Bürgin H, Schmid B, Zbinden G
Toxicology. 1979 Mar-Apr;12(3):251-7. doi: 10.1016/0300-483x(79)90070-2.
The 2 hydrazine derivatives isoniazid (INH) and procarbazine hydrochloride (P) were injected intravenously into rabbits. Radioactive thymidine was injected into both testicles. Rabbits were ejaculated repeatedly, sperms were counted and incorporation of [3H] thymidine into sperm head DNA was determined by liquid scintillation counting. In P-treated rabbits (5 and 50 mg/kg) radioactivity was significantly increased in sperms that were in late phases of spermatocyte and early phases of spermatid maturation at the time of treatment. This indicates that DNA repair synthesis, (unscheduled DNA synthesis, UDS) occurred following drug-induced DNA damage in these germ cells. Normal DNA synthesis in spermatogonia was inhibited by the high dose only. INH (50 and 125 mg/kg) did not cause UDS in spermatocytes and spermatids and did not affect normal DNA synthesis in spermatogonia. The results are in agreement with literature data indicating that P is a potent mutagen and carcinogen. INH, on the other hand, has weak mutagenic and carcinogenic activities that are most apparent in mice.
将两种肼衍生物异烟肼(INH)和盐酸丙卡巴肼(P)静脉注射到兔子体内。将放射性胸苷注射到双侧睾丸。反复刺激兔子射精,对精子进行计数,并通过液体闪烁计数法测定[3H]胸苷掺入精子头部DNA的情况。在接受P治疗的兔子(5和50mg/kg)中,在治疗时处于精母细胞后期和精子细胞成熟早期的精子中的放射性显著增加。这表明在这些生殖细胞中,药物诱导的DNA损伤后发生了DNA修复合成(即非程序性DNA合成,UDS)。仅高剂量时精原细胞中的正常DNA合成受到抑制。INH(50和125mg/kg)在精母细胞和精子细胞中未引起UDS,并且不影响精原细胞中的正常DNA合成。这些结果与文献数据一致,表明P是一种强效诱变剂和致癌物。另一方面,INH具有较弱的诱变和致癌活性,在小鼠中最为明显。