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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Correlation between algogenic effects of calcitonin-gene-related peptide (CGRP) and activation of trigeminal vascular system, in an in vivo experimental model of nitroglycerin-induced sensitization
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Correlation between algogenic effects of calcitonin-gene-related peptide (CGRP) and activation of trigeminal vascular system, in an in vivo experimental model of nitroglycerin-induced sensitization

机译:在硝酸甘油致敏的体内实验模型中,降钙素基因相关肽(CGRP)的促生作用与三叉神经血管系统的激活之间的相关性

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摘要

The neural mechanism(s) underlying migraine remain poorly defined at present; preclinical and clinical studies show an involvement of CGRP in this disorder. However current evidence pointed out that CGRP does not exert an algogenic action per se, but it is able to mediate migraine pain only if the trigeminal-vascular system is sensitized. The present study was addressed to investigate CGRP-evoked behavior in nitric oxide (NO) sensitized rats, using an experimental model of nitroglycerin induced sensitization of trigeminal system, looking at neuropeptide release from different cerebral areas after the intraperitoneal (i.p.) administration of NO-donors. CGRP injected into the rat whisker pad did not induce significant changes in face rubbing behavior compared to controls. On the contrary, CGRP injected in animals pre-treated with 10 mg/kg nitroglycerin significantly increased the time spent in face rubbing. Nitroglycerin pre-treated animals did not show any rubbing behavior after locally injected saline. Furthermore, the i.p. treatment with nitroglycerin produced an increase of CGRP levels in brainstem and trigeminal ganglia, but not in the hypothalamus and hippocampus. The absolute amounts of CGRP produced in the brainstem were lower compared to those in the trigeminal ganglion; however, after nitroglycerin stimulation the percentage increase was higher in the brainstem. In conclusion, findings presented in this study suggest that CGRP induces a painful behavior in rats only after sensitization of trigeminal system; thus supporting the concept that a genetic as well as acquired predisposition to trigemino- vascular activation represents the neurobiological basis of CGRP nociceptive effects in migraineurs. (C) 2014 Elsevier B.V. All rights reserved.
机译:目前,偏头痛的神经机制仍然不清楚。临床前和临床研究表明CGRP参与了这种疾病。然而,目前的证据指出,CGRP本身并不发挥促成生作用,但是只有在三叉神经-血管系统敏化的情况下,它才能介导偏头痛。本研究旨在研究硝酸甘油诱导的三叉神经系统敏化的实验模型,研究一氧化氮(NO)致敏大鼠中CGRP引起的行为,观察腹膜内(ip)给药后不同大脑区域的神经肽释放捐助者。与对照组相比,注射到大鼠晶须垫中的CGRP没有引起面部摩擦行为的明显变化。相反,在用10 mg / kg硝酸甘油进行预处理的动物中注射的CGRP显着增加了面部揉搓所花费的时间。硝酸甘油预处理的动物在局部注射盐水后未显示任何摩擦行为。此外,i.p。硝酸甘油治疗可增加脑干和三叉神经节的CGRP水平,但不会引起下丘脑和海马的CGRP升高。与三叉神经节相比,脑干中产生的CGRP的绝对量要低。然而,硝酸甘油刺激后,脑干中的百分比增加更高。总之,本研究提出的发现表明,CGRP仅在三叉神经系统致敏后才会在大鼠中引起疼痛行为。因此支持了这样的概念,即遗传和后天的三叉神经血管激活易感性代表了偏头痛患者CGRP伤害感受的神经生物学基础。 (C)2014 Elsevier B.V.保留所有权利。

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