Department of Pharmacology & Therapeutics, McGill University, Montréal, Québec, Canada.
Reprod Toxicol. 2010 Jun;29(3):332-8. doi: 10.1016/j.reprotox.2010.01.007. Epub 2010 Jan 22.
The chemotherapeutic agents used to treat non-Hodgkin lymphoma, cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP), have adverse effects on male reproductive function and progeny outcome. To determine the reversibility of these effects, male rats received a CHOP treatment mimicking human exposure. CHOP reduced testicular and epididymal weights; these remained decreased after 9 weeks recovery. This treatment also decreased testicular sperm number and increased spermatozoal DNA damage. Although sperm production returned to control values after 9 weeks recovery, DNA damage persisted. Decreased litter size, and increased pre- and post-implantation losses were observed among litters sired by CHOP-exposed males. Litter size and pre-implantation loss returned to control within 3 weeks post-treatment and post-implantation loss by 6 weeks. Thus, effects of CHOP on progeny outcome were reversed 9 weeks post-treatment, although germ cell DNA breaks remained elevated. These data suggest that the ability to sire viable progeny may not be a sensitive measure of spermatozoal quality in rats.
用于治疗非霍奇金淋巴瘤的化疗药物,环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP),对男性生殖功能和后代结局有不良影响。为了确定这些影响的可逆性,雄性大鼠接受了模拟人类暴露的 CHOP 治疗。CHOP 降低了睾丸和附睾的重量;在 9 周恢复期后,这些重量仍持续下降。这种治疗还降低了睾丸精子数量,并增加了精子 DNA 损伤。尽管在 9 周恢复期后精子生成恢复到对照值,但 DNA 损伤仍然存在。接受 CHOP 暴露雄性大鼠所生育的后代的窝仔数减少,着床前和着床后损失增加。处理后 3 周内窝仔数和着床前损失恢复到对照水平,6 周后着床后损失恢复。因此,CHOP 对后代结局的影响在治疗后 9 周内得到逆转,尽管生殖细胞 DNA 断裂仍然升高。这些数据表明,在大鼠中,生育可育后代的能力可能不是精子质量的敏感衡量标准。