Williams R, Ryves W J, Dalton E C, Eickholt B, Shaltiel G, Agam G, Harwood A J
MRC Laboratory for Molecular Cell Biology and Department of Biology, University College London, Gower St, London WC1E 6BT, UK.
Biochem Soc Trans. 2004 Nov;32(Pt 5):799-802. doi: 10.1042/BST0320799.
Lithium (Li(+)), a mood stabilizer, has profound effects on cultured neurons, offering an opportunity to investigate its cellular biological effects. Here we consider the effect of Li(+) and other psychotropic drugs on growth cone morphology and chemotaxis. Li(+) inhibits GSK-3 (glycogen synthase kinase-3) at a therapeutically relevant concentration. Treated cells show a number of features that arise due to GSK-3 inhibition, such as altered microtubule dynamics, axonal branching and loss of semaphorin 3A-mediated growth cone collapse. Li(+) also causes growth cones to spread; however, a similar effect is seen with two other mood stabilizers, valproic acid and carbamazepine, but without changes in microtubules or axon branching. This common effect of mood stabilizers is mediated by changes in inositol phosphate signalling, not GSK-3 activity. Given the presence of neurogenesis in the adult brain, we speculate that changes in growth cone behaviour could also occur during treatment of mental disorders.
锂(Li(+))作为一种情绪稳定剂,对培养的神经元有深远影响,为研究其细胞生物学效应提供了契机。在此,我们探讨Li(+)及其他精神药物对生长锥形态和趋化性的影响。Li(+)在治疗相关浓度下可抑制糖原合酶激酶-3(GSK-3)。经处理的细胞呈现出一些因GSK-3抑制而产生的特征,如微管动力学改变、轴突分支以及信号素3A介导的生长锥塌陷丧失。Li(+)还会导致生长锥伸展;然而,另外两种情绪稳定剂丙戊酸和卡马西平也有类似效果,但微管或轴突分支并无变化。情绪稳定剂的这种共同效应是由肌醇磷酸信号传导的变化介导的,而非GSK-3活性。鉴于成人大脑中存在神经发生,我们推测在精神障碍治疗过程中生长锥行为也可能发生变化。