一个潜在的临床前偏头痛模型:cgrp致敏小鼠。

Molecular and cellular pharmacology Pub Date : 2009-01-01
Andrew F Russo, Adisa Kuburas, Eric A Kaiser, Ann C Raddant, Ana Recober
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引用次数: 0

摘要

神经肽降钙素基因相关肽(CGRP)在偏头痛中起关键作用。然而,研究CGRP作用的一个主要挑战是缺乏偏头痛的动物模型。临床研究表明,偏头痛患者比没有偏头痛的人对CGRP更敏感。因此,我们产生了对CGRP敏感的转基因小鼠(nestin/hRAMP1小鼠)。小鼠的CGRP受体亚基,人受体活性修饰蛋白1 (hRAMP1)的表达升高。Nestin/hRAMP1小鼠有两种偏头痛症状:畏光和机械异常性疼痛。CGRP脑室内给药可显著增强避光反应。CGRP对小鼠在光照区的运动几乎没有影响,但一旦进入黑暗,小鼠的运动就会比对照组少。与CGRP受体拮抗剂共给药可减轻CGRP诱导的光厌恶。这些发现表明,CGRP作为一种神经调节剂,可以增加感觉反应,而单一基因hRAMP1的调节可能会导致偏头痛的易感性。
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A Potential Preclinical Migraine Model: CGRP-Sensitized Mice.

The neuropeptide calcitonin gene-related peptide (CGRP) plays a key role in migraine. However, a major challenge for studying CGRP actions is the lack of animal models for migraine. Clinical studies suggested that migraineurs are more sensitive to CGRP than people who do not suffer from migraine. We therefore generated a transgenic mouse that is sensitized to CGRP (nestin/hRAMP1 mice). The mice have elevated expression of a subunit of the CGRP receptor, human receptor activity-modifying protein 1 (hRAMP1). Nestin/hRAMP1 mice have two symptoms of migraine: photophobia and mechanical allodynia. The light aversion was greatly enhanced by intracerebroventricular administration of CGRP. CGRP had little effect on motility in the light zone, but once in the dark, the mice moved less than controls. The CGRP-induced light aversion was attenuated by co-administration of the CGRP receptor antagonist olcegepant. These findings suggest that CGRP acts as a neuromodulator to increase sensory responses and that regulation of a single gene, hRAMP1, could potentially contribute to migraine susceptibility.

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