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首页> 外文期刊>Photochemistry and Photobiology: An International Journal >SYNERGISTIC INTERACTION OF PHOTODYNAMIC TREATMENT WITH THE SENSITIZER ALUMINUM PHTHALOCYANINE AND HYPERTHERMIA ON LOSS OF CLONOGENICITY OF CHO CELLS
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SYNERGISTIC INTERACTION OF PHOTODYNAMIC TREATMENT WITH THE SENSITIZER ALUMINUM PHTHALOCYANINE AND HYPERTHERMIA ON LOSS OF CLONOGENICITY OF CHO CELLS

机译:敏铝酞菁和高温对光动力学的协同相互作用对CHO细胞克隆形成力的影响

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摘要

When CHO cells were exposed to hyperthermia and subsequently to photodynamic treatment, the combined effects were additive but in the reverse sequence the interaction was synergistic. The synergistic interaction comprised two quite different components: (1) photodynamically induced sensitization of cellular proteins and/or supramolecular structures for thermal inactivation and (2) a photodynamically induced inhibition of the cellular repair system for sublethal thermal damage, The first component of the synergistic interaction was reflected by a change of the Arrhenius parameters of thermal cell killing, A lowering of the activation energy of this process was responsible for the synergistic interactions, whereas a concomitant decrease of the frequency factor, opposing this effect, actually caused a much lower degree of synergism at higher temperatures, This component of the synergistic interaction did not respond to the insertion of an intermediate incubation period between the two treatments, The second component of the synergistic interaction, viz the interference with the ability of cells to survive sublethal thermal damage, was reversible, as an intermediate incubation between photodynamic treatment and hyperthermia resulted in its repair, The photodynamically induced inhibition of the ability of cells to survive sublethal thermal damage was not related to ATP or glutathione depiction, inhibition of dp novo protein synthesis or impairment of degradation of damaged protein molecules, Restoration of the repair system for sublethal damage depended on a metabolic process and required free intracellular Ca2+, suggesting that a cell signaling pathway may be involved, Thus, in a practical sense the magnitude of the synergistic interaction between photodynamic treatment and hyperthermia depends on the length of the interval between the two treatments and on the temperature and duration of the subsequent thermal treatment, This may have significant consequences for the development of clinical protocols for the combined application of photodynamic therapy and hyperthermia in the treatment of tumors. [References: 37]
机译:当CHO细胞暴露于高温并随后进行光动力处理时,组合的作用是加和的,但在相反的顺序中相互作用是协同的。协同相互作用包括两个完全不同的组成部分:(1)光动力学诱导的细胞蛋白和/或超分子结构对热失活的敏化作用;(2)光动力学诱导的细胞修复系统对亚致死性热损伤的抑制作用,这是协同作用的第一部分相互作用通过热细胞杀伤的阿累尼乌斯参数的变化来反映。该过程的活化能降低是协同相互作用的原因,而与该效应相反的频率因子的降低却导致了较低的程度。较高温度下的协同作用,协同作用的这一组成部分对两种处理之间插入一个中间潜伏期没有反应,协同作用的第二个组成部分,即干扰细胞存活至亚致死性热损伤的能力,是可逆的,作为中间公司光动力治疗和热疗之间的相互影响导致其修复。光动力诱导的细胞对亚致死性热损伤的存活能力的抑制与ATP或谷胱甘肽的描绘,dp novo蛋白质合成的抑制或受损蛋白质分子的降解受损,恢复无关。亚致死性修复系统的功能取决于新陈代谢过程和所需的游离细胞内Ca2 +,提示可能参与了细胞信号转导途径。因此,在实际意义上,光动力治疗与高热之间协同相互作用的强度取决于细胞的长短。两次治疗之间的间隔以及后续热处理的温度和持续时间,这可能对开发将光动力疗法和高温疗法联合用于肿瘤治疗的临床方案的开发产生重大影响。 [参考:37]

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