Very little information is available on the immunological effects of other PAHs. Mice treated with high doses of dibenz[a,h]anthracene exhibited a reduced serum antibody level in response to antigenic
challenge by comparison to controls (Malmgren et al. 1952). The immunosuppressive effects of dibenz[a,h]anthracene were studied in AHH-inducible mice (C57BL/6) and AHH-noninducible mice (DBA/2N) by intraperitoneal and oral administration (Lubet et al. 1984). Immunosuppression occurred in both strains and was more pronounced in the C57BL/6 mice than in the DBA/2N mice, following
intraperitoneal administration. However, the DBA/2N mice were more susceptible to immunosuppression following oral administration. These results suggest that PAHs are rapidly metabolized and excreted following oral administration in AHH-inducible mice, whereas in AHH-noninducible mice, the PAHs are absorbed and distributed to target organs. Based on these results, the authors concluded that AHH inducibility plays an important role in the immunosuppressive
activity of PAHs.
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