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EEG & ECoG

ADInstruments provide various solutions for the recording of electroencephalograph (EEG) and electrocorticograph (ECoG) signals
The cerebral cortex contains large numbers of neurons. Activity of these neurons is to some extent synchronized in regular firing rhythms (‘brain waves’). Electrodes placed in pairs on the scalp can pick up variations in electrical potential that derive from this underlying cortical activity. The electroencephalogram (EEG) and electrocorticogram (ECoG) are recordings of the electrical activity of the brain that occurs between pairs of electrodes in contact with the scalp and represents the sum of a large amount of underlying neural activity.

These EEG signals are affected by the state of arousal of the cerebral cortex, show characteristic changes in different stages of sleep and can be used in the diagnosis of several diseases.

EEG/ECoG recording is technically difficult, mainly because of the small size of the voltage signals (typically 50 µV peak-to-peak). The signals are small because the recording electrodes are separated from the brain’s surface by the scalp, the skull and a layer of cerebrospinal fluid. A specially designed amplifier, such as the Bio Amplifier front-end, is essential. It is also important to use electrodes made of the right material, and to connect them properly. Even with these precautions, recordings may be spoiled by a range of unwanted interfering influences, known as ‘artifacts’.

Simple EEG activity can be recorded with two electrodes: a frontal electrode on the forehead, and an occipital electrode on the scalp at the back of the head and a third (ground or earth) electrode is also attached, to reduce electrical interference.

A simple setup to record of an EEG signal.

Single or dual channel recordings may be useful for the simple recording and identification of alpha activity in conscious subjects or specific waveforms representative of the sleeping subject, whilst multiple channel EEG is used for the identification of neurological functioning and/or abnormalities. Therefore, in clinical EEG, it is usual to record many channels of activity from multiple recording electrodes placed in an array over the head using EEG caps.


Multiple channel EEG recorded using an EEG cap.

ADInstruments EEG Electro-Cap systems includes a cap for EEG, electrode adapter (suits the MLA2540 5-Lead Shielded Bio Amp Cable), body harness, quick insert electrode, ear electrodes (one pair), disposable sponge disks (100), needle/syringe kit, electro-gel (16 oz), head measuring tape, ivory cleaning liquid and a manual. The system is suitable for use with the ADInstruments ML135 Dual Bio Amp, ML138 Octal Bio Amp or the GT201 16 Channel Bio Amp except the ML136 Animal Bio Amp.

To ensure high quality, low noise recordings of EEG/ECoG good subject preparation and application techniques are essential. Excessively high skin impedances (due to inadequate preparation) will cause signal artifacts that can interfere with EEG/ECoG recordings. Therefore, impedances of all electrodes should be checked with a suitable device (i.e. CheckTrode MkIII from UFI) to ensure they are below 10 kOhm.

The EEG signal can be separated and classified into a few distinct waveforms of different frequencies. These waveforms include the Alpha, Beta, Delta, Theta, Gamma and SMR (Sensorimotor Rhythm) waves.


Note: When recording EEG/ECoG it is important to differentiate between "referential" and "differential" recording systems. A "referential system" measures the biopotential of a single electrode site in relation to an electrophysiologically silent electrode (reference). An absolute biopotential is then obtained for each active electrode and the difference between any pair of active electrodes is software-derived at a later stage. In contrast, the ADInstrument's "differential" Bio Amps directly measure the difference between a pair of electrodes and the absolute biopotential at each single electrode site is not provided. The desired channels are determined by hardware electrode connections and cannot be interchanged with software controls. The absolute potential of a single electrode may be obtained with ADInstrument's Bio Amps by linking the negative inputs of all channel connections.

 
LabChart
LabChart software (for Windows and Macintosh) combines the familiar simplicity of a traditional strip chart recorder with the powerful analysis features of a digital acquisition system. LabChart software and a PowerLab data acquisition unit provide data integrity, easy selection of hardware settings, powerful online and offline analysis, procedure automation, seamless extraction of experimental data and flexible display options. Acquisition and analysis capabilities can be further increased with LabChart Extensions and LabChart Modules. LabChart Modules are available as part of LabChart Pro and LabChart Extensions are free for download from the website for existing LabChart users.

