Protective effect of berberine chloride against cisplatin-induced ototoxicity
Background Cisplatin (CP) is an effective anticancer drug broadly used for various types of cancers, but it has shown ototoxicity that results from oxidative stress. Berberine has been reported for its anti-oxidative stress suggesting its therapeutic potential for many diseases such as colitis, diab...
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Published in | Genes & genomics Vol. 44; no. 1; pp. 1 - 7 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Singapore
01.01.2022
Springer Springer Nature B.V 한국유전학회 |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Cisplatin (CP) is an effective anticancer drug broadly used for various types of cancers, but it has shown ototoxicity that results from oxidative stress. Berberine has been reported for its anti-oxidative stress suggesting its therapeutic potential for many diseases such as colitis, diabetes, and vascular dementia.
Objective
Organ of Corti of postnatal day 3 mouse cochlear explants were used to compare hair cells after the treatment with cisplatin alone or with berberine chloride (BC) followed by CP.
Methods
We investigated the potential of the anti-oxidative effect of BC against the cisplatin-induced ototoxicity. We observed a reduced aberrant bundle of stereocilia in hair cells in CP with BC pre-treated group. Caspase-3 immunofluorescence and TUNEL assay supported the hypothesis that BC attenuates the apoptotic signals induced by CP. Reactive oxygen species level in the mitochondria were investigated by MitoSOX Red staining and the mitochondrial membrane potentials were compared by JC-1 assay.
Results
BC decreased ROS generation with preserved mitochondrial membrane potentials in mitochondria as well as reduced DNA fragmentation in hair cells. In summary, our data indicate that BC might act as antioxidant against CP by reducing the stress in mitochondria resulting in cell survival.
Conclusion
Our result suggests the therapeutic potential of BC for prevention of the detrimental effect of CP-induced ototoxicity. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 https://doi.org/10.1007/s13258-021-01157-1 |
ISSN: | 1976-9571 2092-9293 |
DOI: | 10.1007/s13258-021-01157-1 |