- Membrane potential
Membrane potential (also transmembrane potential or membrane voltage) is the difference in electrical potential between the interior and exterior of a biological cell. All animal cells are surrounded by a plasma membrane composed of a lipid bilayer with a variety of types of proteins embedded in it. The membrane potential arises primarily from the interaction between the membrane and the actions of two types of transmembrane proteins embedded in the plasma membrane. The membrane serves as both an insulator and diffusion barrier to the movement of ions. Ion transporter/pump proteins actively push ions across the membrane to establish concentration gradients across the membrane, and ion channels allow ions to move across the membrane down those concentration gradients, a process known as facilitated diffusion. In the most fundamental example of this, the ion transporter Na+/K+-ATPase pumps sodium ions from the inside to the outside, and potassium ions from the outside to the inside of the cell. This establishes two concentration gradients: a gradient for sodium where its concentration is much higher outside than inside the cell, and a gradient for potassium where its concentration is much higher inside the cell than outside. Transmembrane potassium-selective leak channels allow potassium ions to diffuse across the membrane, down the concentration gradient that was established by the ATPase, creating a charge separation, and thus a voltage, across the membrane. In almost all cases, the ion that determines the so-called "resting" membrane potential of a cell, is potassium, although other ions do contribute in more minor ways. By convention, the sign of the membrane potential is designated as the voltage inside relative to ground outside the cell. In the case of potassium, its diffusion down its concentration gradient, toward the outside of the cell, creates transmembrane voltage that is negative relative to the outside of the cell, and typically -60 to -80 milli volts (mV) in amplitude.
Virtually all eukaryotic cells (including cells from animals, plants, and fungi) maintain a nonzero transmembrane potential, usually with a negative voltage in the cell interior as compared to the cell exterior. The membrane potential has two basic functions. First, it allows a cell to function as a battery, providing power to operate a variety of "molecular devices" embedded in the membrane. Second, in electrically excitable cells such as neurons and muscle cells, it is used for transmitting signals between different parts of a cell. Signals are generated by opening or closing of ion channels at one point in the membrane, producing a local change in the membrane potential that causes electric current to flow rapidly to other points in the membrane.
In non-excitable cells, and in excitable cells in their baseline states, the membrane potential is held at a relatively stable value, called the resting potential. For neurons, typical values of the resting potential range from –70 to –80 millivolts; that is, the interior of a cell has a negative baseline voltage of a bit less than one tenth of a volt. The opening and closing of ion channels can induce a departure from the resting potential. This is called a depolarization if the interior voltage becomes more positive (say from –70 mV to –60 mV), or a hyperpolarization if the interior voltage becomes more negative (say from –70 mV to –80 mV). In excitable cells, a sufficiently large depolarization can evoke an action potential, in which the membrane potential changes rapidly and significantly for a short time (on the order of 1 to 100 milliseconds), often reversing its polarity. Action potentials are generated by the activation of certain voltage-gated ion channels.
In neurons, the factors that influence the membrane potential are diverse. They include numerous types of ion channels, some that are chemically gated and some that are voltage-gated. Because voltage-gated ion channels are controlled by the membrane potential, while the membrane potential itself is influenced by these same ion channels, feedback loops arise which allow for complex temporal dynamics, including oscillations and regenerative events such as action potentials.
- 1 Physical basis
- 2 Resting potential
- 3 Graded potentials
- 4 All other values of membrane potential
- 5 Effects and implications
- 6 See also
- 7 Notes
- 8 References
- 9 Further reading
- 10 External links
The membrane potential in a cell derives ultimately from two factors: electrical force and diffusion. Electrical force arises from the mutual attraction between particles with opposite electrical charges (positive and negative) and the mutual repulsion between particles with the same type of charge (both positive or both negative). Diffusion arises from the statistical tendency of particles to redistribute from regions where they are highly concentrated to regions where the concentration is low.
Voltage, which is synonymous with electrical potential, is the ability to drive an electric current across a resistance. Indeed the simplest definition of a voltage is given by Ohm's law: V=IR, where V is voltage, I is current and R is resistance. If a voltage source such as a battery is placed in an electrical circuit, the higher the voltage of the source, the greater the amount of current that it will drive across the available resistance. The functional significance of voltage lies only in potential differences between two points in a circuit. The idea of a voltage at a single point is meaningless. It is conventional in electronics to assign a voltage of zero to some arbitrarily chosen element of the circuit, and then assign voltages for other elements measured relative to that zero point. There is no significance in which element is chosen as the zero point—the function of a circuit depends only on the differences, not on voltages per se. However, in most cases and by convention, the zero level is most often assigned to the portion of a circuit that is in contact with ground.
