Neurotoxicity at the Synaptic Interface, Medical Research Council Toxicology Unit, University of Leicester, Leicester LE1 9HN, United Kingdom.
J Neurosci. 2013 May 22;33(21):9113-21. doi: 10.1523/JNEUROSCI.5043-12.2013.
The central auditory brainstem provides an efferent projection known as the medial olivocochlear (MOC) system, which regulates the cochlear amplifier and mediates protection on exposure to loud sound. It arises from neurons of the ventral nucleus of the trapezoid body (VNTB), so control of neuronal excitability in this pathway has profound effects on hearing. The VNTB and the medial nucleus of the trapezoid body are the only sites of expression for the Kv2.2 voltage-gated potassium channel in the auditory brainstem, consistent with a specialized function of these channels. In the absence of unambiguous antagonists, we used recombinant and transgenic methods to examine how Kv2.2 contributes to MOC efferent function. Viral gene transfer of dominant-negative Kv2.2 in wild-type mice suppressed outward K(+) currents, increasing action potential (AP) half-width and reducing repetitive firing. Similarly, VNTB neurons from Kv2.2 knock-out mice (Kv2.2KO) also showed increased AP duration. Control experiments established that Kv2.2 was not expressed in the cochlea, so any changes in auditory function in the Kv2.2KO mouse must be of central origin. Further, in vivo recordings of auditory brainstem responses revealed that these Kv2.2KO mice were more susceptible to noise-induced hearing loss. We conclude that Kv2.2 regulates neuronal excitability in these brainstem nuclei by maintaining short APs and enhancing high-frequency firing. This safeguards efferent MOC firing during high-intensity sounds and is crucial in the mediation of protection after auditory overexposure.
中枢听觉脑干提供了一种称为内侧橄榄耳蜗(MOC)系统的传出投射,该系统调节耳蜗放大器并介导在暴露于强音时的保护。它源自腹侧梯形体核(VNTB)的神经元,因此该途径中神经元兴奋性的控制对听力有深远的影响。VNTB 和梯形体核内侧是听觉脑干中 Kv2.2 电压门控钾通道唯一的表达部位,这与这些通道的特殊功能一致。由于缺乏明确的拮抗剂,我们使用重组和转基因方法来研究 Kv2.2 如何有助于 MOC 传出功能。在野生型小鼠中,病毒基因转移显性负性 Kv2.2 抑制外向 K(+)电流,增加动作电位(AP)半宽度并减少重复放电。同样,Kv2.2 敲除小鼠(Kv2.2KO)的 VNTB 神经元也显示出 AP 持续时间延长。对照实验表明 Kv2.2 不在耳蜗中表达,因此 Kv2.2KO 小鼠听觉功能的任何变化都必须是中枢起源的。此外,听觉脑干反应的体内记录表明,这些 Kv2.2KO 小鼠对噪声诱导的听力损失更为敏感。我们得出结论,Kv2.2 通过维持短 AP 和增强高频放电来调节这些脑干核中的神经元兴奋性。这在高强度声音下保护传出 MOC 放电,并在听觉过度暴露后的保护中至关重要。