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氨磷汀联合粒细胞集落刺激因子治疗可增强超致死剂量辐射暴露后的恢复能力:动物模型的临床前研究经验

Amifostine plus granulocyte colony-stimulating factor therapy enhances recovery from supralethal radiation exposures: preclinical experience in animals models.

作者信息

Patchen M L

机构信息

Alpha Beta Technologies, Worcester, Massachusetts 01605, USA.

出版信息

Eur J Cancer. 1995;31A Suppl 1:S17-21. doi: 10.1016/0959-8049(95)00147-b.

Abstract

A murine model was used to explore whether the cytoprotective agent amifostine (WR-2721) can be used to protect a critical fraction of haemopoietic stem cells against radiation, and whether granulocyte colony-stimulating factor (G-CSF) can then be used to stimulate the protected cells to proliferate and reconstitute the haematopoietic system. Groups of C3H/HeN mice treated with 200 mg/kg amifostine i.p. 30 min before 60Co irradiation and/or 125 micrograms/kg G-CSF subcutaneously from days 1-16 post irradiation were compared. The dose reduction factor (DRF) of the combination of amifostine and G-CSF from LD50/30 values was greater than the sum of the DRFs for amifostine and G-CSF individually. Acceleration of recovery bone marrow and splenic multipotent stem cells (CFU-s) and granulocyte-macrophage progenitor cells (GM-CFC), as well as of peripheral blood red and white cells and platelets, was greatest in mice treated with amifostine plus G-CSF. These studies suggest that amifostine and recombinant haematopoietic growth factors can be used in combination to reduce myelosuppression and lethality associated with radiation or radiomimetic drugs

摘要

利用小鼠模型来探究细胞保护剂氨磷汀(WR-2721)是否可用于保护一部分关键的造血干细胞免受辐射,以及粒细胞集落刺激因子(G-CSF)随后是否可用于刺激受保护的细胞增殖并重建造血系统。比较了在60Co照射前30分钟腹腔注射200mg/kg氨磷汀和/或在照射后第1 - 16天皮下注射125μg/kg G-CSF的C3H/HeN小鼠组。根据半数致死剂量/30天(LD50/30)值计算,氨磷汀和G-CSF联合使用的剂量降低因子(DRF)大于氨磷汀和G-CSF单独使用时DRF的总和。在接受氨磷汀加G-CSF治疗的小鼠中,骨髓和脾脏多能干细胞(CFU-s)以及粒细胞 - 巨噬细胞祖细胞(GM-CFC)的恢复加速,外周血红细胞、白细胞和血小板的恢复也最为显著。这些研究表明,氨磷汀和重组造血生长因子可联合使用,以减轻与辐射或拟辐射药物相关的骨髓抑制和致死率。

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