降钙素基因相关肽(CGRP)在偏头痛中的作用

Md. Ashraf Ali, H. Rahaman
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引用次数: 0

摘要

偏头痛是第二大头痛。偏头痛在一般人群中的患病率为12%,其中女性为18%,男性为6%。偏头痛可以从童年和青春期开始,并持续一生。这在30多岁和40多岁的人群中最为普遍。偏头痛是一种使人衰弱的半颅性头痛,有搏动,因运动、恶心、呕吐而加重,对光和声音敏感,有或没有先兆。它可以影响生活的方方面面,如工作和学习,养育子女和家庭关系,个人和休闲时间。关于偏头痛的发病机制,有一些理论包括:皮质扩张性抑制、皮质扩张性低血症、三叉神经复合物的激活导致神经炎症和血管修复神经肽的释放,包括降钙素基因相关肽(CGRP)、P物质、血管活性肠多肽(VIP)、一氧化氮(NO)、垂体腺苷酸环化酶激活肽(PACAP)和遗传因子。CGRP是一种有效的血管扩张剂,可引起血管周围血浆蛋白外渗和痛觉性疼痛。较新的药物靶向CGRP用于偏头痛的急性和预防性治疗。孟加拉国神经科学杂志2017;Vol. 33 (1): 39-43
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Calcitonin Gene Related Peptide (CGRP) in Migraine
Migraine is the second most primary headache. The prevalence of Migraine is 12% in the general population, including 18% in women and 6% in men. Migraine can start in childhood and adolescence and continue throughout lifespan. It is most prevalent among people in their 30s and 40s. Migraine is a debilitating hemicranial headache that is pulsating, aggravated by movement, nausea, vomiting and having sensitivity to light and sound, with or without aura. It can affect all aspects of life as work and school, parenting and family relationships and personal and leisure time. There are some theory regarding pathogenesis of migraine which includes cortical spreading depression, cortical spreading oligemia, activation of trigeminocervical complex leading to neuroinflammation & release of vasodialating neuropeptides which include calcitonin gene related peptide (CGRP), substance P, vasoactive intestinal polypeptide (VIP), nitric oxide (NO), and pituitary adenylate cyclase activating peptide (PACAP) & genetic factor. CGRP is a potent vasodilator and causes perivascular plasma protein extravasation and nociceptive pain. Newer medications target CGRP both for acute and preventive treatment of migraine. Bangladesh Journal of Neuroscience 2017; Vol.  33 (1): 39-43
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