The same principle applies to voltage in cell biology. In electrically active tissue, the potential difference between any two points can be measured by inserting an electrode at each point, for example on inside and one outside the cell, and connecting both electrodes to the leads of what is essentially a specialized voltmeter. By convention, the zero potential value is assigned to the outside of the cell and the sign of the potential difference between the outside and inside is determined by the potential of the inside relative to the outside zero.
In mathematical terms, the definition of voltage begins with the concept of an electric field E, a vector field assigning a magnitude and direction to each point in space. In many situations, the electric field is a conservative field, which means that it can be expressed as the gradient of a scalar function V, that is, E = –∇V. This scalar field V is referred to as the voltage distribution. Note that the definition allows for an arbitrary constant of integration—this is why absolute values of voltage are not meaningful. In general electric fields can only be treated as conservative if magnetic fields do not significantly influence them, but this condition usually applies well to biological tissue.
Because the electric field is the gradient of the voltage distribution, rapid changes in voltage within a small region imply a strong electric field; conversely, if the voltage remains approximately the same over a large region, the electric fields in that region must be weak. A strong electric field, equivalent to a strong voltage gradient, implies that a strong force is exerted on any charged particles that lie within the region.
Ions and the forces driving their motionMain articles: Ion, Diffusion, Electrochemical gradient, and Electrophoretic mobility
Electrical signals within biological organisms are, in general, driven by ions. The most important cations for the action potential are sodium (Na+) and potassium (K+). Both of these are monovalent cations that carry a single positive charge. Action potentials can also involve calcium (Ca2+), which is a divalent cation that carries a double positive charge. The chloride anion (Cl−) plays a major role in the action potentials of some algae, but plays a negligible role in the action potentials of most animals.
Ions cross the cell membrane under two influences: diffusion and electric fields. A simple example wherein two solutions—A and B—are separated by a porous barrier illustrates that diffusion will ensure that they will eventually mix into equal solutions. This mixing occurs because of the difference in their concentrations. The region with high concentration will diffuse out toward the region with low concentration. To extend the example, let solution A have 30 sodium ions and 30 chloride ions. Also, let solution B have only 20 sodium ions and 20 chloride ions. Assuming the barrier allows both types of ions to travel through it, then a steady state will be reached whereby both solutions have 25 sodium ions and 25 chloride ions. If, however, the porous barrier is selective to which ions are let through, then diffusion alone will not determine the resulting solution. Returning to the previous example, let's now construct a barrier that is permeable only to sodium ions. Since solution B has a lower concentration of both sodium and chloride, the barrier will attract both ions from solution A. However, only sodium will travel through the barrier. This will result in an accumulation of sodium in solution B. Since sodium has a positive charge, this accumulation will make solution B more positive relative to solution A. Positive sodium ions will be less likely to travel to the now-more-positive B solution. This constitutes the second factor controlling ion flow, namely electric fields. The point at which this electric field completely counteracts the force due to diffusion is called the equilibrium potential. At this point, the net flow of this specific ion (in this case sodium) is zero.
Every animal cell is enclosed in a plasma membrane, which has the structure of a lipid bilayer with many types of large molecules embedded in it. Because it is made of lipid molecules, the plasma membrane intrinsically has a high electrical resistivity, in other words a low intrinsic permeability to ions. However, some of the molecules embedded in the membrane are capable either of actively transporting ions from one side of the membrane to the other, or of providing channels through which they can move.
In electrical terminology, the plasma membrane functions as a combined resistor and capacitor. Resistance arises from the fact that the membrane impedes the movement of charges across it. Capacitance arises from the fact that the lipid bilayer is so thin that an accumulation of charged particles on one side gives rise to an electrical force that pulls oppositely-charged particles toward the other side. The capacitance of the membrane is relatively unaffected by the molecules that are embedded in it, so it has a more or less invariant value estimated at about 2 µF/cm2 (the total capacitance of a patch of membrane is proportional to its area). The conductance of a pure lipid bilayer is so low, on the other hand, that in biological situations it is always dominated by the conductance of alternative pathways provided by embedded molecules. Thus the capacitance of the membrane is more or less fixed, but the resistance is highly variable.
