Extracellular recordings of pharyngeal nerves (AN, MN and PaN) and intracellular recordings of the CDM were performed as previously described in [20 (link)]. In brief, for extracellular recordings of pharyngeal nerves, each nerve was electrically isolated using a petroleum jelly pool surrounding the nerve placed on a piece of Parafilm. Silver wire electrodes were used for measuring with differential recordings motor output of the deafferented nerve. A preamplifier (Model MA103, Ansgar Büschges group electronics lab) connected to a four-channel amplifier/signal conditioner (Model MA 102, Ansgar Büschges group electronics lab) was used. All recorded signals were amplified (amplification factor: 5000) and filtered (bandpass: 0.1–3 kHz). Recordings were sampled at 20 kHz. Data was acquired with Micro3 1401 or Power 1401 mk2 A/D board (Cambridge Electronic Design) and Spike2 software (Cambridge ElectronicDesign). Intracellular muscle recordings of the CDM were recorded using glass microelectrodes filled with 3 M KCl solution (tip resistance: 20–30 MΩ) connected to an intracellular amplifier (BRAMP-01R, npi electronic GmbH). All recordings were digitally sampled by a Power 1401 mk2 A/D board (Cambridge Electronic Design) at 20 kHz. Data was acquired with Spike2 software (Cambridge Electronic Design).
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