磷脂酶A2的抑制剂使雏鸡在被动回避任务中失忆

Christian Hölscher , Steven P.R. Rose
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引用次数: 45

摘要

阻断花生四烯酸(ArA)释放的关键酶磷脂酶A2 (PLA2)对日龄雏鸡记忆保留的影响进行了单试验被动回避实验。双侧脑内注射PLA2和脂氧合酶抑制剂去双氢木脂酸(NDGA) (15 μl 4 mM NDGA/半球,计算得到等效脑内浓度为120 μM)或PLA2抑制剂马兜铃酸(AST) (5 μl 4 mM AST/半球,计算得到等效脑内浓度为~ 40 μM)到中间内侧腹侧高纹状体(IMHV)。在这个任务中,这个区域对小鸡的记忆形成至关重要。训练前注射任何一种抑制剂都会导致雏鸡对回避反应表现出持久的健忘症。NDGA和AST抑制剂均在训练后1.25小时出现健忘症。训练后注射药物对保留率无影响。评估两种药物的时间和剂量依赖性。额外的测试表明,遗忘效果不是由于状态依赖性学习,也不是由于药物对一般运动能力或动机的干扰。研究结果支持了花生四烯酸释放是早期(尽管不是立即)介导与记忆形成相关的突触可塑性事件的必要步骤的理论。这与ArA可能作为突触后和突触前可塑性位点之间的晚期逆行信使的假设是一致的,尽管它不能证明这种作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitors of phospholipase A2 produce amnesia for a passive avoidance task in the chick

The effects of blocking phospholipase A2 (PLA2), a key enzyme in arachidonic acid (ArA) release, on memory retention have been studied in a one-trial passive avoidance task in the day-old chick. Bilateral intracerebral injections of the PLA2 and lipoxygenase inhibitor nordihydroguaiaretic acid (NDGA) (15 μl of 4 mM NDGA/hemisphere, calculated to give an equivalent intracerebral concentration of 120 μM) or the PLA2 inhibitor aristolochic acid (AST) (5 μl of a 4 mM AST/hemisphere, calculated to give an equivalent intracerebral concentration of ∼40 μM) were made into the intermediate medial hyperstriatum ventrale (IMHV), an area that is of crucial importance for memory formation in the chick in this task. Pretraining injections of either inhibitor resulted in the chicks showing lasting amnesia for the avoidance response. The onset of amnesia with both inhibitors NDGA and AST was at 1.25 h post-training. Injection of drugs post-training had no effect on retention. Time and dose dependencies of both drugs were evaluated. Additional tests showed that the amnestic effect is not due to state-dependent learning nor to interference of the drugs with general motor ability or motivation. The results support the theory that arachidonic acid release is a necessary step in the early, although not immediate, events mediating the synaptic plasticity associated with memory formation. This is compatible with the hypothesis that ArA may serve as a late retrograde messenger between post- and presynaptic sites of plasticity, although it is not proof of such a role.

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