| Literature DB >> 32586004 |
Kazuko Shichijo1, Toshihiro Takatsuji2, Zhaslan Abishev3, Darkhan Uzbekov3, Nailya Chaizhunusova3, Dariya Shabdarbaeva3, Daisuke Niino1, Minako Kurisu4, Yoshio Takahashi4, Valeriy Stepanenko5, Almas Azhimkhanov6, Masaharu Hoshi7.
Abstract
Internal radiation exposure from neutron-induced radioisotopes environmentally activated following atomic bombing or nuclear accidents should be considered for a complete picture of pathologic effects on survivors. Inhaled hot particles expose neighboring tissues to locally ultra-high doses of β-rays and can cause pathologic damage. 55MnO2 powder was activated by a nuclear reactor to make 56MnO2 which emits β-rays. Internal exposures were compared with external γ-rays. Male Wistar rats were administered activated powder by inhalation. Lung samples were observed by histological staining at six hours, three days, 14 days, two months, six months and eight months after the exposure. Synchrotron radiation - X-ray fluorescence - X-ray absorption near-edge structure (SR-XRF-XANES) was utilized for the chemical analysis of the activated 56Mn embedded in lung tissues. 56Mn beta energy spectrum around the particles was calculated to assess the local dose rate and accumulated dose. Hot particles located in the bronchiole and in damaged alveolar tissue were identified as accumulations of Mn and iron. Histological changes showed evidence of emphysema, hemorrhage and severe inflammation from six hours through eight months. Apoptosis was observed in the bronchiole epithelium. Our study shows early event damage from the locally ultra-high internal dose leads to pathogenesis. The trigger of emphysema and hemorrhage was likely early event damage to blood vessels integral to alveolar walls.Entities:
Keywords: 56Mn; A-bombing; SR-XRF; X-ray absorption near-edge structure (XANES); apoptosis; elastin; elemental imaging; internal radiation exposure; lung; micro-dosimetry
Year: 2020 PMID: 32586004 DOI: 10.3390/biomedicines8060171
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059