Department of Biology, Sciences and Research Branch, Islamic Azad University, Tehran, Iran.
Neurobiol Learn Mem. 2010 May;93(4):455-62. doi: 10.1016/j.nlm.2010.01.003. Epub 2010 Jan 11.
The present study evaluated the possible role of alpha-adrenergic receptors of the dorsal hippocampus on scopolamine-induced amnesia and scopolamine state-dependent memory in adult male Wistar rats. The animals were bilaterally implanted with chronic cannulae in the CA1 regions of the dorsal hippocampus, trained in a step-through type inhibitory avoidance task, and tested 24h after training to measure step-through latency. Results indicate that post-training or pre-test intra-CA1 administration of scopolamine (1 and 2 microg/rat) dose-dependently reduced the step-through latency, showing an amnestic response. Amnesia produced by post-training scopolamine (2 microg/rat) was reversed by pre-test administration of the scopolamine that is due to a state-dependent effect. Interestingly, pre-test intra-CA1 microinjection of alpha1-adrenergic agonist, phenylephrine (1 and 2 microg/rat) or alpha2-adrenergic agonist, clonidine improved post-training scopolamine (2 microg/rat)-induced retrieval impairment. Furthermore, pre-test intra-CA1 microinjection of phenylephrine (0.25, 0.5 and 1 microg/rat) or clonidine (0.25, 0.5 and 1 microg/rat) with an ineffective dose of scopolamine (0.25 microg/rat), synergistically improved memory performance impaired by post-training scopolamine. On the other hand, pre-test injection of alpha1-receptors antagonist prazosin (1 and 2 microg/rat) or alpha2-receptors antagonist yohimbine (1 and 2 microg/rat) prevented the restoration of memory by pre-test scopolamine. It is important to note that pre-test intra-CA1 administration of the same doses of prazosin or yohimbine, alone did not affect memory retrieval. These results suggest that alpha1- and alpha2-adrenergic receptors of the dorsal hippocampal CA1 regions may play an important role in scopolamine-induced amnesia and scopolamine state-dependent memory.
本研究评估了背海马 CA1 区的α-肾上腺素受体在东莨菪碱诱导的健忘症和东莨菪碱状态依赖性记忆中的可能作用。动物双侧植入背海马 CA1 区的慢性套管,在穿梭式抑制回避任务中进行训练,并在训练后 24 小时进行测试,以测量穿梭潜伏期。结果表明,训练后或测试前 CA1 内给予东莨菪碱(1 和 2μg/大鼠)剂量依赖性地降低穿梭潜伏期,表现出健忘症反应。训练后东莨菪碱(2μg/大鼠)引起的健忘症被测试前给予东莨菪碱逆转,这是由于状态依赖性效应。有趣的是,测试前 CA1 内注射α1-肾上腺素激动剂苯肾上腺素(1 和 2μg/大鼠)或α2-肾上腺素激动剂可乐定可改善训练后东莨菪碱(2μg/大鼠)引起的检索障碍。此外,测试前 CA1 内注射苯肾上腺素(0.25、0.5 和 1μg/大鼠)或可乐定(0.25、0.5 和 1μg/大鼠)与无效剂量的东莨菪碱(0.25μg/大鼠)协同改善了训练后东莨菪碱引起的记忆障碍。另一方面,测试前注射α1-受体拮抗剂哌唑嗪(1 和 2μg/大鼠)或α2-受体拮抗剂育亨宾(1 和 2μg/大鼠)可防止测试前东莨菪碱恢复记忆。重要的是要注意,测试前 CA1 内给予相同剂量的哌唑嗪或育亨宾单独不会影响记忆检索。这些结果表明,背海马 CA1 区的α1-和α2-肾上腺素受体可能在东莨菪碱诱导的健忘症和东莨菪碱状态依赖性记忆中发挥重要作用。