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At least 181 records · Page 10Linked to original sources

Optimization of glass microelectrode properties by response surface methodology.

Glass microelectrodes filled with electrolyte solutions are standard tools for electrophysiological studies. However, for any given application, there are limitations to the properties of the microelectrode, such as impedance and shank length, that can yield satisfactory results. The trial and error approach in pulling electrodes with the desired properties can be time consuming. The use of a response surface procedure which allows the experimenter to change more than one factor at a time and therefore determine the desired puller condition more efficiently is demonstrated. Also, design improvements for the World Precision Instrument, Model PUL-1, Microelectrode puller, used in this study are suggested.

Animals↗

Coincident recording and stimulation of single and multiple neuronal activity with one extracellular microelectrode.

This paper describes how an extracellular microelectrode may be used to stimulate neurons with brief, rectangular pulses and afterwards directly record the resultant activity. Two obstacles are the stimulus artifact lingering in the electrical circuitry and transient tip potentials (TTPs) arising from ion depletion at the electrode-tissue interface. Electronic switching between the stimulus source and the recording amplifier eliminates direct stimulus artifact from the electrical circuitry, although high but acceptable switching artifact remains. TTPs revert with time constants that are prominent in the desired recording (0.1-1 ms) and can reach 50 mV when more than 1 microA passes through a typical electrolyte-filled micropipette (for example 2-4 M omega, filled with 3 M NaCl, and placed in 0.1 M NaCl). They are always negative when cations flow into the tip, they are accompanied by a rise in microelectrode impedance, and they increase as a function of the resting electrode impedance, the duration and amplitude of applied current, and the dilution of the external electrolyte. TTPs were substracted by differential recording and stimulation through matched micropipettes (one in the brain and one in contiguous electrolyte) and in addition were reduced by pressure ejection of electrolyte. Directly elicited spikes (single or multiple) were detected about 0.5 ms after delivery of a rectangular stimulus pulse in the cerebellar cortex of pentobarbital-anesthetized rats. Typically, 3-4 units could be excited by less than 3 microA cathodal currents at any recording site. All-or-nothing properties, thresholds, and refractoriness to a second pulse within 2-4 ms verified the neuronal nature of the recorded signals. Complex wave forms, probably generated synaptically, were also seen. The technique of coincident extracellular recording and stimulation can be used as a universal search stimulus during microelectrode penetrations through the brain and in determining threshold-distance relations for extracellular stimulation. Where cell penetrations are unstable, it might be usefully substituted for intracellular technique in testing a neuron's behavioral or physiological influences or in exploring a cell membrane's response to drugs (in terms of excitability rather than voltage and impedance).

Animals↗

Adaptation of the Reitboeck method of multiple microelectrode recording to the neocortex of the waking monkey.

We adapted to the neocortex of waking monkeys a method for multiple microelectrode recording devised by Reitboeck. A sliding platform allows micropositioning of 7 electrodes independently, in 2 microns steps. Microelectrodes are quartz glass filaments (80 microns o.d.) with central metal cores (30 microns) of tungsten-platinum alloy. Filaments are drawn in a high temperature chamber, and ground to the desired form and tip size. The microdrive is held over the region to be explored, and the microelectrodes passed through 300 microns o.d. guide tubes fixed in implant thimbles of chosen size an and x - y arrangement of tubes, sealed by an O-ring into a small craniotomy opening. A microprocessor controlled recording system provides gain, noise and wave-shape filtering, impedance testing, and differential amplitude discrimination for each channel. Electrode movement is obtained via the microprocessor which displays and updates on the console terminal the electrode depth, impedance, and the channel assignment of each electrode. A second microprocessor based system is used to collect, buffer, and encode in real time all event data, which are transferred whenever convenient to a minicomputer that controls the experiment. Exploratory recordings were made in the posterior parietal, somatic sensory, and motor cortical areas. The system has now been used successfully in a number of investigations.

Action Potentials↗

Neutral carrier sodium ion-selective microelectrode for extracellular studies.

