Yasuda Y, Tanimura T
J Environ Pathol Toxicol. 1980 Aug;4(1):451-6.
In this investigation of the effects of diphenylguanidine (DPG) on pregnancy and fetuses, pregnant mice of the ICR-JCL strain were given dPG orally in a 0.5 percent carboxymethyl cellulose suspension in doses of 0.25, 1.0, 4.0, or 10.0 mg/kg of body weight/day throughout pregnancy. Control mice were fed the vehicle alone. On day 18 of pregnancy, all mice were killed and the fetuses were examined. Disturbances in implantation were seen in the mothers treated with 10 mg/kg/day (the highest dose) of DPG. Retarded ossification of the talus was seen in the fetuses of mothers treated with 4.0 mg/kg/day, but there was no dose-response relationship to this finding. Although malformations such as open eyelids or polydactyly were seen sporadically, these were categorized as spontaneous anomalies. Thus, DPG seems to have no detrimental effects on the development of mouse fetuses in doses of 4 mg/kg or less.
在本次关于二苯基胍(DPG)对妊娠及胎儿影响的研究中,将ICR-JCL品系的怀孕小鼠在整个孕期以0.25、1.0、4.0或10.0毫克/千克体重/天的剂量口服给予溶于0.5%羧甲基纤维素混悬液中的DPG。对照小鼠仅喂食赋形剂。在妊娠第18天,处死所有小鼠并检查胎儿。接受10毫克/千克/天(最高剂量)DPG处理的母鼠出现着床障碍。接受4.0毫克/千克/天处理的母鼠所产胎儿出现距骨骨化迟缓,但该结果不存在剂量反应关系。尽管偶尔可见诸如眼睑开放或多指等畸形,但这些被归类为自发异常。因此,4毫克/千克及以下剂量的DPG似乎对小鼠胎儿发育无有害影响。