Teratogenicity of vitamin A.

B A Underwood
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Abstract

There are few documented reports in humans that link teratogenic consequences to high intakes of supplemental R or RE, taken either acutely or chronically. This is in contrast to the well-documented teratogenicity in humans of RA and some of its synthetic derivatives. Both R and RE are documented teratogens in animals. Therefore, until more is known about the mechanisms of placental transfer and control as well as about the dose-related teratogenicity of vitamin A at different stages of gestation, there are few justifications for routine ingestion by fertile women of supplemental vitamin A in excess of 8-10,000 IU. Exceptions are when clinical signs are evident and habitual diets are unusually deficient. Even then, however, high dosages should be restricted to single administrations followed by frequent or daily dosages not exceeding 10,000 IU. Available evidence indicates that high-dosage supplements of beta-carotene can be safely taken; the dosages probably should be of a level to sustain blood concentrations below 300 micrograms/dl.

维生素A的致畸性
在人类中,很少有文献报道将致畸后果与大量摄入补充R或RE(无论是急性摄入还是长期摄入)联系起来。这与有充分文献记载的类风湿关节炎及其一些合成衍生物对人类的致畸性形成对比。R和RE都是记录在案的动物致畸物。因此,在更多地了解胎盘转移和控制的机制以及维生素A在妊娠不同阶段的剂量相关致畸性之前,很少有理由让育龄妇女常规摄入超过8-10,000 IU的补充维生素A。例外情况是当临床症状明显,习惯性饮食异常不足。然而,即便如此,高剂量也应限制在单次给药之后,频繁或每日给药不超过10,000 IU。现有证据表明,大剂量补充β -胡萝卜素是安全的;剂量可能应该维持在血液浓度低于300微克/分升的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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