The effect of the duration of treatment with antioxidants on age-related hearing loss

References

• Tavanai E, Mohammadkhani G. Role of antioxidants in prevention of age-related hearing loss: a review of literature. Eur Arch Otorhinolaryngol. 2017;274(4):1821–1834.
   PubMed Web of Science ®Google Scholar
• Tavanai E, Mohammadkhani G, Farahani S, et al. Protective effects of Silymarin against age-related hearing loss in an aging rat model. Indian J Otolaryngol Head Neck Surg. 2019;71(S2):1248–1257.
   PubMedGoogle Scholar
• Gates GA, Mills JH. Presbycusis. Lancet. 2005;366(9491):1111–1120.
   PubMed Web of Science ®Google Scholar
• Fetoni AR, Picciotti PM, Paludetti G, et al. Pathogenesis of presbycusis in animal models: a review. Exp Gerontol. 2011;46(6):413–425.
   PubMed Web of Science ®Google Scholar
• Someya S, Rothenberger C, Kim MJ. 2020. Lifestyle intervention to prevent age-related hearing loss: calorie restriction. In: Pucheu S, Radziwon K, Salvi R, editors. New therapies to prevent or cure auditory disorders. Cham: Springer.
   Google Scholar
• Firuzi O, Miri R, Tavakkoli M, et al. Antioxidant therapy: current status and future prospects. Curr Med Chem. 2011;18(25):3871–3888.
   PubMed Web of Science ®Google Scholar
• Bielefeld EC, Coling D, Chen GD, et al. Multiple dosing strategies with acetyl L-carnitine (ALCAR) fail to alter age-related hearing loss in the Fischer 344/NHsd rat. J Negat Results Biomed. 2008;7:4.
   PubMedGoogle Scholar
• Engelhard YN, Gazer B, Paran E. Natural antioxidants from tomato extract reduce blood pressure in patients with grade-1 hypertension: a double-blind, placebo-controlled pilot study. Am Heart J. 2006;151(1):100.
   PubMed Web of Science ®Google Scholar
• Klarod K, Gatterer H, Frontull V, et al. Effects of short-term antioxidant supplementation on oxidative stress and exercise performance in the heat and the cold. Int J Physiol Pathophysiol Pharmacol. 2015;7(2):98–104.
   PubMedGoogle Scholar
• Panemangalore M, Bebe FN. Short- and long-term exposure to low levels of pesticide and flavonoid mixtures modify endogenous antioxidants in tissues of rats. J Environ Sci Health B. 2009;44(4):357–364.
   PubMed Web of Science ®Google Scholar
• Nuttall SL, Martin U, Kendall MJ, et al. Short-term antioxidant supplementation reduces oxidative stress in elderly patients with type 2 diabetes mellitus – a pilot study. Pract Diab Int. 2002;19(7):199–202.
   Google Scholar
• Falsini B, Piccardi M, Iarossi G, et al. Influence of short-term antioxidant supplementation on macular function in age-related maculopathy: a pilot study including electrophysiologic assessment. Ophthalmology. 2003;110(1):51–61.
   PubMed Web of Science ®Google Scholar
• Raitakari OT, Adams MR, McCredie RJ, et al. Oral vitamin C and endothelial function in smokers: short-term improvement, but no sustained beneficial effect. J Am Coll Cardiol. 2000;35(6):1616–1621.
   PubMed Web of Science ®Google Scholar
• Khodr B, Howard J, Watson K, et al. Effect of short-term and long-term antioxidant therapy on primary and secondary ageing neurovascular processes. J Gerontol A Biol Sci Med Sci. 2003;58(8):698–708.
   PubMed Web of Science ®Google Scholar
• Heman-Ackah SE, Juhn SK, Huang TC, et al. A combination antioxidant therapy prevents age-related hearing loss in C57BL/6 mice. Otolaryngol Head Neck Surg. 2010;143(3):429–434.
   PubMed Web of Science ®Google Scholar
• Nevado J, Sanz R, SáNchez-Rodrı’Guez C, et al. Ginkgo biloba extract (EGb761) protects against aging-related caspase-mediated apoptosis in rat cochlear. Acta Otolaryngol. 2010;130(10):1101–111216.
   PubMed Web of Science ®Google Scholar
• Du Z, Yang Y, Hu Y, et al. A long-term high-fat diet increases oxidative stress, mitochondrial damage and apoptosis in the inner ear of D-galactose-induced aging rats. Hear Res. 2012;287(1–2):15–24.
   PubMed Web of Science ®Google Scholar
• Zhong Y, Hu YJ, Yang Y, et al. Contribution of common deletion to total deletion burden in mitochondrial DNA from inner ear of D-galactose-induced aging rats. Mutat Res. 2011;712(1–2):11–19.
   PubMed Web of Science ®Google Scholar
• Kong WJ, Hu YJ, Wang Q, et al. The effect of the mtDNA4834 deletion on hearing. Biochem Biophys Res Commun. 2006;344(1):425–430.
   PubMed Web of Science ®Google Scholar
• Du Z, Han S, Qu T, et al. Age-related insult of cochlear ribbon synapses: an early-onset contributor to D-galactose-induced aging in mice. Neurochem Int. 2020;133:104649.
   PubMed Web of Science ®Google Scholar
• Chen B, Zhong Y, Peng W, et al. Age-related changes in the central auditory system: comparison of D-galactose-induced aging rats and naturally aging rats. Brain Res. 2010;1344:43–53.
   PubMed Web of Science ®Google Scholar
• Chen B, Zhong Y, Peng W, et al. Increased mitochondrial DNA damage and decreased base excision repair in the auditory cortex of D-galactose-induced aging rats. Mol Biol Rep. 2011;38(6):3635–3642.
   PubMed Web of Science ®Google Scholar
• Maxwell S, Thorpe G. Tea flavonoids have little short term impact on serum antioxidant activity. BMJ. 1996;313(7051):229.
   PubMed Web of Science ®Google Scholar
• Surai PF. Silymarin as a natural antioxidant: an overview of the current evidence and perspectives. Antioxidants. 2015;4(1):204–247.
   Web of Science ®Google Scholar
• Draz E, Abdin A, Sarhan N, et al. Neurotrophic and antioxidant effects of silymarin comparable to 4-methylcatechol in protection against gentamicin-induced ototoxicity in guinea pigs. Pharmacol Rep. 2015;67(2):317–325.
   PubMed Web of Science ®Google Scholar
• Cho SI, Lee JE, Yong DN. Protective effect of silymarin against cisplatin-induced ototoxicity. Int J Pediatr Otorhinolaryngol. 2014;78(3):474–478.
   PubMed Web of Science ®Google Scholar
• Tavanai E, Mohammadkhani G. Evaluation of the effects of chronic injection of D-galactose on auditory brainstem responses as a model for studying age-related hearing loss. Acta Med Iran. 2019;57(5):281–288.
   Google Scholar