Individual and Familial Susceptibility to MPTP in a Common Marmoset Model for Parkinson's Disease

被引:6
作者
Franke, Sigrid K. [1 ,2 ]
van Kesteren, Ronald E. [1 ]
Hofman, Sam [2 ]
Wubben, Jacqueline A. M. [2 ]
Smit, August B. [1 ]
Philippens, Ingrid H. C. H. M. [2 ]
机构
[1] Vrije Univ Amsterdam, Neurosci Campus Amsterdam, Ctr Neurogen & Cognit Res, Dept Mol & Cellular Neurobiol, Amsterdam, Netherlands
[2] Biomed Primate Res Ctr, POB 3306, NL-2280 GH Rijswijk, Netherlands
关键词
Parkinson; Marmoset; MPTP; Biochemistry; Behavior; CYNOMOLGUS MONKEYS; SOCIAL-DOMINANCE; PATHOLOGY; DOPAMINE; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE; PERSONALITY; AGGRESSION; MECHANISMS; TOXICITY; CORTISOL;
D O I
10.1159/000442574
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Insight into susceptibility mechanisms underlying Parkinson's disease (PD) would aid the understanding of disease etiology, enable target finding and benefit the development of more refined disease-modifying strategies. Methods: We used intermittent low-dose MPTP (0.5 mg/kg/week) injections in marmosets and measured multiple behavioral and neurochemical parameters. Genetically diverse monkeys from different breeding families were selected to investigate inter- and intrafamily differences in susceptibility to MPTP treatment. Results: We show that such differences exist in clinical signs, in particular nonmotor PD-related behaviors, and that they are accompanied by differences in neurotransmitter levels. In line with the contribution of a genetic component, different susceptibility phenotypes could be traced back through genealogy to individuals of the different families. Conclusion: Our findings show that low-dose MPTP treatment in marmosets represents a clinically relevant PD model, with a window of opportunity to examine the onset of the disease, allowing the detection of individual variability in disease susceptibility, which may be of relevance for the diagnosis and treatment of PD in humans. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:293 / 303
页数:11
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