Schaeffer E L, Bassi F, Gattaz W F
Laboratory of Neuroscience (LIM-27), Department and Institute of Psychiatry, Faculty of Medicine, University of São Paulo, Brazil.
J Neural Transm (Vienna). 2005 May;112(5):641-7. doi: 10.1007/s00702-005-0301-9.
Phospholipase A2 (PLA2) is a family of key enzymes in membrane phospholipid metabolism. In rats, the inhibition of PLA2 activity in the hippocampus was found to impair memory formation. Because memory function is largely dependent on the fluidity of brain membranes, we performed the present study to investigate the effects of in vivo PLA2 inhibition (with PACOCF3) on the fluidity of hippocampal membranes from rats trained in a learning task. Hippocampal tissue from rats injected with 100 microM PACOCF3 showed reduced membrane fluidity as compared to vehicle (p < 0.01), and the reduction of membrane fluidity was highly correlated with PLA2 inhibition (r = .76, p < 0.03). This finding is of interest because reduction of brain membrane fluidity impairs memory formation and both decreased PLA2 activity and reduced membrane fluidity have been reported in the brain from patients with Alzheimer's disease.
磷脂酶A2(PLA2)是膜磷脂代谢中的一类关键酶。在大鼠中,发现海马体中PLA2活性的抑制会损害记忆形成。由于记忆功能在很大程度上依赖于脑膜的流动性,我们进行了本研究,以探讨体内PLA2抑制(使用PACOCF3)对在学习任务中训练的大鼠海马体膜流动性的影响。与注射赋形剂的大鼠相比,注射100微摩尔PACOCF3的大鼠海马组织显示膜流动性降低(p < 0.01),并且膜流动性的降低与PLA2抑制高度相关(r = 0.76,p < 0.03)。这一发现很有趣,因为脑膜流动性的降低会损害记忆形成,并且在阿尔茨海默病患者的大脑中已报道PLA2活性降低和膜流动性降低。