Jaw S P, Su D D, Truong D D
Parkinson and Movement Disorders Laboratory, Department of Neurology, University of California Irvine 92717, USA.
Pharmacol Biochem Behav. 1995 Dec;52(4):667-70. doi: 10.1016/0091-3057(95)00185-y.
Following 10-min cardiac arrest and resuscitation, the central serotonergic system and motor function of rats were found to be affected and later on restored. Astrocyte-derived growth factor (S100 beta) is known to promote survival and neurite outgrowth of serotonergic neurons. In the present study, brain levels of S100 beta were investigated with quantitative immunoblot analysis at various time points following cardiac arrest. Significant reductions of S100 beta were found in the cerebral cortex (30%), midbrain (35%), and cerebellum (46%) of rats 3 days postcardiac arrest. In contrast, at 14 and > 45 days, significant increases of S100 beta were detected in the cerebral cortex (57%; 81%), midbrain (70%; 97%), and cerebellum (84%; 157%). The results indicate that reactive astrocytosis and elevated levels of S100 beta may participate in the recovery processes following hypoxic-ischemic insults to the brain.
在经历10分钟心脏骤停和复苏后,发现大鼠的中枢5-羟色胺能系统和运动功能受到影响,随后恢复。已知星形胶质细胞衍生生长因子(S100β)可促进5-羟色胺能神经元的存活和神经突生长。在本研究中,通过定量免疫印迹分析在心脏骤停后的不同时间点研究了S100β的脑水平。心脏骤停后3天,在大鼠的大脑皮层(30%)、中脑(35%)和小脑(46%)中发现S100β显著降低。相反,在14天和超过45天时,在大脑皮层(57%;81%)、中脑(70%;97%)和小脑(84%;157%)中检测到S100β显著增加。结果表明,反应性星形胶质细胞增生和S100β水平升高可能参与了脑缺氧缺血性损伤后的恢复过程。