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Spike2 data acquisition program

Manufactured by Cambridge Electronic Design
Sourced in United Kingdom

Spike2 is a data acquisition program developed by Cambridge Electronic Design. It is designed to capture and analyze electrophysiological data, such as neural signals and other biological measurements. The program provides a comprehensive set of tools for data acquisition, visualization, and analysis.

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2 protocols using spike2 data acquisition program

1

Abdominal Muscle Activity Monitoring in Mice

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On day 14 post-surgery mice of the SW 1990 and sham groups (SW 1990, n=5; sham, n=5) were anesthetized with isoflurane. An incision was made in the skin of the epigastric region and two silver wires were implanted in the rectus abdominis. The wires were implanted subcutaneously and exteriorized at the back of the neck. The mice were subsequently housed one per cage for 7 days.
Mice were placed individually in the center of an open field arena and the implanted wires were connected to a preamplifier (P5 Series; Grass Technologies, Warwick, RI, USA), electrical activity from the rectus abdominis was relayed to the Spike2 data acquisition program (version 7 for Windows; Cambridge Electronic Design, Cambridge, UK). The processed signal data designated VMRs were exported to Igor Pro software version 6.0 (WaveMetrics, Lake Oswego, OR, USA) for analysis (11 (link),12 (link)), and subtracted from background readings. To normalize VMRs, all VMRs from SW 1990 xenografted mice and sham-operated mice were divided by VMRs from normal mice. For all testing, the mice were habituated for 10 min, and then VMRs were recorded for 30 min. VMRs were recorded 5 times for each mouse, and the mean VMRs were calculated.
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2

Intracellular Recordings in 6-OHDA-Lesioned Rats

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After 3 weeks of recovery, we performed intracellular recordings in 6-OHDA-lesioned and sham rats maintained in narcotized and sedated states with fentanyl (4 µg/kg, i.p.; Janssen-Cilag, Issy-Les-Moulineaux, France), immobilized with gallamine triethiodide (40 mg, i.m., every 2 h; Specia, Paris, France) and artificially ventilated (UMV-03, UNO, Zevenaar, Netherlands). Craniotomies were drilled above M1 (from the interaural line: AP 12.5 mm; ML 3.8 mm) and STN (AP 5.2 mm; ML 2.5 mm). Body temperature was maintained at 36.5 °C with a homeothermic blanket. Intracellular recordings were performed using glass micropipettes filled with 2 M potassium acetate (40–70 MΩ) and the active bridge mode of an Axoclamp 2B amplifier (Molecular Devices, Union City, CA). Data were sampled at 25 kHz via a CED 1401 interface using the Spike2 data acquisition program (Cambridge Electronic Design, Cambridge, UK). The STN ipsilateral to the recorded pyramidal cells was stimulated with a bipolar electrode (SNE-100; Rhodes Medical Instruments, Woodlands Hill, CA) at 8.1 mm depth. Electrical stimulation consisted in either single-shock STN stimulations or 130 Hz DBS (60 µs, 2–4 V), using a stimulus isolator (DS2A, Digitimer, WelWyn Garden City, UK) driven by a pulse stimulator (Pulsemaster A300, WPI, Hitchin, UK).
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