Hemodynamic Correlates of Drug-induced Vascular Injury in the Rat Using High-frequency Ultrasound Imaging

Author:

Swanson Terri A.1,Conte Teri2,Deeley Ben2,Portugal Susan1,Kreeger John M.1,Obert Leslie A.1,Joseph E. Clive1,Wisialowski Todd A.1,Sokolowski Sharon A.1,Rief Catherine3,Nugent Paul1,Lawton Michael P.1,Enerson Bradley E.1

Affiliation:

1. Pfizer Worldwide Research and Development, Groton, Connecticut, USA

2. FUJIFILM VisualSonics, Inc., Toronto, Ontario, Canada

3. Pfizer Worldwide Research and Development, Andover, Massachusetts, USA

Abstract

Several classes of drugs have been shown to cause drug-induced vascular injury (DIVI) in preclinical toxicity studies. Measurement of blood flow and vessel diameter in numerous vessels and across various tissues by ultrasound imaging has the potential to be a noninvasive translatable biomarker of DIVI. Our objective was to demonstrate the utility of high-frequency ultrasound imaging for measuring changes in vascular function by evaluating blood flow and vessel diameter in the superior mesenteric arteries (SMA) of rats treated with compounds that are known to cause DIVI and are known vasodilators in rat: fenoldopam, CI-1044, and SK&F 95654. Blood flow, vessel diameter, and other parameters were measured in the SMA at 4, 8, and 24 hr after dosing. Mild to moderate perivascular accumulations of mononuclear cells, neutrophils in tunica adventitia, and superficial tunica media as well as multifocal hemorrhage and necrosis in the tunica media were found in animals 24 hr after treatment with fenoldopam and SK&F 95654. Each compound caused marked increases in blood flow and shear stress as early as 4 hr after dosing. These results suggest that ultrasound imaging may constitute a functional correlate for the microscopic finding of DIVI in the rat.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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