Voltage

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https://en.wikipedia.org/wiki/Voltage 

 

Voltage
Batteries are sources of voltage in many electric circuits.
Common symbols	V , ∆V , U , ∆U
SI unit	volt
Derivations from other quantities	Voltage = Energy / charge
Dimension	M L2 T−3 I−1

Voltage, electric potential difference, electric pressure or electric tension is the difference in electric potential between two points. The difference in electric potential between two points (i.e., voltage) in a static electric field is defined as the work needed per unit of charge to move a test charge between the two points. In the International System of Units, the derived unit for voltage is named volt. In SI units, work per unit charge is expressed as joules per coulomb, where 1 volt = 1 joule (of work) per 1 coulomb (of charge). The official SI definition for volt uses power and current, where 1 volt = 1 watt (of power) per 1 ampere (of current). This definition is equivalent to the more commonly used 'joules per coulomb'. Voltage or electric potential difference is denoted symbolically by ∆V, but more often simply as V, for instance in the context of Ohm's or Kirchhoff's circuit laws.

Electric potential differences between points can be caused by electric charge, by electric current through a magnetic field, by time-varying magnetic fields, or some combination of these three. A voltmeter can be used to measure the voltage (or potential difference) between two points in a system; often a common reference potential such as the ground of the system is used as one of the points. A voltage may represent either a source of energy (electromotive force) or lost, used, or stored energy (potential drop).

Definition

There are multiple useful ways to define voltage, including the standard definition mentioned at the start of this page. There are also other useful definitions of work per charge.

Roughly speaking, voltage is defined so that negatively charged objects are pulled towards higher voltages, while positively charged objects are pulled towards lower voltages. Therefore, the conventional current in a wire or resistor always flows from higher voltage to lower voltage.

Historically, voltage has been referred to using terms like "tension" and "pressure". Even today, the term "tension" is still used, for example within the phrase "high tension" (HT) which is commonly used in thermionic valve (vacuum tube) based electronics.

Definition as potential of electric field

The voltage increase from some point ${\textstyle x_{A}}$ to some point ${\textstyle x_{B}}$ is given by

${\displaystyle {\begin{aligned}\Delta V_{AB}&=V(x_{B})-V(x_{A})\\&=-\int _{r_{0}}^{x_{B}}{\vec {E}}\cdot d{\vec {l}}-\left(-\int _{r_{0}}^{x_{A}}{\vec {E}}\cdot d{\vec {l}}\right)\\&=-\int _{x_{A}}^{x_{B}}{\vec {E}}\cdot d{\vec {l}}\end{aligned}}}$

The electric field around the rod exerts a force on the charged pith ball, in an electroscope

In this case, the voltage increase from point A to point B is equal to the work which would have to be done per unit charge, against the electric field, to move the charge from A to B without causing any acceleration. Mathematically, this is expressed as the line integral of the electric field along that path. Under this definition, the voltage difference between two points is not uniquely defined when there are time-varying magnetic fields since the electric force is not a conservative force in such cases.

In a static field, the work is independent of the path

If this definition of voltage is used, any circuit where there are time-varying magnetic fields, such as circuits containing inductors, will not have a well-defined voltage between nodes in the circuit. However, if magnetic fields are suitably contained to each component, then the electric field is conservative in the region exterior to the components, and voltages are well-defined in that region. In this case, the voltage across an inductor, viewed externally, turns out to be 

${\displaystyle \Delta V=-L{\frac {dI}{dt}}}$

despite the fact that, internally, the electric field in the coil is zero (assuming it is a perfect conductor).

Definition via decomposition of electric field

Using the above definition, the electric potential is not defined whenever magnetic fields change with time. In physics, it's sometimes useful to generalize the electric potential by only considering the conservative part of the electric field. This is done by the following decomposition used in electrodynamics:

${\displaystyle {\vec {E}}=-\nabla V-{\frac {\partial {\vec {A}}}{\partial t}}}$

where ${\textstyle {\vec {A}}}$ is the magnetic vector potential. The above decomposition is justified by Helmholtz's theorem. 

