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重水和聚(ADP-核糖)合成酶抑制剂对培养的哺乳动物L5178Y细胞中γ射线剂量率效应的抑制作用。

Inhibition of gamma-ray dose-rate effects by D2O and inhibitors of poly(ADP-ribose) synthetase in cultured mammalian L5178Y cells.

作者信息

Ueno A M, Tanaka O, Matsudaira H

出版信息

Radiat Res. 1984 Jun;98(3):574-82.

PMID:6328569
Abstract

Effects of deuterium oxide (D2O) and 3-aminobenzamide, an inhibitor of poly(ADP-ribose) synthetase, on cell proliferation and survival were studied in cultured mammalian L5178Y cells under growing conditions and after acute and low-dose-rate irradiation at about 0.1 to 0.4 Gy/hr of gamma rays. Growth of irradiated and unirradiated cells was inhibited by 45% D2O but not by 3-aminobenzamide at 10 mM, except for treatments longer than 30 hr. The presence of these agents either alone or in combination during irradiation at low dose rates suppressed almost totally the decrease in cell killing due to the decrease in dose rate. The D2O did not inhibit the radiation-induced increase in poly(ADP-ribose) synthesis as measured by the incorporation of [14C]NAD into the acid insoluble fraction, contrary to 3-aminobenzamide. Among other inhibitors tested, theobromine and theophylline were found to be effective in eliminating the dose-rate effects of gamma rays. Possible mechanisms underlying the inhibition are discussed.

摘要

在生长条件下以及在以约0.1至0.4 Gy/小时的剂量率进行急性和低剂量率γ射线照射后,研究了氧化氘(D2O)和聚(ADP - 核糖)合成酶抑制剂3 - 氨基苯甲酰胺对培养的哺乳动物L5178Y细胞增殖和存活的影响。45%的D2O抑制了照射和未照射细胞的生长,但10 mM的3 - 氨基苯甲酰胺在处理时间超过30小时之前未产生抑制作用。在低剂量率照射期间单独或联合使用这些试剂几乎完全抑制了由于剂量率降低导致的细胞杀伤减少。与3 - 氨基苯甲酰胺相反,通过[14C]NAD掺入酸不溶性部分来测量,D2O并未抑制辐射诱导的聚(ADP - 核糖)合成增加。在测试的其他抑制剂中,发现可可碱和茶碱可有效消除γ射线的剂量率效应。讨论了抑制作用背后的可能机制。

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