Cyclohexylamine was found as a metabolite of sodium cyclamate in humans and dogs, which had orally received the sweetener (Kojima and Ichibagase, 1966). Since then, toxicity of cyclohexylamine has been studied by many investigators and it was revealed to cause chromosome aberrations in mammalian cells in vivo as well as in vitro (Legator et al., 1969; Stoltz et al., 1970; Tonmura, 1969, 1970). The present experiment was carried out to examine embryotoxic effects cyclohexylamine in mice. Pregnancy of ICR mice was timed by counting the morning on which the vaginal plug was found as day 0. Cyclohexylamine was diluted with distilled water and given orally to the pregnant mice at 100, 50, and 20 mg/kg/day for six days either from day O to day 5 or from day 6 to day 11 of gestation. Fetuses were removed on day 18 of gestation, all implantation sites counted and the living fetuses weighed and examined for external malformation and then for skeletal abnormality following staining with alizarin red S. Cyclohexylamine at 100 mg/kg/day was mildly embryolethal when administered from day 6 to day 11 of gestation. This dosage, however, was also mildly lethal to the adult female mice when administered for 6~10 days. Body weight of the living fetuses was significantly decreased when 100 mg/kg/day of cyclohexylamine was given from day 6 to day 11 of gestation. Such a growthsuppressing effect of the agent was not so evident in other experimental groups. No teratogenic effect of the agent was revealed in any experimental group. As a result, it was concluded that the level of embryotoxicity of cyclohexylamine is about the same as that of its subacute toxicity in the adult female. Discrepancies in the results of teratological examinations of cyclamate (Tanaka, 1964; Nees and Derse, 1967; Fritz and Hess, 1968; Klotzsche, 1969; Lorke, 1969 a, b) were discussed and it is assumed that cyclamate also has no teratological effect on the offspring when administered to pregnant animals.
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