In this case, the voltage increase from ${\textstyle x_{A}}$ to ${\textstyle x_{B}}$ is given by 

${\displaystyle {\begin{aligned}\Delta V_{AB}&=-\int _{x_{A}}^{x_{B}}{\vec {E}}_{\mathrm {conservative} }\cdot d{\vec {l}}\\&=-\int _{x_{A}}^{x_{B}}\left({\vec {E}}+{\frac {\partial {\vec {A}}}{\partial t}}\right)\cdot d{\vec {l}}\\&=-\int _{x_{A}}^{x_{B}}({\vec {E}}-{\vec {E}}_{\mathrm {induced} })\cdot d{\vec {l}}\end{aligned}}}$

where ${\textstyle {\vec {E}}_{\mathrm {induced} }}$ is the rotational electric field due to time-varying magnetic fields. In this case, the voltage between points is always uniquely defined.

Treatment in circuit theory

In circuit analysis and electrical engineering, the voltage across an inductor is not considered to be zero or undefined, as the standard definition would suggest. This is because electrical engineers use a lumped element model to represent and analyze circuits.

When using a lumped element model, it is assumed that there are no magnetic fields in the region surrounding the circuit and that the effects of these are contained in 'lumped elements', which are idealized and self-contained circuit elements used to model physical components. If the assumption of negligible leaked fields is too inaccurate, their effects can be modelled by parasitic components.

In the case of a physical inductor though, the ideal lumped representation is often accurate. This is because the leaked fields of the inductor are generally negligible, especially if the inductor is a toroid. If leaked fields are negligible, we find that

${\displaystyle \int _{\mathrm {exterior} }{\vec {E}}\cdot d{\vec {l}}=-L{\frac {dI}{dt}}}$

is path-independent, and there is a well-defined voltage across the inductor's terminals. This is the reason that measurements with a voltmeter across an inductor are often reasonably independent of the placement of the test leads.

Volt

The volt (symbol: V) is the derived unit for electric potential, electric potential difference, and electromotive force. The volt is named in honour of the Italian physicist Alessandro Volta (1745–1827), who invented the voltaic pile, possibly the first chemical battery.

Hydraulic analogy

A simple analogy for an electric circuit is water flowing in a closed circuit of pipework, driven by a mechanical pump. This can be called a "water circuit". Potential difference between two points corresponds to the pressure difference between two points. If the pump creates a pressure difference between two points, then water flowing from one point to the other will be able to do work, such as driving a turbine. Similarly, work can be done by an electric current driven by the potential difference provided by a battery. For example, the voltage provided by a sufficiently-charged automobile battery can "push" a large current through the windings of an automobile's starter motor. If the pump isn't working, it produces no pressure difference, and the turbine will not rotate. Likewise, if the automobile's battery is very weak or "dead" (or "flat"), then it will not turn the starter motor.

The hydraulic analogy is a useful way of understanding many electrical concepts. In such a system, the work done to move water is equal to the pressure multiplied by the volume of water moved. Similarly, in an electrical circuit, the work done to move electrons or other charge-carriers is equal to "electrical pressure" multiplied by the quantity of electrical charges moved. In relation to "flow", the larger the "pressure difference" between two points (potential difference or water pressure difference), the greater the flow between them (electric current or water flow).

Applications

Working on high voltage power lines

Specifying a voltage measurement requires explicit or implicit specification of the points across which the voltage is measured. When using a voltmeter to measure potential difference, one electrical lead of the voltmeter must be connected to the first point, one to the second point.

A common use of the term "voltage" is in describing the voltage dropped across an electrical device (such as a resistor). The voltage drop across the device can be understood as the difference between measurements at each terminal of the device with respect to a common reference point (or ground). The voltage drop is the difference between the two readings. Two points in an electric circuit that are connected by an ideal conductor without resistance and not within a changing magnetic field have a voltage of zero. Any two points with the same potential may be connected by a conductor and no current will flow between them.

