Understanding Genotypes and Phenotypes of the Mutations in Voltage- Gated Sodium Channel α Subunits in Epilepsy
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Published:2019-07-17
Issue:4
Volume:18
Page:266-272
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ISSN:1871-5273
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Container-title:CNS & Neurological Disorders - Drug Targets
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language:en
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Short-container-title:CNSNDDT
Author:
Feng Yijun1, Zhang Shuzhang1, Zhang Zhiping1, Guo Jingkang1, Tan Zhiyong2, Zhu Yudan3, Tao Jie3, Ji Yong-Hua1
Affiliation:
1. Laboratory of Neuropharmacology and Neurotoxicology, Shanghai University, Shanghai 200444, China 2. Department of Pharmacology and Toxicology and Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, 46202, United States 3. Central Laboratory, Department of Neurology and Neurosurgery, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
Abstract
Background & Objective:
Voltage-gated sodium channels (VGSCs) are responsible for the
generation and propagation of action potentials in most excitable cells. In general, a VGSC consists of
one pore-forming α subunit and two auxiliary β subunits. Genetic alterations in VGSCs genes, including
both α and β subunits, are considered to be associated with epileptogenesis as well as seizures.
This review aims to summarize the mutations in VGSC α subunits in epilepsy, particularly the pathophysiological
and pharmacological properties of relevant VGSC mutants.
Conclusion:
The review of epilepsy-associated VGSC α subunits mutants may not only contribute to
the understanding of disease mechanism and genetic modifiers, but also provide potential theoretical
targets for the precision and individualized medicine for epilepsy.
Funder
Indiana Spinal Cord and Brain Injury Research grant from the Indiana State Department of Health Project within budget of Shanghai University of Traditional Chinese Medicine Shanghai Municipal Commission of Health and Family Planning Fund National Natural Science Foundation of China
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,General Neuroscience
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