呋喃唑酮对体内外姐妹染色单体交换、细胞增殖动力学和有丝分裂指数的影响。

E Madrigal-Bujaidar, J C Ibañez, M Cassani, G Chamorro
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引用次数: 10

摘要

呋喃唑酮是一种用于人类和兽药的抗菌化合物。本研究的目的是确定其在体外和体内的遗传毒性能力。我们用人淋巴细胞培养系统检测2.0、4.0、6.0、8.0、10.0微克/ml的效果,用小鼠骨髓法检测8.6、30.0、75.0 mg/kg呋喃唑酮的效果。在这两种系统中,我们测定了姐妹染色单体交换频率(SCE)、细胞增殖动力学(CPK)和有丝分裂指数(MI)。体外结果显示,从第二次剂量开始,SCE显著增加,从第三次剂量开始,CPK和MI下降。体内实验结果显示,两种高剂量均使SCE升高,但三种高剂量均未发现CPK和MI有明显变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of furazolidone on sister-chromatid exchanges, cell proliferation kinetics, and mitotic index in vivo and in vitro.

Furazolidone is an antimicrobial compound used in human and veterinary medicine. The aim of this investigation was to determine its genotoxic capacity in vitro and in vivo. We used the human lymphocyte culture system to detect the effect of 2.0, 4.0, 6.0, 8.0, or 10.0 micrograms/ml, and the mouse bone marrow assay to determine the effect of 8.6, 30.0, or 75.0 mg/kg furazolidone. In both systems we determined the frequency of sister-chromatid exchanges (SCE), the cell proliferation kinetics (CPK), and the mitotic index (MI). The in vitro results showed a significant SCE increase starting from the second dose tested and a CPK and MI decrease starting from the third dose. The in vivo results showed a SCE increase with the two high doses tested, but no significant modification was found in the CPK and MI with the three doses tested in the experiment.

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