The Integrated and Powerful Electrophysiology Lab
eLab/eLab+ comprises an innovative wide-band amplifier that is adequate to record all range signals through a 24-bit A to D converter with capabilities of 10K to 50K samples per second.
eLab/eLab+ offers both auditory and visual monitoring features.
A Complete Electrophysiology Lab eLab is a singular data acquisition system for recording the single-unit action potentials (Spikes), Local Field Potential (LFP), LTP, NCV, EEG/ECG, and signal modulation by external digital events.
All adjustments can simply and precisely be added to the software. You can save it as a protocol and share it online with other researchers. You will also have access to our available online protocols.
Olfactory receptors in arthropod antennae
ectroantennography (EAG) is a method for recording electrical potentials from insect antennae. These potentials provide information on the olfactory perception of insects.
The EAG-technique records the ‘slow’ changes of potential that are caused by the superposition of simultaneous membrane depolarisations of numerous receptor cells.
EEG Analysis
stomach and bowel smooth muscle
glottis
An electrogastroenterography (EGG) is based that different organs of a Gastrointestinal tract give different frequency slow wave.
EGEG electrodes are as much as possible removed from a stomach and intestines—usually, three electrodes are placed on the extremities. It allows receiving stabler and comparable results.
EGEG electrodes are as much as possible removed from a stomach and intestines—usually, three electrodes are placed on the extremities. It allows receiving stabler and comparable results
stomach and bowel smooth muscle
glottis
Stomach smooth muscle
Electrogastrography (EGG) is a non-invasive method for the measurement of gastric myoelectrical activity.
Intracardiac electrograms (EGMs) are electrical signals measured within the chambers of the heart, which can be used to locate abnormal cardiac tissue and guide catheter ablations to treat cardiac arrhythmias.
Eye—via the corneoretinal potential
Electronystagmography (ENG or electrooculography) is used to evaluate people with vertigo (a false sense of spinning or motion that can cause dizziness) and certain other disorders that affect hearing and vision. Electrodes are placed at locations above and below the eye to record electrical activity
Electromyography (EMG) allows veterinary neurologists to evaluate the health of nerves and muscles in anesthetized patients. EMG utilizes small needles (<1 mm diameter) to record electrical activity within muscles. When an animal is anesthetized, EMG should not identify any electrical activity within a normal muscle. EMG of animals with either muscle or nerve diseases often identifies each spontaneous electrical activity, which is abnormal. This test is often followed by a nerve conduction velocity (NCV) to further isolate the abnormalities to either the muscle or the nerve.
A muscle disease would have an abnormal EMG and a normal NCV. A nerve disease would have both an abnormal EMG and abnormal NCV.
Electromyography (EMG) is a recording of electrical activity within the muscles after placing a small needle electrode into the muscle. In people, EMG is done fully awake. Since we cannot explain to animals that they might be a little uncomfortable, this procedure is performed under general anesthesia.
a record of the difference in electrical charge between the front and back of the eye that is correlated with eyeball movement (as in REM sleep) and obtained by electrodes placed on the skin near the eye.
An EOG records eye movement by detecting a voltage difference between the cornea and retina. As the eye moves, the vector of this electric field changes recording electrodes placed in the skin at fixed points. These bioelectrical signals are typically very small in amplitude (µV) and an amplifier is required to accurately record the EOG.
Eye—retina specifically
Evaluating retinal function with the electroretinogram (ERG) is an electrical signal that massed response of the retina to light stimulation. ERG is easily recorded from the corneal surface of the mouse eye and is commonly used to assess the integrity of the inner, middle, and outer retinal layers.
An EPSP is received when an excitatory presynaptic cell, connected to the dendrite, fires an action potential. The EPSP signal is propagated down the dendrite and is summed with other inputs at the axon hilllock. The EPSP increases the neurons membrane potential.
ERP and event-related oscillations are extensively used to study the disruption of neuronal circuits underlying sensory encoding, information processing, and attention in neuropsychiatric and neurodegenerative disorders. To date, several sensory-level ERP measures, including the auditory P50 paradigm, mismatch negativity (MMN), and P300 responses have been validated in both human clinical investigations and animal models.
vomeronasal organ
The electrovomeronasogram (EVG) recording technique provides a sensitive means through which ligand-induced activation of populations of VSNs can be recorded from the epithelial surface using an intact, ex vivo preparation of the mouse VNO.
eProbe software provides many scopes, panels, and FFT bars for monitoring and analyzing EXG signals in the different bands and Frequencies.
