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对乙酰氨基酚的致突变活性。一项针对志愿者开展的研究。

Mutagenic activity of paracetamol. A study conducted on volunteers.

作者信息

Srám R J, Kocisová J, Rössner P, Binková B, Topinka J, Bavorová H

机构信息

Research Institute of Psychiatry, Prague.

出版信息

Czech Med. 1990;13(2-3):114-23.

PMID:2245754
Abstract

The mutagenic activity of paracetamol (PC) was studied on a group of healthy persons (3 men, 8 women) after the simultaneous administration of 3 X 1000 mg of PC and an identical dose of PC + 1000 mg of ascorbic acid within a period of 8 hours. Blood sample tests were made at intervals of 0, 24, 72 and 168 hours. A cytogenetic analysis showed that in 24 hours PC had increased the aberrant cell frequency to 2.77 +/- 0.37 per cent as distinct from 1.68 +/- 0.30 per cent (p less than 0.05) prior to the drug. In 72 hours, the rate of buccal mucosa micronuclei had risen to 0.38 +/- 0.07% against 0.19 +/- 0.06% prior to PC (p less than 0.01). Unscheduled DNA synthesis in peripheral lymphocytes had dropped to T/C = 2.06 +/- 0.54 (p less than 0.01) against 3.16 +/- 0.84 before PC. The lipid peroxidation level in the plasma remained unchanged. Ascorbic acid administered simultaneously with PC had no effect on the changes observed. A further follow-up of other PC side effects is recommended.

摘要

对一组健康人(3名男性,8名女性)进行了研究,观察在8小时内同时服用3次1000毫克扑热息痛(PC)以及相同剂量的PC加1000毫克抗坏血酸后扑热息痛的诱变活性。每隔0、24、72和168小时采集血样进行检测。细胞遗传学分析显示,服药24小时后,异常细胞频率从服药前的1.68±0.30%增加到2.77±0.37%(p<0.05)。72小时时,颊黏膜微核率从扑热息痛服药前的0.19±0.06%升至0.38±0.07%(p<0.01)。外周淋巴细胞中DNA的非预定合成降至T/C = 2.06±0.54(p<0.01),而扑热息痛服药前为3.16±0.84。血浆中的脂质过氧化水平保持不变。与扑热息痛同时服用的抗坏血酸对观察到的变化没有影响。建议进一步随访扑热息痛的其他副作用。

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[Mutagenic activity of paracetamol. A study in volunteers].
Cas Lek Cesk. 1989 Sep 22;128(39):1230-4.

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