Hoffer A P, Lisser S P
J Androl. 1984 Nov-Dec;5(6):416-23. doi: 10.1002/j.1939-4640.1984.tb00807.x.
This study evaluates the reversibility of the effects of gossypol on testicular ultrastructure and the motility of epididymal spermatozoa. Adult male rats were treated 6 days weekly with the vehicle alone (Group A), or with 10 (Group B) or 20 (Group C) mg/kg of gossypol for 12 weeks, and then sacrificed six or 12 weeks after cessation of treatment. Although epididymal spermatozoa in Groups B and C were 100% immotile after gossypol treatment, little evidence of abnormality could be detected with the light microscope in the seminiferous tubules or interstitium. By contrast, at the ultrastructural level, there were demonstrable pathognomonic defects in the mitochondrial sheath and axonemes of step 18 and 19 spermatids which were identical to those reported earlier (Hoffer, 1983). In addition, an ultrastructural defect in the flagella of late testicular spermatozoa is described for the first time. This defect consists of an indentation, or constriction, of the mitochondrial sheath at outer dense fibers (ODFs) 1, 2, and 9, resulting in a separation of these 3 ODFs from the other fibers. This defect, though visible in an earlier ultrastructural study (Hoffer, 1983), was not described. In Group B rats allowed to recover from gossypol treatment, ultrastructural defects in step 18 and 19 spermatids could not be detected at six or at 12 weeks after cessation of treatment, and sperm motility also did not differ significantly from controls by the end of either recovery period. In Group C rats, sperm motility returned to the normal range within six weeks after treatment ended, but a few morphological defects in the midpiece and axoneme of late spermatids could still be detected with the electron microscope.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究评估棉酚对睾丸超微结构及附睾精子活力影响的可逆性。成年雄性大鼠每周6天接受单独赋形剂处理(A组),或分别接受10毫克/千克(B组)或20毫克/千克(C组)棉酚处理12周,然后在停药后6周或12周处死。尽管B组和C组大鼠在棉酚处理后附睾精子100%无活力,但在生精小管或间质中,光镜下几乎未检测到异常迹象。相比之下,在超微结构水平,18和19期精子细胞的线粒体鞘和轴丝存在明显的特征性缺陷,与先前报道的相同(霍弗,1983年)。此外,首次描述了晚期睾丸精子鞭毛的超微结构缺陷。该缺陷表现为线粒体鞘在外侧致密纤维1、2和9处出现凹陷或收缩,导致这3条外侧致密纤维与其他纤维分离。这一缺陷虽在早期超微结构研究中可见(霍弗,1983年),但未被描述。在从棉酚处理中恢复的B组大鼠中,停药后6周或12周均未检测到18和19期精子细胞的超微结构缺陷,且在任一恢复期结束时,精子活力与对照组相比也无显著差异。在C组大鼠中,治疗结束后6周内精子活力恢复至正常范围,但电子显微镜下仍可检测到晚期精子细胞的中段和轴丝存在一些形态学缺陷。(摘要截断于250字)