Department of Psychiatry, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0804, United States.
Behav Brain Res. 2011 Sep 12;222(1):183-92. doi: 10.1016/j.bbr.2011.03.054. Epub 2011 Mar 31.
Impairments in attention/vigilance and response disinhibition are commonly observed in several neuropsychiatric disorders. Validating animal models could help in developing therapeutics for cognitive deficits and improving functional outcomes in such disorders. The 5-choice continuous performance test (5C-CPT) in mice offers the opportunity to assess vigilance and two forms of impulsivity. Since reduced dopamine D4 receptor (DRD4) function is implicated in several disorders, DRD4 is a potential therapeutic target for cognition enhancement. We trained wildtype (WT), heterozygous (HT), and knockout (KO) mice of the murine Drd4 to perform the 5C-CPT under baseline and variable stimulus duration conditions. To dissect motor impulsivity (premature responding) from behavioral disinhibition (false alarms), we administered the 5-HT(2C) antagonist SB242084 during an extended inter-trial-interval session. We also examined the preattentive and exploratory profile of these mice in prepulse inhibition (PPI) and the Behavioral Pattern Monitor (BPM). Reduced Drd4 expression in HT mice, as confirmed by quantitative RT-PCR, resulted in response disinhibition and impaired 5C-CPT performance, while premature responding was unaffected. Conversely, SB242084 increased premature responding without affecting response inhibition or attentional measures. No genotypic differences were observed in PPI or BPM behavior. Thus, reduced Drd4 expression impairs attentional performance, but not other behaviors associated with neuropsychiatric disorders. Moreover, the use of signal and non-signal stimuli in the 5C-CPT enabled the differentiation of response disinhibition from motor impulsivity in a vigilance task.
注意力/警觉和反应抑制损伤在多种神经精神疾病中普遍存在。验证动物模型有助于开发治疗认知缺陷的方法,并改善此类疾病的功能结果。小鼠的 5 选择连续作业测试(5C-CPT)提供了评估警觉性和两种冲动形式的机会。由于多巴胺 D4 受体(DRD4)功能降低与多种疾病有关,因此 DRD4 是增强认知的潜在治疗靶标。我们对野生型(WT)、杂合型(HT)和敲除型(KO)小鼠进行了训练,使其在基线和可变刺激持续时间条件下进行 5C-CPT。为了从行为抑制(假警报)中分离出运动冲动(过早反应),我们在延长的试验间间隔期间给予 5-HT(2C)拮抗剂 SB242084。我们还检查了这些小鼠在预注意和探索性方面的表现,包括前脉冲抑制(PPI)和行为模式监测器(BPM)。定量 RT-PCR 证实,HT 小鼠中 Drd4 表达减少导致反应抑制和 5C-CPT 表现受损,而过早反应不受影响。相反,SB242084 增加了过早反应,而不影响反应抑制或注意力测量。在 PPI 或 BPM 行为中未观察到基因型差异。因此,Drd4 表达减少会损害注意力表现,但不会影响与神经精神疾病相关的其他行为。此外,5C-CPT 中使用信号和非信号刺激可在警觉任务中区分反应抑制和运动冲动。