Department of Neurobiology, School of Basic Medical Sciences, Neuroscience Research Institute, Beijing, Peoples Republic of China.
Key Laboratory for Neuroscience, Ministry of Education/National Health and Family Planning Commission, Peking University, Beijing, Peoples Republic of China.
Pain. 2018 Aug;159(8):1550-1561. doi: 10.1097/j.pain.0000000000001240.
One specific behavior can be synergistically modulated by different neural pathways. Medial septal (MS) cholinergic system innervates widespread cortical and subcortical regions and participates in pain modulation, but the underlying neural pathways are not fully understood. This study examined the contribution of MS cholinergic neurons and 2 neural pathways: MS-rostral anterior cingulate cortex (rACC) and MS-ventral hippocampal CA1 (vCA1), in modulating perceptual and affective pain behaviors in a mouse model of chronic inflammatory pain. We found that chronic pain activated MS cholinergic neurons and pyramidal neurons in the rACC, but suppressed pyramidal neuronal activities in the vCA1, all of which contributed to the maintenance of pathological pain. Chemogenetic inhibition of MS cholinergic neurons or the MS-rACC pathway inhibited rACC pyramidal neuronal activities and attenuated perceptual and affective dimensions of chronic pain. By contrast, chemogenetic activation of MS cholinergic neurons also produced analgesia, but by rescuing hypofunctional pyramidal neurons in vCA1. These results clearly demonstrate that the MS cholinergic system differentially modulates chronic inflammatory pain through MS-rACC or MS-vCA1 pathways. More significantly, our research provides evidence for a novel paradigm of neural circuit modulation: MS cholinergic inhibition and activation induce similar analgesia but through distinct neural pathways.
一种特定的行为可以通过不同的神经通路协同调节。内侧隔(MS)胆碱能系统支配广泛的皮质和皮质下区域,并参与疼痛调节,但潜在的神经通路尚不完全清楚。本研究在慢性炎症性疼痛的小鼠模型中,考察了 MS 胆碱能神经元和 2 种神经通路(MS-额前皮质(rACC)和 MS-腹侧海马 CA1(vCA1))对调节感知和情感性疼痛行为的贡献。我们发现,慢性疼痛激活了 MS 胆碱能神经元和 rACC 的锥体神经元,但抑制了 vCA1 中的锥体神经元活动,所有这些都有助于病理性疼痛的维持。MS 胆碱能神经元或 MS-rACC 通路的化学遗传抑制抑制了 rACC 锥体神经元的活动,并减轻了慢性疼痛的感知和情感维度。相比之下,MS 胆碱能神经元的化学遗传激活也产生了镇痛作用,但通过挽救 vCA1 中功能低下的锥体神经元。这些结果清楚地表明,MS 胆碱能系统通过 MS-rACC 或 MS-vCA1 通路对慢性炎症性疼痛进行差异调节。更重要的是,我们的研究为神经回路调节的新范式提供了证据:MS 胆碱能抑制和激活诱导类似的镇痛作用,但通过不同的神经通路。