Torkaman-Boutorabi Anahita, Sheidadoust Hadi, Hashemi-Hezaveh Seyed-Milad, Zarrindast Mohammad-Reza
Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Faculty of Pharmacy, Azad University, Tehran, Iran.
Pharmacol Biochem Behav. 2015 Jun;133:92-8. doi: 10.1016/j.pbb.2015.03.018. Epub 2015 Apr 3.
The prelimbic region of the medial prefrontal cortex (mPFC) is a brain area crucial for memory, attention, and decision making. It has been shown that α2-adreneoceptors (α2-ARs) play a powerful role in regulating memory and attention functions in this region. Since many studies have demonstrated the impairment effect of morphine on memory through mPFC, we aimed to investigate the possible interaction between α2-ARs of the mPFC and morphine induced amnesia in passive avoidance learning in rats. Animals were bilaterally implanted with chronic cannulas in the mPFC, trained in the step-through type passive avoidance task, and tested 24h after training; step-through latencies were measured. Our data indicate that post-training i.p. administration of morphine (2.5, 5 and 7.5mg/kg) dose-dependently reduced the step-through latency, showing an amnesic effect. Post-training intra-mPFC administration of yohimbine (an α2-adrenergic antagonist, 0.125, 0.25 and 0.5μg/rat) and clonidine (an α2-adrenergic agonist, 0.001, 0.01 and 0.2μg/rat), dose dependently impaired memory retrieval. Furthermore, post-training intra-mPFC microinjection of ineffective doses of yohimbine or clonidine significantly reversed the inhibitory effect of morphine on memory retrieval. Furthermore, SKF96365 (a presynaptic calcium channel blocker) reduced yohimbine and showed slight inhibition of clonidine effect. These results suggest that α2-ARs of the mPFC may play an important role in morphine-induced amnesia.
内侧前额叶皮质(mPFC)的前边缘区是一个对记忆、注意力和决策至关重要的脑区。研究表明,α2 -肾上腺素能受体(α2 - ARs)在调节该区域的记忆和注意力功能方面发挥着重要作用。由于许多研究已经证明吗啡通过mPFC对记忆有损害作用,我们旨在研究mPFC的α2 - ARs与吗啡诱导的大鼠被动回避学习失忆之间可能的相互作用。动物双侧在mPFC植入慢性套管,进行穿梭箱式被动回避任务训练,并在训练后24小时进行测试;测量穿梭潜伏期。我们的数据表明,训练后腹腔注射吗啡(2.5、5和7.5mg/kg)剂量依赖性地缩短了穿梭潜伏期,显示出失忆效应。训练后在mPFC内注射育亨宾(一种α2 -肾上腺素能拮抗剂,0.125、0.25和0.5μg/大鼠)和可乐定(一种α2 -肾上腺素能激动剂,0.001、0.01和0.2μg/大鼠),剂量依赖性地损害记忆提取。此外,训练后在mPFC内微量注射无效剂量的育亨宾或可乐定可显著逆转吗啡对记忆提取的抑制作用。此外,SKF96365(一种突触前钙通道阻滞剂)可减弱育亨宾的作用,并对可乐定的作用有轻微抑制。这些结果表明,mPFC的α2 - ARs可能在吗啡诱导的失忆中起重要作用。