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. 2021 Dec 21;2021:3548706. doi: 10.1155/2021/3548706

Table 1.

Studies on the protective effect of antioxidants on various SNHL.

Drug Experimental design Outcome Mechanism Reference
MT Animal experiment: rats DPOAE: M+RT group and RT+M group>RT group Inhibit production of ROS7; enhance the DNA repair process [89]
AMF Animal experiment: guinea pigs Degree of cochlear hair cell damage: IRR + AMF group < RT group.
No difference between 100 mg/kg and 200 mg/kg AMF groups
Be hydrolyzed into active component in vivo, which has sulfhydryl group that scavenges free radicals [90]
LC Animal experiment: guinea pigs Histopathological examination: LC can ameliorate radiation-induced cochlear damage in guinea pigs. Improving mitochondrial oxygen utilization and scavenging free-radicals [91]
MP Clinical trials: NPC patients Pure tone audiometry; DPOAE; ABR: the use of MP during RT can reduce the early RISNHL Mechanisms to protect the OHC:
1. Affects transcription and inhibits caspase-mediated apoptosis
2. Inhibits inflammatory response
3. Promotes GSH synthesis
[92]
PIR Animal experiment: male albino guinea pigs Histopathologic examination: PIR might reduce radiation-induced cochlear damage in guinea pigs Increases oxygenation in the tumor cells with its rheological effects and decreases apoptosis in surrounding healthy cells [93]
EC Cell experiment: HEI-OC1 and UB-OC1
Animal experiment: embryos/rats
EC can increase the survival rate of HEI-OC1 cells after radiotherapy.
EC can inhibit the ABR threshold in the rats.
Inhibits ROS production and MAPK activity [94]

MT: melatonin; AMF: amifostine; LC: L-carnitine; MP: methylprednisolone; PIR: piracetam; EC: epicatechin; GSH: glutathione.