Following metabolism the metabolites are excreted in the urine and faeces. No data on the acute effects of B(a)P in humans were identified and few studies were reported in animals. Following acute exposure of rats to B(a)P, effects on the liver were observed. Following chronic exposure in an occupational setting a decrease in lung function was reported, as well as chest pain, respiratory irritation, cough, dermatitis and depressed immune system, although in most cases it was not possible to evaluate the contribution of B(a)P to such effects. In animals, few adverse effects were observed in rats or hamsters exposed to B(a)P via inhalation. Following ingestion, myelotoxicity was observed in poor affinity Ah-receptor mice but not in high affinity mice. Hepatotoxicity was also reported. Benzo(a)pyrene can cross the placenta and was found to cause adverse developmental and reproductive effects in
Following metabolism the metabolites are excreted in the urine and faeces. No data on the acute effects of B(a)P in humans were identified and few studies were reported in animals. Following acute exposure of rats to B(a)P, effects on the liver were observed. Following chronic exposure in an occupational setting a decrease in lung function was reported, as well as chest pain, respiratory irritation, cough, dermatitis and depressed immune system, although in most cases it was not possible to evaluate the contribution of B(a)P to such effects. In animals, few adverse effects were observed in rats or hamsters exposed to B(a)P via inhalation. Following ingestion, myelotoxicity was observed in poor affinity Ah-receptor mice but not in high affinity mice. Hepatotoxicity was also reported. Benzo(a)pyrene can cross the placenta and was found to cause adverse developmental and reproductive effects in