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Pathological Networks Involving Dysmorphic Neurons in Type ⅡFocal Cortical Dysplasia 被引量:1

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摘要 Focal cortical dysplasia(FCD)is one of the most common causes of drug-resistant epilepsy.Dysmorphic neurons are the major histopathological feature of typeⅡFCD,but their role in seizure genesis in FCD is unclear.Here we performed whole-cell patch-clamp recording and morphological reconstruction of cortical principal neurons in postsurgical brain tissue from drug-resistant epilepsy patients.Quantitative analyses revealed distinct morphological and electrophysiological characteristics of the upper layer dysmorphic neurons in typeⅡFCD,including an enlarged soma,aberrant dendritic arbors,increased current injection for rheobase action potential firing,and reduced action potential firing frequency.Intriguingly,the upper layer dysmorphic neurons received decreased glutamatergic and increased GABAergic synaptic inputs that were coupled with upregulation of the Na^(+)-K^(+)-Cl^(−)cotransporter.In addition,we found a depolarizing shift of the GABA reversal potential in the CamKⅡ-cre::PTENflox/flox mouse model of drug-resistant epilepsy,suggesting that enhanced GABAergic inputs might depolarize dysmorphic neurons.Thus,imbalance of synaptic excitation and inhibition of dysmorphic neurons may contribute to seizure genesis in typeⅡFCD.
出处 《Neuroscience Bulletin》 SCIE CAS CSCD 2022年第9期1007-1024,共18页 神经科学通报(英文版)
基金 supported by grants from the Ministry of Science and Technology(2019YFA0110103) the National Natural Science Foundation of China(81870898,82071287,and 81870916) the Fundamental Research Funds for the Central Universities(2019FZA7009 and 2021FZZX001-37) the Zhejiang Provincial Natural Science Foundation(LR18H090002).
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