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A Comparative Study of Age-Related Hearing Loss in Wild Type and Insulin-Like Growth Factor I Deficient Mice

机译:野生型与胰岛素样生长因子I缺陷型小鼠年龄相关听力损失的比较研究

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摘要

Insulin-like growth factor-I (IGF-I) belongs to the family of insulin-related peptides that fulfils a key role during the late development of the nervous system. Human IGF1 mutations cause profound deafness, poor growth and mental retardation. Accordingly, Igf1−/− null mice are dwarfs that have low survival rates, cochlear alterations and severe sensorineural deafness. Presbycusis (age-related hearing loss) is a common disorder associated with aging that causes social and cognitive problems. Aging is also associated with a decrease in circulating IGF-I levels and this reduction has been related to cognitive and brain alterations, although there is no information as yet regarding the relationship between presbycusis and IGF-I biodisponibility. Here we present a longitudinal study of wild type Igf1+/+ and null Igf1−/− mice from 2 to 12 months of age comparing the temporal progression of several parameters: hearing, brain morphology, cochlear cytoarchitecture, insulin-related factors and IGF gene expression and IGF-I serum levels. Complementary invasive and non-invasive techniques were used, including auditory brainstem-evoked response (ABR) recordings and in vivo MRI brain imaging. Igf1−/− null mice presented profound deafness at all the ages studied, without any obvious worsening of hearing parameters with aging. Igf1+/+ wild type mice suffered significant age-related hearing loss, their auditory thresholds and peak I latencies augmenting as they aged, in parallel with a decrease in the circulating levels of IGF-I. Accordingly, there was an age-related spiral ganglion degeneration in wild type mice that was not evident in the Igf1 null mice. However, the Igf1−/− null mice in turn developed a prematurely aged stria vascularis reminiscent of the diabetic strial phenotype. Our data indicate that IGF-I is required for the correct development and maintenance of hearing, supporting the idea that IGF-I-based therapies could contribute to prevent or ameliorate age-related hearing loss.
机译:胰岛素样生长因子-I(IGF-I)属于胰岛素相关肽家族,在神经系统的晚期发育中起关键作用。人IGF1突变会导致严重的耳聋,生长不良和智力低下。因此,Igf1 -/- null小鼠是侏儒症,它们具有低存活率,耳蜗改变和严重的感音神经性耳聋。老年性耳聋(与年龄有关的听力损失)是与衰老相关的常见疾病,会引起社会和认知问题。衰老还与循环中IGF-I水平的降低有关,并且这种降低与认知和脑部改变有关,尽管目前尚无关于老年性耳聋与IGF-I生物反应性之间关系的信息。在这里,我们对2至12个月大的野生型Igf1 + / + 和无效Igf1 -/-小鼠进行了纵向研究,比较了以下几个参数的时间变化: ,脑形态,耳蜗细胞结构,胰岛素相关因子以及IGF基因表达和IGF-I血清水平。使用互补的侵入性和非侵入性技术,包括听性脑干诱发反应(ABR)记录和体内MRI脑成像。 Igf1 -/-无效的小鼠在所有研究的年龄段都表现出严重的耳聋,而随着年龄的增长,听力参数没有任何明显的恶化。 Igf1 + / + 野生型小鼠随着年龄的增长遭受了与年龄有关的严重听力损失,其听觉阈值和峰值I潜伏期增加,同时IGF-I的循环水平降低。因此,在野生型小鼠中存在与年龄相关的螺旋神经节变性,这在Igf1无效小鼠中不明显。但是,Igf1 -/- null小鼠继而发展出过早衰老的纹状血管,让人联想到糖尿病性纹状表型。我们的数据表明,IGF-I是正确发展和维持听力所必需的,支持基于IGF-I的疗法可能有助于预防或减轻与年龄有关的听力损失的观点。

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