The thickness of a plasma membrane is estimated to be about 7-8 nanometers. Because the membrane is so thin, it does not take a very large transmembrane voltage to create a strong electric field within it. Typical membrane potentials in animal cells are on the order of 100 millivolts (that is, one tenth of a volt), but calculations show that this generates an electric field close to the maximum that the membrane can sustain—it has been calculated that a voltage difference much larger than 200 millivolts could cause dielectric breakdown, that is, arcing across the membrane.
Facilitated diffusion and transport
The resistance of a pure lipid bilayer to the passage of ions across it is very high, but structures embedded in the membrane can greatly enhance ion movement, either actively or passively, via mechanisms called facilitated transport and facilitated diffusion. The two types of structure that play the largest roles are ion channels and ion pumps, both usually formed from assemblages of protein molecules. Ion channels provide passageways through which ions can move. In most cases an ion channel is only permeable to specific types of ions (for example sodium and potassium but not chloride or calcium), and sometimes the permeability varies depending on the direction of ion movement. Ion pumps, also known as ion transporters or carrier proteins, actively transport specific types of ions from one side of the membrane to the other, sometimes using energy derived from metabolic processes to do so.
Ion pumpsMain articles: Ion transporter and Active transport
Ion pumps are integral membrane proteins that carry out active transport, i.e., use cellular energy (ATP) to "pump" the ions against their concentration gradient. Such ion pumps take in ions from one side of the membrane (decreasing its concentration there) and release them on the other side (increasing its concentration there). The ion pump most relevant to the action potential is the sodium–potassium pump, which transports three sodium ions out of the cell and two potassium ions in. As a consequence, the concentration of potassium ions K+ inside the neuron is roughly 20-fold larger than the outside concentration, whereas the sodium concentration outside is roughly ninefold larger than inside. In a similar manner, other ions have different concentrations inside and outside the neuron, such as calcium, chloride and magnesium.
Ion pumps influence the action potential only by establishing the relative ratio of intracellular and extracellular ion concentrations. The action potential involves mainly the opening and closing of ion channels, not ion pumps. If the ion pumps are turned off by removing their energy source, or by adding an inhibitor such as ouabain, the axon can still fire hundreds of thousands of action potentials before their amplitudes begin to decay significantly. In particular, ion pumps play no significant role in the repolarization of the membrane after an action potential.
A major contribution to establishing the membrane potential is made by the sodium-potassium exchange pump. This is a complex of proteins embedded in the membrane that derives energy from ATP in order to transport sodium and potassium ions across the membrane. On each cycle, the pump exchanges three Na+ ions from the intracellular space for two K+ ions from the extracellular space. If the numbers of each type of ion were equal, the pump would be electrically neutral, but because of the three-for-two exchange, it gives a net movement of one positive charge from intracellular to extracellular for each cycle, thereby contributing to a positive voltage difference. The pump has three effects: (1) it makes the sodium concentration high in the extracellular space and low in the intracellular space; (2) it makes the potassium concentration high in the intracellular space and low in the extracellular space; (3) it gives the extracellular space a positive voltage with respect to the intracellular space.
The sodium-potassium exchange pump is relatively slow in operation. If a cell were initialized with equal concentrations of sodium and potassium everywhere, it would take hours for the pump to establish equilibrium. The pump operates constantly, but becomes progressively less efficient as the concentrations of sodium and potassium available for pumping are reduced.
Another functionally important ion pump is the sodium-calcium exchanger. This pump operates in a conceptually similar way to the sodium-potassium pump, except that in each cycle it exchanges three Na+ from the extracellular space for one Ca++ from the intracellular space. Because the net flow of charge is inward, this pump runs "downhill", effectively, and therefore does not require any energy source except the membrane voltage. Its most important effect is to pump calcium outward—it also allows an inward flow of sodium, thereby counteracting the sodium-potassium pump, but because overall sodium and potassium concentrations are much higher than calcium concentrations, this effect is relatively unimportant. The net result of the sodium-calcium exchanger is that in the resting state, intracellular calcium concentrations become very low.
