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偏头痛:分子生物学带来的新治疗选择

Migraine: new treatment options from molecular biology.

作者信息

Stam Anine H, Haan Joost, Frants Rune R, Ferrari Michel D, van den Maagdenberg Arn Mjm

机构信息

Department of Neurology, Leiden University Medical Centre, Leiden, 2300 RC Leiden, The Netherlands.

出版信息

Expert Rev Neurother. 2005 Sep;5(5):653-61. doi: 10.1586/14737175.5.5.653.

Abstract

Migraine is a common, disabling, multifactorial, episodic neurovascular disorder of largely unknown etiology. The disease is typically characterized by recurrent attacks of headaches and associated autonomic and neurologic symptoms. Current acute and prophylactic treatment options are far from optimal and in many cases, empirically chosen. Clearly, improved treatment is desperately needed. New drug targets may emerge from molecular research as the unravelling of the molecular basis of migraine should improve our understanding of the disease, notably why patients experience attacks so frequently. The first two migraine genes discovered in families with hemiplegic migraine encode ion transporters, emphasising that dysfunction of ion transport may be an important factor in migraine. Therefore, ion transporters can be considered as novel targets for the development of future antimigraine drugs. Molecular biologic research will increasingly become important in understanding the pathophysiology of migraine and in identifying potential molecular targets for novel treatments.

摘要

偏头痛是一种常见的、使人丧失能力的、多因素的、发作性神经血管疾病,其病因大多不明。该疾病通常以反复发作的头痛以及相关的自主神经和神经症状为特征。目前的急性和预防性治疗方案远非最佳,在许多情况下是凭经验选择的。显然,迫切需要改进治疗方法。随着偏头痛分子基础的揭示,分子研究可能会出现新的药物靶点,这应该会增进我们对该疾病的理解,特别是为什么患者如此频繁地发作。在偏瘫性偏头痛家族中发现的前两个偏头痛基因编码离子转运体,这强调了离子转运功能障碍可能是偏头痛的一个重要因素。因此,离子转运体可被视为未来抗偏头痛药物开发的新靶点。分子生物学研究在理解偏头痛的病理生理学以及确定新治疗方法的潜在分子靶点方面将变得越来越重要。

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