Neuroanatomical evidence and a mouse calcitonin gene-related peptide model in line with human functional magnetic resonance imaging data support the involvement of peptidergic Edinger-Westphal nucleus in migraine.

IF 5.9 1区 医学 Q1 ANESTHESIOLOGY
PAIN® Pub Date : 2024-12-01 Epub Date: 2024-06-14 DOI:10.1097/j.pain.0000000000003294
Ammar Al-Omari, Balázs Gaszner, Dóra Zelena, Kinga Gecse, Gergely Berta, Tünde Biró-Sütő, Péter Szocsics, Zsófia Maglóczky, Péter Gombás, Erika Pintér, Gabriella Juhász, Viktória Kormos
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引用次数: 0

Abstract

Abstract: The urocortin 1 (UCN1)-expressing centrally projecting Edinger-Westphal (EWcp) nucleus is influenced by circadian rhythms, hormones, stress, and pain, all known migraine triggers. Our study investigated EWcp's potential involvement in migraine. Using RNAscope in situ hybridization and immunostaining, we examined the expression of calcitonin gene-related peptide (CGRP) receptor components in both mouse and human EWcp and dorsal raphe nucleus (DRN). Tracing study examined connection between EWcp and the spinal trigeminal nucleus (STN). The intraperitoneal CGRP injection model of migraine was applied and validated by light-dark box, and von Frey assays in mice, in situ hybridization combined with immunostaining, were used to assess the functional-morphological changes. The functional connectivity matrix of EW was examined using functional magnetic resonance imaging in control humans and interictal migraineurs. We proved the expression of CGRP receptor components in both murine and human DRN and EWcp. We identified a direct urocortinergic projection from EWcp to the STN. Photophobic behavior, periorbital hyperalgesia, increased c-fos gene-encoded protein immunoreactivity in the lateral periaqueductal gray matter and trigeminal ganglia, and phosphorylated c-AMP-responsive element binding protein in the STN supported the efficacy of CGRP-induced migraine-like state. Calcitonin gene-related peptide administration also increased c-fos gene-encoded protein expression, Ucn1 mRNA, and peptide content in EWcp/UCN1 neurons while reducing serotonin and tryptophan hydroxylase-2 levels in the DRN. Targeted ablation of EWcp/UCN1 neurons induced hyperalgesia. A positive functional connectivity between EW and STN as well as DRN has been identified by functional magnetic resonance imaging. The presented data strongly suggest the regulatory role of EWcp/UCN1 neurons in migraine through the STN and DRN with high translational value.

神经解剖学证据和小鼠降钙素基因相关肽模型与人类功能磁共振成像数据一致,支持肽能艾丁格-韦斯特脑核参与偏头痛。
摘要:表达尿皮质素1(UCN1)的中央投射艾丁格-韦斯特脑核(EWcp)受昼夜节律、激素、压力和疼痛的影响,而这些都是已知的偏头痛诱因。我们的研究调查了 EWcp 在偏头痛中的潜在参与。利用 RNAscope 原位杂交和免疫染色法,我们检测了降钙素基因相关肽(CGRP)受体成分在小鼠和人类 EWcp 以及背侧剑突核(DRN)中的表达。追踪研究检验了 EWcp 与脊髓三叉神经核(STN)之间的联系。应用腹腔注射 CGRP 的偏头痛模型并通过光-暗箱进行验证,使用小鼠 von Frey 试验、原位杂交结合免疫染色来评估功能-形态变化。在对照组和发作间期偏头痛患者中使用功能磁共振成像检查了 EW 的功能连接矩阵。我们证实了 CGRP 受体成分在鼠、人 DRN 和 EWcp 中的表达。我们确定了从EWcp到STN的直接尿皮质素能投射。恐光行为、眶周痛觉减退、外侧视网膜灰质和三叉神经节中c-fos基因编码蛋白免疫活性增加以及STN中磷酸化的c-AMP反应元件结合蛋白支持了CGRP诱导的偏头痛样状态的有效性。降钙素基因相关肽也增加了c-fos基因编码蛋白的表达、Ucn1 mRNA和EWcp/UCN1神经元中肽的含量,同时降低了DRN中5-羟色胺和色氨酸羟化酶-2的水平。靶向消融 EWcp/UCN1 神经元可诱导痛觉减退。功能性磁共振成像确定了 EW 和 STN 以及 DRN 之间的正功能连接。这些数据有力地证明了 EWcp/UCN1 神经元通过 STN 和 DRN 在偏头痛中的调节作用,具有很高的转化价值。
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来源期刊
PAIN®
PAIN® 医学-临床神经学
CiteScore
12.50
自引率
8.10%
发文量
242
审稿时长
9 months
期刊介绍: PAIN® is the official publication of the International Association for the Study of Pain and publishes original research on the nature,mechanisms and treatment of pain.PAIN® provides a forum for the dissemination of research in the basic and clinical sciences of multidisciplinary interest.
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