Indocyanine green disposition in healthy dogs and dogs with mild, moderate, or severe dimethylnitrosamine-induced hepatic disease

D. M. Boothe From the Department of Veterinary Physiology and Pharmacology (Boothe, Brown) and the Department of Veterinary Pathology (Green), The Texas Veterinary Medical Center, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4466; Office of the Dean (Jenkins), School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803; Department of Microbiology, Pathology and Parasitology (Cullen), College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606; and USDA, ARS, VTERL (Corrier), College Station, TX 77843.

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S. A. Brown From the Department of Veterinary Physiology and Pharmacology (Boothe, Brown) and the Department of Veterinary Pathology (Green), The Texas Veterinary Medical Center, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4466; Office of the Dean (Jenkins), School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803; Department of Microbiology, Pathology and Parasitology (Cullen), College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606; and USDA, ARS, VTERL (Corrier), College Station, TX 77843.

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W. L. Jenkins From the Department of Veterinary Physiology and Pharmacology (Boothe, Brown) and the Department of Veterinary Pathology (Green), The Texas Veterinary Medical Center, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4466; Office of the Dean (Jenkins), School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803; Department of Microbiology, Pathology and Parasitology (Cullen), College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606; and USDA, ARS, VTERL (Corrier), College Station, TX 77843.

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R. A. Green From the Department of Veterinary Physiology and Pharmacology (Boothe, Brown) and the Department of Veterinary Pathology (Green), The Texas Veterinary Medical Center, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4466; Office of the Dean (Jenkins), School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803; Department of Microbiology, Pathology and Parasitology (Cullen), College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606; and USDA, ARS, VTERL (Corrier), College Station, TX 77843.

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J. M. Cullen From the Department of Veterinary Physiology and Pharmacology (Boothe, Brown) and the Department of Veterinary Pathology (Green), The Texas Veterinary Medical Center, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4466; Office of the Dean (Jenkins), School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803; Department of Microbiology, Pathology and Parasitology (Cullen), College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606; and USDA, ARS, VTERL (Corrier), College Station, TX 77843.

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D. E. Corrier From the Department of Veterinary Physiology and Pharmacology (Boothe, Brown) and the Department of Veterinary Pathology (Green), The Texas Veterinary Medical Center, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4466; Office of the Dean (Jenkins), School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803; Department of Microbiology, Pathology and Parasitology (Cullen), College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606; and USDA, ARS, VTERL (Corrier), College Station, TX 77843.

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Summary

Disposition kinetics of indocyanine green (icg) were used to evaluate hepatic function in healthy Beagles (group 1; n = 6) and Beagles with progressive hepatic disease induced by oral administration of dimethylnitrosamine, a hepatospecific toxin. Three classes of hepatic disease were defined by histologic features: mild (group 2; n = 5), moderate (group 3; n = 6), and severe (group 4; n = 5). Disposition of icg was studied 3 weeks following the last dose of toxin. A rapid iv injection of 0.5 mg of icg/kg was administered and serum samples were obtained at certain intervals during 60-minute periods. Serum icg was analyzed by use of visible spectrophotometry. Disposition kinetics were determined from serum icg concentrations vs 15- and 60-minute time curves and compared between one another and among groups. Data based on 60-minute time curves were not significantly different from those based on 15-minute curves. Area under the curve for icg was greatest in group 3. Clearance of icg was decreased and mean resident time was increased in groups 3 and 4, compared with those in groups 1 and 2. When disposition data (60 minutes) were normalized for differences in hepatic weight among dogs, group-3 mean resident time was significantly greater than that of group 4. This study supports the diagnostic benefits of using icg disposition kinetics as a method of evaluating hepatic function in dogs with progressive liver disease.

Summary

Disposition kinetics of indocyanine green (icg) were used to evaluate hepatic function in healthy Beagles (group 1; n = 6) and Beagles with progressive hepatic disease induced by oral administration of dimethylnitrosamine, a hepatospecific toxin. Three classes of hepatic disease were defined by histologic features: mild (group 2; n = 5), moderate (group 3; n = 6), and severe (group 4; n = 5). Disposition of icg was studied 3 weeks following the last dose of toxin. A rapid iv injection of 0.5 mg of icg/kg was administered and serum samples were obtained at certain intervals during 60-minute periods. Serum icg was analyzed by use of visible spectrophotometry. Disposition kinetics were determined from serum icg concentrations vs 15- and 60-minute time curves and compared between one another and among groups. Data based on 60-minute time curves were not significantly different from those based on 15-minute curves. Area under the curve for icg was greatest in group 3. Clearance of icg was decreased and mean resident time was increased in groups 3 and 4, compared with those in groups 1 and 2. When disposition data (60 minutes) were normalized for differences in hepatic weight among dogs, group-3 mean resident time was significantly greater than that of group 4. This study supports the diagnostic benefits of using icg disposition kinetics as a method of evaluating hepatic function in dogs with progressive liver disease.

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