Hakovirta H, Parvinen M, Lähdetie J
Department of Anatomy, University of Turku, Finland.
Mutat Res. 1993 Mar;301(3):189-93. doi: 10.1016/0165-7992(93)90077-9.
The stage-specific effect of etoposide on spermatogenic DNA synthesis was measured 1, 3 and 18 days after a single intraperitoneal injection of etoposide. Etoposide inhibited premitotic DNA synthesis most effectively at stages II-III and IV-V of the seminiferous epithelial cycle in which DNA synthesis of late spermatogonia takes place. Compared with control levels, DNA synthesis at stages II-III was maximally inhibited 43% and 57% at doses of 5 and 10 mg/kg, respectively, and at stages IV-V the maximal inhibition was 67% and 62%, at doses of 5 and 10 mg/kg respectively. Premeiotic DNA synthesis was not as vulnerable to the etoposide action as premitotic DNA synthesis, the maximal inhibition of premeiotic DNA synthesis was 39% and 41% compared with control at doses of 5 and 10 mg/kg, respectively. Induction of most probably repair-type DNA synthesis was demonstrated in stages I-III, VIIa-b and XII of the cycle. All the effects of etoposide were most apparent 1 and 3 days after treatment but had not totally disappeared 18 days after the treatment.
在单次腹腔注射依托泊苷后的第1、3和18天,测定了依托泊苷对生精DNA合成的阶段特异性影响。依托泊苷在生精上皮周期的II-III期和IV-V期最有效地抑制有丝分裂前DNA合成,晚期精原细胞的DNA合成在此阶段发生。与对照水平相比,在5和10 mg/kg剂量下,II-III期的DNA合成分别被最大程度抑制43%和57%,在IV-V期,在5和10 mg/kg剂量下,最大抑制率分别为67%和62%。减数分裂前DNA合成不如有丝分裂前DNA合成那样易受依托泊苷作用的影响,在5和10 mg/kg剂量下与对照相比,减数分裂前DNA合成的最大抑制率分别为39%和41%。在周期的I-III期、VIIa-b期和XII期证实了很可能是修复型DNA合成的诱导。依托泊苷的所有作用在治疗后1天和3天最为明显,但在治疗后18天尚未完全消失。