Individual differences |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |
Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
Sodium channels are integral membrane proteins that form ion channels, conducting sodium ions (Na+) through a cell's plasma membrane. They may be classified according to the trigger that opens the channel the such ions, i.e. either a voltage-change (voltage-gated sodium channels) or binding of a substance (a ligand) to the channel (ligand-gated sodium channels).
- 1 Voltage-gated
- 2 Ligand-gated
- 3 Role in action potential
- 4 Pharmacologic modulation
- 5 References
- 6 See also
- 7 External links
Sodium channels can often be isolated from cells as a complex of two types of protein subunits, α and β. An α subunit forms the core of the channel. When the α subunit protein is expressed by a cell, it is able to form channels which conduct Na+ in a voltage-gated way, even if β subunits are not expressed. When β subunits assemble with α subunits the resulting complex can display altered voltage dependence and cellular localization.
The α-subunit has four repeat domains, labeled I through IV, each containing six membrane-spanning regions, labeled S1 through S6. The highly conserved S4 region acts as the channel's voltage sensor. The voltage sensitivity of this channel is due to positive amino acids located at every third position. When stimulated by a change in transmembrane voltage, this region moves toward the extracellular side of the cell membrane, allowing the channel to become permeable to ions. The ions are conducted through a pore, which can be broken into two regions. The more external (i.e., more extracellular) portion of the pore is formed by the "P-loops" (the region between S5 and S6) of the four domains. This region is the most narrow part of the pore and is responsible for its ion selectivity. The inner portion (i.e., more cytoplasmic) of the pore is formed by the combined S5 and S6 regions of the four domains. The region linking domains III and IV is also important for channel function. This region plugs the channel after prolonged activation, inactivating it.
Voltage-gated sodium channels have three types of states: deactivated (closed), activated (open), and inactivated (closed). Channels in the deactivated state are thought to be blocked on their intracellular side by an "activation gate", which is removed in response to stimulation that opens the channel. The ability to inactivate is thought to be due to a tethered plug (formed by domains III and IV of the alpha subunit), called an inactivation gate, that blocks the inside of the channel shortly after it has been activated. During an action potential the channel remains inactivated for a few milliseconds after depolarization. The inactivation is removed when the membrane potential of the cell repolarizes following the falling phase of the action potential. This allows the channels to be activated again during the next action potential. Genetic diseases that alter Na+ channel inactivation cause muscle stiffness because of the introduction of a window current.
The temporal behaviour of sodium channels can be described by a Markovian scheme or by the Hodgkin-Huxley-type formalism. In the former scheme, each channel occupies a distinct state with differential equations describing transitions between states; in the latter, the channels are treated as a population that are affected by three independent gating variables. Each of these variables can attain a value between 1 (fully permeant to ions) and 0 (fully non-permeant), the product of these variables yielding the percentage of conducting channels.
Impermeability to other ions
The pore of sodium channels contains a selectivity filter made of negatively charged amino acid residues, which attract the positive Na+ ion and keep out negatively charged ions such as chloride. The cations flow into a more constricted part of the pore that is 0.3 by 0.5 nm wide, which is just large enough to allow a single Na+ ion with a water molecule associated to pass through. The larger K+ ion cannot fit through this area. Differently sized ions also cannot interact as well with the negatively charged glutamic acid residues that line the pore.
Voltage-gated sodium channels normally consist of an alpha subunit which forms the ion conduction pore and one to two beta subunits which have several functions including modulation of channel gating. Expression of the alpha subunit alone is sufficient to produce a functional channel.
The family of sodium channels has nine known members, with amino acid identity >50% in the transmembrane and extracellular loop regions. A standardized nomenclature for sodium channels is currently used and is maintained by the IUPHAR.
The proteins of these channels are named Nav1.1 through Nav1.9. The gene names are referred to as SCN1A through SCN11A (the SCN6/7A gene is part of the Nax sub-family and has uncertain function). The likely evolutionary relationship between these channels, based on the similarity of their amino acid sequences, is shown in figure 1. The individual sodium channels are distinguished not only by differences in their sequence but also by their kinetics and expression profiles. Some of this data is summarized in table 1, below.
