Santana M, Palmér T, Simplício H, Fuentes R, Petersson P
Edmond and Lily Safra International Institute of Neuroscience, Santos Dumont Institute, Macaíba/RN 59280-000, Brazil; Psychobiology Program, Federal Univ. of Rio Grande do Norte, Natal, 59078-970, Brazil; Bacharelado em Ciências Biológicas, Instituto de Ciências e Tecnologia das Águas, Universidade Federal do Oeste do Pará (UFOPA), Santarém, Pará, Brazil.
Integrative Neurophysiology and Neurotechnology, Neuronano Research Center, Department of Experimental Medical Sciences, Lund University, Medicon Village, Building 404 A2 Scheelevägen 8, 223 81 Lund, Sweden; Mathematics LTH Centre for Mathematical Sciences, Faculty of Engineering, Lund University, S-22184 Lund, Sweden.
Behav Brain Res. 2015 Sep 1;290:90-101. doi: 10.1016/j.bbr.2015.04.037. Epub 2015 Apr 28.
Research aimed at developing new therapies for Parkinson's disease (PD) critically depend on valid animal models of the disease that allows for repeated testing of motor disabilities over extended time periods. We here present an extensive characterization of a wide range of motor symptoms in the 6-OHDA marmoset model of PD when tested over several months. The severity of motor deficits was quantified in two ways: (i) through manual scoring protocols appropriately adapted to include species specific motor behavior and (ii) using automated quantitative motion tracking based on image processing of the digital video recordings. We show that the automated methods allow for rapid and reliable characterization of motor dysfunctions, thus complementing the manual scoring procedures, and that robust motor symptoms lasting for several months could be induced when using a two-stage neurotoxic lesioning procedure involving one hemisphere at a time. This non-human primate model of PD should therefore be well suited for long-term evaluation of novel therapies for treatment of PD.
旨在开发帕金森病(PD)新疗法的研究严重依赖于该疾病有效的动物模型,这种模型能够在较长时间段内对运动障碍进行反复测试。我们在此展示了对6-OHDA狨猴PD模型在数月测试期间多种运动症状的广泛特征描述。运动缺陷的严重程度通过两种方式进行量化:(i)通过适当调整的手动评分方案,以纳入特定物种的运动行为;(ii)基于数字视频记录的图像处理使用自动定量运动跟踪。我们表明,自动方法能够快速且可靠地表征运动功能障碍,从而补充手动评分程序,并且当使用一次涉及一个半球的两阶段神经毒性损伤程序时,可以诱导出持续数月的强烈运动症状。因此,这种非人类灵长类动物PD模型应该非常适合用于长期评估治疗PD的新疗法。