Ion channelsMain articles: Ion channel and Passive transport
Ion channels are integral membrane proteins with a pore through which ions can travel between extracellular space and cell interior. Most channels are specific (selective) for one ion; for example, most potassium channels are characterized by 1000:1 selectivity ratio for potassium over sodium, though potassium and sodium ions have the same charge and differ only slightly in their radius. The channel pore is typically so small that ions must pass through it in single-file order. Channel pore can be either open or closed for ion passage, although a number of channels demonstrate various sub-conductance levels. When a channel is open, ions permeate through the channel pore down the transmembrane concentration gradient for that particular ion. Rate of ionic flow through the channel, i.e. single-channel current amplitude, is determined by the maximum channel conductance and electrochemical driving force for that ion, which is the difference between instantaneous value of the membrane potential and the value of the reversal potential.
A channel may have several different states (corresponding to different conformations of the protein), but each such state is either open or closed. In general, closed states correspond either to a contraction of the pore—making it impassable to the ion—or to a separate part of the protein, stoppering the pore. For example, the voltage-dependent sodium channel undergoes inactivation, in which a portion of the protein swings into the pore, sealing it. This inactivation shuts off the sodium current and plays a critical role in the action potential.
Ion channels can be classified by how they respond to their environment. For example, the ion channels involved in the action potential are voltage-sensitive channels; they open and close in response to the voltage across the membrane. Ligand-gated channels form another important class; these ion channels open and close in response to the binding of a ligand molecule, such as a neurotransmitter. Other ion channels open and close with mechanical forces. Still other ion channels—such as those of sensory neurons—open and close in response to other stimuli, such as light, temperature or pressure.
Leakage channels are the simplest type of ion channel, in that their permeability is more or less constant. The types of leakage channels that have the greatest significance in neurons are potassium and chloride channels. It should be noted that even these are not perfectly constant in their properties: first, most of them are voltage-dependent in the sense that they conduct better in one direction than the other (in other words, they are rectifiers); second, some of them are capable of being shut off by chemical ligands even though they do not require ligands in order to operate.
Ligand-gated ion channels are channels whose permeability is greatly increased when some type of chemical ligand binds to the protein structure. Animal cells contain hundreds, if not thousands, of types of these. A large subset function as neurotransmitter receptors—they occur at postsynaptic sites, and the chemical ligand that gates them is released by the presynaptic axon terminal. One example of this type is the AMPA receptor, a receptor for the neurotransmitter glutamate that when activated allows passage of sodium and potassium ions. Another example is the GABAA receptor, a receptor for the neurotransmitter GABA that when activated allows passage of chloride ions.
Neurotransmitter receptors are activated by ligands that appear in the extracellular area, but there are other types of ligand-gated channels that are controlled by interactions on the intracellular side.
Voltage-gated ion channels, also known as voltage dependent ion channels, are channels whose permeability is influenced by the membrane potential. They form another very large group, with each member having a particular ion selectivity and a particular voltage dependence. Many are also time-dependent—in other words, they do not respond immediately to a voltage change, but only after a delay.
One of the most important members of this group is a type of voltage-gated sodium channel that underlies action potentials—these are sometimes called Hodgkin-Huxley sodium channels because they were initially characterized by Alan Lloyd Hodgkin and Andrew Huxley in their Nobel Prize-winning studies of the physiology of the action potential. The channel is closed at the resting voltage level, but opens abruptly when the voltage exceeds a certain threshold, allowing a large influx of sodium ions that produces a very rapid change in the membrane potential. Recovery from an action potential is partly dependent on a type of voltage-gated potassium channel which is closed at the resting voltage level but opens as a consequence of the large voltage change produced during the action potential.
The reversal potential (or equilibrium potential) of an ion is the value of transmembrane voltage at which diffusive and electrical forces counterbalance, so that there is no net ion flow across the membrane. This means that the transmembrane voltage exactly opposes the force of diffusion of the ion, such that the net current of the ion across the membrane is zero and unchanging. The reversal potential is important because it gives the voltage that acts on channels permeable to that ion—in other words, it gives the voltage that the ion concentration gradient generates when it acts as a battery.
