CHANGES IN BODY AND ORGAN WEIGHTS, HEMATOLOGICAL PARAMETERS, AND FREQUENCY OF MICRONUCLEI IN THE PERIPHERAL BLOOD ERYTHROCYTES OF ICR MICE EXPOSED TO LOW-DOSE-RATE $\gamma$-RADIATION

  • Kang, Yu-Mi (Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., Ltd.) ;
  • Shin, Suk-Chul (Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., Ltd.) ;
  • Jin, Young-Woo (Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., Ltd.) ;
  • Kim, Hee-Sun (Radiation Health Research Institute, Korea Hydro & Nuclear Power Co., Ltd.)
  • Published : 2009.09.30

Abstract

We exposed ICR mice to low-dose (0.2 Gy) and low-dose-rate (0.7 mGy/h) $\gamma$-radiation ($^{137}Cs$) in the Low-dose-rate Irradiation Facility at the Radiation Health Research Institute to evaluate systemic effects of low-dose radiation. We compared the body and organ weights, number of blood cells (white and red blood cells and platelets), levels of biochemical markers in serum, and frequency of micronuclei in polychromatic erythrocytes between low-dose irradiated and non-irradiated control mice. The ICR mice irradiated with total doses of 0.2 and 2 Gy showed no changes in body and organ weights, number of blood cells (white and red blood cells), or frequency of micronuclei in the polychromatic erythrocytes of peripheral blood. However, the number of platelets (P = 0.002) and the liver weight (P < 0.01) were significantly increased in mice exposed to 0.2 and 2 Gy, respectively. These results suggest that a low-dose-rate of 0.7 mGy/h does not induce systemic damage. This dose promotes hematopoiesis in the bone marrow microenvironment and the proliferation of liver cells. In the future, the molecular biological effects of lower doses and dose rates need to be evaluated.

Keywords

References

  1. Bennett B, Repacholi M, Carr Z. Health effect of the Chernobyl accident and special health care programmes. Report of the UN Chernobyl Forum Expert Group "Health". 2006
  2. Nomura T. Transgenerational effects of radiation andchemicals in mice and humans. J. Radiat. Res. 2006;47Suppl B:B83-97 https://doi.org/10.1269/jrr.47.B83
  3. Park SH, Lee Y, Jeong K, Yoo SY, Cho CK, Lee YS.Different induction of adaptive response to ionizing radiation in normal and neoplastic cells. Cell Biol. Toxicol. 1999Apr;15:111-119 https://doi.org/10.1023/A:1007525531145
  4. Wu Z, Jiang X, Shen S, Tan S, Xue H. The nature of radiation damage of haemopoietic stem cells under continuous irradiation at low dose rate. Sci. Sin. 1981 Dec;24(12):1744-1751
  5. Nakamura H, Yasui Y, Saito N, Tachibana A, Komatsu K,Ishizaki K. DNA repair defect in AT cells and their hypersensitivity to low-dose-rate radiation. Radiat. Res.2006 Mar;165(3):277-282 https://doi.org/10.1667/RR3519.1
  6. Chen SL, Cai L, Meng QY, Xu S, Wan H, Liu SZ. Lowdosewhole-body irradiation (LD-WBI) change proteinex pression of mouse thymocyte: Effect of a LD-WBIenhanced prote in RIP10 on cell proliferation and spontaneous or radiation induced thymocyte apoptosis. Toxicol. Sci.2000 May;55(1):97-106 https://doi.org/10.1093/toxsci/55.1.97
  7. Takahashi A, Ohnishi K, Asakawa I, Kondo N, NakagawaH, Yonezawa M, Tachibana A, Matsumiti H, Ohnishi T. Radiation response of apoptosis in C57BL/6N mouse spleen after whole-body irradiation. Int. J. Radiat. Biol. 2001 Sep;77(9):939-945 https://doi.org/10.1080/09553000110062873
  8. Ren H, Shen J, Tomiyama-Miyaji C, Watanabe M, Kainuma E, Inoue M, Kuano Y, Abo T. Augmentation of innate immunity by low-dose irradiation. Cell Immunol. 2006Nov;244(1):50-56 https://doi.org/10.1016/j.cellimm.2007.02.009
  9. Takahashi M, Kojima S, Yamaoka K, Niki E. Preventionof type I diabetes by low-dose gamma irradiation in NOD mice. Radiat. Res. 2000 Dec;154(6):680-685 https://doi.org/10.1667/0033-7587(2000)154[0680:POTIDB]2.0.CO;2
  10. Tsuruga M, Taki K, Ishii G, Sasaki Y, Furukawa C, SugiharaT, Nomura T, Ochiai A, Magae J. Amelioration of type IIdiabetes in db/db mice by continuous low-dose-rate gammairradiation. Radiat. Res. 2007 May;167(5):592-599 https://doi.org/10.1667/RR0786.1
  11. Tago F, Tsukimoto M, Nakatsukasa H, Kojima S. Repeated 0.5 Gy gamma irradiation attenuates autoimmune diseasein MRL-lpr/lpr mice with suppression of CD3+CD4-CD8-B220+ T-cell proliferation and up-regulation of CD4+CD25+Foxp3+ regulatory T cells. Radiat. Res. 2008;169(1):59-66 https://doi.org/10.1667/RR1013.1
  12. UNSCER. Volume I and II. United Nations sales publication E.00.IX.3 and E.00.IX.4 United Nations, New York. 2000
  13. Hoshi Y, Nomura T, Oda T, Iwasaki T, Fugita K, IshikawaT, Kato A, Ikegami T, Sakai K, Tanooka H, Yamada T. Application of a newly developed photoluminescenceglass dosimeter for measuring the absorbed dose in individualmice exposed to low-dose rate 137Cs gamma-rays. J. Radiat.Res. 2000 Jun;41(2):129-137 https://doi.org/10.1269/jrr.41.129
  14. Hayashi M, Morita T, Kodama Y, Sofuni T, Ishidate M. The micronucleus assay with mouse peripheral blood recticulocytes using acridine orange-coated slides. Mutat.Res. 1990 Dec;245(4):245-249 https://doi.org/10.1016/0165-7992(90)90153-B
  15. Tsiperson VP, Soloviev MY. The impact of chronicradioactive stress on the immuno-physiological condition ofsmall mammals. Sci. Total Environ. 1997 Sep;203(2):105-113 https://doi.org/10.1016/S0048-9697(97)00138-1
  16. Kim CS, Kim JK, Nam SY, Yang KH, Jeong MS, KimHS, Kim CS, Jin YW, Kim J. Low-dose radiation stimulates the proliferation of normal human lung fibroblasts via a transient activation of Raf and Akt. Mol. Cells 2007Dec;24(3):424-430
  17. Kim CH, Kim JM, Nam SY, Yang KH, Jeong MS, Kim HS, Lim YK, Kim CH, Jin YW, Kim J. Low-dose ionization enhance cell proliferation via transient ERK1/2 and p38 activation in normal human lung fibroblasts. J. Radiat. Res. 2007;48:407-415 https://doi.org/10.1269/jrr.07032
  18. Goodman R, Grate H, Hannon E, Hellman S. Hematopoietic stem cell: Effect of preirradiation, bleeding, and erythropoietin on thrombopoietic differentiation. Blood 1977 Feb;49(2):253-261