Monnerie Hubert, Shashidhara Shalini, Le Roux Peter D
Department of Neurosurgery, University of Pennsylvania, Philadelphia, PA 19104, USA.
Neurosci Lett. 2003 Jul 24;345(3):182-6. doi: 10.1016/s0304-3940(03)00526-3.
During cerebral ischemia, massive glutamate release leads to cell death through ionotropic glutamate receptor activation. An early consequence of this excitotoxicity is dendrite injury, which can precede cell death. We therefore tested whether cells that survived an excitotoxic insult triggered by overactivation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA)/kainate (KA) subtype of ionotropic glutamate receptors displayed altered dendrite growth. We demonstrate that 24 h exposure of cultured cortical neurons to AMPA or KA dramatically reduced dendrite growth from surviving neurons. AMPA or KA exposure decreased primary dendrite number and length, and also reduced dendritic branching. The AMPA/KA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione blocked the deleterious effect of AMPA and KA on dendrite growth. These results suggest that AMPA/KA receptor overactivation may contribute to dendritic injury from neurons that survive an ischemic insult.
在脑缺血期间,大量谷氨酸释放通过离子型谷氨酸受体激活导致细胞死亡。这种兴奋性毒性的早期后果是树突损伤,其可先于细胞死亡出现。因此,我们测试了在离子型谷氨酸受体的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)/海人藻酸(KA)亚型过度激活引发的兴奋性毒性损伤中存活下来的细胞,其树突生长是否发生改变。我们证明,将培养的皮质神经元暴露于AMPA或KA 24小时后,存活神经元的树突生长显著减少。AMPA或KA暴露减少了初级树突的数量和长度,并且也减少了树突分支。AMPA/KA受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮可阻断AMPA和KA对树突生长的有害作用。这些结果表明,AMPA/KA受体过度激活可能导致在缺血性损伤中存活的神经元发生树突损伤。