Piiponniemi Tuukka O, Parkkari Teija, Heikkinen Taneli, Puoliväli Jukka, Park Larry C, Cachope Roger, Kopanitsa Maksym V
Charles River Discovery Services, Kuopio, Finland.
CHDI Management/CHDI Foundation, Los Angeles, CA, United States.
Front Behav Neurosci. 2018 Oct 2;12:226. doi: 10.3389/fnbeh.2018.00226. eCollection 2018.
Cognitive disturbances often predate characteristic motor dysfunction in individuals with Huntington's disease (HD) and place an increasing burden on the HD patients and caregivers with the progression of the disorder. Therefore, application of maximally translational cognitive tests to animal models of HD is imperative for the development of treatments that could alleviate cognitive decline in human patients. Here, we examined the performance of the Q175 mouse knock-in model of HD in the touch screen version of the paired associates learning (PAL) task. We found that 10-11-month-old heterozygous Q175 mice had severely attenuated learning curve in the PAL task, which was conceptually similar to previously documented impaired performance of individuals with HD in the PAL task of the Cambridge Neuropsychological Test Automated Battery (CANTAB). Besides high rate of errors in PAL task, Q175 mice exhibited considerably lower responding rate than age-matched wild-type (WT) animals. Our examination of effortful operant responding during fixed ratio (FR) and progressive ratio (PR) reinforcement schedules in a separate cohort of similar age confirmed slower and unselective performance of mutant animals, as observed during PAL task, but suggested that motivation to work for nutritional reward in the touch screen setting was similar in Q175 and WT mice. We also demonstrated that pronounced sensorimotor disturbances in Q175 mice can be detected at early touch screen testing stages, (e.g., during "Punish Incorrect" phase of operant pretraining), so we propose that shorter test routines may be utilised for more expedient studies of treatments aimed at the rescue of HD-related phenotype.
在患有亨廷顿舞蹈症(HD)的个体中,认知障碍往往早于典型的运动功能障碍出现,并且随着病情的进展,给HD患者及其护理人员带来越来越大的负担。因此,将最大限度可转化的认知测试应用于HD动物模型对于开发能够缓解人类患者认知衰退的治疗方法至关重要。在此,我们在配对联想学习(PAL)任务的触摸屏版本中检测了HD的Q175小鼠基因敲入模型的表现。我们发现,10 - 11月龄的杂合Q175小鼠在PAL任务中的学习曲线严重衰减,这在概念上类似于先前记录的HD患者在剑桥神经心理测试自动化成套系统(CANTAB)的PAL任务中表现受损的情况。除了在PAL任务中错误率高之外,Q175小鼠的反应率也比年龄匹配的野生型(WT)动物低得多。我们在另一组相似年龄的动物中,对固定比率(FR)和累进比率(PR)强化时间表期间的努力操作反应进行了检测,结果证实,如在PAL任务中所观察到的,突变动物的表现较慢且无选择性,但这表明在触摸屏环境中为获取营养奖励而工作的动机在Q175小鼠和WT小鼠中是相似的。我们还证明,在早期触摸屏测试阶段(例如,在操作前训练的“惩罚错误”阶段)就可以检测到Q175小鼠明显的感觉运动障碍,因此我们建议可以采用更短的测试程序,以便更便捷地研究旨在挽救HD相关表型的治疗方法。