Johnson F E, Doubek W G, Tolman K C, Janney C G
Department of Surgery, St. Louis University Medical Center, MO 63110-0250.
Surg Oncol. 1993;2(1):77-81. doi: 10.1016/0960-7404(93)90047-3.
Although the testicular cytotoxicity of procarbazine has been evaluated in the rat, previous models have utilized routes other than the intravenous one, and have generally employed multiple-dose regimens. In this report, we describe testicular toxicity in the Sprague-Dawley rat following a single intravenous bolus of procarbazine (0-700 mg kg body weight), with necropsy 59 +/- 2 days later. Testicular toxicity was evaluated qualitatively by histology and quantitatively by testicular weight, sperm head count, repopulation index and epididymal index. Effects of procarbazine on heart, lung, liver and kidney histology were evaluated qualitatively. Progressive dose-dependent testicular atrophy and oligospermia occurred at low and intermediate dosages of procarbazine. Marked testicular atrophy, oligospermia and germinal hypoplasia were observed at high dosages (500 and 700 mg kg-1 body weight). LD50 at day 59 for procarbazine appears to be approximately 600 mg kg-1 body weight using this regimen. This model will facilitate the study of techniques to avoid drug-induced testicular damage.
尽管已在大鼠中评估了丙卡巴肼的睾丸细胞毒性,但先前的模型采用的是静脉途径以外的其他途径,并且通常采用多剂量方案。在本报告中,我们描述了在单次静脉推注丙卡巴肼(0 - 700 mg/kg体重)后,59±2天后进行尸检的情况下,Sprague-Dawley大鼠的睾丸毒性。通过组织学对睾丸毒性进行定性评估,并通过睾丸重量、精子头计数、再增殖指数和附睾指数进行定量评估。定性评估了丙卡巴肼对心脏、肺、肝脏和肾脏组织学的影响。在低剂量和中等剂量的丙卡巴肼作用下,出现了进行性剂量依赖性睾丸萎缩和少精子症。在高剂量(500和700 mg/kg体重)下观察到明显的睾丸萎缩、少精子症和生精细胞发育不全。使用该方案,丙卡巴肼在第59天的半数致死量似乎约为600 mg/kg体重。该模型将有助于研究避免药物诱导的睾丸损伤的技术。