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Effects of 6-Hydroxydopamine Exposure on Motor Activity and Biochemical Expression in Zebrafish (Danio Rerio) Larvae

机译:6-羟多巴胺暴露对斑马鱼幼虫运动活性和生化表达的影响

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摘要

Parkinson's disease (PD) is a neurodegenerative disease that is characterized by the progressive loss of dopaminergic (DA) neurons in the substantia nigra. However, current treatments for PD are mainly palliative. Recently, researchers discovered that neurotoxins can induce Parkinsonian-like symptoms in zebrafish. No study to date has investigated the characteristics of PD, such as neuroinflammation factors, oxidative stress, or ubiquitin dysfunction, in this model. Therefore, the current study was aimed at utilizing commonly used clinical drugs, minocycline, vitamin E, and Sinemet, to test the usefulness of this model. Previous studies had indicated that DA cell loss was greater with 6-hydroxydopamine (6-OHDA) than with other neurotoxins. Thus, we first challenged zebrafish with 6-OHDA immersion and found a significant reduction in zebrafish locomotor activity; we then reversed the locomotor disruptions by treatment with vitamin E, Sinemet, or minocycline. The present study also analyzed the mRNA expression of parkin, pink1, and cd-11b, because the expression of these molecular targets has been shown to result in attenuation in mammalian models of PD. Vitamin E, Sinemet, and minocycline significantly reversed 6-OHDA-induced changes of parkin, pink1, and cd-11b mRNA expression in zebrafish. Moreover, we assessed tyrosine hydroxylase (TH) expression to confirm the therapeutic effects of vitamin E tested on this PD model and established that vitamin E reversed the 6-OHDA-induced damage on TH expression. Our results provide some support for the validity of this in vivo Parkinson's model, and we hope that this model will be more widely used in the future.
机译:帕金森氏病(PD)是一种神经退行性疾病,其特征是黑质中多巴胺能(DA)神经元的进行性丧失。但是,目前用于PD的治疗主要是姑息治疗。最近,研究人员发现神经毒素可在斑马鱼中诱发帕金森氏样症状。迄今为止,尚无研究在此模型中研究PD的特征,例如神经炎症因子,氧化应激或泛素功能障碍。因此,当前的研究旨在利用常用的临床药物米诺环素,维生素E和Sinemet来测试该模型的有效性。先前的研究表明,6-羟基多巴胺(6-OHDA)的DA细胞损失比其他神经毒素更大。因此,我们首先用6-OHDA浸没攻击斑马鱼,发现斑马鱼的自发活动显着降低。然后,我们通过用维生素E,Sinemet或美满霉素进行治疗来扭转运动障碍。本研究还分析了parkin,pink1和cd-11b的mRNA表达,因为这些分子靶标的表达已显示可导致PD哺乳动物模型的衰减。维生素E,Sinemet和美满霉素可显着逆转6-OHDA诱导的斑马鱼parkin,pink1和cd-11b mRNA表达的变化。此外,我们评估了酪氨酸羟化酶(TH)的表达,以证实在此PD模型上测试的维生素E的治疗效果,并确定维生素E逆转了6-OHDA诱导的TH表达受损。我们的结果为这种体内帕金森模型的有效性提供了一定的支持,我们希望该模型将来会被更广泛地使用。

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