The activity of many cells, in both In vivo and in vitro cases. Also offers you many tools and possibilities for monitoring, discriminating spikes, and analyzing data.
Heart Rate Variability (HRV) is determined by analyzing the time series of beat-to-beat intervals from an electrocardiogram (ECG).
HRV analysis has become one of the most popular methods of ANS evaluation. It is based on the observation that even at rest the duration of RR intervals is not constant but continually fluctuates around the mean value.
ECG, blood pressure, or arterial pulse recordings can be used to investigate the interplay between sympathetic and parasympathetic nervous systems.
Long-term potentiation, or LTP, is a process of synaptic connections between neurons that become stronger with frequent activation.
LTP is thought to be a way in which the brain changes responses to experiments, and thus may be a mechanism underlying learning and memory.
Nerve Conduction Velocity (NCV) testing involves electrical stimulation of peripheral nerves, and recording the electrical response as the nerve impulse is transmitted down the nerve.
By analyzing the degree and type of electrical response, neurologists can better determine whether the nerve is conducting the impulse properly, and which part of the nerve (nerve fibers or myelin coating) is most likely affected.
Nerve conduction testing is used in conjunction with electromyography and biopsy to help diagnose patients with neuromuscular disorders.
Field Potential, NCV Analysis
Heart Rate and Arterial Blood Pressure and Their Variability. The RR interval, the time elapsed between two successive R waves of the QRS signal on the electrocardiogram (and its reciprocal, the HR), is a function of intrinsic properties of the sinus node as well as autonomic influences
eLab lets you have the most precise recordings of action potentials and single neuron activities of the brain and spinal cord. eProbe software also offers you many tools and possibilities for monitoring, discriminating spikes, and analyzing data.
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. The electrode is a microelectrode, with a tip size of about 1 micrometer.
Single-unit potential (spike) analysis
What is the Kindling?
Kindling has been extensively studied as a model of temporal lobe epilepsy (TLE), in many types of research, its advantages and distinctiveness compared to other models remain misunderstood. Through an exquisitely controlled process, kindling induces a predictable sequence of gradually evolving molecular and cellular alterations at every level of biological organization in neural circuits, from gene transcription to patterns of neuronal connectivity.
Studies of kindling had a major influence on understanding the consequences of repeated seizures. It has contributed to an increasing appreciation that affects non-benign seizures.
The alterations induced in remodeled neural circuits by repeated seizures. These seizures are potential therapeutic targets to prevent or delay progressive adverse effects associated with epilepsy.
On this basis, interventions that reduce kindling progression can be regarded as “disease-modifying”. Therapies that slow the rate of kindling can be relatively easily identified by assessing the number of ADs to the first Class V seizure.
Kindling extends a particular translational platform for the evaluation of novel potentially “disease-modifying” therapies, and also for the discovery of novel therapeutic targets among the vast array of potential candidates.
Electrical kindling
In order to study the brain network structures and explore on development parameters of seizures and epilepsy, we need to use a repeated pulse generator and electrical stimulators to make an electrical kindling model, simultaneously recording and analyzing EEG signals.
All you need are provided in eLab and eProbe.
Kindling analysis
Electrophysiological recordings from visceral afferent fibers have demonstrated the occurrence of intestinal receptors that respond to chemical and mechanical stimuli. Most of these recordings have been made from primary afferent fibers in the major visceral nerve trunks. However, physiological anatomical and immunochemical evidence suggests, that in addition to primary afferent fibers with intestinal receptors, there are also intestinal afferent fibers with axons in the mesenteric nerves whose cell bodies are located in the intestinal wall. The cell bodies of these neurons are found in the myenteric and submucous plexuses and their centripetal projections appear to terminate in the abdominal prevertebral sympathetic ganglia. Hence, recordings made from afferent fibers in the mesenteric
Nerves contain information on the receptor properties of both primary afferent and intramural afferent neurons.