|Protein name||Gene||Auxiliary subunits||Expression profile||Associated human channelopathies|
|Navα1.1||SCN1A||β1,β2,β3,β4||Central neurons and cardiac myocytes||Inherited febrile epilepsy, GEFS and myoclonic epilepsy|
|Navα1.2||SCN2A||β1,β2,β3,β4||Central neurons||inherited febrile seizures and epilepsy|
|Navα1.3||SCN3A||β1,β3||Central neurons and cardiac myocytes||none known|
|Navα1.4||SCN4A||β1||Skeletal muscle||hyperkalemic periodic paralysis, Paramyotonia congenita, and potassium-aggravated myotonia|
|Navα1.5||SCN5A||β1,β2,β3,β4||Central neurons, cardiac myocytes||Long QT Syndrome, Brugada syndrome, and idiopathic ventricular fibrillation|
|Navα1.6||SCN8A||β1,β2||Central neurons, dorsal root ganglia, peripheral neurons||none known|
|Navα1.7||SCN9A||β1,β2||Dorsal root ganglia, sympathetic neurons, Schwann cells, and neuroendocrine cells||Erythromelalgia and Channelopathy-associated insensitivity to pain|
|Navα1.8||SCN10A||unknown||Dorsal root ganglia||none known|
|Navα1.9||SCN11A||unknown||Dorsal root ganglia||none known|
|Protein name||Gene link|
Ligand-gated sodium channels are activated by binding of a ligand instead of a change in membrane potential.
Role in action potential
- Main article: Action potential
Voltage-gated sodium channels play an important role in action potentials. If enough channels open when there is a change in the cell's membrane potential, a small but significant number of Na+ ions will move into the cell down their electrochemical gradient, further depolarizing the cell. Thus, the more Na+ channels localized in a region of a cell's membrane, the faster the action potential will propagate, and the more excitable that area of the cell will be. This is an example of a positive feedback loop. The ability of these channels to assume a closed-inactivated state causes the refractory period and is critical for the propagation of action potentials down an axon.
Ligand-gated sodium channels, on the other hand, creates the change in the membrane potential in the first place, in response to the binding of a ligand to it.
The following naturally produced substances block sodium channels by binding to and occluding the extracellular pore opening of the channel:
Drugs which block sodium channels by blocking from the intracellular side of the channel:
- A-803467: specific blockade of Nav1.8 channels, developed by Icagen and Abbott Laboratories
The following naturally produced substances persistently activate (open) sodium channels:
- Alkaloid based toxins
- Diterpene based toxins
The following toxins modify the gating of sodium channels:
- Yu FH, Catterall WA (2003). Overview of the voltage-gated sodium channel family. Genome Biol 4 (3): 207.
- Isom LL (2001). Sodium channel beta subunits: anything but auxiliary. Neuroscientist 7 (1): 42-54.
- Catterall WA, Goldin AL, Waxman SG (2005). International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels.. Pharmacol Rev 57 (4): 397-409.
- Jarvis, Michael F., Prisca Honore and 35 additional coauthors (2007-05-27). A-803467, a potent and selective Nav1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat. PNAS 104 (20): 8520–8525.
- Grolleau F, Stankiewicz M, Birinyi-Strachan L, Wang XH, Nicholson GM, Pelhate M, Lapied B (2001). Electrophysiological analysis of the neurotoxic action of a funnel-web spider toxin, delta-atracotoxin-HV1a, on insect voltage-gated Na+ channels. J. Exp. Biol. 204 (Pt 4): 711-21.
- Eric R. Kandel, Schwartz JH, Jessell TM. Principles of Neural Science, 4th ed., pp.154-169. McGraw-Hill, New York (2000). ISBN 0-8385-7701-6
- Bertil Hille Ion channels of excitable membranes, 3rd ed., Sinauer Associates, Sunderland, MA (2001). ISBN 0-87893-321-2
Membrane transport protein: ion channels
|Ca||Voltage-dependent calcium channel (L-type/CACNA1C, N-type, P-type, Q-type, R-type, T-type) - Inositol triphosphate receptor - Ryanodine receptor - Cation channels of sperm|
|Na: Sodium channel||Nav1.4 - Nav1.5 - Nav1.7 - Epithelial sodium channel|
|K: Potassium channel||Voltage-gated (KvLQT1, KvLQT2, KvLQT3, HERG, Shaker gene, KCNE1) - Calcium-activated (BK channel, SK channel) - Inward-rectifier (ROMK, KCNJ2) - Tandem pore domain|
|Cl: Chloride channel||Cystic fibrosis transmembrane conductance regulator|
|Porin||Aquaporin (1, 2, 3, 4)|
|Transient receptor potential||TRPA - TRPC (TRPC6) - TRPM (TRPM6) - TRPML (Mucolipin-1) - TRPP - TRPV (TRPV1, TRPV6)|
|Other/general||Gap junction - Stretch-activated ion channel - Ligand-gated ion channel - Voltage-gated ion channel - Cyclic nucleotide-gated ion channel - Two-pore channel|
|This page uses Creative Commons Licensed content from Wikipedia (view authors).|