The equilibrium potential of a particular ion is usually designated by the notation Eion.The equilibrium potential for any ion can be calculated using the Nernst equation. For example, reversal potential for potassium ions will be as follows:
- Eeq,K+ is the equilibrium potential for potassium, measured in volts
- R is the universal gas constant, equal to 8.314 joules·K−1·mol−1
- T is the absolute temperature, measured in kelvins (= K = degrees Celsius + 273.15)
- z is the number of elementary charges of the ion in question involved in the reaction
- F is the Faraday constant, equal to 96,485 coulombs·mol−1 or J·V−1·mol−1
- [K+]o is the extracellular concentration of potassium, measured in mol·m−3 or mmol·l−1
- [K+]i is the intracellular concentration of potassium
Even if two different ions have the same charge (i.e. K+ and Na+), they can still have very different equilibrium potentials, provided their outside and/or inside concentrations differ. Take, for example, the equilibrium potentials of potassium and sodium in neurons. The potassium equilibrium potential EK is -84 mV with 5 mM potassium outside and 140 mM inside. The sodium equilibrium potential, on the other hand, ENa is approximately +40 mV with approximately 12 mM sodium inside and 140 mM outside.[note 1]
Electrophysiologists model the effects of ionic concentration differences, ion channels, and membrane capacitance in terms of an equivalent circuit, which is intended to represent the electrical properties of a small patch of membrane. The equivalent circuit consists of a capacitor in parallel with four pathways each consisting of a battery in series with a variable conductance. The capacitance is determined by the properties of the lipid bilayer, and is taken to be fixed. Each of the four parallel pathways comes from one of the principal ions, sodium, potassium, chloride, and calcium. The voltage of each ionic pathway is determined by the concentrations of the ion on each side of the membrane; see the Reversal potential section above. The conductance of each ionic pathway at any point in time is determined by the states of all the ion channels that are potentially permeable to that ion, including leakage channels, ligand-gated channels, and voltage-gated ion channels.
For fixed ion concentrations and fixed values of ion channel conductance, the equivalent circuit can be further reduced, using the Goldman equation as described below, to a circuit containing a capacitance in parallel with a battery and conductance. Electrically this is a type of RC circuit (resistance-capacitance circuit), and its electrical properties are very simple. Starting from any initial state, the current flowing across either the conductance or capacitance decays with an exponential time course, with a time constant of τ = RC, where C is the capacitance of the membrane patch, and R = 1/gnet is the net resistance. For realistic situations the time constant usually lies in the 1—100 millisecond range. In most cases changes in the conductance of ion channels occur on a faster time scale, so an RC circuit is not a good approximation; however the differential equation used to model a membrane patch is commonly a modified version of the RC circuit equation.
When the membrane potential of a cell can go for a long period of time without changing significantly, it is referred to as a resting potential or resting voltage. This term is used for the membrane potential of non-excitable cells, but also for the membrane potential of excitable cells in the absence of excitation. In excitable cells, the other possible states are graded membrane potentials (of variable amplitude), and action potentials, which are large, all-or-nothing rises in membrane potential that usually follow a fixed time course. Excitable cells include neurons, muscle cells, and some secretory cells in glands. Even in other types of cells, though, the membrane voltage can undergo changes in response to environmental or intracellular stimuli. For example, depolarization of the plasma membrane appears to be an important step in programmed cell death.
The interactions that generate the resting potential are modeled by the Goldman equation. This is similar in form to the Nernst equation shown above, in that it is based on the charges of the ions in question, as well as the difference between their inside and outside concentrations. However, it also takes into consideration the relative permeability of the plasma membrane to each ion in question.
The three ions that appear in this equation are potassium (K+), sodium (Na+), and chloride (Cl−). Calcium is omitted, but can be added to deal with situations in which it plays a significant role. Being an anion, the chloride terms are treated differently than the cation terms; the intracellular concentration is in the numerator, and the extracellular concentration in the denominator, which is reversed from the cation terms. Pi stands for the relative permeability of the ion type i.
The Goldman formula essentially expresses the membrane potential as a weighted average of the reversal potentials for the individual ion types, weighted by permeability. In most animal cells, the permeability to potassium is much higher in the resting state than the permeability to sodium. Consequently, the resting potential is usually close to the potassium reversal potential. The permeability to chloride can be high enough to be significant, but unlike the other ions, chloride is not actively pumped, and therefore equilibrates at a reversal potential very close to the resting potential determined by the other ions.
