位置小脑去甲肾上腺素能神经元在急性睡眠障碍与头痛之间的相互作用中的关键作用

Bozhi Li, Ya Cao, Huijuan Yuan, Zhe Yu, Shuai Miao, Chunxiao Yang, Zihua Gong, Wei Xie, Chenhao Li, Wenhao Bai, Wenjing Tang, Dengfa Zhao, Shengyuan Yu
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引用次数: 0

摘要

流行病学和临床研究都表明,头痛和睡眠障碍之间有着复杂的关系。尽管头痛和睡眠有着共同的神经生理学和解剖学基础,但人们对其相互作用的机制仍然知之甚少。间脑和脑干的结构,尤其是小脑定位点(LC),是睡眠和头痛通路交叉的主要部位。为了更好地了解头痛与睡眠之间错综复杂的关系,我们的研究重点是调查在急性头痛和急性睡眠障碍期间,LC 中去甲肾上腺素能神经元的作用和功能。为了探索急性头痛和急性睡眠障碍之间的关系,我们主要采用硝酸甘油(NTG)诱导的偏头痛样头痛和急性睡眠剥夺(ASD)模型。首先,我们通过实验证实了急性睡眠剥夺会增强头痛,并且急性头痛会导致急性睡眠障碍。随后,我们研究了 LC 在睡眠和头痛中的不同作用。我们观察了药物诱导激活和抑制以及化学遗传学操作 LC 去甲肾上腺素能神经元对 ASD 诱导的头痛促进和急性头痛相关睡眠障碍的影响。这种方法使我们能够证明 LC 去甲肾上腺素能神经元的双向功能。我们的研究结果表明,ASD 会促进 NTG 诱导的偏头痛,而急性头痛则会影响睡眠质量。此外,激活低密度脂蛋白胆碱能神经元可降低头痛阈值并增加睡眠潜伏期,而抑制低密度脂蛋白胆碱能神经元则会产生相反的效果。其他研究表明,激活 LC 去甲肾上腺素能神经元会进一步加强 ASD 对疼痛的促进作用,而抑制这些神经元则会降低这种疼痛促进作用。此外,激活 LC 去甲肾上腺素能神经元会加剧急性头痛对睡眠质量的影响,而抑制这些神经元则会减轻这种影响。在急性睡眠障碍和急性头痛的相互作用中,LC 是一个重要的解剖和功能区域。LC去甲肾上腺素能神经元的参与在促进ASD引发的头痛和影响头痛对睡眠质量的影响方面起着关键作用。
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The crucial role of locus coeruleus noradrenergic neurons in the interaction between acute sleep disturbance and headache
Both epidemiological and clinical studies have indicated that headache and sleep disturbances share a complex relationship. Although headache and sleep share common neurophysiological and anatomical foundations, the mechanism underlying their interaction remains poorly understood. The structures of the diencephalon and brainstem, particularly the locus coeruleus (LC), are the primary sites where the sleep and headache pathways intersect. To better understand the intricate nature of the relationship between headache and sleep, our study focused on investigating the role and function of noradrenergic neurons in the LC during acute headache and acute sleep disturbance. To explore the relationship between acute headache and acute sleep disturbance, we primarily employed nitroglycerin (NTG)-induced migraine-like headache and acute sleep deprivation (ASD) models. Initially, we conducted experiments to confirm that ASD enhances headache and that acute headache can lead to acute sleep disturbance. Subsequently, we examined the separate roles of the LC in sleep and headache. We observed the effects of drug-induced activation and inhibition and chemogenetic manipulation of LC noradrenergic neurons on ASD-induced headache facilitation and acute headache-related sleep disturbance. This approach enabled us to demonstrate the bidirectional function of LC noradrenergic neurons. Our findings indicate that ASD facilitated the development of NTG-induced migraine-like headache, while acute headache affected sleep quality. Furthermore, activating the LC reduced the headache threshold and increased sleep latency, whereas inhibiting the LC had the opposite effect. Additional investigations demonstrated that activating LC noradrenergic neurons further intensified pain facilitation from ASD, while inhibiting these neurons reduced this pain facilitation. Moreover, activating LC noradrenergic neurons exacerbated the impact of acute headache on sleep quality, while inhibiting them alleviated this influence. The LC serves as a significant anatomical and functional region in the interaction between acute sleep disturbance and acute headache. The involvement of LC noradrenergic neurons is pivotal in facilitating headache triggered by ASD and influencing the effects of headache on sleep quality.
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