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Developmental stage selective toxicity

The effects of a chemical in a tissue frequently depend on the chemical s interaction with cell surface or cytoplasmic receptors. In some cases, a chemical interacts directly with the cell membrane and alters its permeability. The pharmacodynamic actions of drugs are usually mediated by interactions with a receptor, and a drug often competes with endogenous ligands of a receptor. The toxicity of environmental chemicals can also depend on and be mediated by interactions with receptors. In some cases, the responses are different for chemical exposures at different fetal stages of development, and it is possible to explain the different responses by the chronology of the development of fetal receptor systems. The fetus may develop receptor systems for a compound before it develops the ability to metabolize that compound thus, a low level of an active chemical can have greater and more persistent effects in the fetus than in the mother, whose metabolism limits the duration and extent of the effect. This is one mechanism for selective developmental toxicity of chemicals. [Pg.86]


See other pages where Developmental stage selective toxicity is mentioned: [Pg.360]    [Pg.72]    [Pg.265]    [Pg.214]    [Pg.98]    [Pg.444]    [Pg.336]    [Pg.205]    [Pg.153]    [Pg.2496]    [Pg.155]    [Pg.1291]    [Pg.3]    [Pg.296]    [Pg.462]   
See also in sourсe #XX -- [ Pg.186 ]




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