Elucidation of the toxic mechanism of the plasticizers, phthalic acid esters, putative endocrine disrupters: Effects of dietary di(2-ethylhexyl)phthalate on the metabolism of tryptophan to niacin in rats

• Published in: Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2002-04, Vol.66 (4), p.705-710
• Main Authors: Fukuwatari, T. (Shiga Prefectural Univ., Hikone (Japan)), Suzuki, Y, Sugimoto, E, Shibata, K
• Format: Article
• Language: English
• Subjects: Administration, Oral; Animals; Biological and medical sciences; Body Weight - drug effects; Chemical and industrial products toxicology. Toxic occupational diseases; DIET; Diethylhexyl Phthalate - administration & dosage; Diethylhexyl Phthalate - toxicity; Dose-Response Relationship, Drug; ENDOCRINE GLANDS; Energy Intake - drug effects; Liver - anatomy & histology; Liver - drug effects; Medical sciences; METABOLISM; NAD - metabolism; NADP - metabolism; Niacin - biosynthesis; Niacin - urine; NICOTINAMIDE; Organ Size - drug effects; PHTHALATES; RATS; TOXICITY; Toxicology; TRYPTOPHAN; Tryptophan - metabolism; Various organic compounds
• ISSN: 0916-8451; 1347-6947
• DOI: 10.1271/bbb.66.705

We have previously reported that the administration of a large amount of di(n-butyl)phthalate (DBF) increased the conversion ratio of tryptophan to niacin in rats. In the present experiment, the effect of di(2-ethyl-hexyl)phthalate (DEHP) on the conversion ratio and how altering the conversion ratio of tryptophan to niacin depended on the concentration of DEHP were investigated to elucidate the toxic mechanism of phthalic acid esters (PhE). Rats were fed with a diet containing 0%, 0.01%, 0.05%, 0.1%, 0.5%, 1.0%, or 3.0% DEHP for 21 days. To assess the conversion ratio of tryptophan to niacin, urine samples were collected at the last day of the experiment and measured for metabolites on the tryptophan-niacin pathway. The conversion ratio increased with increasing dietary concentration of DEHP above 0.05%; the conversion ratio was about 2% in the control group, whereas it was 28% in the 3.0% DEHP group. It is suggested that the inhibition of alpha-amino-beta-carboxymuconate-e-semialdehyde decarboxylase (ACMSD) by DEHP or its metabolites caused this increase in the conversion ratio. We conclude that PhE such as DEHP and DBP disturbed the tryptophanniacin metabolism.