Smith Jesse Andrew, Ji Yadong, Lorsung Rebecca, Breault Macauley Smith, Koenig Jeffrey, Cramer Nathan, Masri Radi, Keller Asaf
University of Maryland, Program in Neuroscience, Department of Neurobiology.
Department of Advanced Oral Sciences and Therapeutics, University of Maryland School of Dentistry.
bioRxiv. 2023 May 29:2023.03.22.533230. doi: 10.1101/2023.03.22.533230.
The parabrachial nuclear complex (PBN) is a nexus for aversion, and for the sensory and affective components of pain perception. We have previously shown that, during chronic pain, PBN neurons in anesthetized rodents have amplified activity. We report a method to record from PBN neurons of behaving, head-restrained mice, while applying reproducible noxious stimuli. We find that both spontaneous and evoked activity are higher in awake animals, compared to urethane anesthetized mice. Fiber photometry of calcium responses from CGRP-expressing PBN neurons demonstrates that these neurons respond to nociceptive stimuli. In both males and females with neuropathic or inflammatory pain, responses of PBN neurons remain amplified for at least 5 weeks, in parallel with increased pain metrics. We also show that PBN neurons can be rapidly conditioned to respond to innocuous stimuli, after pairing with nociceptive stimuli. Finally, we demonstrate that changes in PBN neuronal activity are correlated with changes in arousal, measured as changes in pupil diameter.
The parabrachial complex is a nexus of aversion, including pain. We report a method to record from parabrachial nucleus neurons of behaving mice, while applying reproducible noxious stimuli. This allowed, for the first time, tracking the activity of these neurons over time in animals with neuropathic or inflammatory pain. It also allowed us to show that the activity of these neurons correlates with arousal states, and that these neurons can be conditioned to respond to innocuous stimuli.
臂旁核复合体(PBN)是厌恶以及疼痛感知的感觉和情感成分的一个枢纽。我们之前已经表明,在慢性疼痛期间,麻醉啮齿动物的PBN神经元具有增强的活动。我们报告了一种在对行为受限的头部固定小鼠施加可重复的有害刺激时记录PBN神经元活动的方法。我们发现,与氨基甲酸乙酯麻醉的小鼠相比,清醒动物的自发活动和诱发活动都更高。对表达降钙素基因相关肽(CGRP)的PBN神经元的钙反应进行光纤光度测定表明,这些神经元对伤害性刺激有反应。在患有神经性或炎症性疼痛的雄性和雌性动物中,PBN神经元的反应至少持续5周增强,同时疼痛指标增加。我们还表明,在与伤害性刺激配对后,PBN神经元可以快速被训练成对无害刺激做出反应。最后,我们证明PBN神经元活动的变化与以瞳孔直径变化衡量的觉醒变化相关。
臂旁复合体是包括疼痛在内的厌恶的一个枢纽。我们报告了一种在对行为小鼠的臂旁核神经元施加可重复的有害刺激时进行记录的方法。这首次使得在患有神经性或炎症性疼痛的动物中随时间追踪这些神经元的活动成为可能。它还使我们能够表明这些神经元的活动与觉醒状态相关,并且这些神经元可以被训练成对无害刺激做出反应。