Polysomnography is a test conducted to study sleep and to diagnose a variety of sleep disorders. Some people refer to polysomnography (PSG) as a sleep study. Sleep technologists perform the tests which are typically conducted in hospitals, free-standing facilities, or dedicated sleep clinics.
An epileptiform activity in EEG signals including spikes, sharp waves, or spike-and-wave complexes can be evident not only during a seizure (the ictal period) but also a short time before (the preictal period) as well as between seizures (the interictal period).
A burst activity is an activity that is a predecessor to more than one activity. An example of a burst activity is “Database Creation”, which is the predecessor to “Creating Stored Procedures” and “Optimizing Tables”
eLab provides you powerful tools for recording the electrical activities of the heart (ECG/EKG) and cardiovascular in invasive and non-invasive situations. Monitoring and analyzing the high-resolution recorded signals are available in eProbe. Protocol manager in eProbe software, you can carefully investigate the invasive nerve conduction parameters. Also offers you many tools and possibilities for monitoring, discriminating spikes, and analyzing data.
The most frequently used animal species in experimental cardiac electrophysiology are mice, rabbits, and dogs. Murine and human electrocardiograms (ECGs) show salient differences, including the occurrence of a pronounced J-wave and a less distinctive T-wave in the murine ECG. Mouse models can resemble human cardiac arrhythmias, although mice differ from humans in cardiac electrophysiology. Thus, arrhythmia mechanisms in mice may differ from those in humans and should be transferred to the human situation with caution. Further relevant cardiovascular animal models are rabbits, dogs, and minifies, as they show similarities of cardiac ion channel distribution with the human heart and are suitable to study ventricular repolarization or pro- and antiarrhythmic drug effects.
Electrocorticography (ECoG) is the method of recording electroencephalographic signals directly from the surgically exposed cerebral cortex. It detects intraoperatively the cortical regions with substantial epileptiform interictal discharges. Direct cortical stimulation during ECoG provides a method of identifying language, motor, and sensory regions during a craniotomy. Both techniques—the identification of cortex with epileptic activity and cortex with important eloquent functional activity—help determine limits for surgical cortical resection. These are used most commonly during epilepsy and tumor surgery. Anesthetic agents can adversely affect the recording, and ECoG restricts the types of anesthesia that can be used. The amount of spiking from diffuse or remote cortical regions on ECoG can predict the success of postoperative seizure control.
Galvanic Skin Response (GSR) Galvanic Skin Response (GSR) – Technologies The Galvanic Skin Response (GSR), also named Electrodermal Activity (EDA) and Skin Conductance (SC), is the measure of the continuous variations in the electrical characteristics of the skin
the electrical activity of the uterine muscle into a legible tocogram. The EHG signal has a high correlation with the intra-uterine pressure and provides a more accurate assessment of uterine activity compared to external tocodynamometry.
Electroneuronography or electroneurography (ENoG) is a neurological non-invasive test used to study nerve in cases of muscle weakness
An evoked potential or evoked response is an electrical potential in a speculate pattern recorded from a distinct part of the nervous system, especially the brain, of a human or other animals following the presentation of a stimulus such as a light flash or a pure tone.
palatal contact of tongue
Electropalatography (EPG) is a technique used to monitor contacts between the tongue and hard palate, particularly during articulation and speech
Deep brain stimulation (DBS) as a therapy in neurological and psychiatric disorders is applied widely. In this respect, DBS in animal models is performed to study the underlying mechanisms and to evaluate new indications and technology.
The deep brain stimulator is composed of the electrodes implanted in the brain, the implanted pulse generator, and the extended wire connecting the electrodes and pulse generator. The pulse generator is the core part of the system. The pulse generated is transferred to the unilateral or bilateral electrode through the extended wire
eLab helping eProbe gives you a very high accuracy for recording and exploring extracellular field potentials (LFP), that generated by the collective activity of many cells, in both In vivo and in vitro cases. Also offers you many tools and possibilities for monitoring, discriminating spikes, and analyzing data.
Field Potential, NCV Analysis:
Heart Rate Variability (HRV) is determined by analyzing the time series of beat-to-beat intervals from an electrocardiogram (ECG).
