Allan S M, Rothwell N J
School of Biological Sciences, University of Manchester, UK.
J Cereb Blood Flow Metab. 2000 Oct;20(10):1409-13. doi: 10.1097/00004647-200010000-00002.
Striatal coadministration of interleukin-1beta (IL-1beta) with alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (S-AMPA) in rats results in widespread cortical cell death not caused by either treatment alone. This cortical damage was unaffected by cortical infusion of the AMPA-receptor antagonist NBQX. Cortical infusion of an NMDA-receptor antagonist D-AP5 significantly inhibited (57%; P < 0.05) cortical death, but had no effect on the local striatal death. Thus, cortical neuronal death induced by striatal S-AMPA and human recombinant interleukin-1beta (hrIL-1beta) is mediated by activation of NMDA receptors in the cortex. The authors propose that IL-1beta actions on AMPA-receptor mediated cell death may involve the activation of polysynaptic pathways from the striatum to the cortex.
在大鼠纹状体中共同给予白细胞介素 -1β(IL -1β)和α -氨基 -3 -羟基 -5 -甲基 -4 -异恶唑丙酸(S -AMPA)会导致广泛的皮质细胞死亡,而单独使用这两种处理方法均不会引发这种情况。这种皮质损伤不受皮质注入AMPA受体拮抗剂NBQX的影响。皮质注入NMDA受体拮抗剂D -AP5可显著抑制(57%;P < 0.05)皮质细胞死亡,但对局部纹状体细胞死亡没有影响。因此,纹状体S -AMPA和人重组白细胞介素 -1β(hrIL -1β)诱导的皮质神经元死亡是由皮质中NMDA受体的激活介导的。作者提出,IL -1β对AMPA受体介导的细胞死亡的作用可能涉及从纹状体到皮质的多突触途径的激活。