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Long Bones Exhibit Adaptive Responses to Chronic Low-Dose-Rate Ionizing Radiation despite its Lifespan-Shortening and Carcinogenic Effects on C57BL/6 Mice.
Kohzaki, Masaoki; Ootsuyama, Akira; Abe, Toshiaki; Tsukamoto, Manabu; Umata, Toshiyuki; Okazaki, Ryuji.
Afiliación
  • Kohzaki M; Department of Radiobiology and Hygiene Management Institute of Industrial Ecological Sciences, University of Occupational and Environmental Health Kitakyushu Japan.
  • Ootsuyama A; Department of Radiation Biology and Health School of Medicine, University of Occupational and Environmental Health Kitakyushu Japan.
  • Abe T; Radioisotope Research Center Facility for Education and Research Support, University of Occupational and Environmental Health Kitakyushu Japan.
  • Tsukamoto M; Department of Orthopedic Surgery, School of Medicine University of Occupational and Environmental Health Kitakyushu Japan.
  • Umata T; Radioisotope Research Center Facility for Education and Research Support, University of Occupational and Environmental Health Kitakyushu Japan.
  • Okazaki R; Department of Radiobiology and Hygiene Management Institute of Industrial Ecological Sciences, University of Occupational and Environmental Health Kitakyushu Japan.
JBMR Plus ; 6(12): e10688, 2022 Dec.
Article en En | MEDLINE | ID: mdl-36530184
ABSTRACT
Ionizing radiation (IR) is a well-known carcinogen. High-dose-rate (HDR) IR is known to damage long bones (in terms of mass and structure), but the relationships among dose rates (particularly low-dose-rate [LDR] IR), long-bone condition, cancer incidence, and lifespan shortening remain elusive. The aim of this study was to elucidate the effects of LDR-IR on long-bone condition by comparing the long-term consequences of HDR- and LDR-IR exposure in mice. We utilized micro-computed tomography (µCT) scans of the long bones at similar ages (mean 77-96 weeks) to compare mice receiving approximately equivalent total doses of internal LDR-IR or external HDR-IR starting at 4 weeks of age, and their respective control groups. The lifespan-shortening effects of LDR-IR and HDR-IR were similar in these mixed-sex cohorts. Notably, compared to HDR-IR mice, mice internally exposed to chronic LDR-IR with continuous hypohematopoiesis showed a significantly higher trabecular bone connective density [femur 247% (p = 0.0042), tibia 169% (p = 0.0005)] and midshaft cortical bone thickness/area (femur 130% [p = 0.0079]/120% [p = 0.021], tibia 148% [p = 0.0004]/129% [p = 0.002]). Consistent with this result, when comparing 26-32 weeks post-IR with 2-8 weeks post-IR, compared to HDR-IR-treated mice, LDR-IR-treated mice exhibited higher levels of an osteoblast marker (OPG; p = 0.67 for HDR-IR, p = 0.068 for LDR-IR) and lower levels of an osteoclast marker (CTX-I; p = 0.0079 for HDR-IR, p = 0.72 for LDR-IR) despite significantly higher levels of inflammatory markers (CCL2 and CXCL1; p = 0.36-0.8 for HDR-IR, p = 0.013-0.041 for LDR-IR). These results suggest that long bones under chronic LDR-IR stress may exhibit an adaptive response to stresses such as chronic inflammation associated with IR-induced lifespan shortening. © 2022 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
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