Addition of voltages

The voltage between A and C is the sum of the voltage between A and B and the voltage between B and C. The various voltages in a circuit can be computed using Kirchhoff's circuit laws.

When talking about alternating current (AC) there is a difference between instantaneous voltage and average voltage. Instantaneous voltages can be added for direct current (DC) and AC, but average voltages can be meaningfully added only when they apply to signals that all have the same frequency and phase.

Measuring instruments

Multimeter set to measure voltage

Instruments for measuring voltages include the voltmeter, the potentiometer, and the oscilloscope. Analog voltmeters, such as moving-coil instruments, work by measuring the current through a fixed resistor, which, according to Ohm's Law, is proportional to the voltage across the resistor. The potentiometer works by balancing the unknown voltage against a known voltage in a bridge circuit. The cathode-ray oscilloscope works by amplifying the voltage and using it to deflect an electron beam from a straight path, so that the deflection of the beam is proportional to the voltage.

Typical voltages

A common voltage for flashlight batteries is 1.5 volts (DC). A common voltage for automobile batteries is 12 volts (DC). 

Common voltages supplied by power companies to consumers are 110 to 120 volts (AC) and 220 to 240 volts (AC). The voltage in electric power transmission lines used to distribute electricity from power stations can be several hundred times greater than consumer voltages, typically 110 to 1200 kV (AC).

The voltage used in overhead lines to power railway locomotives is between 12 kV and 50 kV (AC) or between 1.5 kV and 3 kV (DC).

Galvani potential vs. electrochemical potential

Inside a conductive material, the energy of an electron is affected not only by the average electric potential, but also by the specific thermal and atomic environment that it is in. When a voltmeter is connected between two different types of metal, it measures not the electrostatic potential difference, but instead something else that is affected by thermodynamics. The quantity measured by a voltmeter is the negative of the difference of the electrochemical potential of electrons (Fermi level) divided by the electron charge and commonly referred to as the voltage difference, while the pure unadjusted electrostatic potential (not measurable with a voltmeter) is sometimes called Galvani potential. The terms "voltage" and "electric potential" are ambiguous in that, in practice, they can refer to either of these in different contexts.

History

The term electromotive force was first used by Volta in a letter to Giovanni Aldini in 1798, and first appeared in a published paper in 1801 in Annales de chimie et de physique. Volta meant by this a force that was not an electrostatic force, specifically, an electrochemical force. The term was taken up by Michael Faraday in connection with electromagnetic induction in the 1820s. However, a clear definition of voltage and method of measuring it had not been developed at this time. Volta distinguished electromotive force (emf) from tension (potential difference): the observed potential difference at the terminals of an electrochemical cell when it was open circuit must exactly balance the emf of the cell so that no current flowed.

Electrophysiology

From Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Electrophysiology 

 

Electrophysiology (from Greek ἥλεκτρον, ēlektron, "amber" [see the etymology of "electron"]; φύσις, physis, "nature, origin"; and -λογία, -logia) is the branch of physiology that studies the electrical properties of biological cells and tissues. It involves measurements of voltage changes or electric current or manipulations on a wide variety of scales from single ion channel proteins to whole organs like the heart. In neuroscience, it includes measurements of the electrical activity of neurons, and, in particular, action potential activity. Recordings of large-scale electric signals from the nervous system, such as electroencephalography, may also be referred to as electrophysiological recordings. They are useful for electrodiagnosis and monitoring.

"Current Clamp" is a common technique in electrophysiology. This is a whole-cell current clamp recording of a neuron firing due to it being depolarized by current injection

Definition and scope

Classical electrophysiological techniques

Principle and mechanisms

Electrophysiology is the branch of physiology that pertains broadly to the flow of ions (ion current) in biological tissues and, in particular, to the electrical recording techniques that enable the measurement of this flow. Classical electrophysiology techniques involve placing electrodes into various preparations of biological tissue. The principal types of electrodes are:

1. simple solid conductors, such as discs and needles (singles or arrays, often insulated except for the tip),
2. tracings on printed circuit boards or flexible polymers, also insulated except for the tip, and
3. hollow tubes filled with an electrolyte, such as glass pipettes filled with potassium chloride solution or another electrolyte solution.

