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DOI: 10.3791/62403-v
Jeffrey Morin*1, Terri A. Swanson*2, Anthony Rinaldi3, Magalie Boucher4, Trenton Ross3, Dinesh Hirenallur-Shanthappa1
1Comparative Medicine,Pfizer Inc., 2Digital Medicine & Translational Imaging,Pfizer Inc., 3Internal Medicine Research Unit,Pfizer Inc., 4Drug Safety Research & Development,Pfizer Inc.
This study employs an enhanced ultrasound technique to non-invasively monitor liver tissue alterations in rodent models of nonalcoholic fatty liver disease. It demonstrates a methodology for observing changes in liver fat and fibrosis, facilitating assessments during drug discovery processes.
This protocol describes the use of an enhanced ultrasound technique to non-invasively observe and quantify liver tissue changes in rodent models of nonalcoholic fatty liver disease.
Use of ultrasound and shear wave elastography enables researchers to measure the changes in liver fat and fibrosis implicit in models of nonalcoholic steatohepatitis. This imaging modality is a non-invasive, high-throughput, and clinically translatable technique, and can be used to assess the disease stage and efficacy in non-alcoholic steatohepatitis models during drug discovery. To begin, place six-to seven-week-old male Wistar Han rats weighing 150 to 175 grams in pairs in individually-ventilated cages with proper bedding at approximately 22 degrees Celsius and 40 to 70%relative humidity with a 12-to-12 hour light/dark cycle.
Provide 20 rats with a choline deficient, high-fat diet with 1%cholesterol, and another 20 rats with the standard lab rodent chow. To set up the imaging instrument, place a warmed surface in the imaging area to keep the animal warm during imaging, and fix the anesthesia nose cone for delivering the inhalant anesthesia. Use the ultrasound probe holder to move the ultrasound probe to the desired location and to prevent the probe from resting on the animal.
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