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Development of a Bacteria-Independent Model of the Multiple Organ Failure Syndrome
Steven Steinberg, MD;
William Flynn, MD;
Kathy Kelley, MD;
Lon Bitzer, MD;
Pramod Sharma;
Cynthia Gutierrez;
James Baxter, PharmD;
David Lalka, PhD;
Amy Sands, MD;
Judy Van Liew, PhD;
James Hassett, MD;
Ray Price, PhD;
Thomas Beam, MD;
Lewis Flint, MD
Arch Surg. 1989;124(12):1390-1395.
Abstract
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Criteria that allow definition of the multiple organ failure syndrome include pulmonary, hepatic, renal, and gut barrier dysfunction along with characteristic histopathologic changes. It has been difficult to study multiple organ failure due to lack of a satisfactory experimental model that would reproduce the pathophysiologic and histopathologic characteristics, would be stable enough to allow study over several days, and would be free of exogenous primary bacterial infection. We have studied pathophysiologic and histopathologic alterations in a potential model of multiple organ failure. Wistar rats received one of the following solutions by intraperitoneal injection: 4 mL of saline, 4 mL of mineral oil, or 1 mg per gram of body weight of zymosan A in 4 mL mL of mineral oil. Animals that received zymosan developed hypoxia, decreased creatinine clearance, and changes in hepatic microsomal cytochrome P450 content and aniline hydroxylase activity. Bacterial translocation occurred in the zymosan group. The lungs, liver, and kidneys of the animals that received zymosan exhibited histopathologic changes. We conclude that this model fulfills our criteria for a model of multiple organ failure.
(Arch Surg. 1989;124:1390-1395)
Author Affiliations
From the Departments of Surgery (Drs Steinberg, Flynn, Kelley, Bitzer, Hassett, Price, and Flint, Mr Sharma, and Ms Gutierrez), Pharmaceutics (Drs Baxter and Lalka), Pathology (Dr Sands), and Medicine (Drs Van Liew and Beam), State University of New York at Buffalo and the Buffalo Veterans Administration Medical Center.
Footnotes
Accepted for publication August 4, 1989.
Read before the Ninth Annual Meeting of the Surgical Infection Society, Denver, Colo, April 13, 1989.
Reprint requests to Surgical Service, 3495 Bailey Ave, Buffalo, NY 14215 (Dr Steinberg).
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