HRV analysis has become one of the most popular methods of ANS evaluation. It is based on the observation that even at rest the duration of RR intervals is not constant but continually fluctuates around the mean value.
ECG, blood pressure, or arterial pulse recordings can be used to investigate the interplay between sympathetic and parasympathetic nervous systems.
eLab provides you a rich setup for nerve conduction studies. Employing the precise stimulator coming with eLab and helping the flexible protocol manager in eProbe software, you can accurately investigate the invasive nerve conduction parameters, also offers you many tools and possibilities for monitoring, discriminating spikes, and analyzing data.
An incredible auditory tool to hear the firing of every single neuron has been presented by eLab.
By employing the eProbe software, you can precisely investigate the invasive nerve conduction parameters.
Visual evoked potential (VEP) is a highly advanced vision test that objectively measures how well the entire vision system is working.
The post-retinal function can be assessed objectively with the visual evoked potential (VEP). The VEP is a gross electrical potential recorded from the visual cortex in response to a visual stimulus. To obtain a normal VEP requires an intact visual pathway from the retina to the primary visual cortex. Thus, any visual pathway disease (e.g., optic neuritis) that alters the function of the central visual pathway will affect the VEP response.
Slice preparation or brain slice is a technique in electrophysiology that allows assessing synapses or neural circuits while isolated from the rest of the brain in control physiological conditions. It involves stimulating or recording from a slice of immersed brain tissue in artificial cerebrospinal fluid.
The technique allows a greater laboratory control on the selected circuit while eliminating the effect of other parts, careful control of the physiological conditions through perfusion of substrates in the incubation fluid, to precise manipulation of neurotransmitter activity through perfusion of agonists and antagonists.
Electrophysiological recordings from visceral afferent fibers have demonstrated the occurrence of intestinal receptors that respond to chemical and mechanical stimuli. Most of these recordings have been made from primary afferent fibers in the major visceral nerve trunks. However, physiological anatomical and immunochemical evidence suggests, that in addition to primary afferent fibers with intestinal receptors, there are also intestinal afferent fibers with axons in the mesenteric nerves whose cell bodies are located in the intestinal wall. The cell bodies of these neurons are found in the myenteric and submucous plexuses and their centripetal projections appear to terminate in the abdominal prevertebral sympathetic ganglia. Hence, recordings made from afferent fibers in the mesenteric
Nerves contain information on the receptor properties of both primary afferent and intramural afferent neurons.
Spinal cord recording is a method for in vivo single-unit extracellular recordings from the dorsal horn of rat or mouse spinal cord. This method allows the complex, dynamic, and plastic circuitry of the dorsal horn to explore in various models and situations. Briefly, in an anesthetized animal, the spinal cord is exposed, while the recording electrode is inserted into the dorsal horn. To isolate a neuron the electrode is moved incrementally through the cord whilst the ipsilateral hind paw (receptive field) is stimulated with a light tap. The neuron can then characterized according to its depth, latency of Abeta-, Adelta- and C-fibre responses and its response to natural (brush, heat, and pressure) and electrical stimulation.
Microarray electrode for any tissue studies
16 channel recording
selectable channel for stimulus
Small size array (less than 1cm)
The pressure is the amount of force exerted on the surface of an object per unit area. Typically pressure measurements are useful when describing a fluid contained inside a solid structure.
Arterial blood pressure measurements are key parameters in studies of autonomic regulation of cardiovascular function. The power of integrative physiological analysis enable by the capability to measure additional parameters concurrently with continuous vascular pressure signals, whether acutely in anesthetized animals or chronically with telemetry implants.
Beat-to-beat invasive blood pressure recording, also assessing the time variance and dynamics of change in data over time.
Small amplitude stable VEP was generated which were entitled “steady-state” visually evoked potentials (SSVEPs) of the human visionary system. There hence, steady-state visual evoked potentials (SSVEPs) are defined as the potential elicited by the change in the visual field with a frequency higher than 6 Hz.
In vitro: The term in vitro refers to a medical study or experiment which is done in the laboratory within the confines of a test tube or laboratory dish.
