Basic Science: Prejunctional and Presynaptic Trigeminovascular Targets: What Preclinical Evidence Is There?

Peter J. Goadsby MD., Ph.D.
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引用次数: 3

Abstract

Inhibition of trigeminovascular nociceptive traffic by a prejunctional/presynaptic mechanism is an attractive approach for the treatment of migraine. It has been shown that blocking the presumed postsynaptic actions of calcitonin gene-related peptide (CGRP) is an effective acute antimigraine strategy, so that blockade of CGRP release by presynaptic inhibition also seems promising. A number of targets are reviewed including serotonin 5-HT1F and 5-HT1D receptor agonists, adenosine A1 receptor agonists, nociceptin, and vanilloid VR1 receptors. For each, the preclinical rationale for their involvement in prejunctional/presynaptic mechanisms is reviewed. Development of one or more such compounds offers the exciting prospect of new nonvasoconstrictor treatments for migraine and cluster headache.

基础科学:神经前和突触前三叉神经血管靶点:有什么临床前证据?
通过突触前/突触前机制抑制三叉神经血管伤害性交通是治疗偏头痛的一种有吸引力的方法。研究表明,阻断降钙素基因相关肽(CGRP)的突触后作用是一种有效的急性抗偏头痛策略,因此通过突触前抑制来阻断CGRP的释放似乎也很有希望。一些靶点包括5-羟色胺5-HT1F和5-HT1D受体激动剂,腺苷A1受体激动剂,痛感肽和香草素VR1受体。对于每一个,临床前的理论基础,他们参与突触前/突触前机制进行了审查。一种或多种此类化合物的开发为偏头痛和丛集性头痛的非血管收缩治疗提供了令人兴奋的前景。
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