Values of resting membrane potential in most animal cells usually vary between the potassium reversal potential (usually around -80 mV) and around -40 mV. The resting potential in excitable cells (capable of producing action potentials) is usually near -60 mV—more depolarized voltages would lead to spontaneous generation of action potentials. Immature or undifferentiated cells show highly variable values of resting voltage, usually significantly more positive than in differentiated cells. In such cells, the resting potential value correlates with the degree of differentiation: undifferentiated cells in some cases may not show any transmembrane voltage difference at all.
Maintenance of the resting potential can be metabolically costly for a cell because of its requirement for active pumping of ions to counteract losses due to leakage channels. The cost is highest when the cell function requires an especially depolarized value of membrane voltage. For example, the resting potential in daylight-adapted blowfly (Calliphora vicina) photoreceptors can be as high as -30 mV. This elevated membrane potential allows the cells to respond very rapidly to visual inputs; the cost is that maintenance of the resting potential may consume more than 20% of overall cellular ATP.
On the other hand, the high resting potential in undifferentiated cells can be a metabolic advantage. This apparent paradox is resolved by examination of the origin of that resting potential. Little-differentiated cells are characterized by extremely high input resistance which implies that few leakage channels are present at this stage of cell life. As an apparent result, potassium permeability becomes similar to that for sodium ions, which places resting potential in-between the reversal potentials for sodium and potassium as discussed above. The reduced leakage currents also mean there is little need for active pumping in order to compensate, therefore low metabolic cost.
As explained above, the potential at any point in a cell's membrane is determined by the ion concentration differences between the intracellular and extracellular areas, and by the permeability of the membrane to each type of ion. The ion concentrations do not normally change very quickly (with the exception of calcium, where the baseline intracellular concentration is so low that even a small inflow may increase it by orders of magnitude), but the permeabilities can change in a fraction of a millisecond, as a result of activation of ligand-gated or voltage-gated ion channels. The change in membrane potential can be large or small, depending on how many ion channels are activated and what type they are. Changes of this type are referred to as graded potentials, in contrast to action potentials, which have a fixed amplitude and time course.
As can be derived from the Goldman equation shown above, the effect of increasing the permeability for a particular type of ion is to shift the membrane potential toward the reversal potential for that ion. Thus, opening sodium channels pulls the membrane potential toward the sodium reversal potential, usually around +100 mV. Opening potassium channels pulls the membrane potential toward about -90 mV; opening chloride channels pulls it toward about -70 mV. Because -90 to +100 mV is the full operating range of membrane potential, the effect is that sodium channels always pull the membrane potential up, potassium channels pull it down, and chloride channels pull it toward the resting potential.
Graded membrane potentials are particularly important in neurons, where they are produced by synapses—a temporary rise or fall in membrane potential produced by activation of a synapse is called a postsynaptic potential. Neurotransmitters that act to open sodium channels cause the membrane potential to rise, while neurotransmitters that act on potassium channels cause it to fall. Because the membrane potential in a neuron must rise past the threshold value to produce an action potential, a rise in membrane potential is excitatory, while a fall is inhibitory. Thus neurotransmitters that act to open sodium channels produce a so-called excitatory postsynaptic potential, or EPSP, whereas neurotransmitters that act to open potassium channels produce an inhibitory postsynaptic potential, or IPSP. When multiple types of channels are open within the same time period, their postsynaptic potentials summate.
All other values of membrane potential
From the viewpoint of biophysics, the resting membrane potential is merely the membrane potential that results from the membrane permeabilities that predominate when the cell is resting. The above equation of weighted averages always applies, but the following approach may be more easily visualized. At any given moment, there are two factors for an ion that determine how much influence that ion will have over the membrane potential of a cell.
- That ion's driving force and,
- That ion's permeability
Intuitively, this is easy to understand. If the driving force is high, then the ion is being "pushed" across the membrane hard (more correctly stated: it is diffusing in one direction faster than the other). If the permeability is high, it will be easier for the ion to diffuse across the membrane. But what are 'driving force' and 'permeability'?
- Driving force: the driving force is the net electrical force available to move that ion across the membrane. It is calculated as the difference between the voltage that the ion "wants" to be at (its equilibrium potential) and the actual membrane potential (Em). So formally, the driving force for an ion = Em - Eion
- For example, at our earlier calculated resting potential of −73 mV, the driving force on potassium is 7 mV : (−73 mV) − (−80 mV) = 7 mV. The driving force on sodium would be (−73 mV) − (60 mV) = −133 mV.
