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树突棘在癫痫发生中的作用。

The role of dendritic spines in epileptogenesis.

作者信息

Jean Gary, Carton Joseph, Haq Kaleem, Musto Alberto E

机构信息

Medical Program, School of Medicine, Eastern Virginia Medical School, Norfolk, VA, United States.

Department of Pathology and Anatomy, Eastern Virginia Medical School, Norfolk, VA, United States.

出版信息

Front Cell Neurosci. 2023 Aug 2;17:1173694. doi: 10.3389/fncel.2023.1173694. eCollection 2023.

Abstract

Epilepsy is a chronic central nervous system (CNS) disease associated with high morbidity. To date, there is no known disease-modifying therapy for epilepsy. A leading hypothesis for a mechanism of epileptogenesis is the generation of aberrant neuronal networks. Although the underlying biological mechanism is not clear, scientific evidence indicates that it is associated with a hyperexcitable synchronous neuronal network and active dendritic spine plasticity. Changes in dendritic spine morphology are related to altered expression of synaptic cytoskeletal proteins, inflammatory molecules, neurotrophic factors, and extracellular matrix signaling. However, it remains to be determined if these aberrant dendritic spine formations lead to neuronal hyperexcitability and abnormal synaptic connections or whether they constitute an underlying mechanism of seizure susceptibility. Focusing on dendritic spine machinery as a potential target for medications could limit or reverse the development of epilepsy.

摘要

癫痫是一种发病率较高的慢性中枢神经系统(CNS)疾病。迄今为止,尚无已知的可改变疾病进程的癫痫治疗方法。癫痫发生机制的一个主要假说是异常神经网络的产生。尽管其潜在的生物学机制尚不清楚,但科学证据表明,它与过度兴奋的同步神经网络和活跃的树突棘可塑性有关。树突棘形态的变化与突触细胞骨架蛋白、炎症分子、神经营养因子和细胞外基质信号的表达改变有关。然而,这些异常的树突棘形成是否导致神经元过度兴奋和异常突触连接,或者它们是否构成癫痫易感性的潜在机制,仍有待确定。将树突棘机制作为药物治疗的潜在靶点可能会限制或逆转癫痫的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f08/10433379/a344c866103e/fncel-17-1173694-g001.jpg

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