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5-羟色胺1样激动剂用于治疗偏头痛的原理。

Rationale for the use of 5-HT1-like agonists in the treatment of migraine.

作者信息

Feniuk W, Humphrey P P, Perren M J, Connor H E, Whalley E T

机构信息

Pharmacology Division, Glaxo Group Research Ltd., Ware, UK.

出版信息

J Neurol. 1991;238 Suppl 1:S57-61. doi: 10.1007/BF01642908.

Abstract

Migraine headache is thought to be associated with a dilatation of cranial blood vessels, particularly those in the dura mater, and an accompanying localized sterile inflammatory response. Sumatriptan is a highly selective 5-HT1-like receptor agonist which selectively constricts cranial blood vessels (including those in the dura mater). It also inhibits neurogenically-mediated plasma protein extravasation in the dura mater. Haemodynamic studies in anaesthetized animals have shown that sumatriptan selectively constricts the carotid arterial circulation and this effect appears to be restricted to an effect on carotid arteriovenous anastomoses. Sumatriptan has a much more selective pharmacological profile than ergot preparations which are also used in the acute treatment of migraine. The development of sumatriptan has been based on a vascular theory of migraine and its high degree of efficacy in the treatment of migraine strengthens the argument that dilatation of cranial blood vessels is the cause of vascular headache.

摘要

偏头痛被认为与颅内血管扩张有关,尤其是硬脑膜中的血管,同时伴有局部无菌性炎症反应。舒马曲坦是一种高度选择性的5-羟色胺1样受体激动剂,可选择性收缩颅内血管(包括硬脑膜中的血管)。它还能抑制硬脑膜中神经源性介导的血浆蛋白外渗。在麻醉动物身上进行的血流动力学研究表明,舒马曲坦能选择性收缩颈动脉循环,且这种作用似乎仅限于对颈动脉动静脉吻合处的影响。与也用于偏头痛急性治疗的麦角制剂相比,舒马曲坦具有更具选择性的药理学特征。舒马曲坦的研发基于偏头痛的血管理论,其在偏头痛治疗中的高度有效性强化了颅内血管扩张是血管性头痛病因这一观点。

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