Sodium Channels

Sodium channels are integral membrane proteins that form a Na+ permeable pore through the plasma membrane and allow ion flux. There are two very different types of sodium channels: voltage-gated sodium channels (NaV) and epithelial sodium channels (ENaC). NaV are present in the membrane of most excitable cells and exist as heterodimers or heterotrimers of 1 α- and 1 or 2 β-subunits. ENaC are present in absorptive epithelia, such as the distal kidney tubule, alveolar epithelium and distal colon, and are responsible for sodium reabsorption. They exist as heterotetramers of α-, β- and γ-subunits, the predominant one being 2α:1β:1γ.

Targets
Literature
Ion Channel Data

Literature for Sodium Channels

Cardiovascular

Cardiovascular Research Product Guide

A collection of over 250 products for cardiovascular research, the guide includes research tools for the study of:

  • Hypertension
  • Thrombosis and Hemostasis
  • Atherosclerosis
  • Myocardial Infarction
  • Ischemia/Reperfusion Injury
  • Arrhythmias
  • Heart Failure
Pain

Pain Research Product Guide

A collection of over 250 products for pain research, the guide includes research tools for the study of:

  • Nociception
  • Ion Channels
  • G-Protein-Coupled Receptors
  • Intracellular Signaling

Properties of Voltage-Gated Sodium Channels

Location Subtype TTX Sensitive? Conductance (pS)
Brain I, II, IIA, III, VI Yes 2.5-25
Skeletal muscle μ1 Yes 2.5-25
Sympathetic ganglia PN1 Yes 6.3-10.7
Heart h1 No (IC50 6 μM) 2.5-25
Dorsal root ganglia PN3/SNS No (IC50 ~ 60 μM) 3.4-6.3

References

Catterall (1992) Cellular and molecular biology of voltage-gated sodium channels. Physiol.Rev. 72 S15. Gordon (1997) Sodium channels as targets for neurotoxins. Mode of action and interaction of neurotoxins with receptor sites on sodium channels. Toxins and Signal Transduction. Eds. Gutman and Lazarovici, pp119-153, Harwood Academic Publishers.