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降钙素基因相关肽受体拮抗剂治疗偏头痛的新疗法。

Novel migraine therapy with calcitonin gene-regulated peptide receptor antagonists.

作者信息

Edvinsson Lars

机构信息

Lund University Hospital, Department of Medicine, Institute of Clinical Sciences, S-221 85 Lund, Sweden.

出版信息

Expert Opin Ther Targets. 2007 Sep;11(9):1179-88. doi: 10.1517/14728222.11.9.1179.

Abstract

Primary headaches, for example, migraine and cluster headaches represent the most prevalent neurological disorders, affecting up to 15-20% of the adult population. There is a clear association between head pain and the release of calcitonin gene-related peptide (CGRP). In this review the role of CGRP in human cranial circulation is described and the role for specific CGRP antagonism elucidated. It is well known that triptans (5-HT(1B/1D) agonist) alleviate headache in part through normalisation of CGRP levels. The central role of CGRP in migraine pathophysiology has resulted in the development of small-molecule CGRP antagonists with no cardiovascular side effects. Such compounds have high selectivity for human CGRP receptors and are efficacious in the relief of acute migraine attacks. Research indicates that they effect the abluminal side of the blood-brain barrier and that they are not vasoconstrictive, providing a new dimension in therapy.

摘要

例如,原发性头痛,如偏头痛和丛集性头痛,是最常见的神经系统疾病,影响高达15%至20%的成年人口。头痛与降钙素基因相关肽(CGRP)的释放之间存在明确关联。在本综述中,描述了CGRP在人体颅循环中的作用,并阐明了特异性CGRP拮抗作用的作用。众所周知,曲坦类药物(5-HT(1B/1D)激动剂)部分通过使CGRP水平正常化来缓解头痛。CGRP在偏头痛病理生理学中的核心作用导致了无心血管副作用的小分子CGRP拮抗剂的开发。此类化合物对人CGRP受体具有高选择性,并且在缓解急性偏头痛发作方面有效。研究表明,它们作用于血脑屏障的管腔外侧,且不具有血管收缩作用,为治疗提供了新的维度。

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