Adinolfi Annalisa, Zelli Silvia, Leo Damiana, Carbone Cristiana, Mus Liudmila, Illiano Placido, Alleva Enrico, Gainetdinov Raul R, Adriani Walter
Center for Behavioural Sciences and Mental Health, Istituto Superiore di Sanità, Viale Regina Elena 299, I-00161 Rome, Italy.
Department of Neurosciences, University of Mons, 20 Place du Parc, B-7000 Mons, Belgium.
Behav Brain Res. 2019 Feb 1;359:516-527. doi: 10.1016/j.bbr.2018.11.028. Epub 2018 Nov 22.
Dopamine (DA) is a key neurotransmitter of the central nervous system, whose availability is regulated by the dopamine transporter (DAT). Deletion of DAT gene leading to hyperdopaminergia was previously performed on mouse models. This enabled recapitulation of the core symptoms of Attention-Deficit / Hyper-activity Disorder (ADHD), which include hyperactivity, inattention and cognitive impairment. We used recently developed DAT knockout (DAT-KO) rats to carry out further behavioral profiling on this novel model of hyperdopaminergia. DAT-KO rats display elevated locomotor activity and restless environmental exploration, associated with a transient anxiety profile. Furthermore, these rats show pronounced stereotypy and compulsive-like behavior at the Marble-Burying test. Homozygous DAT-KO rats mantain intact social interaction when tested in a social-preference task, while heterozygous (HET) rats show high inactivity associated with close proximity to the social stimulus. Ex-vivo evaluation of brain catecholamines highlighted increased levels of norepinephrine in the hippocampus and hypothalamus exclusively of heterozygous rats. Taken together, our data present evidence of unexpected asocial tendencies in heterozygous (DAT-HET) rats associated with neurochemical alterations in norepinephrine neurotransmission. We shed light on the behavioral and neurochemical consequences of altered DAT function in a higher, more complex model of hyperdopaminergia. Unraveling the role of DA neurotransmission in DAT-KO rats has very important implications in the understanding of many psychiatric illnesses, including ADHD, where alterations in DA system have been demonstrated.
多巴胺(DA)是中枢神经系统的一种关键神经递质,其可用性由多巴胺转运体(DAT)调节。先前在小鼠模型上进行了DAT基因缺失导致多巴胺能亢进的实验。这使得能够重现注意力缺陷多动障碍(ADHD)的核心症状,包括多动、注意力不集中和认知障碍。我们使用最近开发的DAT基因敲除(DAT-KO)大鼠,对这种新型多巴胺能亢进模型进行进一步的行为分析。DAT-KO大鼠表现出运动活动增加和不安的环境探索行为,伴有短暂的焦虑状态。此外,这些大鼠在埋球试验中表现出明显的刻板行为和强迫样行为。在社交偏好任务中测试时,纯合子DAT-KO大鼠保持完整的社交互动,而异合子(HET)大鼠表现出高度不活动,且与社交刺激物距离很近。对脑儿茶酚胺的体外评估突出显示,仅在异合子大鼠的海马体和下丘脑去甲肾上腺素水平升高。综上所述,我们的数据表明,异合子(DAT-HET)大鼠存在意想不到的非社交倾向,这与去甲肾上腺素神经传递中的神经化学改变有关。我们揭示了在更高、更复杂的多巴胺能亢进模型中DAT功能改变的行为和神经化学后果。阐明DA神经传递在DAT-KO大鼠中的作用,对于理解许多精神疾病具有非常重要的意义,包括已证明DA系统存在改变的ADHD。