Meßlinger Karl
Institut für Physiologie und Pathophysiologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstraße 17, 91054, Erlangen, Deutschland.
Schmerz. 2020 Apr;34(2):181-187. doi: 10.1007/s00482-020-00448-y.
Calcitonin gene-related peptide (CGRP) is released from trigeminal afferents during migraine and cluster headache attacks and can be detected in the jugular plasma. Infusion of CGRP can induce headache attacks in migraine and cluster patients. Inhibition of the CGRP signal system is therapeutic in migraine and cluster headache. CGRP is a potent dilator of intracranial arteries but does not immediately activate the trigeminal pain system. CGRP may act as a signal molecule between different cells in the trigeminal ganglion and enhances nociceptive transmission in the spinal trigeminal nucleus. Peripheral inhibition of the CGRP system reduces these actions. Outside the trigeminovascular system, CGRP is important for maintaining the perfusion of organs in critical situations, promotes growth and repair functions and is an immunomodulatory factor. These actions should be considered when the CGRP system is suppressed for a long time.
降钙素基因相关肽(CGRP)在偏头痛和丛集性头痛发作时从三叉神经传入纤维释放,并可在颈静脉血浆中检测到。输注CGRP可诱发偏头痛和丛集性头痛患者的头痛发作。抑制CGRP信号系统对偏头痛和丛集性头痛具有治疗作用。CGRP是颅内动脉的强效扩张剂,但不会立即激活三叉神经痛系统。CGRP可能作为三叉神经节中不同细胞之间的信号分子,并增强三叉神经脊束核中的伤害性传递。对CGRP系统的外周抑制可减少这些作用。在三叉神经血管系统之外,CGRP在危急情况下对维持器官灌注很重要,促进生长和修复功能,并且是一种免疫调节因子。当长期抑制CGRP系统时,应考虑这些作用。