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70 protocols using vivid 7 dimension

1

Myocardial Infarction in Mice

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All procedures involving animal use and surgeries were approved by the Institutional Animal Care and Use Committee. MI was produced in 12-week-old mice by a permanent ligation of the left anterior descending coronary artery [23 (link)]. To avoid the potential transient cardiotoxicity by tamoxifen-induced MerCreMer gene deletion [24 (link)], all procedures were performed at least four weeks after the completion of tamoxifen administration. Sham groups had the same procedure without the suture around the coronary artery. Echocardiography was performed without anesthesia to measure left ventricular parameters using GE Vivid 7 Dimension and GE i13L 10–14 MHz transducer. The heart was harvested and stained with 1% triphenyl tetrazolium to calculate infarct size. The harvested heart was paraffin embedded and stained with picrosirius red [23 (link)]. Apoptotic cell death was detected using In Situ Cell Detection Kit (Sigma) and quantified by fluorescence microscopy. Image analyses were performed by ImageJ (NIH Image).
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2

Echocardiographic Analysis of Taco1 Mutant Mice

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Echocardiographic studies to measure left ventricular function were performed on mice under light methoxyflurane anaesthesia with the use of an i13L probe on a Vivid 7 Dimension (GE Healthcare). Echocardiographic measurements were taken on M-mode in triplicate from each mouse. The quantitative measurements represent the average of 30-week-old Taco1wt/wt (n=5) and litter-mate matched 30-week-old Taco1mut/mut (n=5) mice. M-mode recordings were made at a sweep speed of 200 mm s−1. Measurements of left ventricular end diastolic diameter (LVEDD), left ventricular end systolic diameter (LVESD), fractional shortening, left ventricular posterior wall in diastole, left ventricular posterior wall in systole, intraventricular septum in diastole and intraventricular septum in systole were made. Fractional shortening was calculated by the formula [(LVEDD-LVESD)/EDD] × 100.
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3

Echocardiographic Measurements and LV Hypertrophy

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Echocardiographic examinations were performed with a Vivid 7 Dimension equipped with a multi-frequency transducer (GE Healthcare, Vingmed, Norway). Left ventricular (LV) end-diastolic dimension (LVDd), interventricular septal thickness (IVST) and posterior wall thickness (PWT) were measured at end diastole. LV volumes were calculated by the modified Simpson method using the apical 4-chamber view. The LV ejection fraction (LVEF) was defined as low when < 50%. For calculation of the LV mass (LVM), we used the formula proposed by Devereux et al. [21 (link)] with modification as follows: 0.8 x 1.04 x [(LVDd + IVST + PWT)3—LVDd3] + 0.6 [22 (link)]. Body surface area (BSA) was calculated by using the following formula: (body weight)0.425 × (height)0.725 × 0.007184, and the LVM index (LVMI) was calculated as the ratio of LVM to BSA. When the LVMI was greater than 118 g/m2 (men) or 108 g/m2 (women), LV hypertrophy was defined as present [23 (link)].
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4

Echocardiographic Assessment of Cardiac Function

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We assess left ventricle diameters, volumes, systolic and diastolic function according to American Society of Echocardiography guidelines for chamber quantification.[25 (link)] We use Vivid 7 Dimension echocardiographic machine with integrated software (GE, Horten, Norway) for measurements.
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5

Comprehensive Cardiac Evaluation Protocol

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It was performed on an expert class apparatus ‘Vivid-7 Dimension’ (General Electric, USA) by two-dimensional echocardiography, Doppler echocardiography in pulsed and continuous wave mode, color Doppler scanning (CDS) in accordance with the current [9 (link)]. Diameter and thickness of the LV walls were measured in the two-dimensional M-mode. Left heart analysis included assessment of the size and volumetric parameters of the left ventricle, left ventricular mass, the maximum transverse diameter of the left atrium in the diastole (LA). Ejection fraction of the left ventricle (LVEF) was calculated according to the Simpson method.
Left ventricular diastolic parameters were studied using pulsed-wave Doppler imaging, including peak velocity of early (E) and late (A) transmitral filling of the left ventricle and their ratio (E/A) and the isovolumetric relaxation time of the left ventricle. The study was carried out within the first two days from the moment the patient was admitted to the hospital.
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6

