Matsumoto Mariko, Furuhashi Tadakazu, Poncipe Carlo, Ema Makoto
Division of Risk Assessment, Biological Safety Center, National Institute of Health Sciences, 1-1-18 Kamiyoga, Setagaya-ku, Tokyo 185-8501, Japan.
Environ Toxicol. 2008 Apr;23(2):169-83. doi: 10.1002/tox.20321.
In a combined repeated dose toxicity study with reproduction/developmental toxicity screening test, Crj:CD(SD)IGS rats were dosed with dinoseb, 2-sec-butyl-4,6-dinitrophenol, by gavage at 0 (vehicle), 0.78, 2.33, or 7.0 mg/kg bw/day. Six males per group were dosed for a total of 42 days beginning 14 days before mating. Twelve females per group were dosed for a total of 44-48 days beginning 14 days before mating to day 6 of lactation throughout the mating and gestation period. Recovery groups of six males per group and nonpregnant six females per group were dosed for 42 days followed by a 14-day recovery period. No deaths were observed in males of any dose group or in females of the recovery groups. At 7.0 mg/kg bw/day, eight females died and two animals were moribund during late pregnancy, and a significant decrease in body weight gain was found in both sexes. Hematocrit was significantly higher at 0.78 mg/kg bw/day and above in the main group males at the end of administration period. Reduction in extramedullary hematopoiesis in the spleen was significant at 2.33 mg/kg bw/day in the main group females. Sperm analysis revealed a decrease in sperm motility and an increase in the rates of abnormal sperm, abnormal tail, and abnormal head at 7.0 mg/kg bw/day. A number of dams delivered their pups and of dams with live pups at delivery was significantly lowered in the 7.0 mg/kg bw/day group. Based on these findings, the LOAEL for males and NOAEL for females were 0.78 mg/kg bw/day, and the NOAEL for reproductive/developmental toxicity was considered to be 2.33 mg/kg bw/day.
在一项重复给药毒性与生殖/发育毒性筛选联合研究中,对Crj:CD(SD)IGS大鼠经口灌胃给予地乐酚(2-仲丁基-4,6-二硝基苯酚),剂量分别为0(赋形剂)、0.78、2.33或7.0mg/kg体重/天。每组6只雄性大鼠,从交配前14天开始给药,共给药42天。每组12只雌性大鼠,从交配前14天开始给药,直至哺乳期第6天,整个交配和妊娠期共给药44 - 48天。每组6只雄性大鼠和6只未怀孕雌性大鼠作为恢复组,给药42天,随后有14天的恢复期。各剂量组雄性大鼠以及恢复组雌性大鼠均未观察到死亡情况。在7.0mg/kg体重/天剂量组,8只雌性大鼠在妊娠后期死亡,2只濒死,且雌雄两性体重增加均显著降低。在给药期末,主要组雄性大鼠中,0.78mg/kg体重/天及以上剂量组的血细胞比容显著升高。主要组雌性大鼠中,2.33mg/kg体重/天剂量组脾脏的髓外造血减少显著。精子分析显示,7.0mg/kg体重/天剂量组精子活力下降,精子异常率、尾部异常率和头部异常率增加。7.0mg/kg体重/天剂量组分娩的母鼠数量以及分娩时产下活仔的母鼠数量均显著降低。基于这些结果,雄性大鼠的最低观察到有害作用剂量(LOAEL)为0.78mg/kg体重/天,雌性大鼠的未观察到有害作用水平(NOAEL)为0.78mg/kg体重/天,生殖/发育毒性的NOAEL被认为是2.33mg/kg体重/天。