Barrow P C, Olivier P, Marzin D
Pharmakon Europe, Les Oncins, L'Arbresle, France.
Reprod Toxicol. 1995 Jul-Aug;9(4):389-98. doi: 10.1016/0890-6238(95)00026-7.
A 3-generation study with two mating phases per generation and a teratology phase was performed in the rat to assess the reproductive and developmental toxicity of beta-cyclodextrin (beta-CD) in the diet. Transient neonatal growth retardation occurred with 5% beta-CD: a similar, but equivocal, effect was also observed with 2.5%. No permanent defects or other indications of developmental toxicity were found. There was no significant maternal toxicity. The dietary level of 1.25% was found to be a NOAEL for developmental toxicity. Further investigations showed the growth retardation to be specific to dietary administration during lactation: it was not produced by parenteral (i.p.) administration and was not influenced by treatment of the dams or litters during gestation. Slight maternal nutritional deficiency, caused by physico-chemical interactions of beta-CD with nutrients in the gut is proposed as the mechanism of action. No difference in milk composition was found.
在大鼠中进行了一项三代研究,每代有两个交配阶段和一个致畸学阶段,以评估饮食中β-环糊精(β-CD)的生殖和发育毒性。5%的β-CD会导致短暂的新生儿生长迟缓:2.5%的β-CD也观察到了类似但不明确的效果。未发现永久性缺陷或其他发育毒性迹象。未发现明显的母体毒性。发现1.25%的饮食水平是发育毒性的无观察到有害作用水平(NOAEL)。进一步研究表明,生长迟缓是哺乳期饮食给药所特有的:肠胃外(腹腔内)给药不会产生这种情况,并且妊娠期间对母鼠或幼崽的处理也不会影响生长迟缓。有人提出,β-CD与肠道中的营养物质发生物理化学相互作用导致的轻微母体营养缺乏是其作用机制。未发现乳汁成分有差异。