Silva Carla G, Porciúncula Lisiane O, Canas Paula M, Oliveira Catarina R, Cunha Rodrigo A
Center for Neuroscience of Coimbra, Institute of Biochemistry, Faculty of Medicine, University of Coimbra, 3004-504 Coimbra, Portugal.
Neurobiol Dis. 2007 Aug;27(2):182-9. doi: 10.1016/j.nbd.2007.04.018. Epub 2007 May 26.
Since adenosine A(2A) receptor (A(2A)Rs) blockade protects against noxious brain insults involving apoptosis, we directly tested if A(2A)R blockade prevents apoptosis induced by staurosporine (STS). Exposure of rat hippocampal neurons to STS (30 nM, 24 h) decreased neuronal viability while increasing the number apoptotic-like neurons and de-localizing mitochondria and cytochrome c immunoreactivities. This was prevented by the selective A(2A)R antagonists, SCH58261 and ZM241385 (50 nM). Shorter incubation periods (6 h) with STS caused no neuronal loss but decreased synaptophysin and MAP-2 immunoreactivities, which was prevented by SCH58261. Furthermore, STS (100 nM) decreased MTT reduction and increased caspase-3 activity in rat hippocampal nerve terminals, which was prevented by SCH58261. These results show that A(2A)R blockade inhibits STS-induced apoptotic-like neuronal cell death. This begins with an apoptotic-like synaptotoxicity, which later evolved into an overt neurotoxicity, and A(2A)Rs effectively control this initial synaptotoxicity, in agreement with their predominant synaptic localization in the hippocampus.
由于腺苷A(2A)受体(A(2A)Rs)阻断可保护大脑免受涉及细胞凋亡的有害损伤,我们直接测试了A(2A)R阻断是否能预防由星形孢菌素(STS)诱导的细胞凋亡。将大鼠海马神经元暴露于STS(30 nM,24小时)会降低神经元活力,同时增加凋亡样神经元的数量,并使线粒体和细胞色素c免疫反应性发生移位。这可被选择性A(2A)R拮抗剂SCH58261和ZM241385(50 nM)所预防。与STS孵育较短时间(6小时)不会导致神经元丢失,但会降低突触素和MAP-2免疫反应性,这可被SCH58261预防。此外,STS(100 nM)会降低大鼠海马神经末梢的MTT还原并增加caspase-3活性,这可被SCH58261预防。这些结果表明,A(2A)R阻断可抑制STS诱导的凋亡样神经元细胞死亡。这始于一种凋亡样突触毒性,随后发展为明显的神经毒性,并且A(2A)Rs可有效控制这种初始突触毒性,这与其在海马中主要的突触定位一致。