Gallagher M, Rapp P R, Fanelli R J
Brain Res. 1985 Nov 18;347(2):284-90. doi: 10.1016/0006-8993(85)90188-x.
Post-training administration of opiate antagonists improves retention of recent learning in laboratory animals tested on a variety of tasks. We examined the possibility that this effect of opiate antagonist treatment might be due to release of brain norepinephrine (NE) function from opioid peptide inhibition. The behavioral testing procedure in the experiments consisted of one-trial passive avoidance conditioning. Rats received post-training treatments immediately after the training trial and retention was tested 24 h later. Lesions of the dorsal noradrenergic bundle (DNB) that were induced by 6-hydroxydopamine (6-OHDA) were found to prevent the memory enhancing effect of post-training naloxone administration. The memory enhancing effect of naloxone was restored when NE neurons were protected from 6-OHDA by pretreatment with a NE uptake inhibitor. Earlier research indicated that the amygdala complex is one brain site that is sensitive to the effects of opiate manipulations on memory processes. In this study, lesions of the DNB were also found to prevent the memory enhancing effect of intracranial opiate antagonist administration into the amygdala complex.
在训练后给予阿片类拮抗剂可提高在各种任务中接受测试的实验动物对近期学习内容的记忆保持能力。我们研究了阿片类拮抗剂治疗产生这种效果的可能性,即它可能是由于从阿片肽抑制作用中释放了脑去甲肾上腺素(NE)功能。实验中的行为测试程序包括单次被动回避条件反射。大鼠在训练试验后立即接受训练后治疗,并在24小时后测试记忆保持情况。发现由6-羟基多巴胺(6-OHDA)诱导的背侧去甲肾上腺素能束(DNB)损伤可阻止训练后给予纳洛酮的记忆增强作用。当通过用NE摄取抑制剂预处理使NE神经元免受6-OHDA影响时,纳洛酮的记忆增强作用得以恢复。早期研究表明,杏仁核复合体是一个对阿片类药物操作对记忆过程的影响敏感的脑区。在本研究中,还发现DNB损伤可阻止向杏仁核复合体颅内注射阿片类拮抗剂的记忆增强作用。