Valdés-Baizabal Catalina, Soto Enrique, Vega Rosario
Instituto de Fisiología, Benemérita Universidad Autónoma de Puebla, Puebla, México.
PLoS One. 2015 Mar 13;10(3):e0120808. doi: 10.1371/journal.pone.0120808. eCollection 2015.
The cochlear inner hair cells synapse onto type I afferent terminal dendrites, constituting the main afferent pathway for auditory information flow. This pathway receives central control input from the lateral olivocochlear efferent neurons that release various neurotransmitters, among which dopamine (DA) plays a salient role. DA receptors activation exert a protective role in the over activation of the afferent glutamatergic synapses, which occurs when an animal is exposed to intense sound stimuli or during hypoxic events. However, the mechanism of action of DA at the cellular level is still not completely understood. In this work, we studied the actions of DA and its receptor agonists and antagonists on the voltage-gated sodium current (INa) in isolated cochlear afferent neurons of the rat to define the mechanisms of dopaminergic control of the afferent input in the cochlear pathway. Experiments were performed using the voltage and current clamp techniques in the whole-cell configuration in primary cultures of cochlear spiral ganglion neurons (SGNs). Recordings of the INa showed that DA receptor activation induced a significant inhibition of the peak current amplitude, leading to a significant decrease in cell excitability. Inhibition of the INa was produced by a phosphorylation of the sodium channels as shown by the use of phosphatase inhibitor that produced an inhibition analogous to that caused by DA receptor activation. Use of specific agonists and antagonists showed that inhibitory action of DA was mediated both by activation of D1- and D2-like DA receptors. The action of the D1- and D2-like receptors was shown to be mediated by a Gαs/AC/cAMP/PKA and Gαq/PLC/PKC pathways respectively. These results showed that DA receptor activation constitutes a significant modulatory input to SGNs, effectively modulating their excitability and information flow in the auditory pathway.
耳蜗内毛细胞与I型传入终末树突形成突触,构成听觉信息流的主要传入通路。该通路接受来自外侧橄榄耳蜗传出神经元的中枢控制输入,这些神经元释放多种神经递质,其中多巴胺(DA)起显著作用。DA受体激活在传入谷氨酸能突触过度激活时发挥保护作用,这种过度激活发生在动物暴露于强声刺激或缺氧事件期间。然而,DA在细胞水平的作用机制仍未完全明确。在这项研究中,我们研究了DA及其受体激动剂和拮抗剂对大鼠离体耳蜗传入神经元电压门控钠电流(INa)的作用,以确定耳蜗通路中多巴胺能控制传入输入的机制。实验采用电压钳和电流钳技术,在耳蜗螺旋神经节神经元(SGN)原代培养物的全细胞模式下进行。INa记录显示,DA受体激活导致峰值电流幅度显著抑制,导致细胞兴奋性显著降低。如使用磷酸酶抑制剂所显示的,钠通道磷酸化导致INa抑制,该抑制剂产生的抑制作用类似于DA受体激活所引起的抑制作用。使用特异性激动剂和拮抗剂表明,DA的抑制作用是由D1样和D2样DA受体的激活介导的。D1样和D2样受体的作用分别由Gαs/AC/cAMP/PKA和Gαq/PLC/PKC途径介导。这些结果表明,DA受体激活构成了对SGN的重要调节输入,有效调节其兴奋性和听觉通路中的信息流。