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首页> 外文期刊>Chemico-biological interactions >Protective role of chrysin on 6-hydroxydopamine-induced neurodegeneration a mouse model of Parkinson's disease: Involvement of neuroinflammation and neurotrophins
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Protective role of chrysin on 6-hydroxydopamine-induced neurodegeneration a mouse model of Parkinson's disease: Involvement of neuroinflammation and neurotrophins

机译:Chrysin对6-羟基多胺诱导的神经变性的保护作用帕金森病的小鼠模型:神经炎症和神经营养素的参与

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Abstract Chrysin is a natural flavonoid which is found in bee propolis, honey and various plants, and neuroprotective effect of chrysin in mice was previously demonstrated by our group. Neuroinflammation, neurotrophic factors and neuronal recovery factors associated with the neuroprotective effect of this flavonoid require further investigations. Thus, now we investigated the possible involvement of inflammatory cytokines, neurotrophic factors and neuronal recovery in the effect of chrysin in 6-hydroxidopamine (6-OHDA), a well-established model of Parkinson's disease, in striatum of mice. The 6-OHDA microinjection induced behavioral alterations on the rotarod test and apomorphine-induced circling behavior in mice. 6-OHDA administration elevated levels of tumour necrosis factor-α, interferon-gamma, interleukin-1β, interleukin-2, interleukin-6 and nuclear factor-kappa B and decreased the interleukin-10 levels, total reactive antioxidant potential and total antioxidant reactivity in striatum, as well as, modified the calcium-binding protein B (S100B), brain-derived neurotrophic factor, nerve growth factor and glial cell line-derived neurotrophic factor levels. The intrastriatal injection of 6-OHDA also induced an decrease of dopamine, 3,4-dihydroxyphenylacetic acid, homovanylic acid levels and tyrosine hydroxylase content. Oral treatment with chrysin (10?mg/kg, 28 days), culminated with the prevention of these alterations occasioned by 6-OHDA. These results corroborated with the neuroprotective effect of chrysin in the treatment of Parkinson's disease and, indicated the mechanism involved throught the inflammatory cytokines, neurotrophic factors and recovery of dopaminergic neurons in striatum. Highlights ? 6-OHDA microinjection caused dopamine depletion and behavioral deficits. ? Chrysin reversed deficits observed in the Parkinson's disease model. ? Chrysin protected against neurodegeneration in striatum of mice. ? Depletion of tyrosine hydroxylase positive neurons are protected.
机译:摘要Chrysin是一种天然的黄酮,其在蜂蜂胶,蜂蜜和各种植物中发现,并且我们的组先前证明了小鼠蛹的神经保护作用。与该类黄酮的神经保护作用相关的神经炎,神经营养因子和神经元恢复因子需要进一步调查。因此,现在我们调查了炎性细胞因子,神经营养因子和神经元恢复的可能涉及蛹在6-羟基胺(6-OHDA),帕金森病的纹章中的植物纹状体的植物中的效果。 6-OHDA显微注射诱导对小鼠滚子试验的行为改变和甲孔诱导的小鼠中的盘旋行为。 6-OHDA管理升高的肿瘤坏死因子-α,干扰素-γ,白细胞介素-1β,白细胞介素-2,白细胞介素-6和核因子-Kappa B并降低白细胞介素-10水平,总反应性抗氧化势和总抗氧化反应性在纹状体中,以及修饰钙结合蛋白B(S100b),脑衍生的神经营养因子,神经生长因子和胶质细胞系衍生的神经营养因子水平。 6-OHDA的脑内注射也诱导多巴胺,3,4-二羟基苯乙酸,同源酸水平和酪氨酸羟基化酶含量的降低。用蛹(10×mg / kg,28天)的口服处理,终止于预防6-OHDA的这些改变。这些结果与Chrysin治疗帕金森病治疗中的神经保护作用,表明该机制涉及通过纹状体中炎性细胞因子,神经营养因素,多巴胺能神经元的恢复。强调 ? 6-OHDA显微注射导致多巴胺消耗和行为缺陷。还在帕金森病模型中观察到克莱辛逆转赤字。还Chrysin保护小鼠纹状体的神经变性。还保护酪氨酸羟化酶阳性神经元的枯竭。

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