A Na+-selective microelectrode based on a synthetic neutral carrier (ETH 157) is described. The selectivities in respect to K+, Ca2+ and Mg2+ are adequate for extracellular measurements of Na+ activities. Microelectrodes with tip diameters of about 0.7 micron have an electrical resistance of 3 X 10(10) omega and a 90% response time of less than or equal to 3 s. The drift of the potential difference of the Na+-microelectrode cell assembly in aqueous extracellular electrolyte solutions is less than or equal to 0.2 m V/3 h.

Animals↗

Electrodeposition of anchored polypyrrole film on microelectrodes and stimulation of cultured cardiac myocytes.

The electrically conducting polymer polypyrrole (PPy) was electrochemically deposited onto Pt microelectrodes on a polyimide (PI) substrate. Pre-modification of the PI surface with a self-assembled monolayer of octadecyltrichlorosilane-induced anisotropic lateral growth of PPy along the PI surface and enhanced adhesive strength of the PPy film. The lateral growth of PPy film around the electrode anchored the whole film to the substrate. External stimulation of cultured cardiac myocytes was carried out using the PPy-coated microelectrode. The myocytes on the microelectrode substrate were electrically conjugated to form a sheet, and showed synchronized beating upon stimulation. The threshold charge for effective stimulation of a 0.8 cm(2) sheet of myocytes was around 0.2 microC, roughly corresponding to a membrane depolarization of 250 mV.

Animals↗

Sonochemically fabricated microelectrode arrays for biosensors offering widespread applicability: Part I.

A novel and patented procedure is described for the sonochemical fabrication of a new class of microelectrode array based sensor with electrode element populations of up to 2 x 10(5) cm(-2). For some years it has been accepted that microelectrode arrays offer an attractive route for lowering minimum limits of detection and imparting stir (convectional mass transport) independence to sensor responses; despite this no commercial biosensors, to date, have employed microelectrode arrays, largely due to the cost of conventional fabrication routes that have not proved commercially viable for disposable devices. Biosensors formed by our sonochemical approach offer unrivalled sensitivity and impart stir independence to sensor responses. This format lends itself for mass fabrication due to the simplicity and inexpensiveness of the approach; in the first instance impedimetric and amperometric sensors are reported for glucose as model systems. Sensors already developed for ethanol, oxalate and a number of pesticide determinations will be reported in subsequent publications.

Biosensing Techniques↗

Direct electrochemistry of microperoxidase at Pt microelectrodes modified with carbon nanotubes.

Direct electrochemistry of microperoxidase (MP-11) was found at Pt microelectrodes modified with multi-wall carbon nanotubes (MWNTs). The MWNTs used as the immobilization matrix cooperatively promote the bioactivity of MP-11. When MP-11 was immobilized on MWNTs film-modified Pt microelectrodes, a pair of well-defined redox waves was obtained. The resulted stable microelectrode could be used to catalyze the reduction of H2O2 and O2.

Calibration↗

Learning in human neural networks on microelectrode arrays.

This paper describes experiments involving the growth of human neural networks of stem cells on a MEA (microelectrode array) support. The microelectrode arrays (MEAs) are constituted by a glass support in which a set of tungsten electrodes are inserted. The artificial neural network (ANN) paradigm was used by stimulating the neurons in parallel with digital patterns distributed on eight channels, then by analyzing a parallel multichannel output. In particular, the microelectrodes were connected following two different architectures, one inspired by the Kohonen's SOM, the other by the Hopfield network. The output signals have been analyzed in order to evaluate the possibility of organized reactions by the natural neurons.f The results show that the network of human neurons reacts selectively to the subministered digital signals, i.e., it produces similar output signals referred to identical or similar patterns, and clearly differentiates the outputs coming from different stimulations. Analyses performed with a special artificial neural network called ITSOM show the possibility to codify the neural responses to different patterns, thus to interpret the signals coming from the network of biological neurons, assigning a code to each output. It is straightforward to verify that identical codes are generated by the neural reactions to similar patterns. Further experiments are to be designed that improve the hybrid neural networks' capabilities and to test the possibility of utilizing the organized answers of the neurons in several ways.

Embryonic Stem Cells↗

Model-based analysis of cortical recording with silicon microelectrodes.

