Evaluation of the ability of paracetamol to produce chromosome aberrations in man

Ph. Hantson , L. de Saint-Georges , P. Mahieu , E.D. Léonard , M.C. Crutzen-Fayt , A. Léonard
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引用次数: 15

Abstract

The ability of paracetamol to induced structural chrosomed aberrations in human peripheral blood lymphocytes in vivo was evaluated in volunteers who had been administered a single oral dose of 3 g paracetamol, in patients who has received 2 g of propacetamol by intravenous infusion every 6 h for at least 7 days, and in self-poisoned patients who, for suicidal reasons, had ingested more than 15 g paracetamol. In addition to the in vivo observations, the effectiveness of paracetamol to interfere with fusorial microtubule polymerisation was assayed in vitro in order to detect a possible effect of paracetamol on the distribution of chromosomes during cell division. The negative results obtained in all those assays strongly suggest that paracetamol has no mutagenic properties in human. There was, indeed, no significant difference in the percentage of abnormal cells before and after application of paracetamol in volunteers (0.2% before ingestion of 3 g paracetamol, 0.12% after 24 h, 0.04% after 72 h and 0.04% after 168 h) and in patients (0.5% of abnormal cells before treatment versus 0.44% after intravenous infusion of a total of 28 g paracetamol). Moreover, the yield of abnormal cells was not modified in self-poisoned persons (0.24%), in spite of an important decrease in the mitotic index of the PHA stimulated lymphocytes. In the in vitro assay, no inhibition of microtubule polymerisation was detected with concentrations of 2.5, 5 and 10 mM paracetamol.

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对乙酰氨基酚对人染色体畸变能力的评价
对扑热息痛在体内诱导人外周血淋巴细胞结构染色体畸变的能力进行了评估,包括口服单剂量3g扑热息痛的志愿者,每6小时静脉输注2g丙帕他莫至少7天的患者,以及因自杀原因摄入超过15g扑热息痛的自我中毒患者。除了体内观察外,我们还在体外测试了扑热息痛对真菌微管聚合的干扰效果,以检测扑热息痛对细胞分裂过程中染色体分布的可能影响。所有试验结果均为阴性,表明对乙酰氨基酚对人体无致突变性。事实上,在志愿者和患者中,应用扑热息痛前后的异常细胞百分比没有显著差异(服用3 g扑热息痛前为0.2%,24 h后为0.12%,72 h后为0.04%,168 h后为0.04%)(治疗前为0.5%,静脉输注总共28 g扑热息痛后为0.44%)。此外,尽管PHA刺激淋巴细胞的有丝分裂指数显著降低,但自身中毒患者的异常细胞数量并未改变(0.24%)。在体外实验中,2.5、5和10 mM的扑热息痛对微管聚合没有抑制作用。
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