Reitz M, Rumpf M, Knitza R
Department of Physiological Chemistry, University of Mainz, Fed. Rep. of Germany.
Arzneimittelforschung. 1991 Jan;41(1):65-9.
Metronidazole (CAS 443-48-1) induces DNA single strand-breaks in resting human cells (non-stimulated lymphocytes) and in proliferating human cells (phytohemagglutinin-(PHA-)stimulated lymphocytes). The DNA damage depends on metronidazole concentration and time of culture or stimulation. In proliferating lymphocytes the number of DNA single strand-breaks is higher than in resting lymphocytes. In non-stimulated lymphocytes the 3H-thymidine incorporation increases after incubation with metronidazole, possibly due to DNA repair processes. In PHA-stimulated lymphocytes 3H-thymidine incorporation is inhibited by metronidazole. This could be due to the inhibitory effect of DNA damage on cell proliferation. Vitality is not reduced by metronidazole, indeed it may be, as a consequence of DNA repair processes, higher than in controls. DNA repair processes can be also demonstrated after washing out metronidazole from the culture medium.
甲硝唑(CAS 443-48-1)可诱导静息人细胞(未刺激的淋巴细胞)和增殖人细胞(植物血凝素-(PHA-)刺激的淋巴细胞)中的DNA单链断裂。DNA损伤取决于甲硝唑浓度以及培养或刺激时间。在增殖淋巴细胞中,DNA单链断裂的数量高于静息淋巴细胞。在未刺激的淋巴细胞中,与甲硝唑孵育后3H-胸腺嘧啶核苷掺入增加,这可能归因于DNA修复过程。在PHA刺激的淋巴细胞中,甲硝唑抑制3H-胸腺嘧啶核苷掺入。这可能是由于DNA损伤对细胞增殖的抑制作用。甲硝唑不会降低细胞活力,实际上,由于DNA修复过程,其活力可能高于对照组。从培养基中洗去甲硝唑后也可证明DNA修复过程。