Noradrenergic modulation of cognitive function in rat medial prefrontal cortex as measured by attentional set shifting capability

被引:263
作者
Lapiz, MDS
Morilak, DA
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Pharmacol, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Ctr Biomed Neurosci, San Antonio, TX 78229 USA
关键词
arousal; attention; atipamezole; behavioral flexibility; cognition; norepinephrine;
D O I
10.1016/j.neuroscience.2005.09.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The brain noradrenergic system is thought to facilitate neuronal processes that promote behavioral activation, alertness, and attention. One region in which norepinephrine may exert such effects is the medial prefrontal cortex, which has been implicated in many cognitive functions including arousal, attention, motivation, working memory, response inhibition, and behavioral flexibility. The present study addressed the modulatory influence of noradrenergic neurotransmission in medial prefrontal cortex on cognitive function in rats, as measured by performance in an attentional set shifting task. In experiment 1, we tested effects of increasing and decreasing brain noradrenergic neurotransmission by systemic administration of the alpha(2)-adrenergic autoreceptor antagonist and agonist drugs, atipamezole and clonidine, respectively. Atipamezole pretreatment significantly improved performance on the stages of the attentional task requiring an extradimensional shift in attention, and those involving stimulus reversals, whereas clonidine had no effect at any stage. In experiment 2, we then tested effects of microinjecting alpha(1)- or beta-adrenergic receptor antagonists into medial prefrontal cortex on the enhancement of performance on the extradimensional task produced by atiparnezole. The atipamezole-induced enhancement of performance on the extradimensional set shifting task was blocked by alpha(1)-, but not beta-adrenergic receptor antagonists in medial prefrontal cortex. Neither antagonist alone had any effect on extradimensional set shift performance in the absence of atipamezole-induced enhancement. These results indicate that elevating noradrenergic activity at alpha(1)-receptors in medial prefrontal cortex facilitates cognitive performance of rats in an attentional set-shifting task, which may contribute to the role of norepinephrine in behavioral state changes such as arousal, or to the beneficial cognitive effects of psychotherapeutic drugs that target noradrenergic neurotransmission. (c) 2005 Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:1039 / 1049
页数:11
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