Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.
Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322
eNeuro. 2023 Nov 7;10(11). doi: 10.1523/ENEURO.0297-23.2023. Print 2023 Nov.
Sympathetic preganglionic neurons (SPNs) are the final output neurons from the central arm of the autonomic nervous system. Therefore, SPNs represent a crucial component of the sympathetic nervous system for integrating several inputs before driving the postganglionic neurons (PGNs) in the periphery to control end organ function. The mechanisms which establish and regulate baseline sympathetic tone and overall excitability of SPNs and PGNs are poorly understood. The SPNs are also known as the autonomic motoneurons (MNs) as they arise from the same progenitor line as somatic MNs that innervate skeletal muscles. Previously our group has identified a rich repertoire of homeostatic plasticity (HP) mechanisms in somatic MNs of the embryonic chick following synaptic blockade. Here, using the same model system, we examined whether SPNs exhibit similar homeostatic capabilities to that of somatic MNs. Indeed, we found that after 2-d reduction of excitatory synaptic input, SPNs showed a significant increase in intracellular chloride levels, the mechanism underlying GABAergic synaptic scaling in this system. This form of HP could therefore play a role in the early establishment of a setpoint of excitability in this part of the sympathetic nervous system. Next, we asked whether homeostatic mechanisms are expressed in the synaptic targets of SPNs, the PGNs. In this case we blocked synaptic input to PGNs (48-h treatment), or acutely , however neither treatment induced homeostatic adjustments in PGN excitability. We discuss differences in the homeostatic capacity between the central and peripheral component of the sympathetic nervous system.
交感节前神经元 (SPNs) 是自主神经系统中枢臂的最终输出神经元。因此,SPNs 代表交感神经系统的一个关键组成部分,用于整合多个输入,然后驱动外周的节后神经元 (PGNs) 来控制终末器官功能。建立和调节 SPN 和 PGN 的基线交感神经张力和整体兴奋性的机制尚未得到很好的理解。SPNs 也被称为自主运动神经元 (MNs),因为它们起源于与支配骨骼肌的躯体 MNs 相同的祖细胞系。以前,我们的小组已经在胚胎鸡的躯体 MNs 中发现了丰富的稳态可塑性 (HP) 机制,这些机制是在突触阻断后产生的。在这里,我们使用相同的模型系统,研究了 SPN 是否表现出与躯体 MN 相似的稳态能力。事实上,我们发现,在兴奋性突触输入减少 2 天后,SPNs 细胞内氯离子水平显著增加,这是该系统 GABA 能突触缩放的机制。因此,这种形式的 HP 可能在交感神经系统这一部分兴奋性设定值的早期建立中发挥作用。接下来,我们询问 SPN 的突触靶点 PGN 是否表达了稳态机制。在这种情况下,我们阻断 PGN 的突触输入 (48 小时处理),或者急性阻断,但这两种处理都没有诱导 PGN 兴奋性的稳态调节。我们讨论了交感神经系统中枢和外周成分之间的稳态能力差异。