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Mp100a ce

Manufactured by Biopac
Sourced in United States

The MP100A-CE is a multi-purpose data acquisition system designed for laboratory research. It features high-resolution analog-to-digital conversion and provides connectivity for a wide range of sensors and transducers. The device allows for the monitoring and recording of physiological signals and other experimental data.

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6 protocols using mp100a ce

1

Gastric Compliance Measurement Protocol

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Ex vivo gastric compliance was determined according to previously described approaches11 (link),43 (link), 44 (link), 45 (link) with minor modifications. Briefly, intact stomachs were excised, placed in a heated water bath, and connected via the esophagus to a syringe pump (Model 975 Compact Infusion Pump; Harvard Apparatus, Ltd, Cambridge, MA) and a pressure transducer (MP100A-CE; BIOPAC Systems, Inc, Goleta, CA; amplifier: Transbridge 4M; World Precision Instruments, Sarasota, FL) through the pylorus. The stomachs then were filled with Krebs solution46 (link) (37°C) to 1 mL at a rate of 100 μL/min for 10 minutes while recording pressure using ClampFit 10.7.0 software (Molecular Devices, LLC, San Jose, CA).
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2

Arterial Pressure Monitoring in Mice

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Mice were anesthetized with intramuscular injection of ketamine (4.5 mg/kg) + xylazine (0.2 mg/kg) 24 h before the experimental protocol. Polyethylene catheters (PE-10, 0.28 mm ID, 0.61 mm OD, Biocorp Australia, Huntingdale, Victoria, Australia) filled with heparinized saline solution were inserted into the femoral artery for direct measurements of arterial pressure (AP). The body temperature was maintained at 37°C using a heating pad until the full recovery of animals, which were then placed in individual cages and kept in the experimental room for environmental adaptation. Conscious arterial pressure recording was performed following the protocol described previously.13 (link)One day after the surgical procedure, a catheter was connected to a strain-gauge transducer coupled to a computer-based data acquisition system (model MP100 A-CE, Biopac Systems, CA, USA), and pulsatile arterial pressure (PAP) was continuously recorded. Mean arterial pressure (MAP) and HR were simultaneously calculated from the PAP with the software AcqKnowledge (version 3.5.3 for Windows) and continuously acquired. The files were stored and data was analyzed later.
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3

Surgical Implantation of Arterial Catheter and Body Temperature Logger in Rats

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One day before the experiment, the rats received an intraperitoneal injection of ketamine and xylazine for another surgery procedure. This surgery consisted of insertion of a catheter [PE-10 connected to PE-50 (Clay Adams, Parsippany, NJ, USA)] into the abdominal aorta through the femoral artery, to allow pulsatile arterial pressure (PAP) and blood gases measurements. The catheter was externalized in the animal’s dorse close to the neck region. On the experiment day, the catheter was connected to the pressure transducer (TSD 104A, Biopac systems), the signal was amplified (DA 100C, Biopac systems) and digitized on a computer equipped with data acquisition software (MP100ACE; Biopac Systems). Systolic (SAP) and diastolic (DAP) arterial pressure, mean arterial pressure (MAP) and heart rate (HR) were quantified from the PAP recording using the LabChart program (Power-Lab System, ADInstruments®/Chart Software, version 7.3, Sydney, Australia).
For body temperature (TB) measurements, a temperature datalogger (SubCue Dataloggers, Calgary, Canada) was inserted into the abdominal cavity through a midline laparotomy, at the same surgical procedure. The datalogger was programmed to acquire data every 5 min.
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4

Simultaneous Cardiovascular and Ventilation Monitoring in Rats

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In a subgroup of animals, cardiovascular parameters were measured simultaneously to ventilation. To this end, one day before the experiments, the adult rats were anesthetized with ketamine (80 mg kg−1, ip) and xylazine (7 mg kg−1, ip) and a polyethylene catheter (PE-10 connected to PE-50; Clay Adams, Parsippany, NJ, USA) was inserted into the abdominal aorta through the femoral artery for measurements of pulsatile arterial pressure (PAP). The arterial catheter was then tunneled subcutaneously and exteriorized at the animal dorsum. After that, a temperature recorder was also implanted into the abdominal cavity, as previously described. After surgery, animals were treated with antibiotic (enrofloxacin, 10 mg kg−1, im) and analgesic (flunixin meglumine, 2.5 mg kg−1, sc) and monitored until recovered from anesthesia. On the next day, when the animals were recovered from surgical procedures, the arterial catheter was connected to a pressure transducer (TSD 104A; Biopac systems) and to an amplifier (DA 100C; Biopac systems) for the monitoring of PAP in unanesthetized conditions. PAP was recorded using a data acquisition system (MP100 ACE; Biopac systems) at a sampling rate of 1 kHz. Mean arterial pressure (MAP) and heart rate (HR) were derived from PAP signals (Acqknowledge, v 4.2.3, Biopac Systems).
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5

Gastric Slow Wave Monitoring in Diabetes

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Intrinsic gastric slow waves were recorded from the implanted distal serosal electrodes on the greater curvature using a multichannel recorder (Acknowledge 3.7.1, MP100A-CE, Biopac System, Santa Barbara, CA, USA) in all groups before the injection of STZ or vehicle. Before recording, all rats should be quiet for 30 mins; the signals were displayed on a computer monitor and saved on hard disk. The definition of normal gastric slow wave frequency range was 4–6 cycles/min [17 (link)]; it was defined as dysrhythmia if the recording outcome was not in this range. Gastric slow waves were recorded again at 7–14-day diabetes and 56–63-day diabetes before and after stimulation, The age-matched control groups were also recorded again at the same time with diabetic groups.
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6

Gastric Slow Wave Monitoring in Diabetes

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Intrinsic gastric slow waves were recorded from the implanted distal serosal electrodes on the greater curvature using a multichannel recorder (Acknowledge 3.7.1, MP100A-CE, Biopac System, Santa Barbara, CA, USA) in all groups before the injection of STZ or vehicle. Before recording, all rats should be quiet for 30 mins; the signals were displayed on a computer monitor and saved on hard disk. The definition of normal gastric slow wave frequency range was 4–6 cycles/min [17 (link)]; it was defined as dysrhythmia if the recording outcome was not in this range. Gastric slow waves were recorded again at 7–14-day diabetes and 56–63-day diabetes before and after stimulation, The age-matched control groups were also recorded again at the same time with diabetic groups.
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