1.Progress in molecular genetics of epilepsy.
Chinese Journal of Medical Genetics 2002;19(6):505-507
Epilepsy is a group of disorders characterized by recurrent seizures. The etiologies of idiopathic epilepsy commonly have a genetic basis. Gene mutations causing several of the inherited epilepsies have been mapped. In this review, the authors summarize the available information on the genetic basis of human epilepsies and epilepsy syndromes, emphasizing how genetic defects may correlate with the pathophysiological mechanisms of brain hyperexcitability and gene defects can lead to epilepsy by altering multiple and diverse aspects of neuronal function.
Epilepsy
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genetics
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Humans
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KCNQ2 Potassium Channel
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Mutation
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NAV1.1 Voltage-Gated Sodium Channel
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Nerve Tissue Proteins
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genetics
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Potassium Channels
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genetics
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Potassium Channels, Voltage-Gated
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Receptors, Nicotinic
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genetics
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Research
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trends
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Research Design
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Sodium Channels
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genetics
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Voltage-Gated Sodium Channel beta-1 Subunit
2.Progress on structural biology of voltage-gated ion channels.
Journal of Zhejiang University. Medical sciences 2019;48(1):25-33
Ion channels mediate ion transport across membranes, and play vital roles in processes of matter exchange, energy transfer and signal transduction in living organisms. Recently, structural studies of ion channels have greatly advanced our understanding of their ion selectivity and gating mechanisms. Structural studies of voltage-gated potassium channels elucidate the structural basis for potassium selectivity and voltage-gating mechanism; structural studies of voltage-gated sodium channels reveal their slow and fast inactivation mechanisms; and structural studies of transient receptor potential (TRP) channels provide complex and diverse structures of TRP channels, and their ligand gating mechanisms. In the article we summarize recent progress on ion channel structural biology, and outlook the prospect of ion channel structural biology in the future.
Ion Channel Gating
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physiology
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Ion Channels
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Voltage-Gated Sodium Channels
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chemistry
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metabolism
5.Voltage-gated sodium channels are involved in regulating the biological functions of microglial cells.
Bo-Wen LI ; Meng GOU ; Rong XIAO ; Qing-Wei LI
Acta Physiologica Sinica 2015;67(1):41-47
Microglial cells are widely distributed in the brain and spinal cord, and usually act as resident immune cells which could provide continuous monitoring roles within the central nervous system. When the cells in the central nervous system are injured, microglial cells are activated and induce a series of biological effects. Recently, several voltage-gated sodium channel subtypes were found to be expressed on the surface of the microglial cells which are able to participate in the regulation of the activation, phagocytosis, secretion of multiple cytokines/chemokines, migration, invasion of microglial cells, and etc. In the present study, the latest progresses on the regulation of voltage-gated sodium channel isoforms on microglial cells were summarized and analyzed. In addition, the mechanism and future research of the relationship between voltage-gated sodium channels and microglial cells were also discussed.
Animals
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Cytokines
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Humans
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Microglia
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physiology
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Protein Isoforms
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Voltage-Gated Sodium Channels
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physiology
6.Theoretical and simulation studies on voltage-gated sodium channels.
Protein & Cell 2015;6(6):413-422
Voltage-gated sodium (Nav) channels are indispensable membrane elements for the generation and propagation of electric signals in excitable cells. The successes in the crystallographic studies on prokaryotic Nav channels in recent years greatly promote the mechanistic investigation of these proteins and their eukaryotic counterparts. In this paper, we mainly review the progress in computational studies, especially the simulation studies, on these proteins in the past years.
Ion Channel Gating
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Ligands
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Models, Biological
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Permeability
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Substrate Specificity
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Voltage-Gated Sodium Channels
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chemistry
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metabolism
7.Anti-epileptic/pro-epileptic effects of sodium channel modulators from Buthus martensii Karsch.
