Teather L A, Packard M G, Bazan N G
Department of Psychology, University of New Orleans, New Orleans, Louisiana, 70148, USA.
Neurobiol Learn Mem. 1998 Nov;70(3):349-63. doi: 10.1006/nlme.1998.3862.
The present experiments examined the effects of posttraining intrahippocampal injections of the degradative enzyme-resistant methylcarbamyl analog of the bioactive phospholipid platelet-activating factor (mc-PAF) and the platelet-activating factor (PAF) receptor antagonists BN52021 and BN 50730 on memory in male Long-Evans rats trained in a hidden platform version of the Morris water maze. Following an eight-trial training session, rats received a unilateral intrahippocampal injection of mc-PAF (0.5, 1.0, or 2.0 microgram/0.5 microliter), lyso-PAF (1.0 microgram/0.5 microliter), the cell surface PAF receptor antagonist BN 52021 (0.25, 0.5, or 1.0 micrigram/0.5 microliter/, the intracellular PAF receptor antagonist BN 50730 (2.0, 5.0, or 10.0 microgram/0.5 microliter), or vehicle (50% DMSO in 0.9% saline; 0.5 microliter). On a retention test conducted 24 h after training, the escape latencies of rats administered mc-PAF (1.0 or 2.0 microgram) were significantly lower than those of the vehicle-injected controls, demonstrating a memory-enhancing effect of mc-PAF. Injections of lyso-PAF, a structurally similar metabolite of PAF, had no influence on memory, indicating that the memory-enhancing effect of mc-PAF is not caused by membrane perturbation by the phospholipid. The retention test escape latencies of rats administered BN 52021 (0.5 microgram) and BN 50730 (5.0 or 10 microgram) were significantly higher than those of the controls, indicating a memory impairing effect of both PAF antagonists. When mc-PAF, BN 52021, or BN 50730 was administered 2 h posttraining, no effect on retention was observed, indicating a time-dependent effect of the neuroactive substances on memory storage. The findings suggest a role for endogenous PAF in hippocampal-dependent memory processes.
本实验研究了训练后海马内注射生物活性磷脂血小板激活因子(PAF)的抗降解酶甲基氨基甲酰类似物(mc-PAF)以及血小板激活因子(PAF)受体拮抗剂BN52021和BN 50730对在Morris水迷宫隐蔽平台版本中训练的雄性Long-Evans大鼠记忆的影响。经过八次训练后,大鼠接受单侧海马内注射mc-PAF(0.5、1.0或2.0微克/0.5微升)、溶血PAF(1.0微克/0.5微升)、细胞表面PAF受体拮抗剂BN 52021(0.25、0.5或1.0微克/0.5微升)、细胞内PAF受体拮抗剂BN 50730(2.0、5.0或10.0微克/0.5微升)或溶剂(0.9%盐水中50%的二甲亚砜;0.5微升)。在训练后24小时进行的记忆测试中,注射mc-PAF(1.0或2.0微克)的大鼠的逃避潜伏期显著低于注射溶剂的对照组,表明mc-PAF具有增强记忆的作用。注射PAF的结构类似代谢物溶血PAF对记忆没有影响,这表明mc-PAF增强记忆的作用不是由磷脂引起的膜扰动所致。注射BN 52021(0.5微克)和BN 50730(5.0或10微克)的大鼠在记忆测试中的逃避潜伏期显著高于对照组,表明两种PAF拮抗剂均具有损害记忆的作用。当在训练后2小时注射mc-PAF、BN 52021或BN 50730时,未观察到对记忆的影响,这表明神经活性物质对记忆存储具有时间依赖性效应。这些发现表明内源性PAF在海马依赖性记忆过程中发挥作用。