Giles J J, Bannigan J G
Department of Human Anatomy and Physiology, National University of Ireland, University College, Dublin.
J Anat. 1999 Feb;194 ( Pt 2)(Pt 2):197-205. doi: 10.1046/j.1469-7580.1999.19420197.x.
The effects of lithium on vascular development were examined using the chick embryo area vasculosa in shell-less culture as an experimental model. Embryos were explanted after 48 h in ovo and LiC1 (50, 100, 150 and 200 microg in 10 microl water) was applied to the centre of the blastodisc. Controls were untreated or given equimolar amounts of NaCl. At 24 h and 48 h after treatment, untreated and NaCl controls were identical, having well developed extraembryonic vessels. At doses of 100 microg and greater, LiCl significantly inhibited normal vascular development and expansion of the area vasculosa in the majority of explants. In many specimens blood islands continued to form but their assembly into primitive vessels was prevented, indicating that lithium affects the mechanism regulating the assembly of vascular endothelium. At the same time the embryos were alive but retarded in development compared with controls. When LiCl (150 microg) was applied to cultures explanted after 72 h in ovo (when the primary vascular network had already formed through vasculogenesis) no adverse effects were seen. This suggests that lithium affects vasculogenesis but not angiogenesis. Treatment with myo-inositol completely reversed the effects of lithium in a time dependent manner indicating that the phosphatidylinositol second messenger cycle may be involved in the cellular events of vasculogenesis. Finally the results of this study show that the yolk sac vasculature is particularly vulnerable to lithium and the consequent effects of this interference on embryonic development are discussed.
以无壳培养的鸡胚血管区为实验模型,研究了锂对血管发育的影响。在鸡胚孵化48小时后将其移出,将LiC1(50、100、150和200微克溶于10微升水中)施加于胚盘中心。对照组未处理或给予等摩尔量的NaCl。处理后24小时和48小时,未处理组和NaCl对照组情况相同,胚外血管发育良好。在100微克及以上剂量时,LiCl显著抑制了大多数外植体中血管的正常发育以及血管区的扩展。在许多标本中,血岛继续形成,但它们组装成原始血管的过程受到阻碍,这表明锂影响调节血管内皮组装的机制。与此同时,胚胎存活,但与对照组相比发育迟缓。当将LiCl(150微克)施加于孵化72小时后移出的培养物(此时通过血管生成已经形成了初级血管网络)时,未观察到不利影响。这表明锂影响血管生成但不影响血管新生。用肌醇处理能以时间依赖性方式完全逆转锂的作用,这表明磷脂酰肌醇第二信使循环可能参与了血管生成的细胞事件。最后,本研究结果表明卵黄囊血管系统对锂特别敏感,并讨论了这种干扰对胚胎发育的后续影响。