Schuldenzucker Verena, Schubert Robin, Muratori Lisa M, Freisfeld Frauke, Rieke Lorena, Matheis Tamara, Schramke Sarah, Motlik Jan, Kemper Nicole, Radespiel Ute, Reilmann Ralf
George-Huntington-Institute, Technology-Park, Muenster, Germany.
Institute of Zoology, University of Veterinary Medicine Hannover, Hannover, Germany.
PLoS One. 2017 Oct 9;12(10):e0185970. doi: 10.1371/journal.pone.0185970. eCollection 2017.
Large animal models of Huntington's disease (HD) may increase the reliability of translating preclinical findings to humans. Long live expectancy offers opportunities particularly for disease modifying approaches, but also challenges. The transgenic (tg) HD minipig model assessed in this study exhibits a high genetic homology with humans, similar body weight, and comparable brain structures. To test long-term safety, tolerability, and efficacy of novel therapeutic approaches in this model reliable assessments applicable longitudinally for several years are warranted for all phenotypical domains relevant in HD.
To investigate whether the tests proposed assessing motor, cognitive and behavioral domains can be applied repetitively over a 3-year period in minipigs with acceptable variability or learning effects and whether tgHD minipigs reveal changes in these domains compared to wildtype (wt) minipigs suggesting the development of an HD phenotype.
A cohort of 14 tgHD and 18 wt minipigs was followed for three years. Tests applied every six months included a tongue coordination and hurdle test for the motor domain, a color discrimination test for cognition, and a dominance test for assessing behavior. Statistical analyses were performed using repeated ANOVA for longitudinal group comparisons and Wilcoxon-tests for intra-visit differences between tgHD and wt minipigs.
All tests applied demonstrated feasibility, acceptable variance and good consistency during the three-year period. No significant differences between tgHD and wt minipigs were detected suggesting lack of a phenotype before the age of four years.
The assessment battery presented offers measures in all domains relevant for HD and can be applied in long-term phenotyping studies with tgHD minipigs. The observation of this cohort should be continued to explore the timeline of phenotype development and provide information for future interventional studies.
亨廷顿舞蹈症(HD)的大型动物模型可能会提高将临床前研究结果转化至人类研究的可靠性。较长的预期寿命为特别是疾病修饰疗法带来了机遇,但也带来了挑战。本研究中评估的转基因(tg)HD小型猪模型与人类具有高度的基因同源性、相似的体重和相当的脑结构。为了测试该模型中新型治疗方法的长期安全性、耐受性和疗效,对于HD中所有相关表型领域,需要有可靠的评估方法,以便在数年时间内进行纵向评估。
研究针对运动、认知和行为领域提出的测试是否能在3年时间内对小型猪重复应用,且具有可接受的变异性或学习效应,以及与野生型(wt)小型猪相比,tgHD小型猪在这些领域是否显示出变化,提示HD表型的发展。
对一组14只tgHD小型猪和18只wt小型猪进行了为期三年的跟踪研究。每六个月进行的测试包括用于运动领域的舌协调和跨栏测试、用于认知的颜色辨别测试以及用于评估行为的优势测试。使用重复方差分析进行纵向组间比较,使用威尔科克森检验分析tgHD和wt小型猪每次检查之间的差异。
所有应用的测试在三年期间均显示出可行性、可接受的方差和良好的一致性。未检测到tgHD和wt小型猪之间存在显著差异,表明在4岁之前没有表型。
所提出的评估组合提供了与HD相关的所有领域的测量方法,可应用于tgHD小型猪的长期表型研究。应继续观察该队列,以探索表型发展的时间线,并为未来的干预研究提供信息。