Departments of Anesthesiology and Pain Medicine and.
Genetics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030.
J Neurosci. 2018 Jul 11;38(28):6340-6349. doi: 10.1523/JNEUROSCI.2780-17.2018. Epub 2018 Jun 25.
The amygdala is important for processing emotion, including negative emotion such as anxiety and depression induced by chronic pain. Although remarkable progress has been achieved in recent years on amygdala regulation of both negative (fear) and positive (reward) behavioral responses, our current understanding is still limited regarding how the amygdala processes and integrates these negative and positive emotion responses within the amygdala circuits. In this study with optogenetic stimulation of specific brain circuits, we investigated how amygdala circuits regulate negative and positive emotion behaviors, using pain as an emotional assay in male rats. We report here that activation of the excitatory pathway from the parabrachial nucleus (PBN) that relays peripheral pain signals to the central nucleus of amygdala (CeA) is sufficient to cause behaviors of negative emotion including anxiety, depression, and aversion in normal rats. In strong contrast, activation of the excitatory pathway from basolateral amygdala (BLA) that conveys processed corticolimbic signals to CeA dramatically opposes these behaviors of negative emotion, reducing anxiety and depression, and induces behavior of reward. Surprisingly, activating the PBN-CeA pathway to simulate pain signals does not change pain sensitivity itself, but activating the BLA-CeA pathway inhibits basal and sensitized pain. These findings demonstrate that the pain signal conveyed through the PBN-CeA pathway is sufficient to drive negative emotion and that the corticolimbic signal via the BLA-CeA pathway counteracts the negative emotion, suggesting a top-down brain mechanism for cognitive control of negative emotion under stressful environmental conditions such as pain. It remains unclear how the amygdala circuits integrate both negative and positive emotional responses and the brain circuits that link peripheral pain to negative emotion are largely unknown. Using optogenetic stimulation, this study shows that the excitatory projection from the parabrachial nucleus to the central nucleus of amygdala (CeA) is sufficient to drive behaviors of negative emotion including anxiety, depression, and aversion in rats. Conversely, activation of the excitatory projection from basolateral amygdala to CeA counteracts each of these behaviors of negative emotion. Thus, this study identifies a brain pathway that mediates pain-driven negative emotion and a brain pathway that counteracts these emotion behaviors in a top-down mechanism for brain control of negative emotion.
杏仁核对于处理情绪非常重要,包括慢性疼痛引起的负面情绪,如焦虑和抑郁。尽管近年来在杏仁核调节负面(恐惧)和正面(奖励)行为反应方面取得了显著进展,但我们目前对于杏仁核如何在杏仁核回路中处理和整合这些负面和正面情绪反应的理解仍然有限。在这项使用特定脑回路光遗传学刺激的研究中,我们使用疼痛作为雄性大鼠的情感测定,研究了杏仁核回路如何调节负面和正面情绪行为。我们在这里报告,激活中继外周疼痛信号到杏仁核中央核(CeA)的臂旁核(PBN)兴奋性通路足以引起正常大鼠的负面情绪行为,包括焦虑、抑郁和厌恶。相比之下,激活从外侧杏仁核(BLA)传递处理的皮质边缘信号到 CeA 的兴奋性通路强烈反对这些负面情绪行为,减少焦虑和抑郁,并诱导奖励行为。令人惊讶的是,激活 PBN-CeA 通路以模拟疼痛信号本身不会改变疼痛敏感性,但激活 BLA-CeA 通路抑制基础和敏化疼痛。这些发现表明,通过 PBN-CeA 通路传递的疼痛信号足以驱动负面情绪,而通过 BLA-CeA 通路传递的皮质边缘信号对抗负面情绪,表明在疼痛等应激环境条件下,大脑对负面情绪进行认知控制的自上而下机制。目前尚不清楚杏仁核回路如何整合负面和正面情绪反应,以及将外周疼痛与负面情绪联系起来的大脑回路在很大程度上尚不清楚。使用光遗传学刺激,本研究表明,从臂旁核到杏仁核中央核(CeA)的兴奋性投射足以驱动大鼠的负面情绪行为,包括焦虑、抑郁和厌恶。相反,激活从外侧杏仁核到 CeA 的兴奋性投射对抗这些负面情绪行为中的每一种。因此,这项研究确定了一条介导疼痛驱动的负面情绪的大脑通路,以及一条通过自上而下的大脑控制负面情绪的机制来对抗这些情绪行为的大脑通路。