Gilad G M, Gilad V H
Center for Neurosciences and Behavioral Research, Weizmann Institute of Science, Rehovot, Israel.
Int J Dev Neurosci. 1986;4(5):401-5. doi: 10.1016/0736-5748(86)90022-5.
The effects of dansylcadaverine and methylamine, competitive inhibitors of transglutaminase, were examined in primary cultures of dissociated rat cerebellar neurons. Addition of the drugs at plating time resulted 24 hr later in irreversible cytotoxic effects evidenced by failure of aggregation and neurite formation. Cytotoxicity was dose-dependent with methylamine being more potent (IC50 = 20 microM) than dansylcadaverine (IC50 = 30 microM). The cytotoxic effects were less potent when drugs were added 24 hr after plating, the time when neurons had already begun to extend neurites. Drugs were effective in the various sera and heat-inactivated sera tested. We concluded that low doses of methylamine and dansylcadaverine have potent toxic effects on primary neuronal cultures.
在大鼠小脑神经元原代解离培养物中检测了转谷氨酰胺酶的竞争性抑制剂丹磺酰尸胺和甲胺的作用。在接种时添加这些药物,24小时后会产生不可逆的细胞毒性作用,表现为细胞聚集失败和神经突形成受阻。细胞毒性呈剂量依赖性,甲胺比丹磺酰尸胺更具毒性(甲胺的IC50 = 20微摩尔,丹磺酰尸胺的IC50 = 30微摩尔)。在接种24小时后添加药物时,细胞毒性作用较弱,此时神经元已经开始延伸神经突。在测试的各种血清和热灭活血清中,药物均有效果。我们得出结论,低剂量的甲胺和丹磺酰尸胺对原代神经元培养物有强大的毒性作用。