Testing of acetaminophen in support of the international multilaboratory in vivo rat Pig‐a assay validation trial

• Published in: Environmental and molecular mutagenesis 2020-06, Vol.61 (5), p.508-525
• Main Authors: van der Leede, Bas‐jan, Weiner, Sandy, Van Doninck, Terry, De Vlieger, Kathleen, Schuermans, Ann, Tekle, Fetene, Geys, Helena, van Heerden, Marjolein, De Jonghe, Sandra, Van Gompel, Jacky
• Format: Article
• Language: English
• Subjects: Acetaminophen; Acetaminophen - pharmacology; Analgesics; Animals; Assaying; Biocompatibility; Biological Assay; Biomarkers; CD59 antigen; Comet Assay; Damage; DNA damage; Dosage; Erythrocytes; flow cytometry; glycosyl phosphatidylinositol; Hepatocytes; Histopathology; in vivo; In vivo methods and tests; Internationality; Laboratories; Liver; Liver cancer; Male; Micronucleus Tests; Mutagenicity Tests; Mutagens - toxicity; Mutation; mutation assay; Peripheral blood; Rats, Sprague-Dawley; red blood cells; Reproducibility of Results; Reticulocytes; Toxicity
• ISSN: 0893-6692; 1098-2280
• DOI: 10.1002/em.22368

Acetaminophen, a nonmutagenic compound as previously concluded from bacteria, in vitro mammalian cell, and in vivo transgenic rat assays, presented a good profile as a nonmutagenic reference compound for use in the international multilaboratory Pig‐a assay validation. Acetaminophen was administered at 250, 500, 1,000, and 2,000 mg·kg−1·day−1 to male Sprague Dawley rats once daily in 3 studies (3 days, 2 weeks, and 1 month with a 1‐month recovery group). The 3‐Day and 1‐Month Studies included assessments of the micronucleus endpoint in peripheral blood erythrocytes and the comet endpoint in liver cells and peripheral blood cells in addition to the Pig‐a assay; appropriate positive controls were included for each assay. Within these studies, potential toxicity of acetaminophen was evaluated and confirmed by inclusion of liver damage biomarkers and histopathology. Blood was sampled pre‐treatment and at multiple time points up to Day 57. Pig‐a mutant frequencies were determined in total red blood cells (RBCs) and reticulocytes (RETs) as CD59‐negative RBC and CD59‐negative RET frequencies, respectively. No increases in DNA damage as indicated through Pig‐a, micronucleus, or comet endpoints were seen in treated rats. All positive controls responded as appropriate. Data from this series of studies demonstrate that acetaminophen is not mutagenic in the rat Pig‐a model. These data are consistent with multiple studies in other nonclinical models, which have shown that acetaminophen is not mutagenic. At 1,000 mg·kg−1·day−1, Cmax values of acetaminophen on Day 28 were 153,600 ng/ml and 131,500 ng/ml after single and repeat dosing, respectively, which were multiples over that of clinical therapeutic exposures (2.6–6.1 fold for single doses of 4,000 mg and 1,000 mg, respectively, and 11.5 fold for multiple dose of 4,000 mg) (FDA 2002). Data generated were of high quality and valid for contribution to the international multilaboratory validation of the in vivo Rat Pig‐a Mutation Assay.