In vivo: The term in vivo refers to a medical test, experiment, or procedure that is done on (or in) a living organism, such as a laboratory animal or human
invasive procedure A medical procedure that invades (enters) the body, usually by cutting or puncturing the skin or by inserting instruments into the body.
term non-invasive can refer to diseases, procedures, or devices. Noninvasive diseases usually do not spread to or damage other organs and tissues. Noninvasive procedures do not involve tools that break the skin or physically enter the body.
Rodents, especially rats and mice, have been the leading model organisms used in biomedical research for well over a century. … These manipulations have allowed the researcher to study rats or mice genetically suited specifically to the human disease model of their interests.
The physiological similarity between humans and NHPs means there is greater validity of the data obtained from primate models than other animal models (e.g. reproduction and pregnancy, cognition, and cognitive aging). … models of AIDS, lung disorders, and drug metabolism).
The ventrobasal complex (VB) is a relay nucleus of the thalamus for nociceptive stimuli received from nociceptive nerves. The VB consists of the ventral posteromedial nucleus (VPM) and the ventral posterolateral nucleus (VPL). In some species the ventral posterolateral nucleus, pars caudalis is also a part of the VB. The VB gets inputs from the spinothalamic tract, medial lemniscus, and corticothalamic tract. The main output of the VB is the primary somatosensory cortex.
The VB serves as the main relay for nociceptive stimuli and the modulation of that stimuli to the primary somatosensory cortex. The modulation occurs through different types of receptors present in the VB.
Patch-clamp recordings are obtained by electrically isolating a patch of the membrane using an electrolyte-filled glass capillary in close proximity to the cell membrane. A silver or silver chloride electrode inserted at the other end of the capillary will provide electrical continuity with a reference electrode placed in the extracellular bath solution.
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Electrophysiology is a study flow of ions in a living tissue, which is measuring the electrical properties of cells and tissues, the voltage variation of a biological entity from a single ion channel proteins of an organ (for example, heart). Microelectrodes (glass pipette filled with an electrolyte) placing inside a single cell for intracellular measurement and near the surface of a cell for extracellular measurement.
In neuroscience, Electrophysiology recording means measurements of the electrical activity of neurons, and, especially for action potential activity. Recordings of large-scale electric signals from the nervous system, such as electroencephalography, may also be referred to as electrophysiological recordings.
In neuroscience, single-unit recordings provide a method of measuring the electrophysiological responses of single neurons using a microelectrode system. The microelectrode is inserted into the brain, where it can record the rate of change in voltage in time.
Single-Cell Recording is a technique used in research to observe changes in voltage or current in a neuron. The electrode measures the changes in charge as the neuron reaches its action potential. This process is usually concurrent with some stimuli.
Electrophysiology- means recording the electrical activity generated by neurons.
Main techniques:
Single-unit recordings:
probe the activity of a few neurons.
Electroencephalography, perform recording on the activities of large clusters of neurons.
(Single-unit recordings, Basically done on anesthetized animals- want to figure out what’s the smallest part of the brain they can remove- only painful part is opening the skin and skull- no pain receptors in brain Electroencephalography- uses surface-based electrodes that sample electrical activity over a larger area)
– Electroencephalogram (EEG) detects synaptic potentials in an ensemble of neurons- event-related potentials (ERP) tie the electrical response to the presentation of a specific stimulus- trying to study the occurrence of particular brain activity- advantages
The neuron is the cell responsible for the transfer of information and electrical impulses around the body. Neurons work by transferring electrical charges from neuron to neuron (to get from one point to another)
All data is transferred in this electrical method, which is why computer science has become such an important tool in the study of Neuroscience.
To better understand how neurons work, first, we must understand the various parts of a neuron.
Firstly, because the neuron is a cell so it has a nucleus. Nucleus is the center of the neuron and cells will be dead without managing it. The nucleus, in theory, is the brain of the neuron–or any cell.
At the end of each neuron, there are the dendrites. A dendrite is the receiving portion of the neuron. It is an extension that appears on the edge of the neuron, which comes close to other neurons. Dendrites make it possible for neurons to transfer information.
At the opposite end, there is the axon. The axon is the sending extension on the neuron. All information from the neuron leaves through the axon and the terminal buttons at the end of the arms.
Briefly, all information comes into a neuron through the dendrite, flows through the neuron, and then leaves to go to the next neuron through the axon. Arms on each side are required for the neuron to work properly.
