Rizzo Francesca, Nespoli Ester, Abaei Alireza, Bar-Gad Izhar, Deelchand Dinesh K, Fegert Jörg, Rasche Volker, Hengerer Bastian, Boeckers Tobias M
Department for Child and Adolescent Psychiatry and Psychotherapy, Ulm University, Ulm, Germany.
Institute of Anatomy and Cell Biology, Ulm University, Ulm, Germany.
Front Neurol. 2018 Feb 13;9:59. doi: 10.3389/fneur.2018.00059. eCollection 2018.
Tourette's syndrome (TS) is a neurodevelopmental disorder characterized primarily by motor and vocal tics. Comorbidities such as attention deficit and hyperactivity disorder (ADHD) are observed in over 50% of TS patients. We applied aripiprazole in a juvenile rat model that displays motor tics and hyperactivity. We additionally assessed the amount of ultrasonic vocalizations (USVs) as an indicator for the presence of vocal tics and evaluated the changes in the striatal neurometabolism using proton magnetic resonance spectroscopy (1H-MRS) at 11.7T. Thirty-one juvenile spontaneously hypertensive rats (SHRs) underwent bicuculline striatal microinjection and treatment with either aripiprazole or vehicle. Control groups were sham operated and sham injected. Behavior, USVs, and striatal neurochemical profile were analyzed at early, middle, and late adolescence (postnatal days 35 to 50). Bicuculline microinjections in the dorsolateral striatum induced motor tics in SHR juvenile rats. Acute aripiprazole administration selectively reduced both tic frequency and latency, whereas stereotypies, USVs, and hyperactivity remained unaltered. The striatal neurochemical profile was only moderately altered after tic-induction and was not affected by systemic drug treatment. When applied to a young rat model that provides high degrees of construct, face, and predictive validity for TS and comorbid ADHD, aripiprazole selectively reduces motor tics, revealing that tics and stereotypies are distinct phenomena in line with clinical treatment of patients. Finally, our 1H-MRS results suggest a critical revision of the striatal role in the hypothesized cortico-striatal dysregulation in TS pathophysiology.
图雷特综合征(TS)是一种神经发育障碍,主要特征为运动和发声抽动。超过50%的TS患者存在共病,如注意力缺陷多动障碍(ADHD)。我们将阿立哌唑应用于表现出运动抽动和多动的幼年大鼠模型。我们还评估了超声发声(USV)的数量作为发声抽动存在的指标,并使用11.7T的质子磁共振波谱(1H-MRS)评估纹状体神经代谢的变化。31只幼年自发性高血压大鼠(SHR)接受了荷包牡丹碱纹状体微量注射,并接受阿立哌唑或赋形剂治疗。对照组进行假手术和假注射。在青春期早期、中期和晚期(出生后第35至50天)分析行为、USV和纹状体神经化学特征。在SHR幼年大鼠的背外侧纹状体中微量注射荷包牡丹碱可诱发运动抽动。急性给予阿立哌唑可选择性降低抽动频率和潜伏期,而刻板行为、USV和多动保持不变。抽动诱导后纹状体神经化学特征仅发生中度改变,且不受全身药物治疗的影响。当应用于为TS和共病ADHD提供高度结构效度、表面效度和预测效度的幼年大鼠模型时,阿立哌唑可选择性降低运动抽动,表明抽动和刻板行为是与患者临床治疗一致的不同现象。最后,我们的1H-MRS结果提示对TS病理生理学中假设的皮质-纹状体调节异常中纹状体作用进行重大修订。