Possible role of elevation of glutathione in the acquisition of enhanced proliferation of mouse splenocytes exposed to small-dose γ-rays

S. Kojima, S. Matsumori, H. Ishida, Kiyonori Yamaoka

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

Purpose: To examine the relation between the induction of an increased glutathione level and the elevated proliferative response of mouse splenocytes by a small dose of γ-rays. Materials and methods: Male ICR strain mice, 7 weeks of age, were divided into irradiated and non-irradiated control groups. Irradiation was done with γ-rays from 137Cs source at a dose of 50 cGy (1.11 Gy/min). Glutathione content in the splenocytes was measured using a modified spectrophotometric technique. Concanavalin A (Con A)-induced proliferative response of the splenocytes after whole-body γ-ray irradiation was estimated from the 3H-thymidine incorporation into the cells. Results: The glutathione level in mouse splenocytes increased 2 h after whole-body γ-ray irradiation at 50 cGy, peaked at 4 h and thereafter decreased almost to the zero-time level by 12-h post-irradiation. A significant enhancement of Con A-induced proliferation was observed in the splenocytes obtained from the wholebody-irradiated animals between 2 h and 6 h post-irradiation. Glutathione exogenously added to splenocytes obtained from normal mice enhanced the Con A-induced proliferation of splenocytes in a dose-dependent manner. This enhancement was completely blocked by buthionine sulfoximine, a specific inhibitor of the de novo pathway of glutathione synthesis. Conclusions: The induction of endogenous glutathione immediately after low-dose γ-ray irradiation is at least partially responsible for the enhancement of immune function, and may throw light on the mechanisms of carcinostatic effects induced by low dose ionizing radiation.

Original languageEnglish
Pages (from-to)1641-1647
Number of pages7
JournalInternational Journal of Radiation Biology
Volume76
Issue number12
Publication statusPublished - 2000
Externally publishedYes

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glutathione
splenocytes
Glutathione
mice
acquisition
rays
Irradiation
irradiation
dosage
Concanavalin A
concanavalin A
Whole-Body Irradiation
Dosimetry
augmentation
induction
Buthionine Sulfoximine
thymidine
Inbred ICR Mouse
Ionizing radiation
Ionizing Radiation

ASJC Scopus subject areas

  • Agricultural and Biological Sciences (miscellaneous)
  • Radiology Nuclear Medicine and imaging
  • Radiological and Ultrasound Technology
  • Nuclear Energy and Engineering
  • Radiation

Cite this

Possible role of elevation of glutathione in the acquisition of enhanced proliferation of mouse splenocytes exposed to small-dose γ-rays. / Kojima, S.; Matsumori, S.; Ishida, H.; Yamaoka, Kiyonori.

In: International Journal of Radiation Biology, Vol. 76, No. 12, 2000, p. 1641-1647.

Research output: Contribution to journalArticle

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N2 - Purpose: To examine the relation between the induction of an increased glutathione level and the elevated proliferative response of mouse splenocytes by a small dose of γ-rays. Materials and methods: Male ICR strain mice, 7 weeks of age, were divided into irradiated and non-irradiated control groups. Irradiation was done with γ-rays from 137Cs source at a dose of 50 cGy (1.11 Gy/min). Glutathione content in the splenocytes was measured using a modified spectrophotometric technique. Concanavalin A (Con A)-induced proliferative response of the splenocytes after whole-body γ-ray irradiation was estimated from the 3H-thymidine incorporation into the cells. Results: The glutathione level in mouse splenocytes increased 2 h after whole-body γ-ray irradiation at 50 cGy, peaked at 4 h and thereafter decreased almost to the zero-time level by 12-h post-irradiation. A significant enhancement of Con A-induced proliferation was observed in the splenocytes obtained from the wholebody-irradiated animals between 2 h and 6 h post-irradiation. Glutathione exogenously added to splenocytes obtained from normal mice enhanced the Con A-induced proliferation of splenocytes in a dose-dependent manner. This enhancement was completely blocked by buthionine sulfoximine, a specific inhibitor of the de novo pathway of glutathione synthesis. Conclusions: The induction of endogenous glutathione immediately after low-dose γ-ray irradiation is at least partially responsible for the enhancement of immune function, and may throw light on the mechanisms of carcinostatic effects induced by low dose ionizing radiation.

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