Neurons work by conducting electrical signals. It is starting with the axon neurons; send electrical impulses of data through the arms. Neurons have no tangency; they just very close to each other. The space between a neuron axon and another neuron dendrite is known as the synapse. When neurons pass information, the synapse is the portion that is “flinging” the data from one neuron to another. This process is known as synaptic transmission.
Once the synaptic transmission occurs, the data enters through the dendrites. The electrical signal has now successfully transferred from the first neuron to the second one. Then moves to the axon and passes through the synapse to the next neuron’s dendrite. In other words, a neuron works by being the station for the electrical signal or, it can be perceived as railroad tracks, and the signal follows along this track.
Signals require amplification, filtering, isolation, and pre-processed through signal conditioners before being digitized by eProbe.
Record from multiple subjects at the same time in head-fixed or free-moving paradigms. Integrated digital and analog I/O allow for simultaneous communication and control of external behavioral devices, optogenetics light sources, stimulators, compensation delivery devices, or force-feedback devices. On-board processing allows dynamic experiments that change with the animal electrophysiology or behavioral responses. Trellis’ integrated video recording feature provides an easy way to correlate behavior with electrophysiological responses.
By using eWave devices and freely moving, you can simultaneously record and electrically stimulate in freely behaving animals. The eWave device digitizes the signal right on the head of the animal, making the signal immune to artifacts from a swinging cable and other sources of noise. Our commutator is also extremely lightweight, and as a result, can be mounted on a balance to allow a much greater range of motion that retracts the cable to prevent slack. A commutator with a fiber-optic rotary joint is also available, allowing for the integration of high-quality recording, electrical stimulation, and optogenetics stimulation. Our accessories allow connecting multiple inexpensive USB cameras to allow recording from multiple vantage points, with every frame time-stamped and stored with the electrophysiological data. If robust positional tracking or behavioral tracking that is needed, we provide easy integration with mazes.
Field potentials are probably the most common extracellular signals being recorded and include ECG, EMG, and EEG. With an electrode with an even bigger sampling field, the activity of individual neurons can no longer be distinguished, but rather a field potential generated by the activity of many cells. Potentials can either be recorded invasively or non-invasively on the skin.
The phrase “multiunit recording” has been used for the measurement of neuronal activity at a variety of scales, encompassing both averaged measurements of the activity of many thousands (sometimes millions) of neurons, as well as the measurement of the individual action potentials from a handful, perhaps a hundred, of cells
In extracellular recordings, an electrode is not inserted into a single cell, instead, the electrode(s) are placed in the extracellular fluid, near the cell of interest. The type of recording will depend on the type and size of the electrode, and proximity to the signal origin.
A microelectrode near the soma or initial segment. The single-unit discharge is an action potential so that it should be all-or-none, but for catching an action potential the impedance of the recording electrode should be in a range of 4–10 MΩ. The characteristics of the single-unit discharge include fi fixed latency, fi fixed amplitude and a large negative peak
In extracellular recordings, the tip of a microelectrode (typically 1–10 mm in diameter) is positioned immediately adjacent to, but outside of, a neuron. When near the neuron, current fields generated by action potentials in that cell are detected by the microelectrode as small voltage deflections (typically 0.1–1 mV).
The intact, functioning brain is readily explored with microelectrodes in anesthetized animals. In this approach, the animal is anesthetized, most commonly with a barbiturate, urethane, chloralose, or halothane. The animal is then placed in a stereotaxic instrument which positions the skull in an exact position and orientation treating submillimeter scales in three dimensions on the instrument. By positioning the microelectrode tip at the desired coordinate along with these scales, determined by reference to a stereotaxic atlas of the brain of that species, any site within the brain can be found and cellular activity recorded. X-ray or magnetic resonance imaging methods may also be used for this purpose in human studies.
In these experiments, impulse activity of neurons is typically recorded extracellularly, in contrast to the intracellular recordings discussed above. In extracellular recordings, the tip of a microelectrode (typically 1–10 mm in diameter) is positioned immediately adjacent to, but outside of, a neuron. When close to the neuron, current fields generated by action potentials in that cell are detected by the microelectrode as small voltage deflections (typically 0.1–1 mV).
