Inhalation of hydrogen gas attenuates cisplatin-induced ototoxicity via reducing oxidative stress

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• 作者：Juan Qu^a ; Xu Li^a ; Juan Wang^a ; Wenjuan Mi^a ; Keliang Xie^b ; ^{xiekeliang2009@hotmail.com} ; Jianhua Qiu^a ; ^{qiujh@fmmu.edu.cn} ; ^{tougaozy2011@126.com}
• 关键词：8-iso-PGF2¦Á ; 8-iso-prostaglandin F2¦Á ; ABR ; auditory brainstem response ; H2 ; hydrogen gas ; MDA ; malondialdehyde ; OH ; hydroxyl radicals ; OHCs ; outer hair cells ; PBS ; phosphate-buffered saline ; ROS ; reactive oxygen species ; SPL ; sound pressure levels
• 刊名：International Journal of Pediatric Otorhinolaryngology
• 出版年：2012
• 出版时间：January 2012
• 年：2012
• 卷：76
• 期：1
• 页码：111-115
• 全文大小：574 K

文摘

Objective

Cisplatin, an anticancer drug used extensively to treat a broad range of tumors, has strong ototoxic side effects induced by reactive oxygen species (ROS). Recently, it has been reported that hydrogen gas (H₂) is a new antioxidant by selectively reducing hydroxyl radical, the most cytotoxic ROS. The present study was designed to investigate whether H₂ treatment is beneficial to cisplatin-induced ototoxicity via reducing oxidative stress.

Methods

The animals were intraperitoneally given a 30 min infusion of 16 mg/kg cisplatin or the same volume of saline. H₂ treatment was given twice with 2 % H₂ inhalation for 60 min starting at 1 h and 6 h after cisplatin or saline injection, respectively. The hearing status of all animals was evaluated by auditory brainstem responses (ABR). The hair cell damage was observed by phalloidin staining. In addition, the levels of oxidative products in serum and cochlear tissue were measured.

Results

We found that H₂ treatment significantly attenuated cisplatin-induced hearing loss evaluated by click-evoked and tone burst ABR threshold. Furthermore, histological analysis revealed that 2 % H₂ treatment significantly alleviated cisplatin-induced hair cell damage in the organ of corti. In addition, cisplatin significantly increased the levels of malondialdehyde (MDA) and 8-iso-prostaglandin F2¦Á (8-iso-PGF2¦Á) in serum and cochlear tissue, which was attenuated by H₂ treatment.

Conclusion

These results demonstrate that H₂ is beneficial to cisplatin-induced ototoxicity via reducing oxidative stress. Therefore, H₂ has potential for improving the quality of life of patients during chemotherapy by efficiently mitigating the cisplatin ototoxicity.