Grizzle T B, George J D, Fail P A, Heindel J J
Center for Life Sciences and Toxicology, Research Triangle Institute, Research Triangle Park, North Carolina 27709.
Fundam Appl Toxicol. 1995 Jan;24(1):132-9. doi: 10.1006/faat.1995.1014.
Carisoprodol (CARI), a commonly prescribed neuromuscular relaxant, was evaluated for reproductive toxicity in Swiss CD-1 mice using the Reproductive Assessment by Continuous Breeding (RACB) protocol. Male and female mice were given CARI in corn oil suspension by daily gavage at doses of 0, 300, 750, and 1200 mg/kg body wt/day. Clinical signs of general toxicity in F0 animals included sedation, primarily in the high-dose group during the first week of exposure, and reduced body weight in high-dose females. CARI administration for 14 weeks did not affect the ability of the F0 animals to produce litters. However, decreases in proportion of pups born alive (4%) and absolute (5%) and adjusted live pup weight (7%) were observed at 1200 mg/kg CARI when compared to controls. In a crossover mating trial to determine the affected sex, there were no significant differences in the measured reproductive parameters. CARI at the high dose increased the proportion of time spent in proestrus and estrus, but cycle length was unaffected. At F0 necropsy (Week 27 of treatment), all sperm parameters were normal. Right epididymis and liver weights, relative to body weight, were increased (12 and 23%, respectively) over the control group for high-dose males. A mating trial to determine the fertility and reproductive competence of the F1 generation showed no effect of CARI on indices of mating, pregnancy, or fertility, the proportion of F2 pups born alive, the sex ratio of live F2 pups, live F2 pup weight, or gestation length.(ABSTRACT TRUNCATED AT 250 WORDS)
卡立普多(CARI)是一种常用的神经肌肉松弛剂,采用连续繁殖生殖评估(RACB)方案对瑞士CD-1小鼠进行了生殖毒性评估。雄性和雌性小鼠每天经口灌胃给予玉米油混悬液形式的卡立普多,剂量分别为0、300、750和1200 mg/kg体重/天。F0代动物的一般毒性临床体征包括镇静,主要出现在高剂量组暴露的第一周,以及高剂量雌性动物体重减轻。给予卡立普多14周并未影响F0代动物产仔的能力。然而,与对照组相比,在1200 mg/kg卡立普多剂量下观察到活产幼崽比例下降(4%)、绝对体重下降(5%)以及调整后的活幼崽体重下降(7%)。在一项交叉交配试验以确定受影响的性别时,所测量的生殖参数没有显著差异。高剂量的卡立普多增加了动情前期和发情期所占时间比例,但周期长度未受影响。在F0代尸检时(治疗第27周),所有精子参数均正常。高剂量雄性动物的右侧附睾和肝脏重量相对于体重增加(分别比对照组增加12%和23%)。一项确定F1代生育能力和生殖能力的交配试验表明,卡立普多对交配、妊娠或生育指标、F2代活产幼崽比例、F2代活幼崽性别比例、F2代活幼崽体重或妊娠期长度均无影响。(摘要截断于250字)