Inhalation of hydrogen gas attenuates cisplatin-induced ototoxicity via reducing oxidative stress |
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Authors: | Qu Juan Li Xu Wang Juan Mi Wenjuan Xie Keliang Qiu Jianhua |
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Affiliation: | a Department of Otolaryngology, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China b Department of Anesthesiology, General Hospital of Tianjin Medical University, Tianjin 300052, China |
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Abstract: | ObjectiveCisplatin, 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.MethodsThe 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.ResultsWe 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 F2α (8-iso-PGF2α) in serum and cochlear tissue, which was attenuated by H2 treatment.ConclusionThese 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. |
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Keywords: | 8-iso-PGF2α, 8-iso-prostaglandin F2α ABR, auditory brainstem response H2, hydrogen gas MDA, malondialdehyde 0" alt=" radical dot" src=" http://cdn.els-cdn.com/sd/entities/rad" class=" glyphImg" >OH, hydroxyl radicals OHCs, outer hair cells PBS, phosphate-buffered saline ROS, reactive oxygen species SPL, sound pressure levels |
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