Paschen W, Doutheil J, Uto A, Gissel C
Max-Planck-Institute for Neurological Research, Department of Experimental Neurology, Köln, Germany.
Neurosci Lett. 1996 Oct 11;217(1):41-4. doi: 10.1016/0304-3940(96)13066-4.
Transient cerebral ischemia was produced in rats using the four-vessel occlusion model. After 30 min ischemia and 2, 4, 8, or 24 h of recirculation, total RNA was isolated from the cortex, striatum and hippocampus and reverse transcribed into cDNA. Endoplasmic reticulum (ER) calcium-ATPase (SERCA, subunit 2b) cDNA was amplified using appropriate primers. Ischemia-induced changes in SERCA mRNA levels were analyzed by quantitative polymerase chain reaction (PCR). For quantification, each PCR reaction was run in the presence of an internal standard. In control brains SERCA mRNA levels amounted to 392 +/- 43,431 +/- 86, and 409 +/- 21 micrograms mRNA/g total RNA in the cortex, striatum and hippocampus, respectively. SERCA mRNA levels did not change significantly during the first 8 h of recovery. After 24 h of recovery, however, SERCA mRNA levels decreased sharply in the hippocampus and striatum (P < 0.001 versus control) but not in the cortex. It is concluded that in vulnerable brain structures a post-ischemic disturbance in ER calcium homeostasis may limit the recovery of neurons from metabolic stress.
采用四动脉闭塞模型在大鼠中制造短暂性脑缺血。缺血30分钟并再灌注2、4、8或24小时后,从皮质、纹状体和海马体中分离出总RNA,并逆转录成cDNA。使用合适的引物扩增内质网(ER)钙 - ATP酶(SERCA,亚基2b)cDNA。通过定量聚合酶链反应(PCR)分析缺血诱导的SERCA mRNA水平变化。为了进行定量,每个PCR反应在有内标的情况下进行。在对照脑中,皮质、纹状体和海马体中SERCA mRNA水平分别为392±43、431±86和409±21微克mRNA /克总RNA。在恢复的前8小时内,SERCA mRNA水平没有显著变化。然而,恢复24小时后,海马体和纹状体中的SERCA mRNA水平急剧下降(与对照相比,P < 0.001),但皮质中没有下降。结论是,在易损脑结构中,缺血后内质网钙稳态紊乱可能会限制神经元从代谢应激中恢复。