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Visualsonics vevo 3100 imaging system

Manufactured by Fujifilm
Sourced in Canada

The Visualsonics Vevo 3100 Imaging System is a high-resolution, non-invasive in vivo imaging platform designed for preclinical research. The system utilizes high-frequency ultrasound technology to generate real-time, high-quality images of small animal models. The Vevo 3100 provides researchers with a powerful tool for visualizing and analyzing anatomical structures and physiological functions in small animals.

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4 protocols using visualsonics vevo 3100 imaging system

1

Comprehensive Mouse Echocardiography Protocol

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Mouse echocardiography was conducted using a Visualsonics Vevo 3100 Imaging system (FUJIFILM Visualsonics, Toronto, ON, Canada). After initial anesthesia with 4 Vol.-% isoflurane in 1 L/min O2, mice were placed on a heated plate and anesthesia was maintained with 1.5 Vol.-% isoflurane. A rectal probe was introduced, and heart rate, respiratory rate and body temperature were monitored continuously. After hair removal, images of long and short parasternal axis were acquired in M-mode and B-mode. Measurements were analyzed offline by a blinded investigator using Visualsonics VevoLab 3.2.6 software (FUJIFILM Visualsonics, Toronto, ON, Canada). Fractional shortening was determined by comparison of midventricular short-axis enddiastolic and endsystolic volumes. The ejection fraction was calculated using LV tracing on the parasternal short axis [47 (link),48 (link)]. CK and cTnI levels were measured from serum samples using high-sensitive ELISA assays (both Siemens, Erlangen, Germany).
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2

Echocardiographic Analysis of Murine Cardiovascular Function

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Echocardiography was performed using the high-frequency VisualSonics Vevo® 3100 Imaging System (Fujifilm) with a MX550D transducer (22–55 MHz; axial resolution: 40 µm). Mice were prepared and examined under light inhalation anesthesia with oxygen and 1.5% isoflurane through a nose cap. Chest and upper abdominal hair was shaved, and the mice were placed on a warmed platform to maintain physiological conditions. We monitored ECG, heart rate, core temperature, and respiratory frequency. Systolic parameters were obtained by using the B- and M-Mode in parasternal long and short axis views of the left ventricle. Doppler flow profiles were acquired to estimate the isovolumic relaxation time (IVRT), an indicator of diastolic ventricular function. We evaluated the ultrasound imaging data by working with the software Vevo LAB (Fujifilm). Strain analyses via Speckle Tracking were performed by using the Vevo Strain Software (Fujifilm). Younger mice used for echocardiographic investigation were 303 ± 4, older 551 ± 13 days of age.
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3

Echocardiography Measurements in Rat Model

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Baseline and biweekly echocardiography measurements were conducted, recorded and analyzed. Rats were anesthetized with isoflurane/oxygen (see above). A chemical depilator removed chest wall hair and skin was cleansed with warm water. Acoustic gel (non-toxic) was placed on the chest wall and ultrasound image recordings of the heart were collected and stored for analysis (Visual Sonics Vevo 3100 Imaging System, FujiFilm and VevoLab Software v.2.1.0, Toronto, Ontario, Canada). M-mode and B-mode images of LV end-diastolic diameter, interventricular septum and posterior LV wall thicknesses at end diastole were measured and averaged over five beat cycles. Further, we measured the relaxation constant Tau, which reflects LV chamber stiffness (25 (link)) in all groups.
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4

Murine Model of Myocardial Infarction

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Adult mice were anesthetized in a 4% isoflurane chamber and then intubated with a 20G angiocatheter. General anesthesia was maintained with 1.5% to 4% isoflurane during mechanical ventilation at a respiratory rate of 180 breaths per minute. The mice were placed in right lateral decubitus position, and the left chest was shaved and sterilely prepped. 1 mg/kg bupivacaine and 0.5 mg/kg Buprenorphine were injected subcutaneously for perioperative analgesia. A 1 cm left thoracotomy incision was made, and the pericardium was opened. The LCA was identified and permanently ligated using a 6-0 polypropylene suture. The chest was then closed in layers using 5-0 polypropylene sutures. Isoflurane was then weaned off and the mice were extubated after regaining physiological respirations. 5 mg/kg Carprofen was injected subcutaneously daily for the first 3 days after surgery for postoperative analgesia. For adult MI experiments, 2 to 3 months old mice were used (both males and females). To activate Cre, a single dose of 6 mg tamoxifen intraperitoneal injections were administered to each mouse, 2 days before MI. Echocardiograms were obtained from P32/P33 adult mice (sham or MI surgeries at P2) ≈30 days post-MI using VisualSonics Vevo 3100 imaging system (FUJIFILM VisualSonics, Inc) with an MX400 20–46 MHz transducer. Data were analyzed using Vevo LAB Version 3.1.0 (Build 13029).
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