RhG-CSF Improves Radiation-induced Myelosuppression and Survival in the Canine Exposed to Fission Neutron Irradiation
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- YU Zu-Yin
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- LI Ming
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- HAN A-Ru-Na
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- XING Shuang
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- OU Hong-Ling
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- XIONG Guo-Lin
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- XIE Ling
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- ZHAO Yan-Fang
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- XIAO He
- Department of Molecular Immunology, Institute of Basic Medical Sciences
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- SHAN Ya-Jun
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- ZHAO Zhen-Hu
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- LIU Xiao-Lan
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- CONG Yu-Wen
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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- LUO Qing-Liang
- Department of Experimental Therapeutic of Radiation Sickness, Beijing Institute of Radiation Medicine
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抄録
Fission-neutron radiation damage is hard to treat due to its critical injuries to hematopoietic and gastrointestinal systems, and so far few data are available on the therapeutic measures for neutron-radiation syndrome. This study was designed to test the effects of recombinant human granulocyte colony-stimulating factor (rhG-CSF) in dogs which had received 2.3 Gy mixed fission-neutron-γ irradiation with a high ratio of neutrons (~90%). Following irradiation, rhG-CSF treatment induced 100% survival versus 60% in controls. Only two of five rhG-CSF-treated dogs experienced leukopenia (white blood cells [WBC] count < 1.0 × 109/L) and neutropenia (neutrophil [ANC] count < 0.5 × 109/L), whereas all irradiated controls displayed a profound period of leukopenia and neutropenia. Furthermore, administration of rhG-CSF significantly delayed the onset of leukopenia and reduced the duration of leucopenia as compared with controls. In addition, individual dogs in the rhG-CSF-treated group exhibited evident differences in rhG-CSF responsiveness after neutron-irradiation. Finally, histopathological evaluation of the surviving dogs revealed that the incidence and severity of bone marrow, thymus and spleen damage decreased in rhG-CSF-treated dogs as compared with surviving controls. Thus, these results demonstrated that rhG-CSF administration enhanced recovery of myelopoiesis and survival after neutron-irradiation.
収録刊行物
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- Journal of Radiation Research
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Journal of Radiation Research 52 (4), 472-480, 2011
Journal of Radiation Research 編集委員会
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詳細情報 詳細情報について
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- CRID
- 1390001205215260160
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- NII論文ID
- 10029122222
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- NII書誌ID
- AA00705792
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- ISSN
- 13499157
- 04493060
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- NDL書誌ID
- 11164145
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- PubMed
- 21785235
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可