There are many experimental applications of in vivo single-cell electrophysiology. Below we briefly describe three: iontophoresis and local drug application, stimulation recording, and antidromic activation.
There are many experimental applications of in vivo single-cell electrophysiology describe three: iontophoresis and local drug application, stimulation recording, and antidromic activation.
Because these methods have been in wide use for several decades, there are literally hundreds of specific examples that could be described. For example, these methods have been used to determine the origin of the hyperactivity of locus coeruleus neurons during opiate withdrawal and to demonstrate that systemic nicotine potently activates the LC indirectly.
Advantages: in vivo electrophysiology compared to the in vitro methods is obviously due to the intact preparation in vivo. With these in vivo methods, one can study brain regions or neurons in their intact state with its normal complement of inputs and targets, and in their natural milieu of circulating hormones and factors. The cells being studied usually have not been severed or damaged, as is almost always the case with slice studies, and have developed normally in the intact organism, in contrast to the culture preparation. These considerations lend additional credibility and fewer caveats to results concerning neuronal activity in vivo.
Disadvantage: However, there are also several disadvantages of in vivo preparations. In addition to the relative difficulty in performing many of the intracellular and whole-cell studies described above (and therefore in obtaining data on membrane mechanisms of drug action), the researcher does not have as much knowledge as in the in vitro preparations of actual drug concentrations at the cell under study. Therefore, drug and transmitter responses are less confidently identified with a specific receptor or channel. Besides, there may be other confounds, such as the presence of anesthetics (or in awake animals, immobilization stress) that could alter the normal electrophysiological responses to drugs and transmitters.
Yes, you can change it without re-recording the data.
You can create a stimulation protocol with eProbe software, and examples of such simulations can be found in various articles.
You can do this by converting the file to text format.
You can do this by converting the file to text format.
eProbe, used with eLab Data Acquisition Unit, performs an Analog-to-Digital Conversion at a 24-bit full-scale resolution, effectively dividing the Range into 16000000 segments) the Resolution is the size of one of these segments. To calculate the Resolution of any raw signal recorded into eProbe, divide the Total Range that the signal was recorded on by 16000000.
Important Note – The Range extends in both the positive and negative direction. Therefore, a Range of 90mv goes from +90mV to -90mV – a Total Range of 180mV.
ePulse (for animal use only) is designed to be used for simulating the desired points (for example nucleus of a brain and spinal cord and muscle), You can refer to the articles that work with this device.
Glass microelectrodes are used for extra- or intracellular recordings. These have usually a high resistance of 5 to 10 G, glass micropipette filled with electrolyte(2 or 3 M, sodium chloride or potassium chloride)with a tip diameter around 1 micron
A different kind of microelectrode made from a small-diameter strong metal wire (tungsten or stainless steel)
An important characteristic of these electrodes is their electrical resistance, which is related to the exposed tip size. Smaller tips have higher resistance and they restrict the area from which potentials can be recorded, thus permitting the isolation of the activity of either a fiber or a cell .large tip and low resistances to pick up the activity from a number of neuronal elements and are of limited use in efforts to identify the functional properties of single nerve cells.
Extracellular recording generally requires an amplifier designed for a high signal-to-noise ratio.
The most important reason for increasing the signal-to-noise ratio is the low intrinsic noise of the device, including ADC and amplifier, and other equipment.
Device Integrity, Principal Design, Body Shield, Amplifier, and ADC Differentials have Intrinsic Noise less than 1 micron.
No effect of high-frequency signals such as mobile on the device.
Due to the integrated design of the device, Since the minimized wiring and communication, as well as the lack of AC power and the use of a USB cable, the device is susceptible to low frequency and high-frequency noise such as mobile phone. At least there is no problem to use eLab near the recording system, but it should not be placed inside the cage or near the device or animal.
Many factors can contribute to noise during extracellular recording experiments; make sure that everything is properly grounded. You should ground everything (including the Faraday cage) to a single point inside of the cage (you can use either copper wires or even better some mesh), and from there you go to the signal ground of your amplifier using a single wire.
At the top of the device, there is a place for connecting the ground wire, Make sure that the connection is good. Ensure that there is a good connection between active wire and electrode.
These are usually much better than a shield fashioned from aluminum foil.
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