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Window discriminator

Manufactured by World Precision Instruments
Sourced in United States

The Window Discriminator is a laboratory instrument used to analyze and process electrical signals. It functions by isolating a specific range of signal amplitudes, known as the 'window', from an input signal. This allows the user to selectively monitor or process signals within the defined window while ignoring signals outside of that range.

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2 protocols using window discriminator

1

Extracellular Recording of Visual Responses

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For confirming optical imaging results, single- and multi-unit responses to visual stimulation were recorded extracellularly to define the minimum spatial response field (RF), preferred orientation and direction of motion and ocularity using hand-held stimulation at random locations within the mapped area. To this end, glass electrodes (8–10 μm of tip diameter) were filled with 0.5–1 M NaCl (~5 MΩ). The pipettes were advanced perpendicularly to the cortical surface using a manual micro-drive fitted with a digital depth meter (10 μm accuracy, Sylvac SA, Crissier, Switzerland). Along each electrode track single and multi-units were recorded at several depths (300–2000 µm) from the cortical surface. To stabilize recordings, after advancing the electrode into the cortex, the chamber was filled with 3 % agar and covered with low-melting point paraffin (~43 °C, Merck, Darmstadt, Germany). Signals were amplified by AxoClamp-2A (Axon Instruments, Foster City, Canada) and filtered (0.3–10 kHz). Spike activity was monitored using a window discriminator (World Precision Instruments Inc., Sarasota, FL, USA) coupled to an audio monitor. The recorded units had large minimum discharge field (average: 9.5° ± 6.8° of diagonal length, N = 71 from six animals). In some cases RF had large size (maximum, 51°), especially at depths corresponding to layers 5/6.
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2

Extracellular Recordings from mPFC and CeLC

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Extracellular recordings were made from single neurons in the infralimbic part of the mPFC and in the laterocapsular division of the central nucleus of the amygdala (CeLC) with glass-insulated carbon filament electrodes (4–6 MΩ) using the following stereotaxic coordinates (Paxinos and Watson 1998 ): mPFC, 3.0–3.2 mm rostral to bregma, 0.5–1.0 mm lateral to midline, depth 4.5–6.0 mm; CeLC, 2.1–2.8 mm caudal to bregma; 3.8–4.5 mm lateral to midline; depth 7–9 mm. Recordings were made in the right hemisphere because of previous evidence for pain-related lateralization (Carrasquillo and Gereau 2008 (link); Ji and Neugebauer 2009 (link); Goncalves and Dickenson 2012 (link)). Recorded signals were amplified, band-pass filtered (300 Hz – 3 kHz), displayed on analog and digital storage oscilloscopes, fed into a window discriminator (World Precision Instruments), digitized (1401 plus interface, Cambridge Electronic Design), and recorded on a personal computer (PC) using Spike2 software (version 4; Cambridge Electronic Design) to create peristimulus rate histograms online and to store and analyze digital records of single-unit activity offline.
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