Literature DB >> 24723228

Calcium signaling and epilepsy.

Ortrud K Steinlein1.   

Abstract

Calcium signaling is involved in a multitude of physiological and pathophysiological mechanisms. Over the last decade, it has been increasingly recognized as an important factor in epileptogenesis, and it is becoming obvious that the excess synchronization of neurons that is characteristic for seizures can be linked to various calcium signaling pathways. These include immediate effects on membrane excitability by calcium influx through ion channels as well as delayed mechanisms that act through G-protein coupled pathways. Calcium signaling is able to cause hyperexcitability either by direct modulation of neuronal activity or indirectly through calcium-dependent gliotransmission. Furthermore, feedback mechanisms between mitochondrial calcium signaling and reactive oxygen species are able to cause neuronal cell death and seizures. Unravelling the complexity of calcium signaling in epileptogenesis is a daunting task, but it includes the promise to uncover formerly unknown targets for the development of new antiepileptic drugs.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24723228     DOI: 10.1007/s00441-014-1849-1

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  12 in total

1.  Connectivity Mapping Using a Novel sv2a Loss-of-Function Zebrafish Epilepsy Model as a Powerful Strategy for Anti-epileptic Drug Discovery.

Authors:  Yifan Zhang; Lise Heylen; Michèle Partoens; James D Mills; Rafal M Kaminski; Patrice Godard; Michel Gillard; Peter A M de Witte; Aleksandra Siekierska
Journal:  Front Mol Neurosci       Date:  2022-05-24       Impact factor: 6.261

2.  New differentially expressed genes and differential DNA methylation underlying refractory epilepsy.

Authors:  Xi Liu; Shu Ou; Tao Xu; Shiyong Liu; Jinxian Yuan; Hao Huang; Lu Qin; Hui Yang; Lifen Chen; Xinjie Tan; Yangmei Chen
Journal:  Oncotarget       Date:  2016-12-27

Review 3.  SUMOylation and calcium signalling: potential roles in the brain and beyond.

Authors:  Leticia Coelho-Silva; Gary J Stephens; Helena Cimarosti
Journal:  Neuronal Signal       Date:  2017-07-19

Review 4.  Voltage-Dependent Calcium Channels, Calcium Binding Proteins, and Their Interaction in the Pathological Process of Epilepsy.

Authors:  Jie-Hua Xu; Feng-Ru Tang
Journal:  Int J Mol Sci       Date:  2018-09-12       Impact factor: 5.923

5.  Dynamic Transitions of Epilepsy Waveforms Induced by Astrocyte Dysfunction and Electrical Stimulation.

Authors:  Honghui Zhang; Zhuan Shen; Qiangui Zhao; Luyao Yan; Lin Du; Zichen Deng
Journal:  Neural Plast       Date:  2020-11-16       Impact factor: 3.599

6.  Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A.

Authors:  Fang-Mei Luo; Ming-Xing Deng; Rong Yu; Lv Liu; Liang-Liang Fan
Journal:  Front Neurosci       Date:  2021-02-10       Impact factor: 4.677

7.  Dynamic Transitions in Neuronal Network Firing Sustained by Abnormal Astrocyte Feedback.

Authors:  Yangyang Yu; Zhixuan Yuan; Yongchen Fan; Jiajia Li; Ying Wu
Journal:  Neural Plast       Date:  2020-11-22       Impact factor: 3.599

Review 8.  Calcium channelopathies and intellectual disability: a systematic review.

Authors:  Miriam Kessi; Baiyu Chen; Jing Peng; Fangling Yan; Lifen Yang; Fei Yin
Journal:  Orphanet J Rare Dis       Date:  2021-05-13       Impact factor: 4.123

Review 9.  Role of Plant Derived Alkaloids and Their Mechanism in Neurodegenerative Disorders.

Authors:  Ghulam Hussain; Azhar Rasul; Haseeb Anwar; Nimra Aziz; Aroona Razzaq; Wei Wei; Muhammad Ali; Jiang Li; Xiaomeng Li
Journal:  Int J Biol Sci       Date:  2018-03-09       Impact factor: 6.580

10.  In vitro human stem cell derived cultures to monitor calcium signaling in neuronal development and function.

Authors:  Yojet Sharma; Sankhanil Saha; Annu Joseph; Harini Krishnan; Padinjat Raghu
Journal:  Wellcome Open Res       Date:  2020-02-03
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.