EFFECTS OF LIGHT ON THE CYTOTOXICITY AND GENOTOXICITY OF BENZO(A)PYRENE AND AN OIL REFINERY EFFLUENT IN THE NEWT

The genotoxicity and/or toxicity of benzo(a)pyrene (BaP) were evaluated under different lighting conditions in larvae and embryos of the newt Pleurodeles waltl. Visible light alone (1,220 Ix; 2.1 mW/cm(2)), UVA alone (250 mu W/cm(2)), or BaP alone (500, 50, 25, 12.5 ppb) had no toxic effects on the larvae. Conversely, toxic effects were observed in animals exposed to BaP (500 ppb) + daylight, or BaP (greater than or equal to 25 ppb) + UVA. BaP solutions (50 or 12.5 ppb) were irradiated for 24 hr (Irr BaP) prior to being assayed in the dark. The genotoxicity of BaP (50 ppb) as evaluated in the micronucleus test (on day 8) was halved by its previous exposure to UVA, and was abolished at the lowest concentration (12.5 ppb). In other experiments, the larvae were exposed alternatively to BaP or Irr BaP (18 hr in the dark) and UVA (6 hr in water), every day for 8 days. All animals that had accumulated non-irradiated BaP (50 ppb) showed signs of severe toxicity, and 90% died before the end of the test. On the other hand, irradiated BaP (50 ppb) was 4-fold less toxic and half as genotoxic as non-irradiated BaP. In addition, exposure of the animals to UVA alone for 4 days prior to treatment with BaP did not affect the genotoxicity or toxicity of this hydrocarbon. In the dark, the embryotoxicity of BaP was markedly attenuated by the presence of the jelly coats (10% vs. 24%). With dejellied embryos, comparable mortality (24%) was observed after exposure to 25 ppb BaP for 54 or 312 hr. Although UVA alone did not affect growth of the embryos, the toxicity of BaP was enhanced by the combined action of the two agents together or in succession (BaP + UVA or BaP then UVA). Larvae were treated with an oil refinery effluent (EF). At the concentration employed (125 ml/l), EF was not found to be genotoxic in the dark. However, in animals exposed to both EF and UVA, there was a progressive increase in level of micronucleated erythrocytes with increasing duration of daily exposure to UVA (9, 15, 24 hr). Moreover, the genotoxic potential of irradiated EF + UVA was systematically below that of non-irradiated EF + UVA for all durations of exposure to ultraviolet light. Irradiation of this type of effluent might help reduce its harmful effects on aquatic species. Our results also suggest that metabolic activation is not necessary for hydrocarbons to ind vee toxic effects. (C) 1994 Wiley-Liss, Inc.