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耳蜗传出神经的一种新作用:体内反应增强并不需要α9胆碱能受体。

A novel effect of cochlear efferents: in vivo response enhancement does not require alpha9 cholinergic receptors.

作者信息

Maison Stéphane F, Vetter Douglas E, Liberman M Charles

机构信息

Department of Otology and Laryngology, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, MA 02114-3096, USA.

出版信息

J Neurophysiol. 2007 May;97(5):3269-78. doi: 10.1152/jn.00067.2007. Epub 2007 Mar 7.

Abstract

Outer hair cells in the mammalian cochlea receive a cholinergic efferent innervation that constitutes the effector arm of a sound-evoked negative feedback loop. The well-studied suppressive effects of acetylcholine (ACh) release from efferent terminals are mediated by alpha9/alpha10 ACh receptors and are potently blocked by strychnine. Here, we report a novel, efferent-mediated enhancement of cochlear sound-evoked neural responses and otoacoustic emissions in mice. In controls, a slow enhancement of response amplitude to supranormal levels appears after recovery from the classic suppressive effects seen during a 70-s epoch of efferent shocks. The magnitude of post-shock enhancement can be as great as 10 dB and tends to be greater for high-frequency acoustic stimuli. Systemic strychnine at 10 mg/kg eliminates efferent-induced suppression, revealing a purely enhancing effect of efferent shocks, which peaks within 5 s after efferent-stimulation onset, maintains a constant level through the stimulation epoch, and slowly decays back to baseline with a time constant of approximately 100 s. In mice with targeted deletion of the alpha9 ACh receptor subunit, efferent-evoked effects resemble those in wild types with strychnine blockade, further showing that this novel efferent effect is fundamentally different from all cholinergic effects previously reported.

摘要

哺乳动物耳蜗中的外毛细胞接受胆碱能传出神经支配,该神经支配构成了声音诱发的负反馈回路的效应器臂。从传出神经末梢释放的乙酰胆碱(ACh)的抑制作用已得到充分研究,其由α9/α10 ACh受体介导,并被士的宁有效阻断。在此,我们报告了一种新的、由传出神经介导的对小鼠耳蜗声音诱发神经反应和耳声发射的增强作用。在对照组中,在经历70秒传出神经电休克期间出现的经典抑制作用恢复后,对超常水平的反应幅度会出现缓慢增强。休克后增强的幅度可达10分贝,并且对于高频声刺激往往更大。10毫克/千克的全身士的宁消除了传出神经诱导的抑制作用,揭示了传出神经电休克的纯粹增强作用,该作用在传出神经刺激开始后5秒内达到峰值,在刺激期间保持恒定水平,并以约100秒的时间常数缓慢衰减回基线。在α9 ACh受体亚基靶向缺失的小鼠中,传出神经诱发的效应类似于士的宁阻断的野生型小鼠,进一步表明这种新的传出神经效应与先前报道的所有胆碱能效应有根本不同。

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