Toxicity and Residue Studies in Dairy Animals with FireMaster FF-1 (Polybrominated Biphenyls)

• Published in: Environmental health perspectives Vol. 23; pp. 91 - 97
• Main Authors: Robl, M. G., Jenkins, D. H., Wingender, R. J., Gordon, D. E.
• Format: Journal Article
• Language: English
• Published: United States National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare 01-04-1978
• Subjects: "Workshop on Scientific Aspects of Polybrominated Biphenyls," East Lansing, Michigan, October 24-25, 1978: Steven Aust, Conference Chairman; Animals; Biphenyl Compounds - toxicity; Body Weight; Bone Marrow - analysis; Calves; Cattle; Dosage; Dose-Response Relationship, Drug; Feces; Female; Female animals; Flame Retardants - toxicity; Hematologic Tests; Kidneys; Lesions; Leukocyte Count; Lipids - analysis; Liver; Male; Male animals; Milk; Milk - analysis; Polybrominated biphenyls; Polybrominated Biphenyls - analysis; Polybrominated Biphenyls - toxicity; Pregnancy; Spermatogenesis - drug effects; Tissue Distribution
• ISSN: 0091-6765; 1552-9924
• DOI: 10.1289/ehp.782391

Two studies (one in Holstein calves and one in Holstein cows) were conducted to determine potential toxicity and residue levels following oral ingestion of polybrominated biphenyls (PBB). The material was FireMaster FF-1. Administration was by gelatin capsules. Doses in calves were 0.1, 1.0, 10, or 100 mg/kg body weight, while doses in cows were equivalent to 0.01, 0.1, 1.0, or 1C ppm in the diet. The calves were sacrificed after 2, 4, 6, or 12 weeks. The cows were fed 158 or 228 days, and were then in a recovery period for 182 or 112 days. In the calf study, signs of toxicity were observed only in animals fed 100 mg/kg-day. Administration of 10 mg/kg-day or less for up to 12 weeks caused no overt signs of toxicity. Histologic studies were conducted upon selected organs and tissues taken at time of sacrifice. The only treatment-induced lesions among animals fed 0.1 mg/kg-day were minimal lesions in the kidney and skin in the one calf fed at this level for 12 weeks. Treatment-induced lesions were present in the kidneys, skin, and/or liver from some animals fed levels of 1.0 mg/kg-day and above. The relative severity of these lesions was related to the level and length of exposure. Treatment-associated changes were observed in the tests of all males in this study. The hypospermatogenesis observed was consistent with the age of the animals due to prepuberal development of the testes. No clinical signs of toxicity or histologic changes attributed to PBB were observed in the cows. Two cows were pregnant at the initiation of the study and give birth to normal, healthy calves during the study. These calves grew normally and appeared healthy when sacrificed at about 6 months of age. Residue levels were quantitated as the hexabromobiphenyl isomer (BP-6) which is the major isomer present in the PBB mixture. Tissue residue levels in calves increased with dose and duration of administration of PBB with highest levels being found in the fat. At 100 mg/kg the levels in fat were about 6000 to 6300 ppm after 6 to 12 weeks. Residue levels of BP-6 in milk and fat of the cows also increased with dose and duration of administration. Maximum levels in milk were about 1/3 the levels in the diet. In general, the levels plateaued after about 4 to 6 weeks and did not go appreciably higher even though administration of the FireMaster FF-1 was continued. Maximum levels in fat were on the order of approximately 4.5 times the levels in the diet, except at the lowest dose level. Residues decreased in milk after administration of PBB was discontinued, but detectable levels were still present 6 months later. Residues were found in the calves born of treated cows indicating passage of the PBBs through the placental barrier and/or ingestion through the milk.