基于斑马鱼的帕金森病模型:揭示遗传机制和治疗途径。

Rohinee Dodiya, Pratishtha Sharma, Dipa Israni, Mohammad Amjad Kamal, Nigel H Greig
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摘要

斑马鱼被广泛用作活体脊椎动物模型,用于神经发育和神经系统疾病的研究。该物种表现出各种独特的属性,使其非常适合研究神经系统疾病,如帕金森病(PD)。斑马鱼和人类的遗传相似性约为70%,与人类疾病相关的基因中约有84%与斑马鱼相同。基因的相似性和多巴胺等神经递质的存在使科学家能够研究帕金森病的基因和蛋白质。斑马鱼经常受到神经毒素的挑战,以诱导帕金森症状,使研究人员能够评估随之而来的生化途径。斑马鱼还可以修复受损的器官,增加了它们在帕金森病研究中的潜在价值。由于它们的再生能力和与人类的遗传相似性,这些物种可以用于研究多巴胺神经变性和前瞻性PD治疗。除了帕金森病,斑马鱼也是研究亨廷顿氏病、阿尔茨海默病、癫痫、抑郁症、精神分裂症和焦虑症的有用模型。这篇文章强调了与斑马鱼模型PD相关的重要发现,描述了它的挑战和好处。对关键基因、蛋白质通路和神经毒素的研究为了解多巴胺神经递质在帕金森病中的作用提供了机会,并加快了潜在有前景的治疗策略的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zebrafish-Based Parkinson's Disease Models: Unveiling Genetic Mechanisms and Therapeutic Pathways.

The zebrafish (Danio rerio) is widely utilised as a live vertebrate model in research on neurological development and nervous system diseases. This species exhibits various distinctive attributes that render it well-suited for investigating neurological disorders such as Parkinson's disease (PD). Zebrafish and humans have a genetic similarity of around 70%, and approximately 84% of the genes associated with human diseases have zebrafish equivalents. The genetic similarities and presence of neurotransmitters like dopamine allow scientists to study PD genes and proteins. Zebrafish are often challenged with neurotoxins to induce Parkinsonian symptoms, allowing researchers to evaluate attendant biochemical pathways. Zebrafish can also repair damaged organs, increasing their potential value in PD research. Because of their regenerative capacity and genetic resemblance to humans, these species can be used to study dopamine neurodegeneration and prospective PD treatments. In addition to PD, zebrafish are helpful models for studying Huntington's disease, Alzheimer's disease, epilepsy, depression, schizophrenia, and anxiety disorders. This article emphasizes significant findings of relevance to PD using the zebrafish model, describing its challenges and benefits. The investigation of key genes, protein pathways, and neurotoxins provides the opportunity to facilitate understanding of the role of dopamine neurotransmitters in PD and expedite the development of potentially promising therapeutic strategies.

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