeutic effect of the heterocyclic compound quinoxaline (Qx) against ototoxic insults in zebrafish HCs. Animals incubated with Qx were protected against the deleterious effects of cisplatin and gentamicin, and partially against neomycin. In the presence of Qx, there was a reduction in the number of TUNEL-positive HCs. Since Qx did not block the mechanotransduction channels, based on FM1-43 uptake and microphonic potentials, this implies that Qx’s otoprotective effect is at the intracellular level. Together, these results unravel a novel therapeutic role for Qx as an otoprotective drug against the deleterious side effects of cisplatin and aminoglycosides, offering an alternative option for patients treated with these compounds.
AB - Hair cell (HC) death is the leading cause of hearing and balance disorders in humans. It can be triggered by multiple insults, including noise, aging, and treatment with certain therapeutic drugs. As society becomes more technologically advanced, the source of noise pollution and the use of drugs with ototoxic side effects are rapidly increasing, posing a threat to our hearing health. Although the underlying mechanism by which ototoxins affect auditory function varies, they share common intracellular byproducts, particularly generation of reactive oxygen species. Here, we described the therapeutic effect of the heterocyclic compound quinoxaline (Qx) against ototoxic insults in zebrafish HCs. Animals incubated with Qx were protected against the deleterious effects of cisplatin and gentamicin, and partially against neomycin. In the presence of Qx, there was a reduction in the number of TUNEL-positive HCs. Since Qx did not block the mechanotransduction channels, based on FM1-43 uptake and microphonic potentials, this implies that Qx’s otoprotective effect is at the intracellular level. Together, these results unravel a novel therapeutic role for Qx as an otoprotective drug against the deleterious side effects of cisplatin and aminoglycosides, offering an alternative option for patients treated with these compounds.
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U2 - 10.1038/s41598-018-33520-w
DO - 10.1038/s41598-018-33520-w
M3 - Article
C2 - 30310154
AN - SCOPUS:85054773625
SN - 2045-2322
VL - 8
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 15119
ER -