首页> 美国卫生研究院文献>The Journal of Experimental Medicine >The hypoxia imaging agent CuII(atsm) is neuroprotective and improves motor and cognitive functions in multiple animal models of Parkinson’s disease
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The hypoxia imaging agent CuII(atsm) is neuroprotective and improves motor and cognitive functions in multiple animal models of Parkinson’s disease

机译:低氧显像剂CuII(atsm)具有神经保护作用可改善帕金森氏病多种动物模型的运动和认知功能

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摘要

Parkinson’s disease (PD) is a progressive, chronic disease characterized by dyskinesia, rigidity, instability, and tremors. The disease is defined by the presence of Lewy bodies, which primarily consist of aggregated α-synuclein protein, and is accompanied by the loss of monoaminergic neurons. Current therapeutic strategies only give symptomatic relief of motor impairment and do not address the underlying neurodegeneration. Hence, we have identified CuII(atsm) as a potential therapeutic for PD. Drug administration to four different animal models of PD resulted in improved motor and cognition function, rescued nigral cell loss, and improved dopamine metabolism. In vitro, this compound is able to inhibit the effects of peroxynitrite-driven toxicity, including the formation of nitrated α-synuclein oligomers. Our results show that CuII(atsm) is effective in reversing parkinsonian defects in animal models and has the potential to be a successful treatment of PD.
机译:帕金森氏病(PD)是一种进行性慢性疾病,特征在于运动障碍,僵硬,不稳定和震颤。该疾病由路易体的存在定义,路易体主要由聚集的α-突触核蛋白组成,并伴有单胺能神经元的丢失。当前的治疗策略仅能减轻运动障碍的症状,而不能解决潜在的神经变性。因此,我们确定了Cu II (atsm)作为PD的潜在疗法。对四种不同的PD动物模型进行药物给药可改善其运动和认知功能,挽救黑质细胞损失,并改善多巴胺代谢。在体外,该化合物能够抑制过氧亚硝酸盐驱动的毒性作用,包括形成硝化的α-突触核蛋白低聚物。我们的结果表明,Cu II (atsm)可有效逆转动物模型中的帕金森氏病,并且有可能成功治疗PD。

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