Castro Alberto, Raver Charles, Li Ying, Uddin Olivia, Rubin David, Ji Yadong, Masri Radi, Keller Asaf
Department of Anatomy & Neurobiology, Program in Neuroscience, University of Maryland School of Medicine, Baltimore, Maryland 21201, and.
Department of Endodontics, Prosthodontics and Operative Surgery, Baltimore College of Dentistry, Program in Neuroscience, Baltimore, Maryland 21201.
J Neurosci. 2017 Nov 22;37(47):11431-11440. doi: 10.1523/JNEUROSCI.3897-16.2017. Epub 2017 Oct 24.
Pain perception is strongly influenced by descending pathways from "higher" brain centers that regulate the activity of spinal circuits. In addition to the extensively studied descending system originating from the medulla, the neocortex provides dense anatomical projections that directly target neurons in the spinal cord and the spinal trigeminal nucleus caudalis (SpVc). Evidence exists that these corticotrigeminal pathways may modulate the processing of nociceptive inputs by SpVc, and regulate pain perception. We demonstrate here, with anatomical and optogenetic methods, and using both rats and mice (of both sexes), that corticotrigeminal axons densely innervate SpVc, where they target and directly activate inhibitory and excitatory neurons. Electrophysiological recordings reveal that stimulation of primary somatosensory cortex potently suppresses SpVc responses to noxious stimuli and produces behavioral hypoalgesia. These findings demonstrate that the corticotrigeminal pathway is a potent modulator of nociception and a potential target for interventions to alleviate chronic pain. Many chronic pain conditions are resistant to conventional therapy. Promising new approaches to pain management capitalize on the brain's own mechanisms for controlling pain perception. Here we demonstrate that cortical neurons directly innervate the brainstem to drive feedforward inhibition of nociceptive neurons. This corticotrigeminal pathway suppresses the activity of these neurons and produces analgesia. This corticotrigeminal pathway may constitute a therapeutic target for chronic pain.
疼痛感知受到来自“更高”脑区的下行通路的强烈影响,这些通路调节脊髓回路的活动。除了广泛研究的源自延髓的下行系统外,新皮层还提供密集的解剖学投射,直接靶向脊髓和三叉神经脊髓尾核(SpVc)中的神经元。有证据表明,这些皮质-三叉神经通路可能调节SpVc对伤害性输入的处理,并调节疼痛感知。我们在此用解剖学和光遗传学方法,对雌雄大鼠和小鼠进行研究,证明皮质-三叉神经轴突密集地支配SpVc,在那里它们靶向并直接激活抑制性和兴奋性神经元。电生理记录显示,刺激初级体感皮层可有效抑制SpVc对有害刺激的反应,并产生行为性痛觉减退。这些发现表明,皮质-三叉神经通路是伤害感受的有效调节因子,也是缓解慢性疼痛干预的潜在靶点。许多慢性疼痛病症对传统疗法有抗性。有前景的疼痛管理新方法利用大脑自身控制疼痛感知的机制。我们在此证明,皮层神经元直接支配脑干,以驱动对伤害性神经元的前馈抑制。这条皮质-三叉神经通路抑制这些神经元的活动并产生镇痛作用。这条皮质-三叉神经通路可能构成慢性疼痛的治疗靶点。