The principal preparations include:

1. living organisms,
2. excised tissue (acute or cultured),
3. dissociated cells from excised tissue (acute or cultured),
4. artificially grown cells or tissues, or
5. hybrids of the above.

Neuronal electrophysiology is the study of electrical properties of biological cells and tissues within the nervous system. With neuronal electrophysiology doctors and specialists can determine how neuronal disorders happen, by looking at the individual's brain activity. Activity such as which portions of the brain light up during any situations encountered. If an electrode is small enough (micrometers) in diameter, then the electrophysiologist may choose to insert the tip into a single cell. Such a configuration allows direct observation and recording of the intracellular electrical activity of a single cell. However, this invasive setup reduces the life of the cell and causes a leak of substances across the cell membrane. Intracellular activity may also be observed using a specially formed (hollow) glass pipette containing an electrolyte. In this technique, the microscopic pipette tip is pressed against the cell membrane, to which it tightly adheres by an interaction between glass and lipids of the cell membrane. The electrolyte within the pipette may be brought into fluid continuity with the cytoplasm by delivering a pulse of negative pressure to the pipette in order to rupture the small patch of membrane encircled by the pipette rim (whole-cell recording). Alternatively, ionic continuity may be established by "perforating" the patch by allowing exogenous pore-forming agent within the electrolyte to insert themselves into the membrane patch (perforated patch recording). Finally, the patch may be left intact (patch recording). 

The electrophysiologist may choose not to insert the tip into a single cell. Instead, the electrode tip may be left in continuity with the extracellular space. If the tip is small enough, such a configuration may allow indirect observation and recording of action potentials from a single cell, termed single-unit recording. Depending on the preparation and precise placement, an extracellular configuration may pick up the activity of several nearby cells simultaneously, termed multi-unit recording. 

As electrode size increases, the resolving power decreases. Larger electrodes are sensitive only to the net activity of many cells, termed local field potentials. Still larger electrodes, such as uninsulated needles and surface electrodes used by clinical and surgical neurophysiologists, are sensitive only to certain types of synchronous activity within populations of cells numbering in the millions. 

Other classical electrophysiological techniques include single channel recording and amperometry.

Electrographic modalities by body part

Electrophysiological recording in general is sometimes called electrography (from electro- + -graphy, "electrical recording"), with the record thus produced being an electrogram. However, the word electrography has other senses (including electrophotography), and the specific types of electrophysiological recording are usually called by specific names, constructed on the pattern of electro- + [body part combining form] + -graphy (abbreviation ExG). Relatedly, the word electrogram (not being needed for those other senses) often carries the specific meaning of intracardiac electrogram, which is like an electrocardiogram but with some invasive leads (inside the heart) rather than only noninvasive leads (on the skin). Electrophysiological recording for clinical diagnostic purposes is included within the category of electrodiagnostic testing. The various "ExG" modes are as follows:

