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24 protocols using tsd104a

1

Langendorff Isolated Heart Perfusion Technique

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We used the Langendorff isolated heart perfusion technique to monitor intraventricular pressure during cardiac contraction. The aorta is cannulated and perfused in a retrograde manner to drive coronary artery perfusion throughout the heart. This allows measurement of both coronary perfusion pressure and left ventricular (LV) pressure during constant coronary flow controlled by a peristaltic pump (10 mL/min). Changes in coronary resistance are detect as changes in coronary perfusion pressure (CPP, mmHg) measured by a pressure transducer (TSD 104A-Biopac connected to a Funbec MP-100 preamplifier) connected to the perfusion system. For LV pressure, the left atrium was opened and a water inflatable latex balloon connected to a pressure transducer (Biopac TSD 104A-Biopac connected to a preamplifier) was introduced into the LV. This also allowed control of preload by changing end diastolic pressure (DP, mmHg). Left ventricular isovolumetric systolic pressure (LVISP, mmHg) was measured via a data acquisition system (MP 100, Biopac Systems: Inc; CA, including Biopac Student Lab software), using a sampling rate of 2000 samples/s. Hearts were randomly grouped as Control (perfused with normal KHS) and TBT (exposed 5 min to 50 μM TBT). TBT was diluted in ethanol 0.4% plus 99.6% saline.
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2

Measuring Renal Hemodynamics in Anesthetized Rats

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Following the 24-hour period in the metabolic cage, animals were anesthetized with 50 mg/kg body weight (BW) of sodium thiopental and a polyethylene tube (PE-50) was inserted into the right carotid artery to monitor mean arterial pressure (MAP) and heart rate (HR) using an electronic transducer connected to a data acquisition program (TSD104A, BIOPAC Systems Inc., USA). Then, a ventral midline incision was made, exposing the left renal pedicle. The renal artery was then isolated, and a suitable probe was placed around the exposed artery to measure renal blood flow (RBF) [13 (link)].
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3

Hemodynamic Evaluation in Swine Model

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The algorithms described in this section were evaluated using previously reported data (21) . The following is a brief summary of the protocol. Six Yorkshire swine (30-34kg) were studied. The experimental protocol conformed to the Guide for the Care and Use of Laboratory Animals and was approved by the MIT Committee on Animal Care. The animals were pre-anesthetized with intramuscular telazol, xylazine, and atropine prior to endotracheal intubation. The swine were then maintained in a deep plane of anesthesia using inhaled anesthetic isoflurane (0.5-4 %), a mixture of oxygen and ambient air.
Positive-pressure mechanical ventilation at a rate of 10-15 breathes/min, and a tidal volume of 10 ml/kg was employed.
Central ABP (CAP) was measured from the thoracic aorta using a micromanometer-tipped catheter (SPC 350, Millar Instruments, Houston, TX). Femoral ABP (FAP) and radial ABP (RAP) were measured using external fluid-filled pressure transducer (TSD104A, Biopac Systems, Santa Barbara, CA). The
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4

Validation of Bladder Pill Pressure Measurements

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Linear response of the Bladder Pill device was previously characterized in pressure chambers for values up to 300 cm H2O above atmospheric pressure. [11 ] We compared measurement of static water columns by the Bladder Pill and the waistband external device to a fluid-filled catheter system. A PE-50 polyethylene catheter was connected to a fluid pressure transducer (TSD104A, BIOPAC Systems, Goleta, USA). To simulate the effect of bladder contractions on the Bladder Pill measurements, we inserted the device into a syringe and compressed the Pill longitudinally, as shown in Fig 3. Data presented in this section was obtained using the Pill combined with the waistband external device.
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5

Cardiovascular Response to Exercise

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All animals were anesthetized with pentobarbital (50 mg/kg ip) for polyethylene
cannula (PE-50 with saline-heparin solution) implantation in the left carotid artery
to directly measure BP and HR. The cannula was then exteriorized on the animal's
back, allowing 24-hour analysis for all three groups. Thus, the analysis was
performed while the animals were conscious and could move freely during the
experiment.
To measure BP and HR, the cannula was connected to a pressure transducer (TSD104A,
BIOPAC Systems Inc, Goleta, CA, USA) and a signal amplifier (DA100C, BIOPAC Systems
Inc, Goleta, CA, USA). The measures were acquired at a sample rate of 200
samples/second by use of the MP150 system (BIOPAC Systems Inc, Goleta, CA, USA) and
recorded using a specific software (AcqKnowledge 3.7.3 for Windows, BIOPAC Systems
Inc, Goleta, CA, USA). The signals were recorded at rest (10 minutes), during
exercise (every 8 minutes excluding warm-up and deceleration), and up to 90 minutes
after ending the exercise (1 minute every 5 minutes). The signals were analyzed
beat-to-beat to quantify changes in BP and HR. Rate pressure product (RPP),
considered an estimation of myocardial workload, was calculated by multiplying HR by
systolic BP.
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6