OBJECTIVE: The purpose of this study was to use computational modeling to better understand factors that impact neural recordings with silicon microelectrodes used in brain-machine interfaces. METHODS: A non-linear cable model of a layer V pyramidal cell was coupled with a finite-element electric field model with explicit representation of the microelectrode. The model system enabled analysis of extracellular neural recordings as a function of the electrode contact size, neuron position, edema, and chronic encapsulation. RESULTS: The model predicted spike waveforms and amplitudes that were consistent with experimental recordings. Small (< 1000 microm2) and large (10 k microm2) electrode contacts had similar volumes of recording sensitivity, but small contacts exhibited higher signal amplitudes (approximately 50%) when neurons were in close proximity (50 microm) to the electrode. The model results support the notion that acute edema causes a signal decrease ( approximately 24%), and certain encapsulation conditions can result in a signal increase (approximately 17%), a mechanism that may contribute to signal increases observed experimentally in chronic recordings. CONCLUSIONS: Optimal electrode design is application-dependent. Small and large contact sizes have contrasting recording properties that can be exploited in the design process. In addition, the presence of local electrical inhomogeneities (encapsulation, edema, coatings) around the electrode shank can substantially influence neural recordings and requires further theoretical and experimental investigation. SIGNIFICANCE: Thought-controlled devices using cortical command signals have exciting therapeutic potential for persons with neurological deficit. The results of this study provide the foundation for refining and optimizing microelectrode design for human brain-machine interfaces.

Algorithms↗

Painless electroporation with a new needle-free microelectrode array to enhance transdermal drug delivery.

A microelectrode array was designed to minimize the pain sensation of electroporation for enhancing transdermal drug delivery. The influence of the size of the electrode-skin contact area and of the distance between electrodes on the pain sensation was tested on human volunteers. The pain level decreased with the dimension of electrode-skin contact area and with inter-electrode distance. When both reached about 0.5 mm, the pain level was not perceptible even at the threshold of transdermal electroporation level of sixty electric pulses at 150 V, 1 ms at 1-10 Hz. An array of 11 x 11 alternately connected electrodes with 0.6 x 0.6 mm dimension was fabricated. The electric thresholds for effective drug delivery, using toluidine blue O as a marker on mouse skin, was found to be the same for microelectrode arrays as for larger electrodes and wider inter-electrode distances. In vivo transdermal electroporation using microelectrode array with 180 pulses of 150 V, 0.2 ms at 1 Hz, followed by 30 min methotrexate (MTX) occlusion increased more than 4 fold the systemic MTX level in mice. The results demonstrated the potential of painless delivery of significant amounts of chemotherapeutic agents through skin with the new electrode arrays in a clinical setting.

Administration, Cutaneous↗

Simultaneous real-time amperometric measurement of catecholamines and serotonin at carbon fibre 'dident' microelectrodes.

Amperometry allows real-time measurement of in vivo electrochemical signals, albeit with no capacity to identify the constituents of the signal. In the present study, differential amperometry was used to monitor catecholamine and serotonin (5-HT) simultaneously at the same location. 'Dident' carbon fibre microelectrodes (microelectrodes with two working electrodes in a single assembly) were constructed and coated with Nafion to prevent poisoning on contact with brain tissue. One electrode (channel A) was held at +200 mV versus Ag/AgCl to monitor catecholamines selectively. This potential is too low to oxidise 5-HT. The second electrode (channel B), recording faradaic current at +500 mV versus Ag/AgCl, measured the sum of catecholamine and 5-HT oxidation. The 5-HT current component was the difference of channel B minus channel A. With appropriate balancing of the two channels, it is possible to record catecholamines and 5-HT simultaneously at the same dident microelectrode. Examples of measurements in striatum, cortex and locus coeruleus are shown.

Animals↗

The interpretation of current-voltage relations recorded from a spherical cell with a single microelectrode.

