Lu Di, Wan Peng, Liu Yang, Jin Xian-Hua, Chu Chun-Ping, Bing Yan-Hua, Qiu De-Lai
Department of Physiology and Pathophysiology, College of Medicine, Yanbian University, Yanji, China.
Department of Ophthalmology, Affiliated Hospital of Yanbian University, Yanji, China.
Front Cell Neurosci. 2022 Mar 30;16:863342. doi: 10.3389/fncel.2022.863342. eCollection 2022.
Long-term synaptic plasticity in the cerebellar cortex is a possible mechanism for motor learning. Previous studies have demonstrated the induction of mossy fiber-granule cell (MF-GrC) synaptic plasticity under and conditions, but the mechanisms underlying sensory stimulation-evoked long-term synaptic plasticity of MF-GrC in living animals are unclear. In this study, we investigated the mechanism of long-term potentiation (LTP) of MF-GrC synaptic transmission in the cerebellum induced by train of facial stimulation at 20 Hz in urethane-anesthetized mice using electrophysiological recording, immunohistochemistry techniques, and pharmacological methods. Blockade of GABA receptor activity and repetitive facial stimulation at 20 Hz (240 pulses) induced an LTP of MF-GrC synapses in the mouse cerebellar cortical folium Crus II, accompanied with a decrease in paired-pulse ratio (N2/N1). The facial stimulation-induced MF-GrC LTP was abolished by either an -methyl-D-aspartate (NMDA) receptor blocker, i.e., D-APV, or a specific GluNR2A subunit-containing NMDA receptor antagonist, PEAQX, but was not prevented by selective GluNR2B or GluNR2C/D subunit-containing NMDA receptor blockers. Application of GNE-0723, a selective and brain-penetrant-positive allosteric modulator of GluN2A subunit-containing NMDA receptors, produced an LTP of N1, accompanied with a decrease in N2/N1 ratio, and occluded the 20-Hz facial stimulation-induced MF-GrC LTP. Inhibition of nitric oxide synthesis (NOS) prevented the facial stimulation-induced MF-GrC LTP, while activation of NOS produced an LTP of N1, with a decrease in N2/N1 ratio, and occluded the 20-Hz facial stimulation-induced MF-GrC LTP. In addition, GluN2A-containing NMDA receptor immunoreactivity was observed in the mouse cerebellar granular layer. These results indicate that facial stimulation at 20 Hz induced LTP of MF-GrC synaptic transmission the GluN2A-containing NMDA receptor/nitric oxide cascade in mice. The results suggest that the sensory stimulation-evoked LTP of MF-GrC synaptic transmission in the granular layer may play a critical role in cerebellar adaptation to native mossy fiber excitatory inputs and motor learning behavior in living animals.
小脑皮质中的长期突触可塑性是运动学习的一种可能机制。先前的研究已经证明在特定条件下苔藓纤维-颗粒细胞(MF-GrC)突触可塑性的诱导,但活体动物中感觉刺激诱发的MF-GrC长期突触可塑性的潜在机制尚不清楚。在本研究中,我们使用电生理记录、免疫组织化学技术和药理学方法,研究了在乌拉坦麻醉的小鼠中,20Hz面部刺激序列诱导的小脑MF-GrC突触传递长时程增强(LTP)的机制。GABA受体活性阻断和20Hz(240个脉冲)重复面部刺激在小鼠小脑皮质小叶Crus II中诱导了MF-GrC突触的LTP,同时配对脉冲比率(N2/N1)降低。面部刺激诱导的MF-GrC LTP被N-甲基-D-天冬氨酸(NMDA)受体阻断剂即D-APV或含特定GluNR2A亚基的NMDA受体拮抗剂PEAQX消除,但未被含选择性GluNR2B或GluNR2C/D亚基的NMDA受体阻断剂阻止。应用GNE-0723,一种含GluN2A亚基的NMDA受体的选择性且可穿透脑的正变构调节剂,产生了N1的LTP,同时N2/N1比率降低,并阻断了20Hz面部刺激诱导的MF-GrC LTP。一氧化氮合成(NOS)抑制阻止了面部刺激诱导的MF-GrC LTP,而NOS激活产生了N1的LTP,N2/N1比率降低,并阻断了20Hz面部刺激诱导的MF-GrC LTP。此外,在小鼠小脑颗粒层中观察到了含GluN2A的NMDA受体免疫反应性。这些结果表明,20Hz面部刺激在小鼠中通过含GluN2A的NMDA受体/一氧化氮级联诱导了MF-GrC突触传递的LTP。结果表明,颗粒层中感觉刺激诱发的MF-GrC突触传递LTP可能在活体动物中小脑对天然苔藓纤维兴奋性输入的适应和运动学习行为中起关键作用。