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对人类志愿者进行的扑热息痛致突变性研究。II. 非程序性DNA合成及微核试验。

Mutagenicity studies on paracetamol in human volunteers. II. Unscheduled DNA synthesis and micronucleus test.

作者信息

Topinka J, Srám R J, Sirinjan G, Kocisová J, Binková B, Fojtíková I

机构信息

Psychiatric Research Institute, Prague, Czechoslovakia.

出版信息

Mutat Res. 1989 Nov;227(3):147-52. doi: 10.1016/0165-7992(89)90038-9.

Abstract

The possible genotoxic effect of paracetamol (PC) was studied in a group of 11 healthy volunteers. PC was administered in the form of tablets 3 x 1000 mg in the course of 8 h. Blood samples and buccal mucosa cells were taken 0, 24, 72 and 168 h after the first administration of the drug. Each blood sample was used for the termination of the unscheduled DNA synthesis (UDS) in peripheral lymphocytes and ascorbemia in plasma. Buccal mucosa cells were analysed for micronuclei. After PC administration the level of UDS induced by MNNG was decreased to T/C = 4.11 +/- 0.56 after 24 h vs. T/C = 5.02 +/- 0.47 (p less than 0.01) at 0 h. The frequency of micronucleated cells in the buccal mucosa was increased after 72 h to 0.38 +/- 0.07% vs. 0.19 +/- 0.06% (p less than 0.01) before PC administration. If PC was administered simultaneously with ascorbic acid (AA), also in a dose of 3 X 1000 mg, a decreased level of UDS was observed after 24, 72 and 168 h and the increased number of micronuclei was qualitatively the same as the PC alone: 0.38 +/- 0.09% after 72 h vs. 0.20 +/- 0.05% at 0 h AA did not decrease the genotoxic effect of PC, but prolonged the influence of PC on UDS.

摘要

对11名健康志愿者进行了研究,以探讨扑热息痛(PC)可能的遗传毒性作用。以片剂形式给予PC,剂量为3×1000mg,给药时间为8小时。在首次给药后的0、24、72和168小时采集血样和颊黏膜细胞。每份血样用于检测外周淋巴细胞中的非预定DNA合成(UDS)终止情况以及血浆中的抗坏血酸水平。对颊黏膜细胞进行微核分析。给予PC后,24小时时由MNNG诱导的UDS水平降至T/C = 4.11±0.56,而0小时时为T/C = 5.02±0.47(p<0.01)。72小时后颊黏膜中微核化细胞的频率增加至0.38±0.07%,而给药前为0.19±0.06%(p<0.01)。如果同时给予PC和抗坏血酸(AA),剂量也为3×1000mg,则在24、72和168小时后观察到UDS水平降低,微核数量增加的情况与单独使用PC时基本相同:72小时后为0.38±0.09%,而0小时时为0.20±0.05%。AA并未降低PC的遗传毒性作用,但延长了PC对UDS的影响。

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