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N-acetylcysteine Treatment Reduces Age-related Hearing Loss and Memory Impairment in the Senescence-Accelerated Prone 8 (SAMP8) Mouse Model

机译:N-乙酰半胱氨酸治疗减少衰老加速俯卧8(SAMP8)小鼠模型中与年龄有关的听力损失和记忆障碍。

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摘要

Age-related hearing loss (ARHL) is the most common sensory disorder in the elderly population. SAMP8 mouse model presents accelerated senescence and has been identified as a model of gerontological research. SAMP8 displays a progressive age-related decline in brain function associated with a progressive hearing loss mimicking human aging memory deficits and ARHL. The molecular mechanisms associated with SAMP8 senescence process involve oxidative stress leading to chronic inflammation and apoptosis. Here, we studied the effect of N-acetylcysteine (NAC), an antioxidant, on SAMP8 hearing loss and memory to determine the potential interest of this model in the study of new antioxidant therapies. We observed a strong decrease of auditory brainstem response thresholds from 45 to 75 days of age and an increase of distortion product amplitudes from 60 to 75 days in NAC treated group compared to vehicle. Moreover, NAC treated group presented also an increase of memory performance at 60 and 105 days of age. These results confirm that NAC delays the senescence process by slowing the age-related hearing loss, protecting the cochlear hair cells and improving memory, suggesting that antioxidants could be a pharmacological target for age-related hearing and memory loss.
机译:与年龄有关的听力损失(ARHL)是老年人口中最常见的感觉障碍。 SAMP8小鼠模型具有加速衰老的作用,已被确定为老年医学研究的模型。 SAMP8显示出与年龄相关的与大脑功能有关的进行性衰退,与模仿人类衰老的记忆缺陷和ARHL的进行性听力丧失有关。与SAMP8衰老过程相关的分子机制涉及氧化应激,导致慢性炎症和细胞凋亡。在这里,我们研究了抗氧化剂N-乙酰半胱氨酸(NAC)对SAMP8听力损失和记忆的影响,以确定该模型在研究新抗氧化剂中的潜在用途。我们观察到,与媒介物相比,NAC治疗组的听觉脑干反应阈值从45到75天大大降低,畸变产物幅度从60到75天增加。此外,NAC治疗组在60和105天龄时的记忆力也有所提高。这些结果证实,NAC通过减缓与年龄有关的听力丧失,保护耳蜗毛细胞和改善记忆力来延迟衰老过程,表明抗氧化剂可能是与年龄有关的听力和记忆力丧失的药理学靶标。

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