- Permeability: is simply a measure of how easily an ion can cross the membrane. It is normally measured as the (electrical) conductance and the unit, siemens, corresponds to 1 C·s−1·V−1, that is one charge per second per volt of potential.
So in a resting membrane, while the driving force for potassium is low, its permeability is very high. Sodium has a huge driving force, but almost no resting permeability. In this case, potassium carries about 20 times more current than sodium, and thus has 20 times more influence over Em than does sodium.
However, consider another case—the peak of the action potential. Here permeability to Na is high and K permeability is relatively low. Thus the membrane moves to near ENa and far from EK.
The more ions are permeant, the more complicated it becomes to predict the membrane potential. However, this can be done using the Goldman-Hodgkin-Katz equation or the weighted means equation. By simply plugging in the concentration gradients and the permeabilities of the ions at any instant in time, one can determine the membrane potential at that moment. What the GHK equations says, basically, is that at any time, the value of the membrane potential will be a weighted average of the equilibrium potentials of all permeant ions. The "weighting" is the ions relative permeability across the membrane.
Effects and implications
While cells expend energy to transport ions and establish a transmembrane potential, they use this potential in turn to transport other ions and metabolites such as sugar. The transmembrane potential of the mitochondria drives the production of ATP, which is the common currency of biological energy.
Cells may draw on the energy they store in the resting potential to drive action potentials or other forms of excitation. These changes in the membrane potential enable communication with other cells (as with action potentials) or initiate changes inside the cell, which happens in an egg when it is fertilized by a sperm.
In neuronal cells, an action potential begins with a rush of sodium ions into the cell through sodium channels, resulting in depolarization, while recovery involves an outward rush of potassium through potassium channels. Both these fluxes occur by passive diffusion.
- Electrochemical potential
- Goldman Equation
- Saltatory conduction
- Membrane biophysics
- Signal (biology)
- ^ Note that the sign of ENa and EK are opposite. This is because the concentration gradient for potassium is directed out of the cell, while the concentration gradient for sodium is directed into the cell. Membrane potentials are defined relative to the exterior of the cell; thus, a potential of −70 mV implies that the interior of the cell is negative relative to the exterior.
- ^ Campbell Biology, 6th edition
- ^ Johnston and Wu, p. 9.
- ^ a b Bullock, Orkand, and Grinnell, pp. 140–41.
- ^ Bullock, Orkand, and Grinnell, pp. 153–54.
- ^ Mummert H, Gradmann D (1991). "Action potentials in Acetabularia: measurement and simulation of voltage-gated fluxes". Journal of Membrane Biology 124 (3): 265–73. doi:10.1007/BF01994359. PMID 1664861.
- ^ Schmidt-Nielsen, p. 483.
- ^ Lieb WR, Stein WD (1986). "Chapter 2. Simple Diffusion across the Membrane Barrier". Transport and Diffusion across Cell Membranes. San Diego: Academic Press. pp. 69–112. ISBN 0-12-664661-9.
- ^ a b Hodgkin AL, Keynes RD (1955). "Active transport of cations in giant axons from Sepia and Loligo". J. Physiol. 128 (1): 28–60. PMC 1365754. PMID 14368574. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1365754.
- ^ Caldwell PC, Hodgkin AL, Keynes RD, Shaw TI (1960). "The effects of injecting energy-rich phosphate compounds on the active transport of ions in the giant axons of Loligo". J. Physiol. 152: 561–90. PMC 1363339. PMID 13806926. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1363339.
- ^ Steinbach HB, Spiegelman S (1943). "The sodium and potassium balance in squid nerve axoplasm". J. Cell. Comp. Physiol. 22: 187–96. doi:10.1002/jcp.1030220209.
- ^ a b Hodgkin AL (1951). "The ionic basis of electrical activity in nerve and muscle". Biol. Rev. 26: 339–409. doi:10.1111/j.1469-185X.1951.tb01204.x.
- ^ CRC Handbook of Chemistry and Physics, 83rd edition, ISBN 0-8493-0483-0, pp. 12–14 to 12–16.
