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Inactivation by ionizing radiation of ion channels formed by polyene antibiotics amphotericin B and nystatin in lipid membranes: an inverse dose-rate behavior.

机译:通过离子辐射对脂膜中多烯抗生素两性霉素B和制霉菌素形成的离子通道进行辐射灭活:剂量率的反比行为。

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摘要

The phenomena reported are part of a study about the effects of ionizing radiation on membrane transport. We found that the conductance of lipid membranes in the presence of the polyene-antibiotics nystatin or amphotericin B is reduced to virtually zero following irradiation. Ion channels formed by these substances seem to represent extremely sensitive structures being inactivated by radiation doses in the range of a few Centigray (1 cGy = 1 rad) at sufficiently small dose rates. Inactivation shows a so-called inverse dose-rate behavior, i.e., at constant radiation dose the effect increases with decreasing dose rate. Similar to radiation-induced lipid peroxidation the phenomenon may be understood on the basis of a radical chain mechanism initiated by free radicals of water radiolysis. The process--via peroxidation of the polyene part of the molecules--is suggested to modify the hydrophobic exterior and to destabilize the barrel-like structure of the ion channels.
机译:报告的现象是有关电离辐射对膜运输影响的研究的一部分。我们发现在辐照后,多烯抗生素制霉菌素或两性霉素B的存在下脂膜的电导几乎降低为零。由这些物质形成的离子通道似乎代表了非常敏感的结构,该结构在足够小的剂量率下被几厘升(1 cGy = 1 rad)的辐射剂量所灭活。失活显示出所谓的剂量率逆行为,即在恒定辐射剂量下,效果随着剂量率的降低而增加。与辐射诱导的脂质过氧化类似,该现象可以基于水辐射分解自由基引发的自由基链机理来理解。建议通过分子多烯部分的过氧化作用来改变该过程,从而改变疏水性外部并破坏离子通道的桶状结构。

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