Harada S, Sakaguchi Y, Shimada M, Matsuhashi K, Kakihata K, Nomura M, Takayama S
Drug Safety Research Center, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan.
J Toxicol Sci. 1995 Aug;20(3):309-17. doi: 10.2131/jts.20.309.
Sprague-Dawley male rats were administered nefiracetam orally at daily doses of 500 and 1500 mg/kg/day for 4 or 9 weeks. Although the copulation index was not affected by nefiracetam treatment, the fertility index was extremely low in the 1500 mg/kg/day group for both treatment periods. This high dose group consistently exhibited decreased testicular weights. Epididymal and prostate weights were also reduced in the 1500 mg/kg/day group after both 4- and 9-week treatments and in the 500 mg/kg/day group after the 9-week treatment. Severe degenerative changes such as degeneration of germ cells, loss of germ cells and atrophy of seminiferous tubules were observed in all rats of the 1500 mg/kg/day groups after both 4 and 9 weeks of treatment. Retention of spermatids in stage IX, X and XI seminiferous tubules was also noted after the 4- and 9-week treatments at 500 mg/kg/day. The testicular sperm head counts were markedly decreased following the 4- and 9-week treatments at 1500 mg/kg/day, and mildly reduced after the 4-weeks treatment at 500 mg/kg/day. From these results it is concluded that histopathological examination and the testicular sperm head count method are highly useful for detecting testicular toxicity and that testicular lesions caused by nefiracetam can be detected after 4 weeks of exposure.
将500和1500毫克/千克/天的奈非西坦每日口服剂量给予雄性Sprague-Dawley大鼠,持续4周或9周。尽管交配指数不受奈非西坦治疗的影响,但在两个治疗期内,1500毫克/千克/天剂量组的生育指数极低。该高剂量组持续出现睾丸重量下降。在4周和9周治疗后,1500毫克/千克/天剂量组的附睾和前列腺重量也降低,在9周治疗后,500毫克/千克/天剂量组的附睾和前列腺重量也降低。在1500毫克/千克/天剂量组的所有大鼠中,在治疗4周和9周后均观察到严重的退行性变化,如生殖细胞变性、生殖细胞丢失和生精小管萎缩。在500毫克/千克/天剂量组治疗4周和9周后,还注意到IX、X和XI期生精小管中有精子细胞滞留。在1500毫克/千克/天剂量组治疗4周和9周后,睾丸精子头部计数显著降低,在500毫克/千克/天剂量组治疗4周后,睾丸精子头部计数轻度降低。从这些结果可以得出结论,组织病理学检查和睾丸精子头部计数方法对于检测睾丸毒性非常有用,并且在接触奈非西坦4周后可以检测到由其引起的睾丸病变。