Goldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia.
Institute of Chemistry, Komi Science Center, Ural Branch of the Russian Academy of Sciences, Syktyvkar, Komi Republic, Russia.
Bull Exp Biol Med. 2024 Sep;177(5):635-638. doi: 10.1007/s10517-024-06239-0. Epub 2024 Sep 28.
In male C57BL/6 mice (8-12 weeks) and male Wistar rats (12 weeks), the effect of dibornol (2,6-diisobornyl-4-methylphenol) on the level of spontaneous DNA damage in cells of the bone marrow, liver, kidneys, and rectum of mice (series I) and genotoxic effects in rat testicular cells after administration of cytostatic drugs with different mechanisms of action (series II) were studied using the DNA comet assay. In series I, dibornol was intragastrically administered to mice once at doses of 200, 400, and 2000 mg/kg; in series II, dibornol was intragastrically administered to rats at a dose of 10 mg/kg for 5 days before and 5 days after the cytostatic treatment (methotrexate, doxorubicin). It was found that dibornol in all studied doses did not produce the genotoxic (carcinogenic) effect and reduced the level of spontaneous DNA damage in the bone marrow. After combined administration of cytostatic drugs (doxorubicin, methotrexate) and dibornol, the level of DNA breaks was reduced to 38.5 and 49% of the control, respectively.
在雄性 C57BL/6 小鼠(8-12 周)和雄性 Wistar 大鼠(12 周)中,使用 DNA 彗星试验研究了二硼烷(2,6-二异丁基-4-甲基苯酚)对骨髓、肝脏、肾脏和直肠细胞中自发 DNA 损伤水平的影响(系列 I),以及对不同作用机制的细胞抑制剂处理后大鼠睾丸细胞的遗传毒性作用(系列 II)。在系列 I 中,二硼烷以 200、400 和 2000mg/kg 的剂量经胃内给药一次;在系列 II 中,二硼烷以 10mg/kg 的剂量经胃内给药,在细胞抑制剂处理(甲氨蝶呤、阿霉素)之前和之后 5 天给药。结果发现,二硼烷在所有研究剂量下均未产生遗传毒性(致癌性)作用,并降低了骨髓中自发 DNA 损伤的水平。在联合使用细胞抑制剂药物(阿霉素、甲氨蝶呤)和二硼烷后,DNA 断裂水平分别降低至对照的 38.5%和 49%。