Upadhayay Shubham, Yedke Narhari Gangaram, Rahi Vikrant, Singh Surbhi, Kumar Sachin, Arora Anchal, Chandolia Priyanka, Kaur Prabhsharan, Kumar Mandeep, Koshal Prashant, Jamwal Sumit, Kumar Puneet
Department of Pharmacology, Central University of Punjab, Ghudda, Bathinda, 151401, India.
Department of Pharmaceutical Sciences & Technology, Maharaja Ranjit Singh Punjab Technical University, Bathinda, Punjab, India.
Neurochem Res. 2023 Jun;48(6):1631-1647. doi: 10.1007/s11064-023-03868-1. Epub 2023 Feb 4.
Animal models are used to better understand the various mechanisms involved in the pathogenesis of diseases and explore potential pathways that will aid in discovering therapeutic targets. 3-Nitropropionic Acid (3-NPA) is a neurotoxin used to induce Huntington's disease (HD)-like symptoms in experimental animals. The 3-NPA is a fungus toxin that impairs the complex II (succinate dehydrogenase) activity of the mitochondria and reduces ATP synthesis, leading to excessive production of free radicals resulting in the degeneration of GABAergic medium spiny neurons (MSNs) in the striatum. This is characterized by motor impairments a key clinical manifestation of HD. 3-NPA has the potential to alter several cellular processes, including mitochondrial functions, oxidative stress, apoptosis, and neuroinflammation mimicking HD-like pathogenic conditions in animals. This review strives to provide a new insight towards the 3-NPA induced molecular dysfunctioning in developing an animal model of HD. Moreover, we summarise several preclinical studies that support the use of the 3-NPA-induced models for drug discovery and development in HD. This review is a collection of various articles that were published from 1977 to 2022 on Pubmed (1639), Web of Science (2139), and Scopus (2681), which are related to the 3-NPA induced animal model.
动物模型用于更好地理解疾病发病机制中涉及的各种机制,并探索有助于发现治疗靶点的潜在途径。3-硝基丙酸(3-NPA)是一种神经毒素,用于在实验动物中诱导类似亨廷顿舞蹈病(HD)的症状。3-NPA是一种真菌毒素,会损害线粒体的复合物II(琥珀酸脱氢酶)活性并减少ATP合成,导致自由基过度产生,从而导致纹状体中γ-氨基丁酸能中型多棘神经元(MSN)退化。这表现为运动障碍,是HD的关键临床表现。3-NPA有可能改变多种细胞过程,包括线粒体功能、氧化应激、细胞凋亡和神经炎症,在动物中模拟类似HD的致病条件。本综述旨在为3-NPA诱导的分子功能障碍在开发HD动物模型方面提供新的见解。此外,我们总结了几项临床前研究,这些研究支持使用3-NPA诱导的模型进行HD的药物发现和开发。本综述是对1977年至2022年在PubMed(1639篇)、科学网(2139篇)和Scopus(2681篇)上发表的与3-NPA诱导的动物模型相关的各种文章的汇总。