Age-related changes of GAD1 mRNA expression in the central inferior colliculus

Christina C. Koehler , Laila S. Almassri , Nick Tokar , Amir M. Mafi , Mitchell J. O'Hara , Jesse W. Young , Jeffrey G. Mellott
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引用次数: 1

Abstract

Encoding sounds with a high degree of temporal precision is an essential task for the inferior colliculus (IC) to perform and maintain the accurate processing of sounds and speech. However, the age-related reduction of GABAergic neurotransmission in the IC interrupts temporal precision and likely contributes to presbycusis. As presbycusis often manifests at high or low frequencies specifically, we sought to determine if the expression of mRNA for glutamic decarboxylase 1 (GAD1) is downregulated non-uniformly across the tonotopic axis or cell size range in the aging IC. Using single molecule in situ fluorescent hybridization across young, middle age and old Fisher Brown Norway rats (an aging model that acquires low frequency presbycusis) we quantified individual GAD1 mRNA in small, medium and large GABAergic cells. Our results demonstrate that small GABAergic cells in low frequency regions had ∼58% less GAD1 in middle age and continued to decline into old age. In contrast, the amount of GAD1 mRNA in large cells in low frequency regions significantly increased with age. As several studies have shown that downregulation of GAD1 decreases the release of GABA, we interpret our results in two ways. First, the onset of presbycusis may be driven by small GABAergic cells downregulating GAD1. Second, as previous studies demonstrate that GAD67 expression is broadly downregulated in the old IC, perhaps the translation of GAD1 to GAD67 is interrupted in large GABAergic IC cells during aging. These results point to a potential genetic mechanism explaining reduced temporal precision in the aging IC, and in turn, presbycusis.

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中央下丘GAD1 mRNA表达的年龄相关性变化
对声音进行高时间精度的编码是下丘对声音和言语进行准确加工的必要条件。然而,与年龄相关的IC中gaba能神经传递的减少中断了时间精度,并可能导致老年性痴呆。由于老年性痴呆通常以高频率或低频率特异性表现,我们试图确定谷氨酸脱羧酶1 (GAD1) mRNA的表达是否在衰老IC中跨tonotopic轴或细胞大小范围内不均匀下调。利用单分子原位荧光杂交技术,我们在年轻、中年和老年Fisher Brown Norway大鼠(一种获得低频老年性痴呆的衰老模型)中量化了小、中、大gaba能细胞中的个体GAD1 mRNA。我们的研究结果表明,低频区域的小gabaergy细胞在中年时GAD1减少约58%,并在老年时继续下降。相反,大细胞低频区GAD1 mRNA的表达量随着年龄的增长而显著增加。由于一些研究表明,GAD1的下调会减少GABA的释放,我们从两方面解释了我们的结果。首先,小gaba能细胞下调GAD1可能驱动老年性痴呆的发生。其次,先前的研究表明,GAD67的表达在老年IC中广泛下调,可能在衰老过程中,GAD1到GAD67的翻译在大的gabaergy IC细胞中被中断。这些结果指出了一种潜在的遗传机制,可以解释老化IC的时间精度降低,进而导致老年性痴呆。
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来源期刊
Translational Medicine of Aging
Translational Medicine of Aging Medicine-Geriatrics and Gerontology
CiteScore
5.30
自引率
0.00%
发文量
2
审稿时长
103 days
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