Cardiac Assessment by Echocardiography in Rats

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Cardiac morphology and function were assessed by transthoracic echocardiography at week −1, 4, and 8 (Fig. 1). Rats were anesthetized with 2% isoflurane (Forane, AESICA, Queenborough Limited Kent, UK). Then, the chest was shaved, and the rat was placed in a supine position onto a heating pad. Two-dimensional, M-mode, Doppler, and tissue Doppler echocardiographic examinations were performed by the criteria of the American Society of Echocardiography with a Vivid 7 Dimension ultrasound system (General Electric Medical Systems) using a phased array 5.5–12 MHz transducer (10S probe) as described previously63 (link)–65 (link). Data of three consecutive heart cycles were analysed (EchoPac Dimension software; General Electric Medical Systems) by an experienced investigator in a blinded manner. The mean values of three measurements were calculated and used for statistical evaluation.
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7

Noninvasive Assessment of Peripheral Arterial Disease

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The ABI of each foot was calculated by dividing the higher pressure in the posterior tibial or dorsalis pedis arteries by the higher systolic blood pressure in the right or left arm. To record blood pressure, a Doppler probe was placed over the pulsing artery at a 45° to 60° angle to the surface of the skin [20 (link)].
The level and severity of arterial stenosis were assessed by the duplex ultrasound scanning of the lower limb arteries using the Philips Affinity 50 (Philips Ultrasound, Tampa, Florida, USA) and the Vivid 7 Dimension (GE Healthcare, Chicago, Illinois, USA). The ultrasound protocol involved assessing the presence of hemodynamically significant stenoses (at least 50% of the diameter reduction) in 6 main arteries of each lower limb (common femoral artery, deep femoral artery, superficial femoral artery, popliteal artery, anterior tibial artery, posterior tibial artery).
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8

Echocardiographic Assessment of Cardiac Function in Rabbits

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Conventional echocardiography was performed on forty-eight New Zealand white rabbits using the GE Vivid7 Dimension ultrasound machine. Preoperative and postoperative LV end-systolic volume (LVESV), end-diastolic volume (LVEDV), stroke volume (SV) and LV ejection fraction (LVEF) were recorded in the rabbits, and standard high frame rate apical four, three and two-chamber views of three consecutive cardiac cycles were stored for off-line analysis.
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9

Epicardial Echocardiography for Myocardial Ischemia

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Open chest, epicardial echocardiography was performed according to the American Society of Echocardiography Guidelines for Comprehensive Epicardial Echocardiography Examination using GE Vivid 7 Dimension ultrasound system equipped with a 10 MHz phased‐array transducer (GE Vingmed, Horton, Norway). A bovine liver tissue offset was used to enhance image quality; all images were optimized for speckle tracking analysis by manually adjusting sector widths to optimize speckle quality and maintaining frame rates 55–90 frames/sec. Echocardiographic and hemodynamic data were acquired simultaneously at baseline and 1, 5, and 15 minutes after induction of ischemia. Measurements were repeated 1, 15, and 30 minutes after reperfusion. All images were obtained by the same echocardiographer (EM).
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10

Transthoracic Echocardiography of Cardiac Function

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To monitor cardiac function, transthoracic echocardiography was performed using a Vivid 7 Dimension imaging system (GE Medical Systems, Munich, Germany) equipped with a 14 MHz scanning head (i13L Probe). During the procedure, mice were anesthetized with 2% (vol) isoflurane in oxygen (0.5 l/min) via a respiratory mask and placed in dorsal position on a 37°C heating plate. Left ventricular wall and chamber dimensions as well as heart rate were measured in the M-Mode. Ejection fraction (EF) was calculated as described previously [18 (link)]. In TAC and sham mice, the aortic diameter was assessed before and 2 or 4 weeks after surgery.
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