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Bridge amplifier

Manufactured by ADInstruments
Sourced in United States

The Bridge Amplifier is a versatile lab equipment device designed to amplify and condition various types of electrical signals. It features multiple input channels and provides adjustable gain settings to suit a range of input signal levels. The Bridge Amplifier is a core component in many data acquisition and measurement setups, enabling the precise capture and analysis of electrical signals.

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4 protocols using bridge amplifier

1

Langendorff Perfusion of Rabbit Hearts

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Adult New Zealand white rabbits, 3–4 ​kg, were anesthetized with 50 ​mg/kg i. p. pentobarbital sodium and anticoagulated with 1000 U/kg i. p. heparin. Hearts were rapidly removed and retrogradely perfused in a Langendorff apparatus (see Figure S1A) with a constant perfusion pressure of 60–65 ​mmHg at 37 ​°C with oxygenated Tyrode's solution containing (mM): NaCl 136, KCl 5.4, CaCl2 1.8, MgCl2 1.0, NaH2PO4 0.33, HEPES 10, glucose 10, pH adjusted to 7.2 with NaOH. The perfusion pressure was monitored using an in-line physiological pressure transducer connected to the Bridge Amplifier (AD Instruments Inc., Colorado Springs, CO). ECGs were recorded using the Animal Bio Amplifier (AD Instruments Inc.) from perfusion start through to the experiment end using two wire leads, one connected to the right atrium and the other connected to the right ventricular apex. A suture was placed around the LAA and tightened down around the orifice. Thermogel was then injected into the LAA.
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2

Cardiovascular Effects of β-Adrenergic Drugs

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To confirm the functional presence of orally administered β2 agonist clenbuterol along with β1 antagonist atenolol and β3 antagonist SR59230A we measured mean systemic arterial blood pressures and heart rates by attaching an externalized arterial catheter to a physiological pressure transducer that was connected to a PowerLab 8/35 with a bridge amplifier (ADInstruments Inc.). Pressures and heart rates were determined on three separate days and analysed with LabChart software. Pressure transducers were calibrated with a mercury column manometer. Lambs were placed in the sling and physiological pressure transducers were set to the height of the heart. After an acclimation period of at least 10 min, data were recorded for a minimum of eight consecutive minutes under basal conditions. At 29 ± 1 days of age, lambs were challenged with the ADRβ1 agonist dobutamine HCl (12.5 mg ml−1; Hospira, Inc., Lake Forest, IL, USA) to evaluate cardiac responsiveness (Stephens et al. 2011). Data were recorded for 15 min during both basal and dobutamine‐stimulated (10 µg min−1 kg−1) periods.
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3

Telemetric Monitoring of Conscious Blood Pressure

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Conscious BP recording was carried out with a radiotelemetry system, as described previously [21 (link)]. Ten days before making a two-kidney, one-clip (2K1C) model or sham operation, the rats were anesthetized with isoflurane (3%), which was delivered through a nose cone. A telemetry BP probe (model TA11PA-C40, Data Sciences International, St. Paul, MN, USA) was positioned intra-abdominally and secured to the ventral abdominal muscle with the catheter inserted into the lower abdominal aorta. The telemetry signals received by the device were processed and digitized as radiofrequency data, which were recorded and stored in a computer using the Dataquest IV system (Data Sciences International, St. Paul, MN, USA), and the mean values of BP and heart rate (HR) were calculated in a conscious state. Continuous recordings were started 4 days after the probe implantation.
For the microinjection studies, acute BP recording was performed using PE50 catheters under isoflurane (3%) anesthesia. PE50 catheters filled with heparinized saline (100 IU/mL) were placed in the right femoral artery and connected to a BP transducer and a bridge amplifier (AD Instrument, Bella Vista, Australia). The BP and HR data were collected and analyzed with PowerLab software (AD Instrument, Bella Vista, Australia).
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4

Functional Presence of β-Agonist and Antagonists

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To confirm the functional presence of orally administered β2 agonist clenbuterol along with β1 antagonist atenolol and β3 antagonist SR59230A we measured mean systemic arterial blood pressures and heart rates by attaching an externalized arterial catheter to a physiological pressure transducer that was connected to a PowerLab 8/35 with a bridge amplifier (ADInstruments Inc., Colorado Springs CO, USA). Pressures and heart rates were determined on three separate days and analyzed with LabChart software. Pressure transducers were calibrated with a mercury column manometer. Lambs were placed in the sling and physiological pressure transducers were set to the height of the heart. After an acclimation period of at least 10 minutes, data were recorded for a minimum of 8 consecutive minutes under basal conditions. At 29 ± 1 days of age, lambs were challenged with the ADRβ1 agonist dobutamine HCl (12.5 mg/ml; Hospira, Inc., Lake Forest, IL) to evaluate cardiac responsiveness (Stephens et al., 2011 (link)). Data were recorded for 15 minutes during both basal and dobutamine-stimulated (10 μg/min/kg) periods.
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