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缺氧对平台期中国仓鼠卵巢细胞热损伤和辐射损伤恢复的影响。

Effect of hypoxia on recovery from damage induced by heat and radiation in plateau-phase CHO cells.

作者信息

Rao B S, Hopwood L E

出版信息

Radiat Res. 1985 Feb;101(2):312-25.

PMID:3975360
Abstract

The effect of hypoxia on the induction of and recovery from damage by radiation alone and in combination with heat has been investigated using plateau-phase Chinese hamster ovary (CHO) cells. Postirradiation hypoxia reduced the potentially lethal damage recovery (PLDR) in cells irradiated under an euoxic state and completely eliminated PLDR in cells irradiated under hypoxia. Cells which were maintained under hypoxia during both irradiation and a 4-hr recovery period and then incubated for a further period of 4 hr under euoxic conditions showed PLDR, suggesting that the inhibition of PLDR by hypoxia is reversible. Oligomycin, an inhibitor of energy metabolism, completely eliminated PLDR when present at a concentration of 1 microM during the postirradiation period. Pre- or postirradiation heat treatment at 42.5 degrees C for 30 min appreciably sensitized the cells to the induction of lethality. Thermal enhancement ratio (TER) was 1.7 for cells irradiated and heat treated under hypoxic conditions. The same heat treatment reduced the oxygen enhancement ratio (OER) associated with gamma radiation from 3.1 to 2.5. Cells subjected to this postirradiation heat treatment showed a small extent of PLDR, whereas the pre-heat-treated cells showed as much recovery as non-heat-treated cells. When hypoxic conditions prevailed during the post-treatment incubation period, PLDR was reduced in preheated cells and completely eliminated in postheated cells. The kinetics of interaction between heat and radiation damage were studied by introducing a time gap of 4 hr between the treatments. Cells maintained under euoxic conditions between the treatments showed an appreciable decrease in interaction, suggesting recovery from damage induced by the first treatment. Hypoxic conditions intervening the two treatments largely inhibited the loss of sensitization. Analysis of the results suggests that cells fail to recover from sublethal heat damage when held for 4 hr under hypoxic conditions. Cells held under hypoxic conditions partly recover from the radiation damage which subsequently interacts with sublethal heat damage, resulting in cell lethality.

摘要

利用处于平台期的中国仓鼠卵巢(CHO)细胞,研究了缺氧对单独辐射以及辐射与热联合作用所致损伤的诱导和恢复的影响。照射后缺氧降低了在常氧状态下照射的细胞中潜在致死性损伤的恢复(PLDR),并完全消除了在缺氧状态下照射的细胞中的PLDR。在照射和4小时恢复期均处于缺氧状态,然后在常氧条件下再培养4小时的细胞显示出PLDR,这表明缺氧对PLDR的抑制是可逆的。能量代谢抑制剂寡霉素在照射后阶段以1 microM的浓度存在时,完全消除了PLDR。在42.5℃下进行30分钟的照射前或照射后热处理,可明显使细胞对致死性诱导敏感。在缺氧条件下照射并热处理的细胞的热增强比(TER)为1.7。相同的热处理使与γ辐射相关的氧增强比(OER)从3.1降至2.5。接受这种照射后热处理的细胞显示出较小程度的PLDR,而预热处理的细胞显示出与未热处理的细胞相同程度的恢复。当在后处理孵育期普遍存在缺氧条件时,预加热细胞中的PLDR降低,而后加热细胞中的PLDR完全消除。通过在处理之间引入4小时的时间间隔,研究了热与辐射损伤之间的相互作用动力学。在处理之间保持在常氧条件下的细胞显示出相互作用明显降低,表明从第一次处理诱导的损伤中恢复。介于两次处理之间的缺氧条件在很大程度上抑制了敏化作用的丧失。结果分析表明,细胞在缺氧条件下保持4小时后无法从亚致死性热损伤中恢复。在缺氧条件下保持的细胞部分从辐射损伤中恢复,随后与亚致死性热损伤相互作用,导致细胞死亡。

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