In addition, LabChart software can:
  • Rectify and integrate the raw EEG signal and display the results on a separate channel.
  • Calculate and display the RMS power content of the signal.
  • Display the power spectrum (FFT) of a selected region of data using Spectrum command
  • Include a digital filter that allows the user to record at the highest sampling rate and apply filtering online or offline.
  • Apply filtering options such as low-pass, high-pass, notch, narrow band-pass, band-pass and band-stop. This is very useful for EEG recording and analysis because specific waveform frequencies such as alpha, delta and theta etc can be easily identified.


Scope
Scope software, supplied with PowerLab systems, provides powerful display, recording and analysis features to transform your computer into a two-channel storage oscilloscope, XY plotter or Power Spectrum (FFT) analyser. Scope is used commonly to measure any high-frequency signal that is time-locked to a stimulus such as action potentials and evoked responses. For analyzing Evoked EEG Potentials, the Scope Software is recommended because it provides signal averaging functions that are necessary to extract the evoked response from background noise.

This software:
  • Provides the ability to record, display and analyze any high frequency signal that is time-locked to a stimulus
  • Synchronizes sweeps with recorded or built-in stimulation patterns
  • Provides a range of real-time and offline analysis features
  • Generates stimuli of differing intensities and waveform structures (i.e. single-pulse, multiple pulse, simple ramps) and controls an external stimulator using the analog output on the front of the PowerLab.

GLP and 21 CFR Part 11
For those researchers working within a laboratory requiring GLP and 21 CFR Part 11 compliance the GLP Client and GLP Server are available for use with LabChart (Windows only) and PowerLab data acquisition systems. For more information, visit the Good Laboratory Practice application page or contact your nearest ADInstruments representative.

Bio Amplifiers

The EEG biopotentials are typically very small in amplitude (µV). Therefore accurate recording, display and analysis of an EEG requires a suitable bioamplifier. ADInstruments offer a range of Bio Amplifiers that when connected to a PowerLab data acquisition unit are certified safe for use with humans or animals. These bioamplifiers are fully software-controlled using LabChart or Scope. The following ADInstruments' biological amplifiers are fully isolated for connection to human or animal subjects:

Human EEG

The following ADInstruments' biological amplifiers are independently certified to comply with international safety standards and are fully isolated for connection to human subjects:

ML132 Bio Amp
ML135 Dual Bio Amp
ML408 Dual Bio Amp/Stimulator

The Bio Amp, Dual Bio Amp and Dual Bio Amp/Stimulator are manufactured for use with PowerLab data acquisition systems and are fully software-controlled by LabChart or Scope. These Bio Amps cannot be used for recording 3 or more biopotentials on a single subject; however, they may be used for multiple subjects that have separate grounding leads. For recording more than 3 biopotentials from a single subject see below:

Multiple-Channel EEG/ECoG Recordings

ADInstruments also provides multiple channel bioamplifiers that connect directly to PowerLab data acquisition systems. These units are also fully-isolated, and independently certified, for connection to human subjects.

ML138 Octal Bio Amp
  • A differential amplifier that consists of eight electrically isolated differential input AC amplifiers
  • A shared ground connection across all eight inputs.
  • Supplied with two packets of MLA0310 Lead Wires (1.8 m, 10 snap on)

GT201/F 16 Channel Bio Amp Animal EEG
The following ADInstruments' biological amplifiers for use with animals (i.e. pithed toad, or anaesthetized rat/mouse) only:

ML136 Animal Bio Amp

Multiple channel EEG may be recorded using the ML138 Octal Bio Amp or GT201/F 16 Channel Bio Amps that connect directly to the MLA1505 Lead Wires that terminate in alligator clips or the MLA1203 Needle Electrodes.

