Back to Search Start Over

Apoptosis-inducing factor and calpain upregulation in glutamate-induced injury of rat spiral ganglion neurons

Authors :
Xiaodong Chen
Xin Chen
Fu‑Quan Chen
Zhong‑Jia Ding
Wen‑Juan Mi
Ren‑Feng Wang
Jian Wang
Jian‑Hua Qiu
Yong‑Li Song
Xiao‑Xu Tang
Xi Wang
Source :
Molecular Medicine Reports
Publication Year :
2015
Publisher :
D.A. Spandidos, 2015.

Abstract

Spiral ganglion neuron (SGN) damage and apoptosis can lead to noise-induced hearing loss, age-associated hearing loss and, in certain cases, auditory neuropathy. The apoptosis-inducing factor (AIF)-associated pathway may be important in this process. The present study aimed to investigate the expression levels of AIF and calpain in damaged SGNs. Glutamate (Glu) perfusion and cell culture in different concentrations of Glu were performed to damage the SGNs of Sprague-Dawley (SD) rats, with saline water used as a control Different concentrations (5, 10, 20 and 40 mM) of Glu were injected into the cochlear tympanic canal of 18 SD rats, and 10, 20 and 40 mM Glu were added to SGN cultures. Auditory brainstem responses (ABR) were measured prior to and 2 days following the injection of Glu. Immunofluorescent staining was used to detect the SGN damage and the expression levels of AIF and calpain in vivo and in in vitro. Transmission electron microscopy (TEM) was used to measure cell apoptosis and reverse transcription-quantitative polymerase chain reaction was used to analyse the gene expression levels of AIF and calpain in the damaged SGNs. The TEM identified mitochondrial vacuolisation, swelling of the SGN and hetero-chromatin formation. Injection of Glu reduced the number of SGNs and induced apoptosis. AIF was observed to translocate into the nuclei of the SGNs in the 20 and 40 mM Glu groups, and the expression levels of AIF and calpain were markedly upregulated in the modiolus of the Glu-damaged SGNs. The upregulation of AIF and calpain may be important in the process of SGN damage and apoptosis.

Details

Language :
English
ISSN :
17913004 and 17912997
Volume :
12
Issue :
2
Database :
OpenAIRE
Journal :
Molecular Medicine Reports
Accession number :
edsair.doi.dedup.....7413158670171ef7cbe892fe6f0ef29e