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Sonos4500

Manufactured by Philips

The SONOS4500 is a high-performance laboratory ultrasound system designed for advanced imaging and analysis. It features a digital beamformer, advanced signal processing, and a wide range of transducers to accommodate diverse applications.

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17 protocols using sonos4500

1

Echocardiography Assessment of Cardiac Function in Rats

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Echocardiography is a non-invasive method used for the assessment of left ventricular function. Rats were lightly anesthetized (2% Isoflurane with oxygen, via inhalation), then the chest was shaved and they were placed in a supine position. After echocardiography transmission gel was applied, an echocardiography probe (S12, Hewlett Packard) which was connected to an echocardiograph (SONOS4500, Philips), was used for collecting the data from the heart. Signals from M-mode echocardiography at the papillary muscle level were recorded. Parameters obtained from echocardiography were: 1) RVDd = right ventricular dimension during diastole; (2) IVSs,d = systolic and diastolic interventricular septum; (3) LVIDs,d = systolic and diastolic left ventricular internal dimension; and (4) LVPWs,d = left ventricular posterior wall thickness during systole and diastole. Fractional shortening (FS) and ejection fraction (EF) were calculated by the following formula; %FS = ((LVIDd − LVIDs)/LVIDd)*100, and % EF = ((LVEDV − LVESV)/LVEDV)*10051 . After investigation, animals were allowed to fully recover and then returned to the cages.
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2

Echocardiographic Assessment of Cardiac Function in I/R Injury

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Prior to the I/R protocol, left ventricular function was assessed using an echocardiograph (SONOS4500, Philips). The chest area was shaved and rats were stabilized in a supine position. The probe was gently placed on the chest and moved to enable the collecting of data along the short and long axes of the heart. Signals from M-mode echocardiography at the level of the papillary muscles were recorded. Parameters obtained from the echocardiogram including left ventricular internal dimensions during systole (LVIDs) and diastole (LVIDd), and left ventricular posterior wall thickness during systole (LVPWs) and diastole (LVPWd) were recorded. Fractional shortening (FS) was calculated using the formula: %FS = (LVIDd—LVIDs) x 100 / LVIDd.
At the end of the experiment, left ventricular pressure during I/R injury was evaluated using an intravascular pressure catheter. The right carotid artery was canulated and the pressure in the LV chamber was recorded using a LabScribe2 program (iWorx Systems Inc., Dover, NH, USA) [23 (link), 28 (link)]. Heart rate (HR), left ventricular end-systolic pressure (LVESP) and left ventricular end-diastolic pressure (LVEDP) were assessed prior to the occlusion of the LAD, at the end of ischemic period and at the end of reperfusion period.
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3

Echocardiographic Assessment of Murine Cardiac Function

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Echocardiography was performed on conscious mice using an ultrasonography equipped with a 15-MHz linear transducer (SONOS-4500, Philips Medical Systems). An M-mode echocardiogram of the midventricle was recorded at the level of the papillary muscles in the two-dimensional parasternal short-axis view. The following parameters were obtained to assess LV size and function: heart rate (HR), end-diastolic interventricular septal and LV posterior wall thickness (IVSd and LVPWd), end-diastolic and end-systolic internal dimensions of LV (LVDd and LVDs) and fractional shortening of LV dimension (FS) and LV mass. FS and LV mass were calculated as 100 × (LVDd—LVDs)/LVDd and 1.05 × [(LVDd + IVSd + LVPWd)3 (link)—(LVDd)3 (link)], respectively.
The 8‒11-week-old male mice underwent TAC surgery using 26-gauge needles22 (link). Non-invasive measurements of blood pressure were performed on mice anaesthetized with 2.5% avertin using a blood pressure monitor for mice (Model MK-2000, Muromachi Kikai), according to the manufacturer’s instructions as previously described22 (link).
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4

