Comprehensive Analysis of Neurotoxin-Induced Ablation of Dopaminergic Neurons in Zebrafish Larvae

被引:31
|
作者
Kalyn, Michael [1 ]
Hua, Khang [1 ]
Noor, Suzita Mohd [2 ]
Wong, Chee Ern David [2 ]
Ekker, Marc [1 ]
机构
[1] Dept Biol, Fac Sci, Ottawa, ON K1N 6N5, Canada
[2] Univ Malaya, Dept Biomed Sci, Fac Med, Kuala Lumpur 50603, Malaysia
基金
加拿大自然科学与工程研究理事会;
关键词
Parkinson's disease; neurotoxins; dopaminergic neurons; ventral diencephalon; locomotor; zebrafish; PARKINSONS-DISEASE; PARAQUAT NEUROTOXICITY; EXPOSURE; MPTP; MODELS; ROTENONE; TRANSPORTER; VALIDATION; EXPRESSION; FEATURES;
D O I
10.3390/biomedicines8010001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurotoxin exposure of zebrafish larvae has been used to mimic a Parkinson's disease (PD) phenotype and to facilitate high-throughput drug screening. However, the vulnerability of zebrafish to various neurotoxins was shown to be variable. Here, we provide a direct comparison of ablative effectiveness in order to identify the optimal neurotoxin-mediated dopaminergic (DAnergic) neuronal death in larval zebrafish. Transgenic zebrafish, Tg(dat:eGFP), were exposed to different concentrations of the neurotoxins MPTP, MPP+, paraquat, 6-OHDA, and rotenone for four days, starting at three days post-fertilization. The LC50 of each respective neurotoxin concentration was determined. Confocal live imaging on Tg(dat:eGFP) showed that MPTP, MPP+, and rotenone caused comparable DAnergic cell loss in the ventral diencephalon (vDC) region while, paraquat and 6-OHDA caused fewer losses of DAnergic cells. These results were further supported by respective gene expression analyses of dat, th, and p53. Importantly, the loss of DAnergic cells from exposure to MPTP, MPP+, and rotenone impacted larval locomotor function. MPTP induced the largest motor deficit, but this was accompanied by the most severe morphological impairment. We conclude that, of the tested neurotoxins, MPP+ recapitulates a substantial degree of DAnergic ablation and slight locomotor perturbations without systemic defects indicative of a Parkinsonian phenotype.
引用
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页数:16
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