Giles James J, Bannigan John G
Department of Human Anatomy and Physiology and Conway Institute of Biomolecular and Biomedical Research, National University of Ireland, Dublin, Ireland.
Curr Pharm Des. 2006;12(12):1531-41. doi: 10.2174/138161206776389804.
A review is presented on the effects of lithium in therapeutic doses on the outcome of human pregnancy. The results of various studies including cohort, prospective, retrospective and small number case reports indicate that lithium is a "weak" teratogen in humans. The main effects attributable to lithium are, cardiac malformations and babies with increased birth weight. There is a possibility that, in particular, lithium may be associated with the Ebstein anomaly but present evidence cannot definitely affirm or deny this association. Animal studies with lithium using doses comparable to human therapeutic serum levels have not reported any abnormalities. However, higher doses have produced exencephaly, skeletal and craniofacial defects and abnormalities of blood vessel development. Experiments with other vertebrates have shown that lithium affects dorsoventral specification and inhibition of vasculogenesis. Both these effects can be prevented by pretreatment with myo-inositol indicating that lithium interferes with the phosphatidyl inositol cycle. More recent findings have shown that the effects of lithium on invertebrates may be mediated through inhibition of GSK-3beta in the Wnt-GSK-3 pathway.
本文综述了治疗剂量的锂对人类妊娠结局的影响。包括队列研究、前瞻性研究、回顾性研究及少量病例报告在内的各项研究结果表明,锂在人类中是一种“弱”致畸剂。锂的主要影响包括心脏畸形和出生体重增加的婴儿。特别是,锂有可能与埃布斯坦畸形有关,但目前的证据不能明确肯定或否定这种关联。使用与人类治疗血清水平相当的剂量进行的锂的动物研究未报告任何异常。然而,更高剂量会导致无脑畸形、骨骼和颅面缺陷以及血管发育异常。对其他脊椎动物的实验表明,锂会影响背腹轴的特化并抑制血管生成。这两种作用都可以通过用肌醇预处理来预防,这表明锂会干扰磷脂酰肌醇循环。最近的研究结果表明,锂对无脊椎动物的影响可能是通过抑制Wnt-GSK-3信号通路中的GSK-3β介导的。