Ex vivo stimulation of the trigeminal nucleus caudalis induces peripheral CGRP release in the trigeminal ganglion and reveals a distinct dopamine-endocannabinoid mechanism relevant to migraine.

IF 7.3 1区 医学 Q1 CLINICAL NEUROLOGY
Isabella Mai Christiansen, Philip Victor Reducha, Lars Edvinsson, Anja Holm, Kristian Agmund Haanes
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引用次数: 0

Abstract

Background: Calcitonin gene-related peptide (CGRP) release from trigeminal structures is central to migraine pathophysiology. This study employed an ex vivo model preserving anatomical continuity between the trigeminal nucleus caudalis (TNC) and trigeminal ganglion (TG) to investigate (1) whether TNC stimulation induces peripheral CGRP release from the TG and (2) the potential involvement of a distinct dopamine-endocannabinoid mechanism.

Methods: Tissues were dissected as a single unit and placed in custom 3D-printed chambers, allowing targeted stimulation of either the TNC or the TG while measuring CGRP in both compartments. Pharmacological tools, including capsaicin (TRPV1 agonist), KCl (depolarizing agent), dopamine, and selective enzyme inhibitors or receptor antagonists, were used to elucidate underlying signalling pathways. CGRP levels were quantified via enzyme-linked immunosorbent assay.

Results: Stimulation of the TNC elicited a significant rise in CGRP release locally and in the TG compartment, whereas directly stimulating the TG did not trigger CGRP release in the TNC. Subsequent experiments showed that applying dopamine to the TNC further enhanced CGRP release. TRPV1 blockade or pharmacological inhibition of N-acyl phosphatidylethanolamine phospholipase D (NAPE-PLD), an enzyme important for anandamide biosynthesis, markedly attenuated dopamine-induced CGRP release, indicating that an endocannabinoid-driven mechanism is involved.

Conclusion: Activating the TNC alone was sufficient to evoke CGRP release in the peripheral trigeminal compartment, underscoring a potential central-to-peripheral mechanism that may be relevant to migraine. Moreover, a dopamine-endocannabinoid-TRPV1 axis appears to modulate CGRP signalling in this system, indicating additional complexity and providing potential new strategies for migraine therapy.

体外刺激三叉神经尾核诱导三叉神经节外周CGRP释放,揭示了与偏头痛相关的多巴胺-内源性大麻素机制。
背景:从三叉神经结构释放降钙素基因相关肽(CGRP)是偏头痛病理生理的核心。本研究采用体外模型保持三叉神经尾核(TNC)和三叉神经节(TG)之间的解剖连续性,以研究(1)TNC刺激是否诱导外周CGRP从TG释放;(2)多巴胺-内源性大麻素的潜在参与机制。方法:将组织作为一个单元解剖,并放置在定制的3d打印腔室中,允许靶向刺激TNC或TG,同时测量两个腔室中的CGRP。包括辣椒素(TRPV1激动剂)、KCl(去极化剂)、多巴胺和选择性酶抑制剂或受体拮抗剂在内的药理学工具被用来阐明潜在的信号通路。采用酶联免疫吸附法定量CGRP水平。结果:刺激TNC可引起局部和TG室CGRP释放显著升高,而直接刺激TG不触发TNC中CGRP释放。随后的实验表明,多巴胺作用于TNC进一步增强了CGRP的释放。TRPV1阻断或药物抑制n -酰基磷脂酰乙醇胺磷脂酶D (NAPE-PLD),显著减弱多巴胺诱导的CGRP释放,表明内源性大麻素驱动的机制参与其中。结论:单独激活TNC足以引起三叉神经外周腔室CGRP的释放,强调了可能与偏头痛相关的潜在中枢到外周机制。此外,多巴胺-内源性大麻素- trpv1轴似乎调节该系统中的CGRP信号,这表明了额外的复杂性,并为偏头痛治疗提供了潜在的新策略。
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来源期刊
Journal of Headache and Pain
Journal of Headache and Pain 医学-临床神经学
CiteScore
11.80
自引率
13.50%
发文量
143
审稿时长
6-12 weeks
期刊介绍: The Journal of Headache and Pain, a peer-reviewed open-access journal published under the BMC brand, a part of Springer Nature, is dedicated to researchers engaged in all facets of headache and related pain syndromes. It encompasses epidemiology, public health, basic science, translational medicine, clinical trials, and real-world data. With a multidisciplinary approach, The Journal of Headache and Pain addresses headache medicine and related pain syndromes across all medical disciplines. It particularly encourages submissions in clinical, translational, and basic science fields, focusing on pain management, genetics, neurology, and internal medicine. The journal publishes research articles, reviews, letters to the Editor, as well as consensus articles and guidelines, aimed at promoting best practices in managing patients with headaches and related pain.
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