Modality	Abbreviation	Body part	Prevalence in clinical use
electrocardiography	ECG or EKG	heart (specifically, the cardiac muscle), with cutaneous electrodes (noninvasive)	1—very common
electroatriography	EAG	atrial cardiac muscle	3—uncommon
electroventriculography	EVG	ventricular cardiac muscle	3—uncommon
intracardiac electrogram	EGM	heart (specifically, the cardiac muscle), with intracardiac electrodes (invasive)	2—somewhat common
electroencephalography	EEG	brain (usually the cerebral cortex), with extracranial electrodes	2—somewhat common
electrocorticography	ECoG or iEEG	brain (specifically the cerebral cortex), with intracranial electrodes	2—somewhat common
electromyography	EMG	muscles throughout the body (usually skeletal, occasionally smooth)	1—very common
electrooculography	EOG	eye—entire globe	2—somewhat common
electroretinography	ERG	eye—retina specifically	2—somewhat common
electronystagmography	ENG	eye—via the corneoretinal potential	2—somewhat common
electroolfactography	EOG	olfactory epithelium in mammals	3—uncommon
electroantennography	EAG	olfactory receptors in arthropod antennae	4—not applicable clinically
electrocochleography	ECOG or ECochG	cochlea	2—somewhat common
electrogastrography	EGG	stomach smooth muscle	2—somewhat common
electrogastroenterography	EGEG	stomach and bowel smooth muscle	2—somewhat common
electroglottography	EGG	glottis	3—uncommon
electropalatography	EPG	palatal contact of tongue	3—uncommon
electroarteriography	EAG	arterial flow via streaming potential detected through skin[2]	3—uncommon
electroblepharography	EBG	eyelid muscle	3—uncommon
electrodermography	EDG	skin	3—uncommon
electrohysterography	EHG	uterus	3—uncommon
electroneuronography	ENeG or ENoG	nerves	3—uncommon
electropneumography	EPG	lungs (chest movements)	3—uncommon
electrospinography	ESG	spinal cord	3—uncommon
electrovomerography	EVG	vomeronasal organ	3—uncommon

Optical electrophysiological techniques

Optical electrophysiological techniques were created by scientists and engineers to overcome one of the main limitations of classical techniques. Classical techniques allow observation of electrical activity at approximately a single point within a volume of tissue. Essentially, classical techniques singularize a distributed phenomenon. Interest in the spatial distribution of bioelectric activity prompted development of molecules capable of emitting light in response to their electrical or chemical environment. Examples are voltage sensitive dyes and fluorescing proteins.

After introducing one or more such compounds into tissue via perfusion, injection or gene expression, the 1 or 2-dimensional distribution of electrical activity may be observed and recorded.

Intracellular recording

Intracellular recording involves measuring voltage and/or current across the membrane of a cell. To make an intracellular recording, the tip of a fine (sharp) microelectrode must be inserted inside the cell, so that the membrane potential can be measured. Typically, the resting membrane potential of a healthy cell will be -60 to -80 mV, and during an action potential the membrane potential might reach +40 mV. In 1963, Alan Lloyd Hodgkin and Andrew Fielding Huxley won the Nobel Prize in Physiology or Medicine for their contribution to understanding the mechanisms underlying the generation of action potentials in neurons. Their experiments involved intracellular recordings from the giant axon of Atlantic squid (Loligo pealei), and were among the first applications of the "voltage clamp" technique. Today, most microelectrodes used for intracellular recording are glass micropipettes, with a tip diameter of < 1 micrometre, and a resistance of several megohms. The micropipettes are filled with a solution that has a similar ionic composition to the intracellular fluid of the cell. A chlorided silver wire inserted into the pipet connects the electrolyte electrically to the amplifier and signal processing circuit. The voltage measured by the electrode is compared to the voltage of a reference electrode, usually a silver chloride-coated silver wire in contact with the extracellular fluid around the cell. In general, the smaller the electrode tip, the higher its electrical resistance, so an electrode is a compromise between size (small enough to penetrate a single cell with minimum damage to the cell) and resistance (low enough so that small neuronal signals can be discerned from thermal noise in the electrode tip).

Voltage clamp

The voltage clamp uses a negative feedback mechanism. The membrane potential amplifier measures membrane voltage and sends output to the feedback amplifier. The feedback amplifier subtracts the membrane voltage from the command voltage, which it receives from the signal generator. This signal is amplified and returned into the cell via the recording electrode.

The voltage clamp technique allows an experimenter to "clamp" the cell potential at a chosen value. This makes it possible to measure how much ionic current crosses a cell's membrane at any given voltage. This is important because many of the ion channels in the membrane of a neuron are voltage-gated ion channels, which open only when the membrane voltage is within a certain range. Voltage clamp measurements of current are made possible by the near-simultaneous digital subtraction of transient capacitive currents that pass as the recording electrode and cell membrane are charged to alter the cell's potential.

Current clamp

Not to be confused with Current clamp in electronics.

