Effects of memantine on aminoglycoside-induced apoptosis of spiral ganglion cells in guinea pigs

BY Kim, WY Bae, DY Hur, JR Kim… - … --Head and Neck …, 2016 - journals.sagepub.com
BY Kim, WY Bae, DY Hur, JR Kim, TK Koh, TH Lee, GB Park
Otolaryngology--Head and Neck Surgery, 2016journals.sagepub.com
Objective To explore whether memantine, an N-methyl-D-aspartate receptor antagonist,
exerts a neuroprotective effect against apoptosis of spiral ganglion cells (SGCs) induced by
gentamicin. Study Design An animal experiment. Setting Dong-A University College of
Medicine, Busan, Korea. Subjects and Methods Gentamicin was injected into the left
cochleae of guinea pigs to induce apoptosis of SGCs; the contralateral cochleae served as
controls. Memantine was intraperitoneally injected 12 hours and 1 hour prior to gentamicin …
Objective
To explore whether memantine, an N-methyl-D-aspartate receptor antagonist, exerts a neuroprotective effect against apoptosis of spiral ganglion cells (SGCs) induced by gentamicin.
Study Design
An animal experiment.
Setting
Dong-A University College of Medicine, Busan, Korea.
Subjects and Methods
Gentamicin was injected into the left cochleae of guinea pigs to induce apoptosis of SGCs; the contralateral cochleae served as controls. Memantine was intraperitoneally injected 12 hours and 1 hour prior to gentamicin injection. At 1 week after gentamicin and/or memantine injection, the cochleae were removed and stained with hematoxylin and eosin to evaluate morphologic changes and apoptosis. Western blotting was performed to measure FasL expression and the extent of caspase activation in SGCs.
Results
SGC numbers remained stable after memantine treatment. Western blotting showed that FasL expression and activation of caspases 3, 8, and 9 were reduced in SGCs after memantine treatment.
Conclusion
Memantine attenuated the gentamicin-induced apoptosis of SGCs in guinea pigs. Moreover, memantine may affect Fas-FasL signaling in the receptor-mediated apoptotic pathway and caspase activation involved in the receptor-mediated and mitochondrial apoptotic pathways.
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