Treatment of irradiated mice with high-dose ascorbic acid reduced lethality

PLoS One. 2015 Feb 4;10(2):e0117020. doi: 10.1371/journal.pone.0117020. eCollection 2015.

Abstract

Ascorbic acid is an effective antioxidant and free radical scavenger. Therefore, it is expected that ascorbic acid should act as a radioprotectant. We investigated the effects of post-radiation treatment with ascorbic acid on mouse survival. Mice received whole body irradiation (WBI) followed by intraperitoneal administration of ascorbic acid. Administration of 3 g/kg of ascorbic acid immediately after exposure significantly increased mouse survival after WBI at 7 to 8 Gy. However, administration of less than 3 g/kg of ascorbic acid was ineffective, and 4 or more g/kg was harmful to the mice. Post-exposure treatment with 3 g/kg of ascorbic acid reduced radiation-induced apoptosis in bone marrow cells and restored hematopoietic function. Treatment with ascorbic acid (3 g/kg) up to 24 h (1, 6, 12, or 24 h) after WBI at 7.5 Gy effectively improved mouse survival; however, treatments beyond 36 h were ineffective. Two treatments with ascorbic acid (1.5 g/kg × 2, immediately and 24 h after radiation, 3 g/kg in total) also improved mouse survival after WBI at 7.5 Gy, accompanied with suppression of radiation-induced free radical metabolites. In conclusion, administration of high-dose ascorbic acid might reduce radiation lethality in mice even after exposure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / administration & dosage*
  • Apoptosis / drug effects
  • Apoptosis / radiation effects
  • Ascorbic Acid / administration & dosage*
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / radiation effects
  • Hematopoiesis / drug effects
  • Hematopoiesis / radiation effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Radiation, Ionizing
  • Radiation-Protective Agents / administration & dosage*
  • Survival Analysis
  • Whole-Body Irradiation

Substances

  • Antioxidants
  • Radiation-Protective Agents
  • Ascorbic Acid

Grants and funding

This work was supported by a grant-in-aid for Special Research Program (Host stress responses to internal and external factors) from the National Defense Medical College to M.K. and S.S. and a grant-in-aid for Promoted Research Program of Defense Medicine (Host defense against radiation) from the Ministry of Defense to M.K. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.