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神经肽Y受体配体在癫痫治疗中的临床潜力。

Clinical potential of neuropeptide Y receptor ligands in the treatment of epilepsy.

作者信息

Meurs Alfred, Clinckers Ralph, Ebinger Guy, Michotte Yvette, Smolders Ilse

机构信息

Department of Neurology, University Hospital Brussels, Laarbeeklaan 101, 1090 Brussels, Belgium.

出版信息

Curr Top Med Chem. 2007;7(17):1660-74. doi: 10.2174/156802607782340975.

Abstract

A substantial amount of experimental evidence implicates neuropeptide Y (NPY) in the pathophysiology of epilepsy. Over the past 20 years, remarkable progress has been made in unraveling the mechanisms and receptors involved in the anticonvulsant effect of this abundantly expressed neuropeptide. Activation of Y(2) and/or Y(5) receptors and blockade of Y(1) receptors in the central nervous system suppresses seizures in a variety of animal seizure models. Orally available, brain penetrating Y(2) and/or Y(5) agonists, and possibly Y(1) antagonists, may therefore constitute a novel class of antiepileptic drugs, which could greatly benefit patients with medically refractory epilepsy. Significant progress has been made in identifying non-peptidergic Y(1) antagonists that fulfill these criteria, but suitable Y(2) and/or Y(5) agonists have proven to be more elusive. Innovative oral and parental drug delivery strategies which are currently under development may offer a means of using the more readily available peptidergic NPY receptor ligands in a clinical setting. Finally, gene therapy, antisense probes or RNA interference strategies which alter the expression of NPY or its receptors in specific brain regions may also be of use in the treatment of epilepsy, but will probably benefit a smaller subgroup of epilepsy patients, since they typically require an invasive procedure.

摘要

大量实验证据表明神经肽Y(NPY)与癫痫的病理生理学有关。在过去20年里,在揭示这种大量表达的神经肽的抗惊厥作用所涉及的机制和受体方面取得了显著进展。中枢神经系统中Y(2)和/或Y(5)受体的激活以及Y(1)受体的阻断在多种动物癫痫模型中可抑制癫痫发作。因此,口服可穿透脑的Y(2)和/或Y(5)激动剂,以及可能的Y(1)拮抗剂,可能构成一类新型抗癫痫药物,这将使药物难治性癫痫患者大大受益。在鉴定符合这些标准的非肽类Y(1)拮抗剂方面已取得重大进展,但事实证明,合适的Y(2)和/或Y(5)激动剂更难找到。目前正在开发的创新口服和经皮给药策略可能提供一种在临床环境中使用更容易获得的肽类NPY受体配体的方法。最后,改变特定脑区中NPY或其受体表达的基因治疗、反义探针或RNA干扰策略也可能用于癫痫治疗,但可能只会使一小部分癫痫患者受益,因为它们通常需要侵入性操作。

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