Conscious Echocardiography in Mice

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To exclude the influence imposed by the anaesthesia drug, mice underwent transthoracic echocardiography in a conscious state with a Sonos 4500 and a 15–6 L MHz transducer (Philips, Amsterdam, the Netherlands) over time as described elsewhere48 (link)50 (link).
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5

Echocardiography and Ultrasound Hemodynamics

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Hemodynamics measurements were assessed immediately after each study period by echocardiography and head ultrasound using a Philips Sonos 4500 ultrasound machine (Philips Medical Systems, Andover, MA) with a 5 to 12 MHz transducer (S12, 21380A, Philips Medical Systems, Andover, MA). The patients continued the study ventilation during measurements. The scans were recorded on a hard disk, and measurements were analyzed offline to minimize patient handling time. The investigator performing the offline analyses was blinded to the treatment mode and not involved in the randomization or the recording of the intervention.
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6

Echocardiographic Assessment of Cardiac Function

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Animals were lightly anesthetized and placed in a supine position. An echocardiography probe (S12, Hewlett Packard) which was connected to an echocardiography machine (SONOS 4500, Philips) was gently placed on the chest and moved for collecting the data along short axis of the heart. Signals from M-mode echocardiography at the level of papillary muscles were recorded. Then, the percentage of the fractional shortening (%FS) was calculated17 (link). Echocardiogram was recorded at baseline, 12, 16, 20 and 24 weeks.
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7

Echocardiographic Assessment of Cardiac Function

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Mice were anesthetized with 0.5–2.0% isoflurane (AErrane, Baxter, USA) mixed with oxygen. Echocardiography was performed with a 15-MHz high-frequency transducer (Agilent Technologies SONOS 4500, Philips Medical System). A two-dimensional short-axis view of the left ventricle was obtained at the level of the papillary muscles, and two-dimensionally targeted M-mode tracings were recorded at a sweep speed of 100 mm/s. Fractional shortening (FS) was calculated as: FS (%) = [(LVEDD − LVESD) / LVEDD] × 100, where LVEDD and LVESD indicate LV end-diastolic and end-systolic dimension, respectively. Data from three to five consecutive selected cardiac cycles were analyzed and averaged.
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8

In Vivo Cardiac Morphology Assessment

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In vivo cardiac morphology was assessed in non-anesthetized mice using transthoracic echocardiography with an ultrasound machine (SONOS 4500; Philips Medical System, Santa Clara, CA). The M-mode left ventricular end-systolic and end-diastolic dimensions, intraventricular septum wall width, and posterior wall width were averaged from 3 to 5 beats. The left ventricular percentage of fractional shortenings was calculated as described in earlier reports12 (link).
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9

Transthoracic Echocardiography in Mice

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Transthoracic echocardiography was performed with a Sonos 4500 and a 15-6 L MHz transducer (Philips, the Netherlands) or a Sequoia 512 system with a 17L-5 probes (Siemens, Germany). Mice were weighed, anesthetized with 2.5% avertin (0.06 ml/10 g), and settled in the left decubitus or supine position. Good two-dimensional short-axis views of the left ventricle were obtained for guided M-mode measurements of the left ventricular posterior wall thickness (LVPWd), left ventricular end-diastolic diameter (LVEDd), and left ventricular end-systolic diameter (LVESd). Left ventricular fractional shortening (LVFS) was calculated: LVFS = (LVEDd–LVESd)/LVEDd × 100.
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10

Left Ventricular Dimension Quantification

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Two‐dimensional echocardiography (Sonos‐4500; Philips Medical Systems, Andover, MA) was used for assessment of left ventricular (LV) dimensions including LV internal diameter during diastole, interventricular septal thickness during diastole, and posterior wall thickness during diastole, according to previously described protocols16 based on the recommendations of the American Society of Echocardiography. LV mass (grams) was calculated using the American Society of Echocardiography formula.24 LVMI was calculated by dividing LV mass (grams) by estimated body surface area (m2).
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