It has been reported in the previous paper that the myelotoxicity of benzene is related to its metabolic changes.
In the present paper, benzene metabolites were tested for myelotoxicity similar to that of benzene. Metabolites were administered to seven-week-old, 130 g male Donryu rats subcutaneously on the back daily. Doses of metabolites were determined by using the results of Parke's experiment. Criteria used for the evaluation were body weight, erythrocyte count, leucocyte count, thrombocyte count, and hemoglobin content of the blood taken from the tail. Reversal experiment was applied to the present studies in three sections, each for seven days, to eliminate the time factor.
Phenol (0.20 g/kg) caused leucocytosis; hydroquinone (0.05 g/kg), decrease of body weight; pyrocatechol (0.03 g/kg), erythropenia and leucopenia; hydroxyhydroquinone (0.005 g/kg), t-t muconic acid (0.013 g/kg), and D, L-phenylmercapturic acid (0.01 g/kg), no changes. Conjugated phenol was tested at the same time. Potassium phenylsulfate (0.50 g/kg) caused an increase in body weight and leucocytosis.
From the above results, the likely cause of hemopoietic disturbance in chronic benzene poisoning is the formation of pyrocatechol via benzeneglycol.
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