M.V. Lomonosov Moscow State University, A.N. Belozersky Institute of Physico-Chemical Biology, Biological Faculty, Leninskiye gory, 1, b. 40, 119991 Moscow, Russia; Research Center of Neurology, Volokolamskoe Shosse 80, 125367 Moscow, Russia.
Research Center of Neurology, Volokolamskoe Shosse 80, 125367 Moscow, Russia.
Toxicol Appl Pharmacol. 2018 Jun 1;348:99-104. doi: 10.1016/j.taap.2018.04.024. Epub 2018 Apr 20.
Streptozotocin (STZ) is a glucosamine-nitrosourea compound that is particularly toxic to the insulin-producing beta-cells of the pancreas in mammals; it is used for experimental simulation of sporadic Alzheimer's disease by means of intracerebroventricular administration in vivo. Here we show that the application of 3-4 mM STZ to primary culture for 48 h induces neuronal death in immature (2-3 days in vitro) cultures of rat cerebellar granule cells. Mature cultures (7-8 days in vitro) were poorly sensitive to this toxic treatment. Immature cultures demonstrated a high expression of the protein PSA-NCAM, the marker of immature neurons, and they were insensitive to the toxic effect of glutamate. In mature cultures, this protein was poorly expressed, whereas neurons showed a very high sensitivity to the toxic effect of glutamate. Measurements of the concentration of intracellular free calcium ions ([Ca]) showed that the STZ-induced [Ca] increase in young neurons was six times higher than that in mature neurons. Our results show that STZ is very toxic for immature neurons and probably it can significantly impair neurogenesis.
链脲佐菌素(STZ)是一种氨基葡萄糖-亚硝脲化合物,对哺乳动物胰腺中产生胰岛素的β细胞具有特别的毒性;通过在体颅内给药,STZ 被用于实验性模拟散发性阿尔茨海默病。在这里,我们发现,将 3-4mM 的 STZ 应用于原代培养 48 小时,会诱导大鼠小脑颗粒细胞未成熟(体外培养 2-3 天)培养物中的神经元死亡。成熟的培养物(体外培养 7-8 天)对这种毒性处理的敏感性较差。未成熟的培养物表现出高水平的 PSA-NCAM 蛋白表达,这是未成熟神经元的标志物,它们对谷氨酸的毒性作用不敏感。在成熟的培养物中,这种蛋白质表达水平较低,而神经元对谷氨酸的毒性作用非常敏感。细胞内游离钙离子浓度([Ca])的测量表明,STZ 诱导的年轻神经元中[Ca]的增加是成熟神经元的六倍。我们的结果表明,STZ 对未成熟神经元非常有毒,可能会显著损害神经发生。