Induction of mRNAs for glutathione synthesis-related proteins in mouse liver by low doses of gamma-rays

Biochim Biophys Acta. 1998 Aug 24;1381(3):312-8. doi: 10.1016/s0304-4165(98)00043-9.

Abstract

We examined the elevation of the reduced form of glutathione (GSH)level and the induction of MRNAs for proteins involved in the synthesis and regeneration of GSH in the liver of mice after low-dose gamma-ray irradiation. The liver GSH level increased soon after irradiation with 50 cGy of gamma-rays, reached a maximum at around 12 h post-treatment. The mRNA of gamma-glutamylcysteine synthetase (gamma-GCS), the rate-limiting enzyme for de novo synthesis for GSH, showed a small increase that peaked at 6 h after gamma-ray irradiation at a dose of 50 cGy. Only a small increase in gamma-GCS activity was observed throughout the 24-h post-irradiation period. In the case of glutathione reductase (GR), which is involved in the regeneration of GSH from the oxidized form (GSSG), the mRNA level peaked strongly at 1 h, while the activity peaked at twice the control level 12 h after irradiation. The level of mRNA for thioredoxin (TRX), which contributes to GSH biosynthesis by supplying cysteine to the de novo pathway, peaked at 1 h and declined thereafter, while the activity peaked at 3 h and then declined sharply. These results indicate that the increase in endogenous GSH immediately following low-dose gamma-ray irradiation is predominantly due to operation of the regeneration cycle and not de novo synthesis. We also examined the dependence of mRNA induction on the gamma-ray dose.

MeSH terms

  • Animals
  • Female
  • Gamma Rays
  • Glutamate-Cysteine Ligase / genetics
  • Glutathione / biosynthesis*
  • Glutathione Reductase / genetics
  • Kinetics
  • Liver / metabolism*
  • Liver / radiation effects*
  • Mice
  • Mice, Inbred C57BL
  • RNA, Messenger / biosynthesis*
  • Thioredoxins / genetics

Substances

  • RNA, Messenger
  • Thioredoxins
  • Glutathione Reductase
  • Glutamate-Cysteine Ligase
  • Glutathione