Oldreive Ceri E, Doherty Gayle H
School of Biology, Bute Building, West Burn Lane, St. Andrews, Fife KY16 9TS, United Kingdom.
Neurosci Lett. 2007 Feb 8;413(1):52-7. doi: 10.1016/j.neulet.2006.11.031. Epub 2006 Dec 6.
Whilst a plethora of studies that describe the toxicity of homocysteine to CNS neurons have been published, the effects of homocysteine on the Purkinje neurons of the cerebellum that play a vital role in motor function remain wholly unexplored. We have therefore established cultures of embryonic cerebellar Purkinje neurons and exposed them to a range of concentrations of homocysteine and determined its effects on their survival. The experiments revealed that all concentrations of homocysteine studied, from 50 to 500microM, caused a significant decrease in cerebellar Purkinje neuron number. This loss could be counteracted by the pan-caspase inhibitor z-VAD-fmk in the first 24h following homocysteine exposure, revealing that the initial loss was apoptotic. However, z-VAD-fmk could not prevent homocysteine-mediated loss of cerebellar Purkinje neurons in the longer term, after 6 days in vitro. In addition to its effects on Purkinje neuron survival, homocysteine markedly reduced both the overall magnitude and the complexity of the neurite arbor extended by the cerebellar Purkinje neurons, following 6 days incubation with this agent in vitro. Taken together our data reveal that homocysteine is toxic to cerebellar Purkinje neurons in vitro, inhibiting both their survival and the outgrowth of neurites.
虽然已经发表了大量描述同型半胱氨酸对中枢神经系统神经元毒性的研究,但同型半胱氨酸对在运动功能中起关键作用的小脑浦肯野神经元的影响仍完全未被探索。因此,我们建立了胚胎小脑浦肯野神经元培养物,并将它们暴露于一系列浓度的同型半胱氨酸中,以确定其对神经元存活的影响。实验表明,所研究的所有同型半胱氨酸浓度,从50到500微摩尔,都会导致小脑浦肯野神经元数量显著减少。在同型半胱氨酸暴露后的最初24小时内,泛半胱天冬酶抑制剂z-VAD-fmk可以抵消这种损失,这表明最初的损失是凋亡性的。然而,在体外培养6天后的长期实验中,z-VAD-fmk并不能阻止同型半胱氨酸介导的小脑浦肯野神经元损失。除了对浦肯野神经元存活的影响外,在体外与该试剂孵育6天后,同型半胱氨酸还显著降低了小脑浦肯野神经元延伸的神经突分支的总体大小和复杂性。综合我们的数据表明,同型半胱氨酸在体外对小脑浦肯野神经元有毒性,抑制它们的存活和神经突生长。