Inhibition of δ-aminolevulinate dehydratase in trichloroethylene-exposed rats, and the effects on heme regulation

Hiroyoshi Fujita, Akio Koizumi, Masayuki Yamamoto, Miho Kumai, Tetsuo Sadamoto, Masayuki Ikeda

研究成果: Article査読

23 被引用数 (Scopus)

抄録

A pronounced and irreversible depression of the erythroid and liver δ-aminolevulinate dehydratase (porphobilinogen synthase; 5-aminolevulinate hydro-lyase, EC 4.2.1.24) activity was observed in rats exposed to trichloroethylene, a widely used solvent. The depression could not be restored after the treatment with dithiothreitol and zinc; however, radioimmunoassay of δ-aminolevulinate dehydratase indicated that trichloroethylene exposure did not essentially decrease the amount of enzyme. The depression of the enzyme activity thus proved to be due to a reduction in the enzyme amount but to enzyme inhibition. The purified holoenzyme (fully activated δ-aminolevulinate dehydratase with 1 atom zinc per subunit) and apoenzyme (fully activated enzyme with the remaining zinc less than 0.1 atom per subunit) were prepared to investigate the in vitro inhibition of the enzyme by trichloroethylene. Incubation with trichloroethylene did not inhibit the holoenzyme, but inhibited the apoenzyme dose-dependently. Trichloroethylene inhibited the holoenzyme when incubated with the mixed function oxidase system. The in vitro experiments reported here indicate two mechanisms of the enzyme inhibition by trichloroethylene. In the liver of rats exposed to trichloroethylene, cytochrome P-450 concentration and heme saturation of tryptophan pyrrolase (EC 1.13.11.11) are reduced; in addition, the activity of δ-aminolevulinate synthase (EC 2.3.1.37) increased. After exposure to trichloroethylene at 2.14 g/m3, urinary δ-aminolevulinic acid increased to 142% of the control, while the excretion of coproporphyrin was reduced to 19.6% of the control.

本文言語English
ページ(範囲)1-10
ページ数10
ジャーナルBBA - General Subjects
800
1
DOI
出版ステータスPublished - 1984 7 16

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

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