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Multiport

Manufactured by Blackrock Microsystems

The MultiPort is a modular, multi-channel interface system designed for a wide range of laboratory applications. It provides simultaneous data acquisition and control capabilities across multiple channels. The core function of the MultiPort is to enable seamless integration of various sensors and devices within a laboratory environment.

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Lab products found in correlation

2 protocols using multiport

1

Ketamine-Induced LFP Changes in Macaque Frontal Cortex

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All procedures in non-human primates reported here followed the guidelines of the National Institutes of Health and were approved by the Massachusetts Institute of Technology’s Committee on Animal Care.
The local field potential (LFP) was recorded from a rhesus macaque (Macaca mulatta) aged 8 years (female, 6.6 kg). Ketamine was administered as a single 20 mg/kg bolus intramuscular dose. Fifteen minutes prior to ketamine administration, glycopyrrolate (0.01 mg/kg) was delivered to reduce salivation and airway secretions. The LFP was recorded from an 8 × 8 iridium-oxide contact microelectrode array (‘Utah array’, MultiPort: 1.0 mm shank length, 400 μm spacing, Blackrock Microsystems, Salt Lake City, UT) implanted in the frontal cortex (vlPFC). The LFP was continuously recorded from 1–5 minutes prior to ketamine injection up to 18–20 minutes following ketamine injection. The LFP recorded at 30 kHz, was low-pass filtered to 250 Hz and then downsampled to 1 kHz. The LFP was bandpass filtered between 0.5–100 Hz using a 2nd order butterworth filter and plotted. The spectrogram was derived using the discrete fourier transform.
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2

Ketamine-Induced LFP Dynamics in Macaque Cortex

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LFPs were recorded in multiple separate recording sessions from two rhesus macaques (Macaca mulatta) aged 14 years (NHP MJ, male, 13.0 kg) and 8 years (NHP LM, female, 6.6 kg). LFP recordings from 4 sessions in NHP MJ and 5 sessions in NHP LM were analyzed in this study. During each recording session, ketamine was administered as a single 20 mg/kg bolus intramuscular dose. This is a putative high dose for sedation and low dose for surgical anesthesia in NHPs [59 –61 ]. Fifteen minutes prior to ketamine administration, glycopyrrolate (0.01 mg/kg) was delivered to reduce salivation and airway secretions. In both NHPs, LFPs were recorded from a 8 × 8 iridium-oxide contact microelectrode array (“Utah array”, MultiPort: 1.0 mm shank length, 400 μm spacing, Blackrock Microsystems, Salt Lake City, UT) implanted in the frontal cortex (vlPFC). LFPs, recorded at 30 kHz, were low-pass filtered to 250 Hz and then downsampled to 1 kHz. LFPs were continuously recorded from 1–5 minutes prior to ketamine injection up to 18–20 minutes following ketamine injection. In the ensuing figures representing neural timeseries data, the time 0 denotes the time-point when the ketamine bolus was administered.
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