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Mechanisms of Intrinsic Epileptogenesis in Human Gelastic Seizures with Hypothalamic Hamartoma

机译:下丘脑血肿形成的人全能性癫痫发作的内在癫痫发生机制。

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Summary Human hypothalamic hamartoma ( HH ) is a rare developmental malformation often characterized by gelastic seizures, which are refractory to medical therapy. Ictal EEG recordings from the HH have demonstrated that the epileptic source of gelastic seizures lies within the HH lesion itself. Recent advances in surgical techniques targeting HH have led to dramatic improvements in seizure control, which further supports the hypothesis that gelastic seizures originate within the HH . However, the basic cellular and molecular mechanisms of epileptogenesis in this subcortical lesion are poorly understood. Since 2003, Barrow Neurological Institute has maintained a multidisciplinary clinical program to evaluate and treat patients with HH . This program has provided a unique opportunity to investigate the basic mechanisms of epileptogenesis using surgically resected HH tissue. The first report on the electrophysiological properties of HH neurons was published in 2005. Since then, ongoing research has provided additional insights into the mechanisms by which HH generate seizure activity. In this review, we summarize this progress and propose a cellular model that suggests that GABA ‐mediated excitation contributes to epileptogenesis in HH lesions.
机译:总结人类下丘脑错构瘤(HH)是一种罕见的发育畸形,通常以弹力性癫痫发作为特征,这些药物难以治疗。 HH的部分EEG记录表明,HH病变本身是癫痫性发作的来源。针对HH的外科手术技术的最新进展已导致癫痫发作控制的显着改善,这进一步支持了在HH内发生地弹性癫痫发作的假说。然而,这种皮层下病变中癫痫发生的基本细胞和分子机制了解甚少。自2003年以来,巴罗神经病学研究所一直保持一项多学科临床计划,以评估和治疗HH患者。该程序提供了一个独特的机会来研究使用手术切除的HH组织进行癫痫发生的基本机制。关于HH神经元的电生理特性的第一份报告发表于2005年。从那时起,正在进行的研究为HH引起癫痫发作的机制提供了更多见解。在这篇综述中,我们总结了这一进展并提出了一种细胞模型,该模型表明,GABA介导的兴奋有助于HH病变的癫痫发生。

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