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双氢麦角胺可抑制猫三叉神经血管通路的中枢激活。一项c-Fos和电生理研究。

Central activation of the trigeminovascular pathway in the cat is inhibited by dihydroergotamine. A c-Fos and electrophysiological study.

作者信息

Hoskin K L, Kaube H, Goadsby P J

机构信息

Institute of Neurology, The National Hospital for Neurology and Neurosurgery, London, UK.

出版信息

Brain. 1996 Feb;119 ( Pt 1):249-56. doi: 10.1093/brain/119.1.249.

Abstract

Recent studies have delineated a clear role for the trigeminal innervation of pain-sensitive intracranial structures in the pathophysiology of migraine. The development of new compounds for the treatment of the acute attack of migraine has led to a greater understanding of serotonin (5-hydroxytryptamine; 5HT) receptor diversity. The ergot alkaloids have been used in the treatment of acute attacks of migraine for many years and parenteral administration of dihydroergotamine (DHE) can be a useful treatment strategy. In this study, the question of a possible central site of action of DHE is considered using both anatomical and physiological approaches. The c-Fos method has been used to map functional activation of central neurons in response to stimulation of the superior sagittal sinus (SSS) in the cat. This structure has been used as it refers pain to the ophthalmic division of the trigeminal nerve in humans, and in cats induces changes in neuropeptides and cranial blood flow similar to those seen in migraine. In addition, the temporal aspects of the effect of DHE have been studied by making extracellular recordings from cells in the most caudal aspect of the trigeminal nuclear complex. Stimulation of the SSS results in Fos expression in the superfical laminae of the trigeminal nucleus caudalis and in the dorsal horn of C1 and C2. This activation is blocked by a clinically relevant dose of DHE. Similarly, cells can be recorded in this region that respond to SSS stimulation. This linked cellular activity can be inhibited by the same intravenous dose of DHE. Together, these studies show that DHE can inhibit activity in central trigeminal neurons. Since the sinus and its nerve supply are directly stimulated, the peripheral nerve/vessel innervation is bypassed and this inhibition cannot have happened at any other site. These data imply that drugs acting at the central trigeminal neurons may have a role in the treatment of acute attacks of migraine.

摘要

最近的研究已经明确了疼痛敏感的颅内结构的三叉神经支配在偏头痛病理生理学中的作用。用于治疗偏头痛急性发作的新化合物的开发使人们对血清素(5-羟色胺;5HT)受体多样性有了更深入的了解。麦角生物碱多年来一直用于治疗偏头痛急性发作,胃肠外给予双氢麦角胺(DHE)可能是一种有效的治疗策略。在本研究中,使用解剖学和生理学方法探讨了DHE可能的中枢作用位点问题。c-Fos方法已被用于绘制猫的上矢状窦(SSS)刺激后中枢神经元的功能激活情况。选择该结构是因为它在人类中会将疼痛传导至三叉神经的眼支,并且在猫中会引起与偏头痛中所见类似的神经肽和颅血流量变化。此外,通过对三叉神经核复合体最尾端的细胞进行细胞外记录,研究了DHE作用的时间方面。刺激SSS会导致三叉神经尾侧核浅层以及C1和C2背角中Fos表达。这种激活被临床相关剂量的DHE阻断。同样,在该区域可以记录到对SSS刺激有反应的细胞。这种相关的细胞活动可以被相同静脉剂量的DHE抑制。这些研究共同表明,DHE可以抑制中枢三叉神经神经元的活动。由于窦及其神经供应直接受到刺激,外周神经/血管支配被绕过,这种抑制不可能在其他任何部位发生。这些数据表明,作用于中枢三叉神经神经元的药物可能在偏头痛急性发作的治疗中发挥作用。

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