Department of Molecular and Cell Biology and Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA, USA.
MOE Frontier Science Center for Brain Research and Brain-Machine Integration, Zhejiang University Medical Center, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China.
Nat Neurosci. 2021 Oct;24(10):1402-1413. doi: 10.1038/s41593-021-00903-8. Epub 2021 Aug 9.
Pain decreases the activity of many ventral tegmental area (VTA) dopamine (DA) neurons, yet the underlying neural circuitry connecting nociception and the DA system is not understood. Here we show that a subpopulation of lateral parabrachial (LPB) neurons is critical for relaying nociceptive signals from the spinal cord to the substantia nigra pars reticulata (SNR). SNR-projecting LPB neurons are activated by noxious stimuli and silencing them blocks pain responses in two different models of pain. LPB-targeted and nociception-recipient SNR neurons regulate VTA DA activity directly through feed-forward inhibition and indirectly by inhibiting a distinct subpopulation of VTA-projecting LPB neurons thereby reducing excitatory drive onto VTA DA neurons. Correspondingly, ablation of SNR-projecting LPB neurons is sufficient to reduce pain-mediated inhibition of DA release in vivo. The identification of a neural circuit conveying nociceptive input to DA neurons is critical to our understanding of how pain influences learning and behavior.
疼痛会降低腹侧被盖区 (VTA) 多巴胺 (DA) 神经元的活动,然而,将疼痛信号传递到 DA 系统的神经回路尚不清楚。在这里,我们发现外侧臂旁核 (LPB) 的一个亚群神经元对于将脊髓的伤害性信号传递到黑质网状部 (SNR) 至关重要。伤害性刺激激活了投射到 SNR 的 LPB 神经元,沉默这些神经元可以阻断两种不同疼痛模型中的疼痛反应。LPB 靶向和伤害性接受的 SNR 神经元通过前馈抑制直接调节 VTA DA 活动,通过抑制 LPB 投射神经元的另一亚群间接调节 VTA DA 活动,从而减少对 VTA DA 神经元的兴奋性驱动。相应地,SNR 投射 LPB 神经元的消融足以减少体内疼痛介导的 DA 释放抑制。传递伤害性输入到 DA 神经元的神经回路的鉴定对于我们理解疼痛如何影响学习和行为至关重要。