An analysis is presented of the displacement of potential recorded when one microelectrode is used both to apply current to and record potential from a spherical cell. There are three significant components of the displacement in potential: a component produced inside the microelectrode, a time-independent component representing the spatially nonuniform flow of current in the immediate vicinity of the microelectrode, and a time-dependent spatially uniform component representing the average potential across the cell membrane. The second component describes changes in the potential across the cell membrane as well as potential drops in the interior of the cell, the importance of each factor being dependent on the location of the electrode. Simple expressions, derived by a theoretical treatment, are given for each component of potential. The implications for the interpretation of experimental results determined with the "single-electrode bridge" technique are discussed and an optimal balancing procedure is suggested.

Cell Membrane↗

Ovarian function after incision of the ovary by scalpel, CO2 laser, and microelectrode.

OBJECTIVE: The objective was to evaluate the relative effects of a standardized surgical incision performed with scalpel, CO2 laser, or microelectrode on ovarian tissue and function. DESIGN: Thirty sexually mature female rabbits were randomly assigned to one of three surgical groups. The injury consisted of a linear incision along the long axis of both ovaries, from the cortex to the hilum, followed by immediate unilateral oophorectomy for evaluation of the acute tissue damage. The opposite ovary was left in situ to evaluate subsequent healing, steroidogenesis, folliculogenesis, and ovulation. RESULTS: Minimal damage was observed after surgery with either laser or microelectrode. The ovarian stroma and follicles adjacent to the surgical site appeared normal both immediately and 15 days after all surgeries. Steroidogenesis, folliculogenesis, and luteinization were similar among the three groups. The number of ovulated oocytes after human chorionic gonadotropin was significantly reduced after scalpel and laser surgery compared with microelectrode (P less than 0.05). The former groups appeared to have a higher incidence of unruptured luteinized follicles with untrapped oocytes, which were often covered with a cellular fibrous membrane. CONCLUSIONS: These findings suggest that surgical trauma is well tolerated by the ovaries and does not impair subsequent ovarian function. However, rupture of the preovulatory follicle and its release of the oocyte may be influenced by the presence of ovarian adhesions and/or surgical trauma.

Analysis of Variance↗

Dependence of dopamine calibration factors on media Ca2+ and Mg2+ at carbon-fiber microelectrodes used with fast-scan cyclic voltammetry.

Carbon-fiber microelectrodes and voltammetric methods have been used extensively for the detection of dopamine in brain tissue in vivo and in vitro. Voltammetric microelectrodes are often calibrated in non-physiological media, like phosphate-buffered saline, rather than in oxygenated physiological media. Here, we determined dopamine calibration factors (nA microM-1) in several defined solutions for two types of carbon-fiber electrode used with fast-scan cyclic voltammetry. For both electrode types, dopamine calibration factors, and thus electrode sensitivities, were 2-3-fold higher in phosphate- or HEPES-buffered saline than in a bicarbonate-based artificial CSF (ACSF) that reflected that normal ionic composition of brain extracellular fluid. Removal of Ca2+ and Mg2+ from ACSF eliminated this difference. Because extracellular Ca2+ concentration ([Ca2+]o) can fall under stimulation conditions used to elicit dopamine release, we also evaluated the size of stimulated [Ca2+]o shifts in guinea pig midbrain slices using ion-selective microelectrodes. The [Ca2+]o decreases were less than 100 microM, which was well below the mM decreases observed to alter DA sensitivity. Consequently, calibration data obtained in normal physiological solutions should be valid under conditions of mild stimulation. Moreover, calibration in divalent cation-free media will cause calculated DA levels to be underestimated and should be avoided, unless appropriate for a given experimental paradigm.

Animals↗

Quantitation of in vivo measurements with carbon fiber microelectrodes.

Fast-scan cyclic voltammetry (FSCV) at carbon fiber disk microelectrodes and quantitative microdialysis were used to measure striatal concentration changes of N-acetyl-p-aminophenol (APAP, acetaminophen) following an intraperitoneal injection of 75 mg/kg APAP in rats. The goal of this work was to determine which in vitro calibration procedure, precalibration or postcalibration, gave the most accurate results when using carbon fiber microelectrodes in vivo. Voltammetric detection of APAP in vivo was complicated with normal electrodes by interference from pH changes. An electrode treatment was used to minimize electrode sensitivity to pH and this allowed successful APAP detection. In vitro calibrations of the treated carbon fiber disk microelectrodes before and after the in vivo experiment were used to calculate APAP concentration changes measured in vivo and compared to microdialysis results. The maximal striatal APAP concentration determined by microdialysis, adjusted for in vitro recovery, was 23.1 microM. The electrochemical results were approximately two times greater (postcalibration) or smaller (precalibration) than the microdialysis result.

