Effects of Androgen Receptor Inhibition on Kanamycin-Induced Hearing Loss in Rats

• Published in: International journal of molecular sciences Vol. 22; no. 10; p. 5307
• Main Authors: Chun, Kyung-Ju, Lee, Chang-Ho, Kim, Kyung-Woon, Lee, So-Min, Kim, So-Young
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 18.05.2021; MDPI
• Subjects: Aminoglycosides; Androgen receptors; Androgens; Antiandrogens; Apoptosis; Brain stem; Caspase-3; Cochlea; Cytochrome P450; Cytochromes P450; Estrogens; Flutamide; Gene expression; Hearing; Hearing loss; Homeostasis; Inflammation; Kanamycin; low-density lipoprotein receptor-related protein-2; Metallothionein; Oxidative stress; Polymerase chain reaction; Protein expression; Proteins; receptors, androgen; RNA-directed DNA polymerase; Signal transduction; Testosterone; Tumor necrosis factor-α; Western blotting
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22105307

Megalin has been proposed as an endocytic receptor for aminoglycosides as well as estrogen and androgen. We aimed to investigate the otoprotective effects of antiandrogens (flutamide, FM) on kanamycin (KM)-induced hearing loss in rats. Rats were divided into four groups. The KM group was administered KM (20 mg/kg/day) for 5 days, while the FM group received FM (15 mg/kg/day) for 10 days. In the KM + FM group, KM and FM (15 mg/kg/day) were simultaneously injected for 5 days and then FM was injected for 5 days. Auditory brainstem responses were measured. Western blotting and/or quantitative reverse transcriptase-polymerase chain reaction were performed for megalin, cytochrome P450 1A1 (Cyp1a1), Cyp1b1, metallothionein 1A (MT1A), MT2A, tumor necrosis factor (TNF)-α, caspase 3, and cleaved caspase 3. The FM + KM group showed attenuated auditory thresholds when compared with the KM group at 4, 8, 16, and 32 kHz (all p < 0.05). The KM + FM group showed lower megalin and Cyp1b1 levels than the KM group (all p < 0.05). The KM + FM group revealed lower MT1A, TNFα, and caspase 3 protein levels, compared with those in the KM group (all p < 0.05). Androgen receptor inhibition protects against cochlear injuries in KM-induced hearing loss rats by attenuating megalin expression, revealing anti-inflammatory and anti-apoptotic effects.