 

The current clamp technique records the membrane potential by injecting current into a cell through the recording electrode. Unlike in the voltage clamp mode, where the membrane potential is held at a level determined by the experimenter, in "current clamp" mode the membrane potential is free to vary, and the amplifier records whatever voltage the cell generates on its own or as a result of stimulation. This technique is used to study how a cell responds when electric current enters a cell; this is important for instance for understanding how neurons respond to neurotransmitters that act by opening membrane ion channels. 

Most current-clamp amplifiers provide little or no amplification of the voltage changes recorded from the cell. The "amplifier" is actually an electrometer, sometimes referred to as a "unity gain amplifier"; its main purpose is to reduce the electrical load on the small signals (in the mV range) produced by cells so that they can be accurately recorded by low-impedance electronics. The amplifier increases the current behind the signal while decreasing the resistance over which that current passes. Consider this example based on Ohm's law: A voltage of 10 mV is generated by passing 10 nanoamperes of current across 1 MΩ of resistance. The electrometer changes this "high impedance signal" to a "low impedance signal" by using a voltage follower circuit. A voltage follower reads the voltage on the input (caused by a small current through a big resistor). It then instructs a parallel circuit that has a large current source behind it (the electrical mains) and adjusts the resistance of that parallel circuit to give the same output voltage, but across a lower resistance.

Patch-clamp recording

The cell-attached patch clamp uses a micropipette attached to the cell membrane to allow recording from a single ion channel.

This technique was developed by Erwin Neher and Bert Sakmann who received the Nobel Prize in 1991. Conventional intracellular recording involves impaling a cell with a fine electrode; patch-clamp recording takes a different approach. A patch-clamp microelectrode is a micropipette with a relatively large tip diameter. The microelectrode is placed next to a cell, and gentle suction is applied through the microelectrode to draw a piece of the cell membrane (the 'patch') into the microelectrode tip; the glass tip forms a high resistance 'seal' with the cell membrane. This configuration is the "cell-attached" mode, and it can be used for studying the activity of the ion channels that are present in the patch of membrane. If more suction is now applied, the small patch of membrane in the electrode tip can be displaced, leaving the electrode sealed to the rest of the cell. This "whole-cell" mode allows very stable intracellular recording. A disadvantage (compared to conventional intracellular recording with sharp electrodes) is that the intracellular fluid of the cell mixes with the solution inside the recording electrode, and so some important components of the intracellular fluid can be diluted. A variant of this technique, the "perforated patch" technique, tries to minimise these problems. Instead of applying suction to displace the membrane patch from the electrode tip, it is also possible to make small holes on the patch with pore-forming agents so that large molecules such as proteins can stay inside the cell and ions can pass through the holes freely. Also the patch of membrane can be pulled away from the rest of the cell. This approach enables the membrane properties of the patch to be analysed pharmacologically.

Sharp electrode recording

In situations where one wants to record the potential inside the cell membrane with minimal effect on the ionic constitution of the intracellular fluid a sharp electrode can be used. These micropipettes (electrodes) are again like those for patch clamp pulled from glass capillaries, but the pore is much smaller so that there is very little ion exchange between the intracellular fluid and the electrolyte in the pipette. The resistance of the micropipette electrode is tens or hundreds of MΩ. Often the tip of the electrode is filled with various kinds of dyes like Lucifer yellow to fill the cells recorded from, for later confirmation of their morphology under a microscope. The dyes are injected by applying a positive or negative, DC or pulsed voltage to the electrodes depending on the polarity of the dye.

Extracellular recording

Single-unit recording

An electrode introduced into the brain of a living animal will detect electrical activity that is generated by the neurons adjacent to the electrode tip. If the electrode is a microelectrode, with a tip size of about 1 micrometre, the electrode will usually detect the activity of at most one neuron. Recording in this way is in general called "single-unit" recording. The action potentials recorded are very much like the action potentials that are recorded intracellularly, but the signals are very much smaller (typically about 1 mV). Most recordings of the activity of single neurons in anesthetized and conscious animals are made in this way. Recordings of single neurons in living animals have provided important insights into how the brain processes information. For example, David Hubel and Torsten Wiesel recorded the activity of single neurons in the primary visual cortex of the anesthetized cat, and showed how single neurons in this area respond to very specific features of a visual stimulus. Hubel and Wiesel were awarded the Nobel Prize in Physiology or Medicine in 1981.