CVBG Revascularization in Ameroid Model

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Two weeks after ameroid placement, the animals in Group I underwent CVBG. By this time, the ameroid constrictor had already created nearly 100% stenosis of the LAD artery (corroborated by angiography). The animals in Group II did not undergo CVBG and served as control. Two days before the CVBG surgery was performed, the animals received daily Aspirin 325 mg, PO, and Clopidogrel 75 mg, PO. On the day of the procedure, the right femoral artery was percutaneously accessed with a 6F introducer sheath and connected to a pressure transducer (TSD104A – Biopac Systems, Inc, Goleta, CA) for arterial pressure monitoring. Heparin 100–200 IU/kg was administered IV before further instrumentation and was then supplemented as needed to keep an activated clotting time over 200 s. The chest was reopened through the previous sternotomy and the LIMA was dissected from its bed in a skeletonized fashion (without a muscular pedicle). An end-to-side anastomosis between the LIMA and the arterialized GCV in the anterior longitudinal sulcus was performed without the aid of cardiopulmonary bypass. The off-pump technique included insertion of an intra-venous shunt to aid in the creation of the anastomosis. This allowed oxygenated blood to reach the ischemic myocardium in a retrograde fashion. After the revascularization procedure, the animals were recovered for 8 additional weeks.
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7

Extremity ECG and Hemodynamic Monitoring

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The standard extremity electrocardiography leads were placed into four extremities near the thoracic and abdominal regions, where the electrocardiography waves were recorded best. Electrocardiograms were monitored (MP36, BIOPAC Systems, Inc., California, USA) continuously during the experiment. The heart rate was calculated from the electrocardiographic records. Ventricular arrhythmias and QT prolongation were analyzed according to the guidelines of the Lambeth Conventions for the determination of experimental arrhythmias (36 (link)). Also, arterial blood pressure was continuously recorded by a transducer (TSD104A, BIOPAC Systems, Inc., California, USA) from a catheter that was inserted into the left carotid artery. All data were analyzed by a computer program (AcqKnowledge BIOPAC Systems, Inc., California, USA).
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8

Gastric Motility Measurement Protocol

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Gastric motility recording was performed as described previously by Gao et al. [23 (link)]. The abdomen was opened by a longitudinal incision (5–6 cm in length) right below the diaphragm. The stomach was exposed entirely. A balloon (0.5 cm in diameter) attached to a catheter (1.5 mm OD and 1.1 mm ID) was inserted into the stomach by making a small hole at the duodenum close to the pylorus. The balloon was placed in the antrum to record the gastric motility. Subsequently, the hole was securely tied to avoid bloodletting and balloon shifting. Another end of the catheter was connected to a pressure transducer (TSD 104A; BIOPAC Systems, Inc., USA) via a three-way tube. The three-way tube was also connected to a syringe. The internal pressure of the balloon was maintained at 80–100 mmHg by injecting 0.3–0.4 ml of warm saline with the syringe. The pressure varied in accordance with the gastric motility changes. Therefore, it was an indicator of gastric motility. The pressure signal was recorded by the data acquisition system (MP150; BIOPAC Systems, Inc., USA) with the EGG transducer module. The acquisition parameter settings were LP: 1.0 Hz, HP: 0.005 Hz, and sampling frequency: 1000 Hz.
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9

Rat Liver Perfusion with Compounds

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Rat livers were perfused via the portal vein with carbogen-saturated Krebs Henseleit buffer (Biochrom, Berlin, Germany) containing 2 gÁL À1 glucose, using a body weight-adapted constant flow rate of 100 mlÁ(kg body weightÁmin) À1 . Z-BOX A, Z-BOX B, or vehicle was individually administered to the main flow. In parallel to bile sampling, portal pressure was measured (TSD104A, 10 or 20 Hz, Biopac Systems, Goleta, CA, USA) and 0.01 Hz low-pass filtered (OriginLab, Northampton, USA).
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10

Measuring Right Ventricular Pressure in Rats

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Every rat was performed with right heart catheter after MR procedures. Rats were weighed and anesthetized with 1.0 g/kg urethane (Sigma-Aldrich), administered intraperitoneally. A polyethylene catheter (PE10, 427400; BD Biosciences,) and heparinsaline (125 U/ml; Changzhou Yinsheng Pharmaceutical Co., Ltd.) was inserted into the right jugular vein and advanced into the right ventricle. The catheter was connected to an MPA Acquisition and Analysis system (MP100; BIOPAC Systems, Inc.) by a pressure transducer (TSD104A; BIOPAC Systems Inc.). The right ventricular systolic pressure (RVSP) was recorded using a multiparameter monitor PM-8000 (Zhuhai Joyful Medical Equipment Co.) [11] .
Following measurements of hemodynamic parameters and blood sample collection, the rats were sacri ced by cervical dislocation, and the thorax was opened. The heart was removed and the right ventricle (RV), left ventricle (LV) were separated. The mass ratio of RV to LV (RV/LV) was evaluated.
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