Administration of nitro-oleic acid mitigates radiation-induced hematopoietic injury in mice

Life Sci. 2022 Dec 1:310:121106. doi: 10.1016/j.lfs.2022.121106. Epub 2022 Oct 20.

Abstract

Aims: Limited number of agents that provide protection against hematopoietic acute radiation syndrome led us to the evaluation of nitro-oleic acid (NO2OA) as a potential protector/mitigator against radiation-induced hematopoietic injury in C57/BL6 mice.

Materials and methods: NO2OA was administered before and after sub-lethal total body irradiation (TBI) and hematological parameters were evaluated 3 or 7 days after TBI.

Key findings: Our results show that NO2OA significantly increase bone marrow cellularity including the granulocyte-macrophage colony-forming cells and erythroid progenitors on the 3rd day after TBI. In addition, NO2OA enhanced recovery of white blood cells (lymphocytes, neutrophils, and monocytes) in peripheral blood 7 days after irradiation. These effects may be in part attributed to NO2OA-induced granulocyte colony-stimulating factor production after TBI. On the other hand, radiation-induced impairment of peripheral red blood cells, hemoglobin, and platelets were not affected with NO2OA treatment up to 7 days post TBI.

Significance: In conclusion, our data show that NO2OA significantly protects hematopoiesis after irradiation, and thus showed a high potential to act as an agent for medical radiation countermeasure.

Keywords: Acute radiation syndrome; Bone marrow cells; G-CSF; Hematopoiesis; Nitro-oleic acid.

MeSH terms

  • Animals
  • Bone Marrow*
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Hematopoiesis / radiation effects
  • Hematopoietic Stem Cells*
  • Mice
  • Mice, Inbred C57BL
  • Recombinant Proteins / pharmacology
  • Whole-Body Irradiation

Substances

  • CXA-10
  • Granulocyte Colony-Stimulating Factor
  • Recombinant Proteins