Multi-unit recording

If the electrode tip is slightly larger, then the electrode might record the activity generated by several neurons. This type of recording is often called "multi-unit recording", and is often used in conscious animals to record changes in the activity in a discrete brain area during normal activity. Recordings from one or more such electrodes that are closely spaced can be used to identify the number of cells around it as well as which of the spikes come from which cell. This process is called spike sorting and is suitable in areas where there are identified types of cells with well defined spike characteristics. If the electrode tip is bigger still, in general the activity of individual neurons cannot be distinguished but the electrode will still be able to record a field potential generated by the activity of many cells.

Field potentials

A schematic diagram showing a field potential recording from rat hippocampus. At the left is a schematic diagram of a presynaptic terminal and postsynaptic neuron. This is meant to represent a large population of synapses and neurons. When the synapse releases glutamate onto the postsynaptic cell, it opens ionotropic glutamate receptor channels. The net flow of current is inward, so a current sink is generated. A nearby electrode (#2) detects this as a negativity. An intracellular electrode placed inside the cell body (#1) records the change in membrane potential that the incoming current causes.

Extracellular field potentials are local current sinks or sources that are generated by the collective activity of many cells. Usually, a field potential is generated by the simultaneous activation of many neurons by synaptic transmission. The diagram to the right shows hippocampal synaptic field potentials. At the right, the lower trace shows a negative wave that corresponds to a current sink caused by positive charges entering cells through postsynaptic glutamate receptors, while the upper trace shows a positive wave that is generated by the current that leaves the cell (at the cell body) to complete the circuit. For more information, see local field potential.

Amperometry

Amperometry uses a carbon electrode to record changes in the chemical composition of the oxidized components of a biological solution. Oxidation and reduction is accomplished by changing the voltage at the active surface of the recording electrode in a process known as "scanning". Because certain brain chemicals lose or gain electrons at characteristic voltages, individual species can be identified. Amperometry has been used for studying exocytosis in the nervous and endocrine systems. Many monoamine neurotransmitters; e.g., norepinephrine (noradrenalin), dopamine, and serotonin (5-HT) are oxidizable. The method can also be used with cells that do not secrete oxidizable neurotransmitters by "loading" them with 5-HT or dopamine.

Planar patch clamp

Planar patch clamp is a novel method developed for high throughput electrophysiology. Instead of positioning a pipette on an adherent cell, cell suspension is pipetted on a chip containing a microstructured aperture. A single cell is then positioned on the hole by suction and a tight connection (Gigaseal) is formed. The planar geometry offers a variety of advantages compared to the classical experiment:

• It allows for integration of microfluidics, which enables automatic compound application for ion channel screening.
• The system is accessible for optical or scanning probe techniques.
• Perfusion of the intracellular side can be performed.

• 

  Schematic drawing of the classical patch clamp configuration. The patch pipette is moved to the cell using a micromanipulator under optical control. Relative movements between the pipette and the cell have to be avoided in order to keep the cell-pipette connection intact.
  
• 

  Scanning electron microscope image of a patch pipette.
  
• 

  In planar patch configuration, the cell is positioned by suction. Relative movements between cell and aperture can then be excluded after sealing. An antivibration table is not necessary.
  
• 

  Scanning electron microscope image of a planar patch clamp chip. Both the pipette and the chip are made from borosilicate glass.
  

