Gamma-ray glow preceding downward terrestrial gamma-ray flash

Wada, Yuki*; Enoto, Teruaki*; Nakamura, Yoshitaka*; Furuta, Yoshihiro; Yuasa, Takayuki*; Nakazawa, Kazuhiro*; Morimoto, Takeshi*; Sato, Mitsuteru*; Matsumoto, Takahiro*; Yonetoku, Daisuke*; et al.

Communications Physics (Internet), 2(1), p.67_1 - 67_9, 2019/06

https://doi.org/10.1038/s42005-019-0168-y

Induction of DNA DSB and its rejoining in clamped and non-clamped tumours after exposure to carbon ion beams in comparison to X-rays

Hirayama, Ryoichi*; Uzawa, Akiko*; Matsumoto, Yoshitaka*; Noguchi, Miho; Kase, Yuki*; Takase, Nobuhiro*; Ito, Atsushi*; Koike, Sachiko*; Ando, Koichi*; Okayasu, Ryuichi*; et al.

Radiation Protection Dosimetry, 143(2-4), p.508 - 512, 2011/02

https://doi.org/10.1093/rpd/ncq478

We studied double-strand breaks (DSB) induction and rejoining in clamped and non-clamped transplanted tumours in mice leg after exposure to 80 keV/m carbon ions and X-rays. The yields of DSB in the tumours were analysed by a static-field gel electrophoresis. The OER of DSB after X-rays was 1.68, and this value was not changed after 1 h rejoining time (1.40). These damages in oxygenated conditions were rejoined 60-70% within 1 h in situ. No difference was found between the exposure to X-rays and carbon ions for the induction and rejoining of DSB. Thus, the values of OER and rejoined fraction after exposure to carbon ions were similar to those after X-rays, and the calculated relative biological effectivenesses of carbon ion were around 1 under both oxygen conditions. The yields of DSB in vivo depend on exposure doses, oxygen conditions and rejoining time, but not on the types of radiation quality.

Contributions of direct and indirect actions in cell killing by high-LET radiations

Hirayama, Ryoichi*; Ito, Atsushi*; Tomita, Masanori*; Tsukada, Teruyo*; Yatagai, Fumio*; Noguchi, Miho; Matsumoto, Yoshitaka*; Kase, Yuki*; Ando, Koichi*; Okayasu, Ryuichi*; et al.

Radiation Research, 171(2), p.212 - 218, 2009/02

https://doi.org/10.1667/RR1490.1

The biological effects of radiation originate principally in damages to DNA. DNA damages by X-rays as well as heavy ions are induced by a combination of direct and indirect actions. The contribution of indirect action in cell killing can be estimated from the maximum degree of protection by dimethylsulfoxide (DMSO), which suppresses indirect action without affecting direct action. Exponentially growing Chinese hamster V79 cells were exposed to high-LET radiations of 20 to 2106 keV/m in the presence or absence of DMSO and their survival was determined using a colony formation assay. The contribution of indirect action to cell killing decreased with increasing LET. However, the contribution did not reach zero even at very high LETs and was estimated to be 32% at an LET of 2106 keV/m. Therefore, even though the radiochemically estimated G value of OH radicals was nearly zero at an LET of 1000 keV/m, indirect action by OH radicals contributed to a substantial fraction of the biological effects of high-LET radiations. The RBE determined at a survival level of 10% increased with LET, reaching a maximum value of 2.88 at 200 keV/m, and decreased thereafter. When the RBE was estimated separately for direct action (RBE(D)) and indirect action (RBE(I)); both exhibited an LET dependence similar to that of the RBE, peaking at 200 keV/m. However, the peak value was much higher for RBE(D) (5.99) than RBE(I) (1.89). Thus direct action contributes more to the high RBE of high-LET radiations than indirect action does.

Study on the prediction accuracy of nuclide generation and depletion with JENDL

Okumura, Keisuke; Oki, Shigeo*; Yamamoto, Munenari*; Matsumoto, Hideki*; Ando, Yoshihira*; Tsujimoto, Kazufumi; Sasahara, Akihiro*; Katakura, Junichi; Matsumura, Tetsuo*; Aoyama, Takafumi*; et al.

JAERI-Research 2004-025, 154 Pages, 2005/01

JAERI-Research-2004-025.pdf:19.46MB

This report summarizes the activity (FY2000-2003) of Working Group (WG) on Evaluation of Nuclide Generation and Depletion under Subcommittee on Nuclear Fuel Cycle of Japanese Nuclear Data Committee. In the WG, analyses of Post Irradiation Examinations have been carried out for UO and MOX fuels irradiated in PWRs, BWRs and FBRs, and for actinide samples irradiated in fast reactors, by using ORIGEN or more detailed calculation codes with their libraries based on JENDL-3.2, JENDL-3.3 and other foreign nuclear data files. From these results, current prediction accuracy and problems for evaluation of nuclide generation and depletion are discussed. Furthermore, this report covers other products of our activity; development of the ORIGEN libraries for PWR, BWR and FBR based on JENDL-3.3, study on introduction of neutron spectrum index to ORIGEN calculations, and results of questionnaire survey on desirable accuracy of ORIGEN calculations.

Burnup code for fuel assembly by Monte Carlo code; MKENO-BURN

Naito, Yoshitaka; Suyama, Kenya; Masukawa, Fumihiro; Matsumoto, Kiyoshi; Kurosawa, Masayoshi; *

JAERI-Data/Code 96-037, 70 Pages, 1996/12

JAERI-Data-Code-96-037.pdf:1.68MB

no abstracts in English

Bystander effect and radiation quality with microbeams on cells

Furusawa, Yoshiya*; Matsumoto, Yoshitaka*; Hamada, Nobuyuki*; Wada, Seiichi*; Kobayashi, Yasuhiko; Funayama, Tomoo; Sakashita, Tetsuya; Kakizaki, Takehiko

no journal, , 

no abstracts in English

Rejoining of DNA double-strand breaks in hypoxic cells following irradiation by X-rays and heavy ions

Hirayama, Ryoichi*; Matsumoto, Yoshitaka*; Noguchi, Miho; Uzawa, Akiko*; Koda, Kana*; Furusawa, Yoshiya*

no journal, , 

The presence or absence of molecular oxygen dramatically influences the biological effect of low LET radiations. To produce oxygen effect, molecular oxygen must be present during the radiation exposure or at least during the lifetime of the free radicals generated by the radiation. Little study has been done to actually investigate the influence of oxygen after the radiation exposure. The present study was undertaken in order to explore the rejoining activity of DNA-DSB induced by anaerobic X-ray or carbon ion (80 keV/m) irradiations under oxic and hypoxic holdings (37 C). DNA-DSB in CHO cells were analyzed by a static-field gel electrophoresis. The kinetics of the rejoining could be described by a sum of fast and slow components. The slow component of DNA-DSB induced by X-ray under oxic incubation was faster than that under hypoxic incubation. Furthermore, the percentages of non-reparable DNA damage were 5% and 20% under oxic and hypoxic incubation conditions, respectively. However, no difference between oxic and hypoxic incubation conditions was found for carbon ion irradiation. There results indicate that molecular oxygen influences the rejoining of DNA-DSB after low LET radiation exposure.