Accessories

Bio Amp cables:

Leads compatible with both shielded (MLA2340 & MLA2540) and unshielded (MLA1340 & MLA1540) cables:

Leads compatible with shielded cables (MLA2340 & MLA2540) only:

Leads that directly connect to the Dual Bio Amp

Leads that directly connect to the Animal Bio Amp

Electrodes:

Consummables:

EEG Caps (Not suitable for use with the ML136 Animal Bio Amp):

Electroencephalographic activation by fluoxetine in rats: role of 5-HT1A receptors and enhancement of concurrent acetylcholinesterase inhibitor treatment
H C Dringenberg and P Diavolitsis, Neuropharmacology, 154-161, 2002
In adult rats (400–500 g) a chronic neocortical recording electrode (Teflon coated wire, 125 µm diameter) was implanted on the surface of the sensory-motor cortex (AP-1.0 from bregma; L+2.0 from midline). Additional reference and ground connections (jewelry screw attached to a miniature female connector) were placed in the bone over the cerebellum. All electrodes were held in place by dental cement built around the electrodes and anchor screws placed in the bone around the electrodes. Neocortical EEG activity was recorded in awake, freely moving rats placed in a Plexiglas cage. Lightweight cables were connected to the implanted electrodes and cortical activity was recorded differentially against the cerebellar connection. The neocortical signal was amplified using Grass P511 amplifiers (half-amplitude set at 0.3 Hz and 10 kHz). Initial filtering (low pass filter set at 47 Hz) and digitizing (100 Hz) of the raw EEG signal was carried out by a PowerLab/4s system for the Macintosh (ADInstruments, Milford, MA). The digitized EEG signal was displayed on one EEG channel. Further, it was passed through additional software-controlled band-pass filters to separate and display the following frequency bands on four additional channels: delta: 0.5–4 Hz; theta: 4–8 Hz; alpha: 8–12 Hz; beta: 12–30 Hz.
Influence of a dietary n-3 fatty acid deficiency on the cerebral catecholamine contents, EEG and learning ability in rat
T Takeuchi; Y Fukumoto and E Harada, Behavioural Brain Research, 193-203, 2002
N newborn rats EEG electrodes were implanted chronically. Recording electrodes, Teflon-coated multi strand stainless-steel wire (7935, A-M Systems Inc, USA), were bilaterally implanted extra-durally over the frontal and occipital areas. Ground and reference electrodes were also implanted over the frontal sinus and at an intermediate position between the frontal sinus and frontal bone, respectively. Each electrode was connected to a socket, and fixed on the surface of the skull with dental resin…….. Monopolar EEG recordings were made from bilateral occipital areas, using a polygraph (1A74, NEC San-ei, Tokyo) with time constant at 0.3 s and high frequency 60 Hz filter. The EEG signals were recorded on paper (3 cm/s) for visual analysis and stored on magnetic tape (MR-10, TEAC, Tokyo) which enabled off-line computer analysis……….. On the basis of visual analysis, parts of the EEG recording lasting 1 min each, were selected for computer (MacLab, AD Instruments, USA) analysis. Prior to spectral analysis, each digitized epoch of EEG was filtered by application of a Hanning window cosine transform. The EEG signal was sampled at a rate of 128 Hz and then digitally low-pass filtered at 60 Hz. Frequency analyses were carried out by means of a fast Fourier transformation. The EEG was sampled and transformed directly in epochs of 2 s. Each digitized 2 s epoch of EEG thereby yielded a power spectrum having a Fourier resolution of 0.5 Hz over a frequency range of 1–30 Hz. The average power spectrum of 30 of these epochs for each 1.5 min EEG sample was plotted in the range from 1 to 30 Hz with a resolution of 0.5 Hz.

The material on this page is provided in good faith and believed accurate at the time of writing. No responsibility will be taken, or liability accepted, for damages arising from the use of information herein. Readers are urged to check with respective manufacturers the accuracy of all product related information.


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