Acetaminophen↗

Phase correlation among rhythms present at different frequencies: spectral methods, application to microelectrode recordings from visual cortex and functional implications.

In classical EEG analysis rhythms with different frequencies occurring at separable regions and states of the brain are analysed. Rhythms in different frequency bands have often been assumed to be independent and their occurrence was interpreted as a sign of different functional operations. Independence has scarcely been proved because of conceptual and computational difficulties. It is, on the other hand, probable that different rhythmic brain processes are coupled because of the broad recurrent connectivity among brain structures. We, therefore, set out to find interactions among rhythmic signals at different frequencies. We were particularly interested in interactions between lower frequency bands and gamma-activities (30-90 Hz), because the latter have been analysed in our laboratory in great detail and had properties suggesting their involvement in perceptual feature linking. Fast oscillations occurred synchronized in a stimulus-specific way in the visual cortex of cat and monkey. Their presence was often accompanied by lower frequency components at considerable power. Such multiple spectral peaks are known from many cortical and subcortical structures. Despite their well known occurrence, coupling among different frequencies has not been established, apart from harmonic components. For the present investigation we extended existing analytical tools to detect non-linear correlations among signal pairs at any frequency (including incommensurate ones). These methods were applied to multiple microelectrode recordings from visual cortical areas 17 and 18 of anesthetized cats and V1 of awake monkeys. In particular, we assessed non-linear correlations by means of higher order spectral analysis of multi-unit spike activities (MUA) and local slow wave field potentials (LFP, 1-120 Hz) recorded with microelectrodes. Non-linear correlations among signal components at different frequencies were investigated in the following steps. First, the frequency content of short (approximately 250 ms) sliding window signal epochs was analyzed for simultaneously occurring rhythms of significant power at different frequencies. This was done by a newly developed method derived from the trispectrum using separate averaging of the products of short-epoch power spectra for any possible combination of frequency pairs. Second, non-linear (quadratic) phase coupling between different frequencies was assessed by the methods of bispectrum and bicoherence. We found phase correlations at different frequencies in the visual cortex of the cat and monkey. These couplings were significant in about 60% of the investigated MUA and LFP recordings, including several cases of coupling among incommensurate (i.e. non-harmonic) frequencies. Significant phase correlations were present: (1) within the gamma-frequency range; (2) between gamma- and low frequency ranges (1-30 Hz, including alpha- and beta-rhythms); and (3) within the low frequency range. Phase correlations depended, in most cases, on specific visual stimulation. We discuss the possible functional significance of phase correlations among high and low frequencies by including proposals from previous work about potential roles of single-frequency rhythms of the EEG. Our suggestions include: (1) visual feature linking across different temporal and spatial scales provided by coherent oscillations at high and low frequencies; (2) linking of visual cortical representations (high frequencies) to subcortical centers (low frequencies) like the thalamus and hippocampus; and (3) temporal segmentation of the sustained stream of incoming visual information into separate frames at different temporal resolutions in order to prevent perceptual smearing due to shifting retinal images. These proposals are, at present, merely speculative. However, they can, in principle, be proved by microelectrode recordings from trained behaving animals.

Animals↗

Tapered tungsten fine-wire microelectrode for chronic single unit recording.

A new fine-wire microelectrode made from tungsten wire is described. The electrode design provides for strength as well as flexibility due to the stiffness of tungsten wire and a gradually tapering profile. Unlike previously-used fine wire electrodes, microelectrodes of the new design can be singly implanted under electrophysiological control into deep brain structures of larger animals such as cats. The flexibility of the fine diameter terminal portion of the microelectrode permits stable recording from caudal brain stem single units during vigorous behavioral activity.

Animals↗