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重新审视偏头痛中的P物质:一种受抗降钙素基因相关肽和抗垂体腺苷酸环化酶激活肽成功启发的方法学途径。

Revisiting substance P in migraine: a methodological approach inspired by anti-CGRP and anti-PACAP success.

作者信息

Pellesi Lanfranco, Edvinsson Lars

机构信息

Clinical Pharmacology, Pharmacy and Environmental Medicine, Department of Public Health, University of Southern Denmark, Odense, 5230, Denmark.

Department of Medicine, Institute of Clinical Sciences, Lund University, Lund, Sweden.

出版信息

J Headache Pain. 2025 Jan 31;26(1):22. doi: 10.1186/s10194-025-01959-8.

Abstract

Substance P, previously dismissed as a therapeutic target for migraine due to the failure of neurokinin-1 receptor antagonists, warrants renewed attention. Building on the success of therapies targeting the calcitonin gene-related peptide (CGRP) system and pituitary adenylate cyclase-activating peptide (PACAP) in migraine prevention, which highlight the importance of targeting peptides, this proposal reexamines substance P as a mediator in migraine pathophysiology. Using an established methodological framework, migraine-inducing properties of substance P can be evaluated through randomized, double-blind, placebo-controlled crossover studies involving healthy volunteers and individuals with a history of migraine. This approach aims to establish proof of concept for substance P's role in migraine, laying the groundwork for investigations with animal and cell-based models and advancing the development of innovative treatments for patients refractory to current therapies.

摘要

由于神经激肽-1受体拮抗剂的失败,P物质先前被排除在偏头痛治疗靶点之外,现在值得重新关注。基于靶向降钙素基因相关肽(CGRP)系统和垂体腺苷酸环化酶激活肽(PACAP)预防偏头痛疗法的成功,这些疗法突出了靶向肽的重要性,本提议重新审视P物质作为偏头痛病理生理学中的一种介质。使用既定的方法框架,可以通过涉及健康志愿者和有偏头痛病史个体的随机、双盲、安慰剂对照交叉研究来评估P物质的偏头痛诱发特性。这种方法旨在确立P物质在偏头痛中作用的概念验证,为基于动物和细胞模型的研究奠定基础,并推动针对当前疗法难治患者的创新治疗方法的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1f/11786519/2ef46478f376/10194_2025_1959_Fig1_HTML.jpg

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