Department of Pain & Migraine Research, Merck Research Laboratories, West Point, PA 19486, USA.
Curr Pharm Biotechnol. 2011 Oct;12(10):1671-80. doi: 10.2174/138920111798357401.
Migraine remains one of the most prevalent and disabling neurological disorders that often affects a person during their most productive years. Migraine afflicts approximately 11% of the adult population globally, causes substantial disability, which translates into lost productivity both at home and at work. Clearly there remains a need for new approaches to treat migraine and calcitonin gene-related peptide (CGRP) receptor antagonists have the potential to be a major advance in antimigraine therapy. CGRP was first proposed to play a role in migraine pathophysiology a little over 20 years ago and today there is considerable evidence that CGRP plays a key role in the pathogenesis of migraine. CGRP is a 37 amino acid vasoactive neuropeptide largely expressed in sensory neurons. It was observed that plasma levels of CGRP were elevated during the headache phase of migraine and the levels were normalized concomitantly with pain relief. This observation, along with other evidence, suggested that CGRP receptor antagonists might represent a novel approach to migraine treatment. The advent of small molecule CGRP receptor antagonists has clearly demonstrated a clinical link between blocking the CGRP receptor and effectiveness in treating migraine. This review will highlight the biology of CGRP as it pertains to migraine; discuss the CGRP receptor; spotlight the development of CGRP receptor antagonists; and examine site of action.
偏头痛仍然是最常见和最具致残性的神经疾病之一,通常在人们最具生产力的年龄段影响他们。偏头痛影响全球约 11%的成年人,导致严重的残疾,这意味着在家中和工作中都会失去生产力。显然,我们仍然需要新的方法来治疗偏头痛,降钙素基因相关肽(CGRP)受体拮抗剂有可能成为偏头痛治疗的重大进展。CGRP 大约在 20 多年前首次被提出在偏头痛病理生理学中发挥作用,如今有相当多的证据表明 CGRP 在偏头痛的发病机制中起着关键作用。CGRP 是一种 37 个氨基酸的血管活性神经肽,主要在感觉神经元中表达。研究观察到,CGRP 的血浆水平在偏头痛的头痛阶段升高,并且随着疼痛缓解而同时正常化。这一观察结果以及其他证据表明,CGRP 受体拮抗剂可能代表治疗偏头痛的一种新方法。小分子 CGRP 受体拮抗剂的出现清楚地表明,阻断 CGRP 受体与治疗偏头痛的有效性之间存在临床联系。这篇综述将重点介绍 CGRP 与偏头痛相关的生物学;讨论 CGRP 受体;强调 CGRP 受体拮抗剂的发展;并检查作用部位。