Hvoslef-Eide Martha, Oomen C A, Fisher B M, Heath C J, Robbins T W, Saksida L M, Bussey T J
Department of Psychology, University of Cambridge, Downing Street, Cambridge, CB2 3EB, UK.
MRC and Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, CB2 3EB, UK.
Psychopharmacology (Berl). 2015 Nov;232(21-22):4005-16. doi: 10.1007/s00213-015-4038-3. Epub 2015 Aug 12.
Spatial working memory is dependent on the appropriate functioning of the prefrontal cortex (PFC). PFC activity can be modulated by noradrenaline (NA) released by afferent projections from the locus coeruleus. The coreuleo-cortical NA system could therefore be a target for cognitive enhancers of spatial working memory. Of the three classes of NA receptor potentially involved, the α2 and α1 classes seem most significant, though agents targeting these receptors have yielded mixed results. This may be partially due to the use of behavioural assays that do not translate effectively from the laboratory to the clinical setting. Use of a paradigm with improved translational potential may be essential to resolve these discrepancies.
The objective of this study was to assess the effects of PFC-infused α2 and α1 adrenergic receptor agonists on spatial working memory performance in the touchscreen continuous trial-unique non-matching to location (cTUNL) task in rats.
Young male rats were trained in the cTUNL paradigm. Cannulation of the mPFC allowed direct administration of GABA agonists for task validation, and phenylephrine and guanfacine to determine the effects of adrenergic agonists on task performance.
Infusion of muscimol and baclofen resulted in a delay-dependent impairment. Administration of the α2 agonist guanfacine had no effect, whilst infusion of the α1 agonist phenylephrine significantly improved working memory performance.
Spatial working memory as measured in the rat cTUNL task is dependent on the mPFC. Enhancement of noradrenergic signalling enhanced performance in this paradigm, suggesting a significant role for the α1 receptor in this facilitation.
空间工作记忆依赖于前额叶皮质(PFC)的正常功能。PFC的活动可由蓝斑传入投射释放的去甲肾上腺素(NA)调节。因此,蓝斑-皮质NA系统可能是空间工作记忆认知增强剂的作用靶点。在可能涉及的三类NA受体中,α2和α1类似乎最为重要,尽管针对这些受体的药物产生了不同的结果。这可能部分是由于使用的行为测定方法无法有效地从实验室转化到临床环境。使用具有更好转化潜力的范式可能对于解决这些差异至关重要。
本研究的目的是评估向PFC注入α2和α1肾上腺素能受体激动剂对大鼠触摸屏连续试验-位置独特不匹配(cTUNL)任务中空间工作记忆表现的影响。
对年轻雄性大鼠进行cTUNL范式训练。通过向内侧前额叶皮质插管可直接给予GABA激动剂以验证任务,并给予去氧肾上腺素和胍法辛以确定肾上腺素能激动剂对任务表现的影响。
注入蝇蕈醇和巴氯芬导致延迟依赖性损伤。给予α2激动剂胍法辛没有效果,而注入α1激动剂去氧肾上腺素显著改善了工作记忆表现。
在大鼠cTUNL任务中测量的空间工作记忆依赖于内侧前额叶皮质。去甲肾上腺素能信号增强在该范式中提高了表现,表明α1受体在这种促进作用中起重要作用。