In 1964, Bleiberg
et al. reported high prevalence of porphyria cutanea tarda (PCT) among the workers in a 2, 4-D and 2, 4, 5-T producing plant. Since then, like chlorinated benzenes, some of the poly-chlorinated phenols have been suspected as a possible inducer of PCT, but the experimental evidence is as yet lacking.
A series of feeding experiments of 2, 4-di-, 2, 4, 5-tri-, and penta-chlorophenol (2, 4-DCP, 2, 4, 5-TCP, PCP) to rats was carried out in order to determine whether these chemicals themselves are really able to induce hepatic porphyria. In the first experiment, a short term experiment with a large dose, the chemicals were administered to rats in the doses of 200-1, 000 mg/kg every day for 3 weeks, and in the second a small dose of chemicals, 10 mg/day/capita (30-70 mg/kg), was administered every day for 17 weeks. All of the rats including the control were fasted for 3 days in the last week of each experiment. The results obtained are summarized as follows.
Urinary excretion of ALA and coproporphyrin did not increase, or rather decreased in the rats treated with the chlorinated phenols during the course of both experiments. No uroporphyrinuria was found in all of the rats. In the groups treated with each of the chlorinated phenols, the average values of urinary PBG and fecal porphyrin showed no significant increase compared with those in the control. Abnormal accumulation of porphyrins in the liver and kidneys was not observed in all of the rats, and uroporphyrin contents in these organs were under the limit of detection. Histologic examination revealed only a slight liver damage with vacuole degeneration and intralobular leucocytic infiltration in about half of the rats treated with chlorinated phenols.
From these results, it seems unlikely that the poly-chlorinated phenols have potency to induce hepatic porphyria. However, it should be noted that improvement and control of working environment are necessary in the factories producing these organochloric herbicides because there are some possibilities of the presence of highly hepatotoxic chemicals having the induction potency of porphyria, such as chlorinated benzenes and tetrachlorodibenzo-
p-dioxin, in their synthesizing process as pre-compounds or by-products.
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