Aix Marseille Univ, CNRS, IBDM, Marseille, France.
J Neurosci Res. 2022 Jun;100(6):1370-1385. doi: 10.1002/jnr.25046. Epub 2022 Mar 31.
Accumulating evidence implicates the parafascicular nucleus of the thalamus (Pf) in basal ganglia (BG)-related functions and pathologies. Despite Pf connectivity with all BG components, most attention is focused on the thalamostriatal system and an integrated view of thalamic information processing in this network is still lacking. Here, we addressed this question by recording the responses elicited by Pf activation in single neurons of the substantia nigra pars reticulata (SNr), the main BG output structure in rodents, in anesthetized mice. We performed optogenetic activation of Pf neurons innervating the striatum, the subthalamic nucleus (STN), or the SNr using virally mediated transcellular delivery of Cre from injection in either target in Rosa26-LoxP-stop-ChR2-EYFP mice to drive channelrhodopsin expression. Photoactivation of Pf neurons connecting the striatum evoked an inhibition often followed by an excitation, likely resulting from the activation of the trans-striatal direct and indirect pathways, respectively. Photoactivation of Pf neurons connecting the SNr or the STN triggered one or two early excitations, suggesting partial functional overlap of trans-subthalamic and direct thalamonigral projections. Excitations were followed in about half of the cases by an inhibition that might reflect recruitment of intranigral inhibitory loops. Finally, global Pf stimulation, electrical or optogenetic, elicited similar complex responses comprising up to four components: one or two short-latency excitations, an inhibition, and a late excitation. These data provide evidence for functional connections between the Pf and different BG components and for convergence of the information processed through these pathways in single SNr neurons, stressing their importance in regulating BG outflow.
越来越多的证据表明丘脑束旁核(Pf)与基底神经节(BG)相关功能和病理学有关。尽管 Pf 与所有 BG 成分都有连接,但大多数注意力都集中在丘脑纹状体系统上,而对于该网络中丘脑信息处理的综合观点仍然缺乏。在这里,我们通过在麻醉小鼠中记录单个黑质网状部(SNr)神经元对 Pf 激活的反应来解决这个问题,SNr 是啮齿动物中 BG 的主要输出结构。我们使用病毒介导的 Cre 从纹状体、底丘脑核(STN)或 SNr 中的目标注射进行 Pf 神经元的光遗传学激活,以驱动通道蛋白表达在 Rosa26-LoxP-stop-ChR2-EYFP 小鼠中。连接纹状体的 Pf 神经元的光激活诱发了抑制,通常随后是兴奋,这可能是由于直接和间接纹状体通路的激活分别导致的。连接 SNr 或 STN 的 Pf 神经元的光激活引发了一个或两个早期兴奋,这表明跨 STN 和直接丘脑苍白球投射的部分功能重叠。在大约一半的情况下,兴奋之后是抑制,这可能反映了苍白球内抑制环的募集。最后,Pf 的全局刺激,电刺激或光遗传学刺激,引起了类似的复杂反应,包括多达四个成分:一个或两个短潜伏期兴奋、抑制和晚期兴奋。这些数据为 Pf 与不同 BG 成分之间的功能连接提供了证据,并为通过这些途径在单个 SNr 神经元中处理的信息的汇聚提供了证据,强调了它们在调节 BG 输出中的重要性。