- ^ Eisenman G (1961). "On the elementary atomic origin of equilibrium ionic specificity". In A Kleinzeller, A Kotyk, eds.. Symposium on Membrane Transport and Metabolism. New York: Academic Press. pp. 163–79. Eisenman G (1965). "Some elementary factors involved in specific ion permeation". Proc. 23rd Int. Congr. Physiol. Sci., Tokyo. Amsterdam: Excerta Med. Found.. pp. 489–506.
* Diamond JM, Wright EM (1969). "Biological membranes: the physical basis of ion and nonekectrolyte selectivity". Annual Review of Physiology 31: 581–646. doi:10.1146/annurev.ph.31.030169.003053. PMID 4885777.
- ^ Junge, pp. 33–37.
- ^ Cai SQ, Li W, Sesti F (2007). "Multiple modes of a-type potassium current regulation". Curr. Pharm. Des. 13 (31): 3178–84. doi:10.2174/138161207782341286. PMID 18045167.
- ^ Goldin AL (2007). "Neuronal Channels and Receptors". In Waxman SG. Molecular Neurology. Burlington, MA: Elsevier Academic Press. pp. 43–58. ISBN 978-0-12-369509-3.
- ^ Purves et al., pp. 28–32; Bullock, Orkand, and Grinnell, pp. 133–134; Schmidt-Nielsen, pp. 478–480, 596–597; Junge, pp. 33–35
- ^ Franco R, Bortner CD, Cidlowski JA (January 2006). "Potential roles of electrogenic ion transport and plasma membrane depolarization in apoptosis". J. Membr. Biol. 209 (1): 43–58. doi:10.1007/s00232-005-0837-5. PMID 16685600.
- ^ Purves et al., pp. 32–33; Bullock, Orkand, and Grinnell, pp. 138–140; Schmidt-Nielsen, pp. 480; Junge, pp. 35–37
- ^ Spangler SG (1972). "Expansion of the constant field equation to include both divalent and monovalent ions". Ala J Med Sci 9 (2): 218–23. PMID 5045041.
- ^ Purves et al., p. 34; Bullock, Orkand, and Grinnell, p. 134; Schmidt-Nielsen, pp. 478–480.
- ^ Purves et al., pp. 33–36; Bullock, Orkand, and Grinnell, p. 131.
- ^ a b Magnuson DS, Morassutti DJ, Staines WA, McBurney MW, Marshall KC. (1995 Jan 14). "In vivo electrophysiological maturation of neurons derived from a multipotent precursor (embryonal carcinoma) cell line". Brain Res Dev Brain Res. 84 (1): 130–41. doi:10.1016/0165-3806(94)00166-W. PMID 7720212.
- ^ Juusola M, Kouvalainen E, Järvilehto M, Weckström M. (1994 Sep). "Contrast gain, signal-to-noise ratio, and linearity in light-adapted blowfly photoreceptors". J Gen Physiol. 104 (3): 593–621. doi:10.1085/jgp.104.3.593. PMC 2229225. PMID 7807062. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2229225.
- ^ Laughlin SB, de Ruyter van Steveninck RR, Anderson JC (1998 May). "The metabolic cost of neural information". Nat Neurosci. 1 (1): 36–41. doi:10.1038/236. PMID 10195106.
- Alberts et al. Molecular Biology of the Cell. Garland Publishing; 4th Bk&Cdr edition (March, 2002). ISBN 0-8153-3218-1. Undergraduate level.
- Guyton, Arthur C., John E. Hall. Textbook of medical physiology. W.B. Saunders Company; 10th edition (August 15, 2000). ISBN 0-7216-8677-X. Undergraduate level.
- Hille, B. Ionic Channel of Excitable Membranes Sinauer Associates, Sunderland, MA, USA; 1st Edition, 1984. ISBN 0-87893-322-0
- Nicholls, J.G., Martin, A.R. and Wallace, B.G. From Neuron to Brain Sinauer Associates, Inc. Sunderland, MA, USA 3rd Edition, 1992. ISBN 0-87893-580-0
- Ove-Sten Knudsen. Biological Membranes: Theory of Transport, Potentials and Electric Impulses. Cambridge University Press (September 26, 2002). ISBN 0-521-81018-3. Graduate level.
- National Medical Series for Independent Study. Physiology. Lippincott Williams & Wilkins. Philadelphia, PE, USA 4th Edition, 2001. ISBN 0-638-30603-0
- Cell communication
- Cell signaling
- Cellular neuroscience
- Contractile cells
- Membrane biology
- Signal transduction
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