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Toxicology of Industrial Compounds

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1979), such as tetrazole or a sulphonamide moiety (Eacho et al., 1986;<br />

Lock et al., 1989).<br />

It should be noted that rodent liver peroxisome proliferators exhibit<br />

marked compound potency differences. While potent peroxisome<br />

proliferators include compounds developed as hypolipidaemic agents (e.g.<br />

cipr<strong>of</strong>ibrate, Wy-14,643), plasticisers such as DEHP are less potent and<br />

chemicals such as acetylsalicylic acid are even less potent (Reddy et al.,<br />

1986; Barber et al., 1987; Lake and Lewis, 1993). For example, in a 30day<br />

feeding study, a similar magnitude <strong>of</strong> induction <strong>of</strong> palmitoyl-CoA<br />

oxidation was observed in rats fed 0.001 per cent cipr<strong>of</strong>ibrate and 0.5 per<br />

cent DEHP diets, whereas for DEHA a dietary level <strong>of</strong> >1.0 per cent but

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