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Adenosine Amine Congener as a Cochlear Rescue Agent

We have previously shown that adenosine amine congener (ADAC), a selective A(1) adenosine receptor agonist, can ameliorate noise- and cisplatin-induced cochlear injury. Here we demonstrate the dose-dependent rescue effects of ADAC on noise-induced cochlear injury in a rat model and establish the tim...

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Detalles Bibliográficos
Autores principales: Vlajkovic, Srdjan M., Chang, Hao, Paek, Song Yee, Chi, Howard H.-T., Sreebhavan, Sreevalsan, Telang, Ravindra S., Tingle, Malcolm, Housley, Gary D., Thorne, Peter R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160640/
https://www.ncbi.nlm.nih.gov/pubmed/25243188
http://dx.doi.org/10.1155/2014/841489
Descripción
Sumario:We have previously shown that adenosine amine congener (ADAC), a selective A(1) adenosine receptor agonist, can ameliorate noise- and cisplatin-induced cochlear injury. Here we demonstrate the dose-dependent rescue effects of ADAC on noise-induced cochlear injury in a rat model and establish the time window for treatment. Methods. ADAC (25–300 μg/kg) was administered intraperitoneally to Wistar rats (8–10 weeks old) at intervals (6–72 hours) after exposure to traumatic noise (8–16 kHz, 110 dB sound pressure level, 2 hours). Hearing sensitivity was assessed using auditory brainstem responses (ABR) before and 12 days after noise exposure. Pharmacokinetic studies investigated ADAC concentrations in plasma after systemic (intravenous) administration. Results. ADAC was most effective in the first 24 hours after noise exposure at doses >50 μg/kg, providing up to 21 dB protection (averaged across 8–28 kHz). Pharmacokinetic studies demonstrated a short (5 min) half-life of ADAC in plasma after intravenous administration without detection of degradation products. Conclusion. Our data show that ADAC mitigates noise-induced hearing loss in a dose- and time-dependent manner, but further studies are required to establish its translation as a clinical otological treatment.