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Voltage-gated Sodium Channels: Structure, Function and Channelopathies

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Cover of 'Voltage-gated Sodium Channels: Structure, Function and Channelopathies'

Table of Contents

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    Book Overview
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    Chapter 43 Cardiac Arrhythmias Related to Sodium Channel Dysfunction
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    Chapter 44 Structural Models of Ligand-Bound Sodium Channels
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    Chapter 45 The Cardiac Sodium Channel and Its Protein Partners
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    Chapter 46 Effects of Benzothiazolamines on Voltage-Gated Sodium Channels
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    Chapter 47 Sodium Channel Trafficking
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    Chapter 48 Voltage-Gated Sodium Channel β Subunits and Their Related Diseases
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    Chapter 52 Sodium Channelopathies of Skeletal Muscle
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    Chapter 53 Regulation of Cardiac Voltage-Gated Sodium Channel by Kinases: Roles of Protein Kinases A and C
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    Chapter 54 Gating Pore Currents in Sodium Channels
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    Chapter 61 Structural and Functional Analysis of Sodium Channels Viewed from an Evolutionary Perspective
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    Chapter 63 Calculating the Consequences of Left-Shifted Nav Channel Activity in Sick Excitable Cells
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    Chapter 66 Toxins That Affect Voltage-Gated Sodium Channels
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    Chapter 69 Posttranslational Modification of Sodium Channels
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    Chapter 70 Evolutionary History of Voltage-Gated Sodium Channels
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    Chapter 73 Mechanisms of Drug Binding to Voltage-Gated Sodium Channels
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    Chapter 75 Mining Protein Evolution for Insights into Mechanisms of Voltage-Dependent Sodium Channel Auxiliary Subunits
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    Chapter 91 Translational Model Systems for Complex Sodium Channel Pathophysiology in Pain
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    Chapter 97 Selective Ligands and Drug Discovery Targeting the Voltage-Gated Sodium Channel Nav1.7
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    Chapter 99 pH Modulation of Voltage-Gated Sodium Channels
Attention for Chapter 70: Evolutionary History of Voltage-Gated Sodium Channels
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Chapter title
Evolutionary History of Voltage-Gated Sodium Channels
Chapter number 70
Book title
Voltage-gated Sodium Channels: Structure, Function and Channelopathies
Published in
Handbook of experimental pharmacology, January 2017
DOI 10.1007/164_2017_70
Pubmed ID
Book ISBNs
978-3-31-990283-8, 978-3-31-990284-5
Authors

Atsuo Nishino, Yasushi Okamura, Nishino, Atsuo, Okamura, Yasushi

Abstract

Every cell within living organisms actively maintains an intracellular Na+ concentration that is 10-12 times lower than the extracellular concentration. The cells then utilize this transmembrane Na+ concentration gradient as a driving force to produce electrical signals, sometimes in the form of action potentials. The protein family comprising voltage-gated sodium channels (NaVs) is essential for such signaling and enables cells to change their status in a regenerative manner and to rapidly communicate with one another. NaVs were first predicted in squid and were later identified through molecular biology in the electric eel. Since then, these proteins have been discovered in organisms ranging from bacteria to humans. Recent research has succeeded in decoding the amino acid sequences of a wide variety of NaV family members, as well as the three-dimensional structures of some. These studies and others have uncovered several of the major steps in the functional and structural transition of NaV proteins that has occurred along the course of the evolutionary history of organisms. Here we present an overview of the molecular evolutionary innovations that established present-day NaV α subunits and discuss their contribution to the evolutionary changes in animal bodies.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 29 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 17%
Student > Bachelor 4 14%
Student > Doctoral Student 2 7%
Professor 2 7%
Researcher 2 7%
Other 7 24%
Unknown 7 24%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 10 34%
Agricultural and Biological Sciences 5 17%
Neuroscience 3 10%
Nursing and Health Professions 1 3%
Medicine and Dentistry 1 3%
Other 1 3%
Unknown 8 28%