Other methods

Solid-supported membrane (SSM)-based

With this electrophysiological approach, proteoliposomes, membrane vesicles, or membrane fragments containing the channel or transporter of interest are adsorbed to a lipid monolayer painted over a functionalized electrode. This electrode consists of a glass support, a chromium layer, a gold layer, and an octadecyl mercaptane monolayer. Because the painted membrane is supported by the electrode, it is called a solid-supported membrane. It is important to note that mechanical perturbations, which usually destroy a biological lipid membrane, do not influence the life-time of an SSM. The capacitive electrode (composed of the SSM and the absorbed vesicles) is so mechanically stable that solutions may be rapidly exchanged at its surface. This property allows the application of rapid substrate/ligand concentration jumps to investigate the electrogenic activity of the protein of interest, measured via capacitive coupling between the vesicles and the electrode.

Bioelectric recognition assay (BERA)

The bioelectric recognition assay (BERA) is a novel method for determination of various chemical and biological molecules by measuring changes in the membrane potential of cells immobilized in a gel matrix. Apart from the increased stability of the electrode-cell interface, immobilization preserves the viability and physiological functions of the cells. BERA is used primarily in biosensor applications in order to assay analytes that can interact with the immobilized cells by changing the cell membrane potential. In this way, when a positive sample is added to the sensor, a characteristic, "signature-like" change in electrical potential occurs. BERA is the core technology behind the recently launched pan-European FOODSCAN project, about pesticide and food risk assessment in Europe. BERA has been used for the detection of human viruses (hepatitis B and C viruses and herpes viruses), veterinary disease agents (foot and mouth disease virus, prions, and blue tongue virus), and plant viruses (tobacco and cucumber viruses) in a specific, rapid (1–2 minutes), reproducible, and cost-efficient fashion. The method has also been used for the detection of environmental toxins, such as pesticides and mycotoxins in food, and 2,4,6-trichloroanisole in cork and wine, as well as the determination of very low concentrations of the superoxide anion in clinical samples.

A BERA sensor has two parts:

• The consumable biorecognition elements
• The electronic read-out device with embedded artificial intelligence.

A recent advance is the development of a technique called molecular identification through membrane engineering (MIME). This technique allows for building cells with defined specificity for virtually any molecule of interest, by embedding thousands of artificial receptors into the cell membrane.

Computational electrophysiology

While not strictly constituting an experimental measurement, methods have been developed to examine the conductive properties of proteins and biomembranes in silico. These are mainly molecular dynamics simulations in which a model system like a lipid bilayer is subjected to an externally applied voltage. Studies using these setups have been able to study dynamical phenomena like electroporation of membranes and ion translocation by channels.

The benefit of such methods is the high level of detail of the active conduction mechanism, given by the inherently high resolution and data density that atomistic simulation affords. There are significant drawbacks, given by the uncertainty of the legitimacy of the model and the computational cost of modeling systems that are large enough and over sufficient timescales to be considered reproducing the macroscopic properties of the systems themselves. While atomistic simulations may access timescales close to, or into the microsecond domain, this is still several orders of magnitude lower than even the resolution of experimental methods such as patch-clamping.

Clinical electrophysiology

Clinical electrophysiology is the study of how electrophysiological principles and technologies can be applied to human health. For example, clinical cardiac electrophysiology is the study of the electrical properties which govern heart rhythm and activity. Cardiac electrophysiology can be used to observe and treat disorders such as arrhythmia (irregular heartbeat). For example, a doctor may insert a catheter containing an electrode into the heart to record the heart muscle's electrical activity.

Another example of clinical electrophysiology is clinical neurophysiology. In this medical specialty, doctors measure the electrical properties of the brain, spinal cord, and nerves. Scientists such as Duchenne de Boulogne (1806–1875) and Nathaniel A. Buchwald (1924–2006) are considered to have greatly advanced the field of neurophysiology, enabling its clinical applications.

Clinical reporting guidelines

Minimum Information (MI) standards or reporting guidelines specify the minimum amount of meta data (information) and data required to meet a specific aim or aims in a clinical study. The "Minimum Information about a Neuroscience investigation" (MINI) family of reporting guideline documents aims to provide a consistent set of guidelines in order to report an electrophysiology experiment. In practice a MINI module comprises a checklist of information that should be provided (for example about the protocols employed) when a data set is described for publication.