4.7 Article

Degranulation of Murine Resident Cochlear Mast Cells: A Possible Factor Contributing to Cisplatin-Induced Ototoxicity and Neurotoxicity

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MDPI
DOI: 10.3390/ijms24054620

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ototoxicity; cisplatin; mast cells; cromoglicic acid; cromolyn; cochlea; mouse

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Our research group discovered resident mast cells in rodents' cochleae and found that adding cisplatin changed their number. We further observed that murine cochlear mast cells degranulate in response to cisplatin and that the mast cell stabilizer cromolyn inhibits this process. Additionally, cromolyn significantly prevented cisplatin-induced loss of auditory hair cells and spiral ganglion neurons, providing evidence for mast cell participation in cisplatin-induced damage to the inner ear.
Permanent hearing loss is one of cisplatin's adverse effects, affecting 30-60% of cancer patients treated with that drug. Our research group recently identified resident mast cells in rodents' cochleae and observed that the number of mast cells changed upon adding cisplatin to cochlear explants. Here, we followed that observation and found that the murine cochlear mast cells degranulate in response to cisplatin and that the mast cell stabilizer cromoglicic acid (cromolyn) inhibits this process. Additionally, cromolyn significantly prevented cisplatin-induced loss of auditory hair cells and spiral ganglion neurons. Our study provides the first evidence for the possible mast cell participation in cisplatin-induced damage to the inner ear.

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