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抗癫痫药物通过 T 型钙通道延缓与年龄相关的螺旋神经节神经元的丢失。

Anti-epileptic drugs delay age-related loss of spiral ganglion neurons via T-type calcium channel.

机构信息

Department of Otolaryngology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Hear Res. 2011 Aug;278(1-2):106-12. doi: 10.1016/j.heares.2011.05.010. Epub 2011 May 26.

Abstract

Loss of spiral ganglion neurons is a major cause of age-related hearing loss (presbycusis). Despite being the third most prevalent condition afflicting elderly persons, there are no known medications to prevent presbycusis. Because calcium signaling has long been implicated in age-related neuronal death, we investigated T-type calcium channels. This family is comprised of three members (Ca(v)3.1, Ca(v)3.2, and Ca(v)3.3), based on their respective main pore-forming alpha subunits: α1G, α1H, and α1I. In the present study, we report a significant delay of age-related loss of cochlear function and preservation of spiral ganglion neurons in α1H null and heterozygous mice, clearly demonstrating an important role for Ca(v)3.2 in age-related neuronal loss. Furthermore, we show that anticonvulsant drugs from a family of T-type calcium channel blockers can significantly preserve spiral ganglion neurons during aging. To our knowledge, this is the first report of drugs capable of diminishing age-related loss of spiral ganglion neurons.

摘要

螺旋神经节神经元的丧失是与年龄相关的听力损失(老年性聋)的主要原因。尽管它是困扰老年人的第三大常见疾病,但目前尚无已知的药物可以预防老年性聋。由于钙信号在与年龄相关的神经元死亡中一直被牵连,我们研究了 T 型钙通道。该家族由三个成员(Ca(v)3.1、Ca(v)3.2 和 Ca(v)3.3)组成,基于它们各自的主要孔形成α亚基:α1G、α1H 和α1I。在本研究中,我们报告了 α1H 缺失和杂合小鼠与年龄相关的耳蜗功能丧失和螺旋神经节神经元保存的显著延迟,这清楚地表明 Ca(v)3.2 在与年龄相关的神经元丧失中起着重要作用。此外,我们还表明,来自 T 型钙通道阻滞剂家族的抗惊厥药物在衰老过程中可以显著保护螺旋神经节神经元。据我们所知,这是首次报道能够减少与年龄相关的螺旋神经节神经元丧失的药物。

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