首页> 美国卫生研究院文献>Frontiers in Aging Neuroscience >The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP+-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture
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The Association of Iron and the Pathologies of Parkinson’s Diseases in MPTP/MPP+-Induced Neuronal Degeneration in Non-human Primates and in Cell Culture

机译:铁与非人灵长类动物和细胞培养物中MPTP / MPP +诱导的神经元变性的帕金森氏病病理学关联

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摘要

Despite much efforts in the last few decades, the mechanism of degeneration of dopamine (DA) neurons in the substantia nigra (SN) in Parkinson’s disease (PD) remains unclear. This represents a major knowledge gap in idiopathic and genetic forms of PD. Among various possible key factors postulated, iron metabolism has been widely suggested to be involved with fueling oxidative stress, a known factor in the pathogenesis of PD. However, the correlation between iron and DA neuron loss, specifically in the SN, has not been described in experimental animal models with great detail, with most studies utilizing rodents and, rarely, non-human primates. In the present study, aiming to gain further evidence of a pathological role of iron in PD, we have examined the correlation of iron with DA neuron loss in a non-human primate model of PD induced by MPTP. We report a significant iron accumulation accompanied by both DA degeneration in the SN and motor deficits in the monkey that displayed the most severe PD pathology and behavioral deficits. The other two monkeys subjected to MPTP displayed less severe PD pathologies and motor deficits, however, their SN iron levels were significantly lower than controls. These findings suggest that high iron may indicate and contribute to heightened MPP+-induced PD pathology in late or severe stages of PD, while depressed levels of iron may signal an early stage of disease. Similarly, using a cell culture preparation, we have found that high doses of ferric ammonium citrate (FAC), a factor known to enhance iron accumulation, increased MPP+-induced cell death in U251 and SH-SY5Y cells, and even in control cells. However, at low dose FAC restored or increased the viability of U251 and SH-SY5Y cells in the absence or presence of MPP+. These observations imply that high levels of iron likely contribute to or heighten MPP+ toxicity in the later stages of PD. While we report reduced iron levels in the earlier stages of MPTP induced PD, the significance of these changes remains to be determined.
机译:尽管在过去的几十年中付出了很多努力,但帕金森氏病(PD)中黑质(SN)中多巴胺(DA)神经元的变性机制仍不清楚。这代表了PD的特发性和遗传形式的主要知识鸿沟。在推测的各种可能的关键因素中,铁代谢已被广泛认为与促进氧化应激有关,氧化应激是PD发病机理中的已知因素。但是,铁和DA神经元丧失之间的相关性,特别是在SN中,尚未在实验动物模型中进行详细描述,大多数研究都利用啮齿动物,而很少使用非人类灵长类动物。在本研究中,旨在获得铁在PD中的病理作用的进一步证据,我们在MPTP诱导的PD的非人类灵长类动物模型中研究了铁与DA神经元丢失的相关性。我们报告了大量的铁积累,伴随着SN中的DA变性和猴子中的运动缺陷,这显示了最严重的PD病理和行为缺陷。其他两只遭受MPTP的猴子表现出较不严重的PD病变和运动功能障碍,但是它们的SN铁水平显着低于对照组。这些发现表明,高铁可能预示着PD的晚期或重度阶段中MPP + 引起的PD病理的加剧,而铁水平下降可能预示着疾病的早期。同样,使用细胞培养制剂,我们发现高剂量的柠檬酸铁铵(FAC)是已知的增强铁蓄积的因子,可增加U251和SH-SY5Y中MPP + 诱导的细胞死亡。细胞,甚至在对照细胞中。然而,在不存在或存在MPP + 的情况下,低剂量FAC可以恢复或增加U251和SH-SY5Y细胞的活力。这些观察结果表明,高水平的铁可能会在PD的晚期导致或增加MPP + 毒性。虽然我们报告了MPTP诱导的PD早期铁水平降低,但这些变化的重要性尚待确定。

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