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New AMPA antagonists in epilepsy

机译:癫痫新的AMPA拮抗剂

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Introduction: Epilepsy is a common neurological disorder; however, its therapy is not satisfactory because a large number of patients suffer from refractory seizures and/or has a low quality of life due to antiepileptic drug (AED) side effects. Glutamate is the major excitatory neurotransmitter in the brain, AMPA receptors (AMPARs) represent a validated target for AEDs' development. Evidences support their role during seizures and neurodegeneration. Development of AMPAR ligands has led to two different branches of research, with the identification of competitive and noncompetitive antagonists. Areas covered: We herein describe the architecture of AMPAR and the main structureactivity relationships of antagonists. Finally, we report the effects of AMPAR antagonists in preclinical models and clinical trials in epileptic patients. We reviewed the most relevant research in the field, focusing on research advances for the oldest AMPA antagonists and the new most promising molecules identified. Expert opinion: Overall, the development of AMPAR antagonists confirms their great clinical potential; their arrival to clinical practice has been slowed down by their unfavorable pharmacokinetic profile and tolerability; however, their clinical use might be justified by their efficacy and the new drugs developed such as perampanel have been greatly ameliorated from both points of view.
机译:简介:癫痫病是一种常见的神经系统疾病;但是,由于抗癫痫药(AED)的副作用,大量患者患有难治性癫痫发作和/或生活质量低下,因此其治疗效果不理想。谷氨酸是大脑中主要的兴奋性神经递质,AMPA受体(AMPAR)代表AEDs的发展目标。证据支持它们在癫痫发作和神经退行性变中的作用。 AMPAR配体的发展导致了两个不同的研究领域,即鉴定竞争性和非竞争性拮抗剂。涵盖的领域:我们在此描述AMPAR的体系结构和拮抗剂的主要结构活性关系。最后,我们报告了AMPAR拮抗剂在癫痫患者的临床前模型和临床试验中的作用。我们回顾了该领域最相关的研究,重点研究了最古老的AMPA拮抗剂和鉴定出的最有希望的新分子的研究进展。专家意见:总体而言,AMPA拮抗剂的开发证实了其巨大的临床潜力;由于不良的药代动力学和耐受性,它们进入临床实践的速度已经减慢。然而,它们的临床效果可能因其功效而合理,从这两种观点来看,开发的新药(如perampanel)都得到了极大的改善。

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