Chemogenetic Activation of Midbrain Dopamine Neurons Affects Attention, but not Impulsivity, in the Five-Choice Serial Reaction Time Task in Rats

被引:36
作者
Boekhoudt, Linde [1 ]
Voets, Elisa S. [1 ]
Flores-Dourojeanni, Jacques P. [1 ,2 ]
Luijendijk, Mieneke C. M. [1 ]
Vanderschuren, Louk J. M. J. [2 ]
Adan, Roger A. H. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Translat Neurosci, Brain Ctr Rudolf Magnus, Univ Weg 100, NL-3584 CG Utrecht, Netherlands
[2] Univ Utrecht, Div Behav Neurosci, Dept Anim Sci & Soc, Fac Vet Med, Utrecht, Netherlands
关键词
MEDIAL PREFRONTAL CORTEX; NUCLEUS-ACCUMBENS; DORSAL STRIATUM; ORBITOFRONTAL CORTEX; CEREBRAL-CORTEX; PERFORMANCE; RECEPTORS; LESIONS; SYSTEMS; ORGANIZATION;
D O I
10.1038/npp.2016.235
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Attentional impairments and exaggerated impulsivity are key features of psychiatric disorders, such as attention-deficit/hyperactivity disorder, schizophrenia, and addiction. These deficits in attentional performance and impulsive behaviors have been associated with aberrant dopamine (DA) signaling, but it remains unknown whether these deficits result from enhanced DA neuronal activity in the midbrain. Here, we took a novel approach by testing the impact of chemogenetically activating DA neurons in the ventral tegmental area (VTA) or substantia nigra pars compacta (SNc) on attention and impulsivity in the five-choice serial reaction time task (5-CSRTT) in rats. We found that activation of DA neurons in both the VTA and SNc impaired attention by increasing trial omissions. In addition, SNc DA neuron activation decreased attentional accuracy. Surprisingly, enhanced DA neuron activity did not affect impulsive action in this task. These results show that enhanced midbrain DA neuronal activity induces deficits in attentional performance, but not impulsivity. Furthermore, DA neurons in the VTA and SNc have different roles in regulating attention. These findings contribute to our understanding of the neural substrates underlying attention deficits and impulsivity, and provide valuable insights to improve treatment of these symptoms.
引用
收藏
页码:1315 / 1325
页数:11
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