Qian XIAO ; Zhi-Ping ZHANG ; Yang-Bo HOU ; Dong-Xiao QU ; Le-Le TANG ; Li-Ji CHEN ; Guo-Yi LI ; Yong-Hua JI ; Jie TAO ; Yu-Dan ZHU
Acta Physiologica Sinica 2022;74(4):621-632
The East Asian scorpion Buthus martensii Karsch (BmK) is one of the classical traditional Chinese medicines for treating epilepsy for over a thousand years. Neurotoxins purified from BmK venom are considered as the main active ingredients, acting on membrane ion channels. Voltage-gated sodium channels (VGSCs) play a crucial role in the occurrence of epilepsy, which make them become important drug targets for epilepsy. Long chain toxins of BmK, composed of 60-70 amino acid residues, could specifically recognize VGSCs. Among them, α-like neurotoxins, binding to the receptor site-3 of VGSC, induce epilepsy in rodents and can be used to establish seizure models. The β or β-like neurotoxins, binding to the receptor site-4 of VGSC, have significant anticonvulsant effects in epileptic models. This review aims to illuminate the anticonvulsant/convulsant effects of BmK polypeptides by acting on VGSCs, and provide potential frameworks for the anti-epileptic drug-design.
Animals
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Anticonvulsants/therapeutic use*
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Neurotoxins/pharmacology*
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Scorpion Venoms/pharmacology*
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Scorpions/chemistry*
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Voltage-Gated Sodium Channels
8.Long QT syndrome gene diagnosis by haplotype analysis.
Jiang-fang LIAN ; Chang-cong CUI ; Xiao-lin XUE ; Chen HUANG ; Han-bing CUI ; Hai-zhu ZHANG
Chinese Journal of Medical Genetics 2004;21(3):272-273
OBJECTIVEThree long QT syndrome(LQTS) pedigrees were brought together for genetic diagnosis by using short tandem repeat(STR) markers.
METHODSGenomic DNA was extracted from blood samples. STR markers (D7S1824, D7S2439, D7S483, D3S1298, D3S1767, D3S3521) in or spanning the HERG and SCN5A gene were amplified; the haplotype analysis for LQTS was performed.
RESULTSClinical diagnosis showed that 15 are LQTS patients (3 died) and 11 are probable patients. Linkage analysis showed that LQTS patients are linked with the SCN5A gene in family 1, HERG is linked with the disease in family 2 and 3. Fourteen gene carriers were identified, 2 patients and 7 probable patients were excluded.
CONCLUSIONLinkage analysis using STR markers can serve as useful tool for presymptomatic diagnosis.
ERG1 Potassium Channel ; Ether-A-Go-Go Potassium Channels ; Female ; Genetic Linkage ; Haplotypes ; Humans ; Long QT Syndrome ; genetics ; Male ; NAV1.5 Voltage-Gated Sodium Channel ; Pedigree ; Potassium Channels ; genetics ; Potassium Channels, Voltage-Gated ; Sodium Channels ; genetics ; Tandem Repeat Sequences
10.Research status of genodermatoses in China.
Xue-Jun ZHANG ; Jian-jun CHEN ; Min GAO
Acta Academiae Medicinae Sinicae 2005;27(3):408-414
Among over 300 genodernatoses, causative genes have been identified in 170 monogenetic diseases, while gene mapping has been performed in over 100 monogenetic and polygenctic skin diseases. Researches in genodermatoses has rapidly advanced in China in recent ten years. The causative genes involved in multiple familial trichoepithelioma and primary erythermalgia have been found. Two independent genome-wide scans with DNA markers have been performed to detect genetic linkage related to psoriasis and vitiligo. In this review article, we summarize these most recent findings.
Erythromelalgia
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genetics
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HLA Antigens
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genetics
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Humans
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NAV1.7 Voltage-Gated Sodium Channel
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Proteins
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genetics
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Psoriasis
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genetics
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Sodium Channels
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genetics
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Vitiligo
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genetics