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降钙素基因相关肽受体拮抗剂治疗偏头痛。它们也是淀粉样蛋白受体拮抗剂吗?

CGRP receptor antagonists for migraine. Are they also AMY receptor antagonists?

机构信息

Department of Pharmacology and Toxicology, University of Otago, Dunedin, New Zealand.

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

出版信息

Br J Pharmacol. 2022 Feb;179(3):454-459. doi: 10.1111/bph.15585. Epub 2021 Jun 24.

Abstract

The development of several drugs that target the calcitonin gene-related peptide (CGRP) system has been a major breakthrough in the pharmacological management of migraine. These are divided into two major classes, antibodies which bind to the CGRP peptide, preventing it from activating CGRP receptors and receptor antagonists. Within the receptor antagonist class, there are two mechanisms of action, small molecule receptor antagonists and an antibody antagonist. This mini-review considers the pharmacology of these receptor targeted antagonist drugs at the CGRP receptor and closely related AMY receptor, at which CGRP may also act. The antagonists are most potent at the CGRP receptor but can also show antagonism of the AMY receptor. However, important data are missing and selectivity parameters cannot be provided for all antagonists. The clinical implications of AMY receptor antagonism are unknown, but we urge consideration of this receptor as a potential contributing factor to CGRP and antagonist drug actions. LINKED ARTICLES: This article is part of a themed issue on Advances in Migraine and Headache Therapy (BJP 75th Anniversary). To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.3/issuetoc.

摘要

几种靶向降钙素基因相关肽 (CGRP) 系统的药物的开发是偏头痛药物治疗的重大突破。这些药物分为两类,一类是与 CGRP 肽结合的抗体,阻止其激活 CGRP 受体,另一类是受体拮抗剂。在受体拮抗剂类中,有两种作用机制,小分子受体拮抗剂和抗体拮抗剂。这篇小型综述考虑了这些靶向 CGRP 受体和密切相关的 AMY 受体的受体靶向拮抗剂药物的药理学,CGRP 也可能在这些受体上发挥作用。这些拮抗剂在 CGRP 受体上最有效,但也可以表现出对 AMY 受体的拮抗作用。然而,重要的数据缺失,无法为所有拮抗剂提供选择性参数。AMY 受体拮抗的临床意义尚不清楚,但我们敦促考虑该受体作为 CGRP 和拮抗剂药物作用的潜在影响因素。相关文章:本文是关于偏头痛和头痛治疗进展的专题(BJP 75 周年纪念)的一部分。要查看本部分的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.3/issuetoc.

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